Search by Gene
| geneid | 26122 |
|---|---|
| ensemblid | ENSG00000135999.12 |
| hgncid | 24543 |
| symbol | EPC2 |
| name | enhancer of polycomb homolog 2 |
| refseq_nuc | NM_015630.4 |
| refseq_prot | NP_056445.3 |
| ensembl_nuc | ENST00000258484.11 |
| ensembl_prot | ENSP00000258484.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 148644751 |
| end | 148787569 |
| strand | + |
| ver | v1.2 |
| region | chr2:148644751-148787569 |
| region5000 | chr2:148639751-148792569 |
| regionname0 | EPC2_chr2_148644751_148787569 |
| regionname5000 | EPC2_chr2_148639751_148792569 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 807 | 304 | 81 | 40 | 145 | 6 | 30 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0002 | 0/0 | 807 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0003 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2424 | 296 | 73 | 40 | 145 | 6 | 30 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| c0002 | 0/0 | 2424 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| c0003 | 0/0 | 2424 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| c0004 | 0/0 | 2424 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| c0005 | 0/0 | 2424 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| c0006 | 0/0 | 2424 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| c0007 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1461 | 204 | 81 | 19 | 81 | 3 | 19 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0002 | 0/0 | 1462 | 84 | 1 | 17 | 52 | 3 | 11 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0003 | 0/0 | 1462 | 6 | 0 | 2 | 4 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0004 | 0/0 | 1461 | 6 | 0 | 0 | 6 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0005 | 0/0 | 1458 | 3 | 0 | 2 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0006 | 1/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0007 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0008 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0009 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| t0010 | 0/0 | 1461 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 296 | 73 | 40 | 145 | 6 | 30 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 193 | 71 | 19 | 80 | 3 | 19 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 84 | 1 | 17 | 52 | 3 | 11 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0002c0002t0007 | a0002 | c0002 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0238 | a0001 | c0001 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0239 | a0001 | c0001 | t0001 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0260 | a0001 | c0001 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0261 | a0001 | c0001 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0262 | a0001 | c0001 | t0001 | g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0265 | a0001 | c0001 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0266 | a0001 | c0001 | t0001 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0267 | a0001 | c0001 | t0001 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0273 | a0001 | c0001 | t0001 | g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0275 | a0001 | c0001 | t0001 | g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0277 | a0001 | c0001 | t0001 | g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0279 | a0001 | c0001 | t0001 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0280 | a0001 | c0001 | t0001 | g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0281 | a0001 | c0001 | t0001 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0284 | a0001 | c0001 | t0001 | g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0285 | a0001 | c0001 | t0001 | g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0286 | a0001 | c0001 | t0001 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0288 | a0001 | c0001 | t0001 | g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0289 | a0001 | c0001 | t0001 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0292 | a0001 | c0001 | t0001 | g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0293 | a0001 | c0001 | t0001 | g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0295 | a0001 | c0001 | t0001 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0297 | a0001 | c0001 | t0001 | g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0298 | a0001 | c0001 | t0001 | g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0299 | a0001 | c0001 | t0001 | g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0300 | a0001 | c0001 | t0001 | g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0301 | a0001 | c0001 | t0001 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0302 | a0001 | c0001 | t0001 | g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0304 | a0001 | c0001 | t0001 | g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0305 | a0001 | c0001 | t0001 | g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0306 | a0001 | c0001 | t0001 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0001g0307 | a0001 | c0001 | t0001 | g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0057 | a0001 | c0001 | t0002 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0062 | a0001 | c0001 | t0002 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0063 | a0001 | c0001 | t0002 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0067 | a0001 | c0001 | t0002 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0069 | a0001 | c0001 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0075 | a0001 | c0001 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0082 | a0001 | c0001 | t0002 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0084 | a0001 | c0001 | t0002 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0087 | a0001 | c0001 | t0002 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0102 | a0001 | c0001 | t0002 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0104 | a0001 | c0001 | t0002 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0105 | a0001 | c0001 | t0002 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0106 | a0001 | c0001 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0108 | a0001 | c0001 | t0002 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0109 | a0001 | c0001 | t0002 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0111 | a0001 | c0001 | t0002 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0112 | a0001 | c0001 | t0002 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0124 | a0001 | c0001 | t0002 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0003g0061 | a0001 | c0001 | t0003 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0003g0083 | a0001 | c0001 | t0003 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0003g0086 | a0001 | c0001 | t0003 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0003g0090 | a0001 | c0001 | t0003 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0003g0107 | a0001 | c0001 | t0003 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0003g0120 | a0001 | c0001 | t0003 | g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0004g0172 | a0001 | c0001 | t0004 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0004g0175 | a0001 | c0001 | t0004 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0004g0176 | a0001 | c0001 | t0004 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0004g0180 | a0001 | c0001 | t0004 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0004g0181 | a0001 | c0001 | t0004 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0004g0182 | a0001 | c0001 | t0004 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0005g0010 | a0001 | c0001 | t0005 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0005g0216 | a0001 | c0001 | t0005 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0005g0228 | a0001 | c0001 | t0005 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0006g0019 | a0001 | c0001 | t0006 | g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0008g0211 | a0001 | c0001 | t0008 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0009g0038 | a0001 | c0001 | t0009 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0001t0010g0296 | a0001 | c0001 | t0010 | g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0003t0001g0250 | a0001 | c0003 | t0001 | g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0003t0001g0270 | a0001 | c0003 | t0001 | g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0003t0001g0271 | a0001 | c0003 | t0001 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0004t0001g0022 | a0001 | c0004 | t0001 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0004t0001g0025 | a0001 | c0004 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0005t0001g0008 | a0001 | c0005 | t0001 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0005t0001g0187 | a0001 | c0005 | t0001 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0001c0006t0001g0006 | a0001 | c0006 | t0001 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0002c0002t0001g0254 | a0002 | c0002 | t0001 | g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0002c0002t0001g0308 | a0002 | c0002 | t0001 | g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0002c0002t0007g0255 | a0002 | c0002 | t0007 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| a0003c0007t0001g0137 | a0003 | c0007 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | FIN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0022 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0216 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CDX | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0006 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0271 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0187 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0211 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | EPC2_chr2_148639751_148792569 | EPC2 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | STU | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18939 | hp1 | a0001 | c0001 | t0009 | g0038 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0025 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19056 | hp2 | a0001 | c0001 | t0010 | g0296 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19086 | hp2 | a0003 | c0007 | t0001 | g0137 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | EPC2_chr2_148639751_148792569 | EPC2 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | EPC2_chr2_148639751_148792569 | EPC2 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | EPC2_chr2_148639751_148792569 | EPC2 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | EPC2_chr2_148639751_148792569 | EPC2 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | GIH | EPC2_chr2_148639751_148792569 | EPC2 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0270 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 |
| NA20300 | hp1 | a0002 | c0002 | t0007 | g0255 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0168 | REF | REF | EPC2_chr2_148639751_148792569 | EPC2 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0019 | REF | REF | EPC2_chr2_148639751_148792569 | EPC2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148762780
|
A | G | 1 | a0003 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.926A>G | p.Lys309Arg | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/14 | 1193/3883 | 926/2424 | 309/807 | chr2 | 148762780 | ||
| chr2:148771169
|
A | G | 1 | a0002 | 3 | HG02965.hp1 NA20300.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1502A>G | p.Asn501Ser | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/14 | 1769/3883 | 1502/2424 | 501/807 | chr2 | 148771169 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148645035
|
C | T | 1 | a0001c0003 | 3 | HG01884.hp1 HG02109.hp1 HG02622.hp2 |
synonymous_variant | LOW | c.18C>T | p.Phe6Phe | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/14 | 285/3883 | 18/2424 | 6/807 | chr2 | 148645035 | ||
| chr2:148761868
|
T | A | 1 | a0001c0006 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.753T>A | p.Ile251Ile | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/14 | 1020/3883 | 753/2424 | 251/807 | chr2 | 148761868 | ||
| chr2:148761874
|
A | G | 1 | a0001c0005 | 2 | HG02257.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.759A>G | p.Arg253Arg | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/14 | 1026/3883 | 759/2424 | 253/807 | chr2 | 148761874 | ||
| chr2:148781756
|
G | A | 1 | a0001c0004 | 2 | HG01891.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1833G>A | p.Ser611Ser | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/14 | 2100/3883 | 1833/2424 | 611/807 | chr2 | 148781756 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148644835
|
C | CG | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | 307 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(304): Show |
5_prime_UTR_variant | MODIFIER | c.-182dupG | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/14 | 181 | INFO_REALIGN_3_PRIME | chr2 | 148644835 | ||||
| chr2:148786476
|
A | G | 1 | a0001c0001t0010 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*99A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 99 | chr2 | 148786476 | |||||
| chr2:148786517
|
T | C | 1 | a0001c0001t0003 | 6 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*140T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 140 | chr2 | 148786517 | |||||
| chr2:148786993
|
C | A | 1 | a0001c0001t0004 | 6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*616C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 616 | chr2 | 148786993 | |||||
| chr2:148787031
|
A | G | 1 | a0001c0001t0009 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 654 | chr2 | 148787031 | |||||
| chr2:148787062
|
TAAA | T | 1 | a0001c0001t0005 | 3 | HG01943.hp2 HG02273.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689_*691delAAA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 689 | INFO_REALIGN_3_PRIME | chr2 | 148787062 | ||||
| chr2:148787079
|
G | GA | 3 | a0001c0001t0002a0001c0001t0003a0001c0001t0009 | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*708dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 709 | INFO_REALIGN_3_PRIME | chr2 | 148787079 | ||||
| chr2:148787170
|
G | A | 1 | a0002c0002t0007 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 793 | chr2 | 148787170 | |||||
| chr2:148787337
|
A | C | 1 | a0001c0001t0008 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 960 | chr2 | 148787337 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148645492
|
C | T | 1 | a0002c0002t0001g0308 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.153+322C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645492 | ||||||
| chr2:148645516
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+346C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645516 | ||||||
| chr2:148645644
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153+474C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645644 | ||||||
| chr2:148645809
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.153+639G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645809 | ||||||
| chr2:148645817
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+647G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645817 | ||||||
| chr2:148645826
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+656G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645826 | ||||||
| chr2:148645826
|
G | C | 1 | a0001c0006t0001g0006 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+656G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645826 | ||||||
| chr2:148645827
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+657C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645827 | ||||||
| chr2:148645842
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+672C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645842 | ||||||
| chr2:148646051
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.153+881G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646051 | ||||||
| chr2:148646238
|
G | A | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+1068G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646238 | ||||||
| chr2:148646470
|
AATAG | A | 15 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(12): Show | 15 | HG00673.hp2 HG02074.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.153+1304_153+1307d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148646470 | |||||
| chr2:148646493
|
A | G | 6 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | NA18747.hp1 NA18947.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1323A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646493 | ||||||
| chr2:148646601
|
C | CT | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 288 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.153+1441dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148646601 | |||||
| chr2:148646917
|
C | T | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+1747C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646917 | ||||||
| chr2:148646924
|
G | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+1754G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646924 | ||||||
| chr2:148646955
|
C | T | 98 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(95): Show | 98 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.153+1785C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646955 | ||||||
| chr2:148646982
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.153+1812C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646982 | ||||||
| chr2:148647002
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+1832C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647002 | ||||||
| chr2:148647387
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+2217A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647387 | ||||||
| chr2:148647496
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.153+2326C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647496 | ||||||
| chr2:148647609
|
G | A | 41 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.153+2439G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647609 | ||||||
| chr2:148647619
|
C | CT | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0130others(4): Show | 7 | HG02647.hp1 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+2476dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | |||||
| chr2:148647619
|
CT | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0134others(103): Show | 106 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.153+2476delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | |||||
| chr2:148647619
|
CTT | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(42): Show | 45 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.153+2475_153+2476d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | |||||
| chr2:148647619
|
CTTT | C | 81 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0291others(78): Show | 81 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.153+2474_153+2476d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | |||||
| chr2:148647619
|
CTTTT | C | 6 | a0001c0001t0001g0035a0001c0001t0002g0036a0001c0001t0002g0037others(3): Show | 6 | HG01070.hp2 HG02895.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+2473_153+2476d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | |||||
| chr2:148647619
|
CTTTTTT | C | 8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+2471_153+2476d others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | |||||
| chr2:148647646
|
T | A | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.153+2476T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647646 | ||||||
| chr2:148647661
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+2491T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647661 | ||||||
| chr2:148647709
|
T | G | 5 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+2539T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647709 | ||||||
| chr2:148647910
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.153+2740G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647910 | ||||||
| chr2:148647976
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.153+2806A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647976 | ||||||
| chr2:148648025
|
A | C | 1 | a0001c0001t0002g0119 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.153+2855A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648025 | ||||||
| chr2:148648071
|
A | G | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+2901A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648071 | ||||||
| chr2:148648072
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153+2902G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648072 | ||||||
| chr2:148648234
|
TTTTCTTT others(3): Show |
T | 1 | a0001c0001t0001g0256 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.153+3074_153+3083d others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148648234 | |||||
| chr2:148648275
|
T | C | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+3105T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648275 | ||||||
| chr2:148648288
|
A | C | 36 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(33): Show | 36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+3118A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648288 | ||||||
| chr2:148648528
|
A | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+3358A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648528 | ||||||
| chr2:148648555
|
A | G | 1 | a0001c0006t0001g0006 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+3385A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648555 | ||||||
| chr2:148648822
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+3652T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648822 | ||||||
| chr2:148648860
|
C | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+3690C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648860 | ||||||
| chr2:148649061
|
G | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+3891G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649061 | ||||||
| chr2:148649072
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.153+3902A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649072 | ||||||
| chr2:148649133
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+3963T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649133 | ||||||
| chr2:148649311
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+4141T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649311 | ||||||
| chr2:148649394
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.153+4224G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649394 | ||||||
| chr2:148649472
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+4302G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649472 | ||||||
| chr2:148649746
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+4576T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649746 | ||||||
| chr2:148650089
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.153+4919C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650089 | ||||||
| chr2:148650181
|
T | C | 8 | a0001c0001t0002g0036a0001c0001t0002g0044a0001c0001t0002g0045others(5): Show | 8 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+5011T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650181 | ||||||
| chr2:148650368
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.153+5198T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650368 | ||||||
| chr2:148650382
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.153+5212A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650382 | ||||||
| chr2:148650670
|
A | G | 165 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(162): Show | 165 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.153+5500A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650670 | ||||||
| chr2:148650748
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+5578G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650748 | ||||||
| chr2:148650766
|
G | GT | 104 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(101): Show | 104 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.153+5597dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148650766 | |||||
| chr2:148650899
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+5729A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650899 | ||||||
| chr2:148651263
|
C | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+6093C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651263 | ||||||
| chr2:148651355
|
G | A | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+6185G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651355 | ||||||
| chr2:148651392
|
C | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+6222C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651392 | ||||||
| chr2:148651466
|
G | C | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.153+6296G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651466 | ||||||
| chr2:148651552
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+6382C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651552 | ||||||
| chr2:148651553
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6383T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651553 | ||||||
| chr2:148651555
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6385G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651555 | ||||||
| chr2:148651561
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6391T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651561 | ||||||
| chr2:148651562
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6392G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651562 | ||||||
| chr2:148651564
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6394A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651564 | ||||||
| chr2:148651565
|
GGGT | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+6399_153+6401d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148651565 | |||||
| chr2:148651567
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6397G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651567 | ||||||
| chr2:148651569
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6399G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651569 | ||||||
| chr2:148651573
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6403T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651573 | ||||||
| chr2:148651574
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6404A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651574 | ||||||
| chr2:148651575
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6405G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651575 | ||||||
| chr2:148651583
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6413A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651583 | ||||||
| chr2:148651590
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6420A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651590 | ||||||
| chr2:148651593
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6423T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651593 | ||||||
| chr2:148651594
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6424A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651594 | ||||||
| chr2:148651596
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6426G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651596 | ||||||
| chr2:148651598
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6428T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651598 | ||||||
| chr2:148651599
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6429T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651599 | ||||||
| chr2:148651600
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6430C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651600 | ||||||
| chr2:148651602
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6432G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651602 | ||||||
| chr2:148651611
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6441G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651611 | ||||||
| chr2:148651615
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6445C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651615 | ||||||
| chr2:148651618
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6448G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651618 | ||||||
| chr2:148651619
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6449T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651619 | ||||||
| chr2:148651623
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6453G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651623 | ||||||
| chr2:148651624
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6454G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651624 | ||||||
| chr2:148651625
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6455T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651625 | ||||||
| chr2:148651629
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6459C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651629 | ||||||
| chr2:148651631
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6461T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651631 | ||||||
| chr2:148651632
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6462G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651632 | ||||||
| chr2:148651633
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6463G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651633 | ||||||
| chr2:148651634
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6464A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651634 | ||||||
| chr2:148651637
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6467A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651637 | ||||||
| chr2:148651639
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6469C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651639 | ||||||
| chr2:148651640
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6470C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651640 | ||||||
| chr2:148651644
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6474T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651644 | ||||||
| chr2:148651650
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6480C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651650 | ||||||
| chr2:148651651
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6481T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651651 | ||||||
| chr2:148651656
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6486G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651656 | ||||||
| chr2:148651657
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6487G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651657 | ||||||
| chr2:148651658
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6488G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651658 | ||||||
| chr2:148651662
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6492A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651662 | ||||||
| chr2:148651666
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6496G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651666 | ||||||
| chr2:148651671
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6501A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651671 | ||||||
| chr2:148651680
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6510A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651680 | ||||||
| chr2:148651681
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6511A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651681 | ||||||
| chr2:148651682
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6512G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651682 | ||||||
| chr2:148651686
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6516C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651686 | ||||||
| chr2:148651744
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.153+6574T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651744 | ||||||
| chr2:148651772
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+6602A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651772 | ||||||
| chr2:148651842
|
T | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+6672T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651842 | ||||||
| chr2:148651876
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+6706T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651876 | ||||||
| chr2:148651886
|
C | T | 5 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+6716C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651886 | ||||||
| chr2:148651901
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.153+6731G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651901 | ||||||
| chr2:148651936
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153+6766C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651936 | ||||||
| chr2:148652070
|
G | A | 5 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(2): Show | 5 | HG01106.hp1 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+6900G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652070 | ||||||
| chr2:148652499
|
G | A | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+7329G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652499 | ||||||
| chr2:148652506
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.153+7336C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652506 | ||||||
| chr2:148652542
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.153+7372T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652542 | ||||||
| chr2:148652572
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.153+7402T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652572 | ||||||
| chr2:148652621
|
C | T | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+7451C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652621 | ||||||
| chr2:148652664
|
TGAAAA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+7498_153+7502d others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148652664 | |||||
| chr2:148652757
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.153+7587C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652757 | ||||||
| chr2:148652773
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+7603G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652773 | ||||||
| chr2:148653087
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153+7917A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653087 | ||||||
| chr2:148653350
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.153+8180A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653350 | ||||||
| chr2:148653363
|
C | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+8193C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653363 | ||||||
| chr2:148653363
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+8193C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653363 | ||||||
| chr2:148653583
|
T | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.153+8413T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653583 | ||||||
| chr2:148653681
|
A | G | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+8511A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653681 | ||||||
| chr2:148653791
|
TGAA | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+8623_153+8625d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148653791 | |||||
| chr2:148653950
|
G | GT | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG02071.hp1 HG02135.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+8794dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148653950 | |||||
| chr2:148653950
|
GT | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(98): Show | 101 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.153+8794delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148653950 | |||||
| chr2:148653990
|
C | A | 1 | a0001c0001t0003g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.153+8820C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653990 | ||||||
| chr2:148654004
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+8834A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654004 | ||||||
| chr2:148654030
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.153+8860C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654030 | ||||||
| chr2:148654105
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.153+8935C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654105 | ||||||
| chr2:148654325
|
T | C | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+9155T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654325 | ||||||
| chr2:148654642
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153+9472A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654642 | ||||||
| chr2:148654731
|
C | A | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+9561C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654731 | ||||||
| chr2:148654787
|
G | C | 1 | a0001c0001t0001g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.153+9617G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654787 | ||||||
| chr2:148654832
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG01884.hp1 HG02040.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+9662C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654832 | ||||||
| chr2:148654998
|
G | C | 1 | a0001c0001t0001g0159 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.153+9828G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654998 | ||||||
| chr2:148655188
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.153+10018C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655188 | ||||||
| chr2:148655508
|
T | C | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+10338T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655508 | ||||||
| chr2:148655906
|
T | G | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+10736T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655906 | ||||||
| chr2:148655960
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+10790C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655960 | ||||||
| chr2:148656001
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0002g0058a0001c0001t0002g0060a0001c0001t0002g0114others(4): Show | 7 | HG00423.hp2 HG02273.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+10848_153+1085 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTGT others(3): Show |
53 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0043others(50): Show | 53 | HG00280.hp2 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+10846_153+1085 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTGT others(5): Show |
24 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0044others(21): Show | 24 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.153+10844_153+1085 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0002g0056 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.153+10842_153+1085 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0003g0107 | 3 | NA18959.hp1 NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.153+10840_153+1085 others(20): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0002g0108 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.153+10838_153+1085 others(22): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTT | 11 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 11 | HG00639.hp2 HG02040.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTTT others(1): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG02257.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656001
|
C | CTGTGTTT others(15): Show |
1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+10836_153+1083 others(26): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | |||||
| chr2:148656003
|
G | GTGTT | 15 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00639.hp1 HG00642.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656003 | |||||
| chr2:148656005
|
G | GTT | 57 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0133others(54): Show | 57 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656005 | |||||
| chr2:148656007
|
G | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.153+10837G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656007 | ||||||
| chr2:148656022
|
T | G | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.153+10852T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656022 | ||||||
| chr2:148656022
|
T | TG | 5 | a0001c0001t0001g0011a0001c0001t0001g0252a0001c0001t0001g0293others(2): Show | 5 | HG02723.hp1 HG03130.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+10853dupG | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656022 | |||||
| chr2:148656024
|
T | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0189others(17): Show | 20 | HG00642.hp1 HG01517.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+10854T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656024 | ||||||
| chr2:148656024
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.153+10855_153+1085 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656024 | |||||
| chr2:148656025
|
G | GT | 42 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0145others(39): Show | 42 | HG00423.hp1 HG00544.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.153+10855_153+1085 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656025 | ||||||
| chr2:148656025
|
G | GTGT | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(9): Show | 12 | HG02080.hp1 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+10855_153+1085 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656025 | ||||||
| chr2:148656025
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0002g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+10855_153+1085 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656025 | ||||||
| chr2:148656026
|
G | T | 143 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.153+10856G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656026 | ||||||
| chr2:148656027
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.153+10857G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656027 | ||||||
| chr2:148656028
|
G | T | 112 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.153+10858G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656028 | ||||||
| chr2:148656029
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0002g0112 | 2 | NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.153+10859G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656029 | ||||||
| chr2:148656030
|
G | T | 103 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.153+10860G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656030 | ||||||
| chr2:148656031
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0002g0112 | 2 | NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.153+10861G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656031 | ||||||
| chr2:148656032
|
G | T | 103 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.153+10862G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656032 | ||||||
| chr2:148656033
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+10863G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656033 | ||||||
| chr2:148656034
|
G | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(99): Show | 102 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.153+10864G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656034 | ||||||
| chr2:148656035
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+10865G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656035 | ||||||
| chr2:148656036
|
G | T | 5 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+10866G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656036 | ||||||
| chr2:148656171
|
G | A | 1 | a0001c0001t0004g0175 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.153+11001G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656171 | ||||||
| chr2:148656187
|
A | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+11017A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656187 | ||||||
| chr2:148656200
|
A | G | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18939.hp2 NA18945.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+11030A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656200 | ||||||
| chr2:148656403
|
AAAAT | A | 105 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+11234_153+1123 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656403 | ||||||
| chr2:148656477
|
A | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+11307A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656477 | ||||||
| chr2:148656539
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+11369T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656539 | ||||||
| chr2:148656620
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.153+11450A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656620 | ||||||
| chr2:148656737
|
C | T | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+11567C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656737 | ||||||
| chr2:148656870
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 170 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.153+11700A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656870 | ||||||
| chr2:148656881
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+11711G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656881 | ||||||
| chr2:148656970
|
A | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+11800A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656970 | ||||||
| chr2:148657175
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.153+12005G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657175 | ||||||
| chr2:148657319
|
T | G | 1 | a0001c0001t0003g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.153+12149T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657319 | ||||||
| chr2:148657358
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.153+12188A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657358 | ||||||
| chr2:148657377
|
A | C | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+12207A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657377 | ||||||
| chr2:148657440
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.153+12270A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657440 | ||||||
| chr2:148657487
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.153+12317C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657487 | ||||||
| chr2:148657549
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153+12379A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657549 | ||||||
| chr2:148657586
|
T | G | 36 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(33): Show | 36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+12416T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657586 | ||||||
| chr2:148657768
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153+12598C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657768 | ||||||
| chr2:148657796
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153+12626G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657796 | ||||||
| chr2:148657859
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+12689A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657859 | ||||||
| chr2:148657884
|
T | TTG | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(47): Show | 50 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.153+12736_153+1273 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148657884 | |||||
| chr2:148657884
|
T | TTGTG | 69 | a0001c0001t0001g0030a0001c0001t0002g0036a0001c0001t0002g0039others(66): Show | 69 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.153+12734_153+1273 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148657884 | |||||
| chr2:148657973
|
C | T | 3 | a0001c0001t0002g0062a0001c0001t0002g0094a0001c0001t0002g0095 | 3 | HG00673.hp1 HG02040.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.153+12803C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657973 | ||||||
| chr2:148658016
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.153+12846G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658016 | ||||||
| chr2:148658060
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153+12890G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658060 | ||||||
| chr2:148658087
|
A | T | 94 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(91): Show | 94 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.153+12917A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658087 | ||||||
| chr2:148658150
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0242 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.153+12980G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658150 | ||||||
| chr2:148658311
|
C | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+13141C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658311 | ||||||
| chr2:148658342
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.153+13172C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658342 | ||||||
| chr2:148658503
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+13333G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658503 | ||||||
| chr2:148658552
|
G | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+13382G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658552 | ||||||
| chr2:148658593
|
CTG | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+13437_153+1343 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658593 | |||||
| chr2:148658605
|
GTGTA | G | 13 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+13437_153+1344 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658605 | |||||
| chr2:148658607
|
G | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+13437G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658607 | ||||||
| chr2:148658607
|
G | GTA | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00673.hp2 HG01943.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+13461_153+1346 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATA | 23 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(20): Show | 23 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.153+13459_153+1346 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATA | 20 | a0001c0001t0001g0291a0001c0001t0002g0045a0001c0001t0002g0051others(17): Show | 20 | HG00558.hp2 HG01123.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.153+13457_153+1346 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATAT others(1): Show |
19 | a0001c0001t0002g0040a0001c0001t0002g0066a0001c0001t0002g0067others(16): Show | 19 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+13455_153+1346 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATAT others(3): Show |
9 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0073others(6): Show | 9 | HG01884.hp2 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+13453_153+1346 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0002g0062a0001c0001t0002g0072 | 2 | HG00673.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.153+13449_153+1346 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATAT others(9): Show |
4 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0063others(1): Show | 4 | HG00735.hp1 HG03704.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+13447_153+1346 others(20): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATAT others(11): Show |
2 | a0001c0001t0002g0070a0001c0001t0002g0097 | 2 | NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.153+13445_153+1346 others(22): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+13443_153+1346 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTGTA | 5 | a0001c0001t0002g0055a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00423.hp2 HG02135.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+13438_153+1343 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
G | GTGTATA | 12 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(9): Show | 12 | HG00741.hp1 HG01106.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+13438_153+1343 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
GTA | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(26): Show | 29 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.153+13461_153+1346 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
GTATA | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(70): Show | 73 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.153+13459_153+1346 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658607
|
GTATATA | G | 56 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(53): Show | 56 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.153+13457_153+1346 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | |||||
| chr2:148658611
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.153+13441A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658611 | ||||||
| chr2:148658613
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 71 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.153+13443A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658613 | ||||||
| chr2:148658615
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 106 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.153+13445A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658615 | ||||||
| chr2:148658617
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0266 | 2 | HG03098.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.153+13447A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658617 | ||||||
| chr2:148658776
|
TTAC | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.153+13611_153+1361 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658776 | |||||
| chr2:148658819
|
ATATG | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+13655_153+1365 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658819 | |||||
| chr2:148658982
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153+13812C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658982 | ||||||
| chr2:148659251
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+14081G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659251 | ||||||
| chr2:148659252
|
C | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+14082C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659252 | ||||||
| chr2:148659436
|
T | C | 94 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(91): Show | 94 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.153+14266T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659436 | ||||||
| chr2:148659820
|
GACATTA | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+14654_153+1465 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148659820 | |||||
| chr2:148659889
|
G | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+14719G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659889 | ||||||
| chr2:148659903
|
T | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+14733T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659903 | ||||||
| chr2:148660055
|
A | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0120 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.153+14885A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660055 | ||||||
| chr2:148660184
|
C | A | 105 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+15014C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660184 | ||||||
| chr2:148660299
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153+15129T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660299 | ||||||
| chr2:148660335
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.153+15165G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660335 | ||||||
| chr2:148660340
|
G | T | 18 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(15): Show | 18 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.153+15170G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660340 | ||||||
| chr2:148660473
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+15303A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660473 | ||||||
| chr2:148660537
|
A | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+15367A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660537 | ||||||
| chr2:148660573
|
G | GT | 6 | a0001c0001t0001g0189a0001c0001t0001g0222a0001c0001t0001g0251others(3): Show | 6 | HG00642.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+15416dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148660573 | |||||
| chr2:148660586
|
T | A | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+15416T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660586 | ||||||
| chr2:148660605
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153+15435G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660605 | ||||||
| chr2:148660606
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153+15436C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660606 | ||||||
| chr2:148660680
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.153+15510T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660680 | ||||||
| chr2:148660706
|
T | A | 1 | a0001c0001t0002g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.153+15536T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660706 | ||||||
| chr2:148661056
|
T | C | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.153+15886T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661056 | ||||||
| chr2:148661068
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.153+15898T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661068 | ||||||
| chr2:148661130
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+15960C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661130 | ||||||
| chr2:148661202
|
T | C | 2 | a0001c0004t0001g0022a0001c0004t0001g0025 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.153+16032T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661202 | ||||||
| chr2:148661234
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.153+16064A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661234 | ||||||
| chr2:148661403
|
C | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+16233C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661403 | ||||||
| chr2:148661522
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.153+16352T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661522 | ||||||
| chr2:148661626
|
C | G | 111 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.153+16456C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661626 | ||||||
| chr2:148661635
|
G | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+16465G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661635 | ||||||
| chr2:148661640
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18941.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.153+16470G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661640 | ||||||
| chr2:148661661
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.153+16491A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661661 | ||||||
| chr2:148661667
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153+16497A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661667 | ||||||
| chr2:148661695
|
T | TTATG | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+16528_153+1653 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148661695 | |||||
| chr2:148661772
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+16602A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661772 | ||||||
| chr2:148661866
|
C | T | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+16696C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661866 | ||||||
| chr2:148662058
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+16888A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662058 | ||||||
| chr2:148662059
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+16889T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662059 | ||||||
| chr2:148662079
|
C | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.153+16909C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662079 | ||||||
| chr2:148662222
|
G | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.153+17052G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662222 | ||||||
| chr2:148662250
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+17080T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662250 | ||||||
| chr2:148662271
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 17 | HG00639.hp2 HG02040.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.153+17101G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662271 | ||||||
| chr2:148662401
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+17231A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662401 | ||||||
| chr2:148662421
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.153+17251C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662421 | ||||||
| chr2:148662495
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153+17325T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662495 | ||||||
| chr2:148662501
|
G | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+17331G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662501 | ||||||
| chr2:148662561
|
G | A | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+17391G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662561 | ||||||
| chr2:148662616
|
A | G | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+17446A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662616 | ||||||
| chr2:148662619
|
A | T | 1 | a0001c0001t0001g0239 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.153+17449A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662619 | ||||||
| chr2:148662705
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+17535A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662705 | ||||||
| chr2:148662812
|
T | TATA | 130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(127): Show | 130 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.153+17653_153+1765 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148662812 | |||||
| chr2:148662828
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+17658T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662828 | ||||||
| chr2:148662834
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.153+17664T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662834 | ||||||
| chr2:148662835
|
A | T | 1 | a0001c0001t0001g0290 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.153+17665A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662835 | ||||||
| chr2:148662989
|
T | A | 1 | a0001c0001t0001g0290 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.153+17819T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662989 | ||||||
| chr2:148663038
|
T | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+17868T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663038 | ||||||
| chr2:148663193
|
T | TTTA | 3 | a0001c0001t0004g0172a0001c0001t0004g0176a0001c0001t0004g0182 | 3 | HG00544.hp2 HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.153+18023_153+1802 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663193 | ||||||
| chr2:148663194
|
G | GTAT | 61 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0026others(58): Show | 61 | HG00280.hp2 HG00639.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.153+18068_153+1807 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
G | GTATTAT | 36 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0032others(33): Show | 36 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+18065_153+1807 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
G | GTATTATT others(2): Show |
22 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0028others(19): Show | 22 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.153+18062_153+1807 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
G | GTATTATT others(5): Show |
2 | a0001c0001t0001g0198a0001c0001t0002g0052 | 2 | HG01258.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.153+18059_153+1807 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
G | T | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+18024G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663194 | ||||||
| chr2:148663194
|
GTAT | G | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 53 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.153+18068_153+1807 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
GTATTAT | G | 67 | a0001c0001t0001g0139a0001c0001t0001g0152a0001c0001t0001g0166others(64): Show | 67 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.153+18065_153+1807 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
GTATTATT others(2): Show |
G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+18062_153+1807 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663194
|
GTATTATT others(5): Show |
G | 4 | a0001c0001t0002g0051a0001c0001t0002g0060a0001c0001t0002g0088others(1): Show | 4 | HG03654.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+18059_153+1807 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | |||||
| chr2:148663346
|
G | A | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+18176G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663346 | ||||||
| chr2:148663411
|
G | T | 1 | a0001c0001t0001g0257 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.153+18241G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663411 | ||||||
| chr2:148663575
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG00558.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.153+18405T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663575 | ||||||
| chr2:148663581
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+18411T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663581 | ||||||
| chr2:148663592
|
A | AT | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+18450dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663592
|
AT | A | 67 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(64): Show | 67 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.153+18450delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663592
|
ATT | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(161): Show | 164 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.153+18449_153+1845 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663592
|
ATTTTTTT | A | 8 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+18444_153+1845 others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663592
|
ATTTTTTT others(1): Show |
A | 13 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(10): Show | 13 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.153+18443_153+1845 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663592
|
ATTTTTTT others(2): Show |
A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+18442_153+1845 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663592
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+18439_153+1845 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | |||||
| chr2:148663643
|
G | GAA | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+18474_153+1847 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663643 | |||||
| chr2:148663690
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.153+18520C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663690 | ||||||
| chr2:148663783
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+18613C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663783 | ||||||
| chr2:148663875
|
A | G | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0056 | 3 | HG01106.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.153+18705A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663875 | ||||||
| chr2:148663879
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+18709T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663879 | ||||||
| chr2:148663934
|
C | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+18764C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663934 | ||||||
| chr2:148663981
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153+18811C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663981 | ||||||
| chr2:148664342
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+19172T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664342 | ||||||
| chr2:148664458
|
G | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+19288G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664458 | ||||||
| chr2:148664558
|
A | G | 3 | a0001c0001t0002g0075a0001c0001t0002g0079a0001c0001t0002g0080 | 3 | NA18975.hp1 NA19077.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.153+19388A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664558 | ||||||
| chr2:148664981
|
G | C | 1 | a0002c0002t0007g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.153+19811G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664981 | ||||||
| chr2:148665188
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.153+20018G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665188 | ||||||
| chr2:148665358
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+20188A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665358 | ||||||
| chr2:148665475
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153+20305A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665475 | ||||||
| chr2:148665521
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.153+20351G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665521 | ||||||
| chr2:148665683
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+20513T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665683 | ||||||
| chr2:148665762
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.153+20592A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665762 | ||||||
| chr2:148665818
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+20648C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665818 | ||||||
| chr2:148665907
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+20737A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665907 | ||||||
| chr2:148666078
|
G | A | 13 | a0001c0001t0001g0168a0001c0001t0001g0203a0001c0001t0001g0219others(10): Show | 13 | HG00609.hp1 HG01346.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.153+20908G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666078 | ||||||
| chr2:148666201
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.153+21031C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666201 | ||||||
| chr2:148666465
|
T | A | 1 | a0001c0003t0001g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+21295T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666465 | ||||||
| chr2:148666530
|
T | C | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+21360T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666530 | ||||||
| chr2:148666563
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.153+21393A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666563 | ||||||
| chr2:148666687
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+21517T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666687 | ||||||
| chr2:148666768
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.153+21598A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666768 | ||||||
| chr2:148666851
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.153+21681T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666851 | ||||||
| chr2:148666853
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+21683A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666853 | ||||||
| chr2:148666869
|
CT | C | 276 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0035others(273): Show | 276 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.153+21714delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148666869 | |||||
| chr2:148666961
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.153+21791T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666961 | ||||||
| chr2:148667137
|
C | G | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+21967C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667137 | ||||||
| chr2:148667235
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.153+22065T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667235 | ||||||
| chr2:148667356
|
G | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+22186G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667356 | ||||||
| chr2:148667400
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.153+22230T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667400 | ||||||
| chr2:148667420
|
G | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+22250G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667420 | ||||||
| chr2:148667513
|
G | GT | 6 | a0001c0001t0002g0057a0001c0001t0002g0064a0001c0005t0001g0187others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+22352dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148667513 | |||||
| chr2:148667827
|
G | C | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.154-22387G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667827 | ||||||
| chr2:148668105
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154-22109G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668105 | ||||||
| chr2:148668616
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-21598G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668616 | ||||||
| chr2:148668630
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-21584G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668630 | ||||||
| chr2:148668666
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.154-21548G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668666 | ||||||
| chr2:148668852
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-21362A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668852 | ||||||
| chr2:148668864
|
G | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.154-21350G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668864 | ||||||
| chr2:148668892
|
T | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-21322T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668892 | ||||||
| chr2:148668894
|
T | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-21320T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668894 | ||||||
| chr2:148668975
|
A | G | 1 | a0001c0001t0002g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.154-21239A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668975 | ||||||
| chr2:148669002
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.154-21212A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669002 | ||||||
| chr2:148669205
|
G | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-21009G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669205 | ||||||
| chr2:148669428
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-20786G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669428 | ||||||
| chr2:148669673
|
A | G | 1 | a0002c0002t0001g0308 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154-20541A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669673 | ||||||
| chr2:148669683
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-20531C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669683 | ||||||
| chr2:148669703
|
C | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-20511C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669703 | ||||||
| chr2:148669735
|
T | C | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-20479T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669735 | ||||||
| chr2:148669804
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.154-20410A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669804 | ||||||
| chr2:148669855
|
T | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-20359T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669855 | ||||||
| chr2:148669905
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-20309T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669905 | ||||||
| chr2:148669998
|
G | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.154-20216G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669998 | ||||||
| chr2:148670159
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-20055T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670159 | ||||||
| chr2:148670225
|
G | T | 133 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(130): Show | 133 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.154-19989G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670225 | ||||||
| chr2:148670321
|
AT | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-19890delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148670321 | |||||
| chr2:148670331
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-19883T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670331 | ||||||
| chr2:148670339
|
CT | C | 31 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00673.hp2 HG01069.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.154-19863delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148670339 | |||||
| chr2:148670506
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.154-19708C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670506 | ||||||
| chr2:148670520
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.154-19694C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670520 | ||||||
| chr2:148670640
|
T | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-19574T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670640 | ||||||
| chr2:148670688
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154-19526C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670688 | ||||||
| chr2:148670791
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-19423C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670791 | ||||||
| chr2:148670847
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-19367C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670847 | ||||||
| chr2:148670879
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-19335C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670879 | ||||||
| chr2:148670923
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-19291A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670923 | ||||||
| chr2:148671286
|
G | GT | 27 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(24): Show | 27 | HG00609.hp2 HG00735.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.154-18928_154-1892 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671286 | ||||||
| chr2:148671286
|
G | GTT | 3 | a0001c0001t0001g0306a0001c0001t0002g0048a0001c0001t0004g0176 | 3 | HG00544.hp2 HG01346.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.154-18928_154-1892 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671286 | ||||||
| chr2:148671286
|
G | GTTTTT | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131 | 3 | HG00639.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.154-18928_154-1892 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671286 | ||||||
| chr2:148671287
|
A | AT | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(30): Show | 33 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.154-18907dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | |||||
| chr2:148671287
|
A | ATT | 15 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.154-18908_154-1890 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | |||||
| chr2:148671287
|
A | ATTT | 17 | a0001c0001t0001g0186a0001c0001t0001g0222a0001c0001t0001g0273others(14): Show | 17 | HG00673.hp2 HG02074.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.154-18909_154-1890 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | |||||
| chr2:148671287
|
A | T | 106 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(103): Show | 106 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.154-18927A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671287 | ||||||
| chr2:148671287
|
AT | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG01981.hp1 HG02155.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-18907delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | |||||
| chr2:148671287
|
ATT | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(13): Show | 16 | HG01891.hp1 HG02040.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.154-18908_154-1890 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | |||||
| chr2:148671310
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.154-18904A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671310 | ||||||
| chr2:148671340
|
A | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-18874A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671340 | ||||||
| chr2:148671608
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-18606C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671608 | ||||||
| chr2:148671610
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.154-18604T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671610 | ||||||
| chr2:148671617
|
A | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.154-18597A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671617 | ||||||
| chr2:148671731
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-18483G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671731 | ||||||
| chr2:148671847
|
A | C | 1 | a0001c0001t0001g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.154-18367A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671847 | ||||||
| chr2:148672118
|
C | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-18096C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672118 | ||||||
| chr2:148672635
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG01891.hp1 HG02258.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-17579C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672635 | ||||||
| chr2:148672760
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.154-17454A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672760 | ||||||
| chr2:148672990
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-17224C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672990 | ||||||
| chr2:148673032
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-17182G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673032 | ||||||
| chr2:148673235
|
T | C | 110 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.154-16979T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673235 | ||||||
| chr2:148673259
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-16955T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673259 | ||||||
| chr2:148673657
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.154-16557C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673657 | ||||||
| chr2:148673902
|
T | A | 1 | a0001c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.154-16312T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673902 | ||||||
| chr2:148674167
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02155.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.154-16047A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674167 | ||||||
| chr2:148674356
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-15858A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674356 | ||||||
| chr2:148674376
|
C | CAGAATT | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-15835_154-1583 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148674376 | |||||
| chr2:148674510
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG02027.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-15704A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674510 | ||||||
| chr2:148674576
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.154-15638C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674576 | ||||||
| chr2:148674641
|
G | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.154-15573G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674641 | ||||||
| chr2:148674908
|
C | G | 2 | a0001c0001t0002g0094a0001c0001t0002g0095 | 2 | HG02040.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.154-15306C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674908 | ||||||
| chr2:148674929
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.154-15285C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674929 | ||||||
| chr2:148674933
|
G | A | 106 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(103): Show | 106 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.154-15281G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674933 | ||||||
| chr2:148675179
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-15035A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675179 | ||||||
| chr2:148675322
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-14892G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675322 | ||||||
| chr2:148675499
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.154-14715G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675499 | ||||||
| chr2:148675501
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.154-14713T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675501 | ||||||
| chr2:148675516
|
A | G | 110 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.154-14698A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675516 | ||||||
| chr2:148675705
|
T | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0165 | 2 | HG02080.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.154-14509T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675705 | ||||||
| chr2:148675966
|
C | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-14248C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675966 | ||||||
| chr2:148676079
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.154-14135C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676079 | ||||||
| chr2:148676115
|
A | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0226 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.154-14099A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676115 | ||||||
| chr2:148676127
|
G | GT | 108 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0173others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.154-14074dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676127 | |||||
| chr2:148676127
|
GT | G | 12 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0275others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-14074delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676127 | |||||
| chr2:148676416
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-13798G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676416 | ||||||
| chr2:148676603
|
T | C | 6 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-13611T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676603 | ||||||
| chr2:148676740
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.154-13474T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676740 | ||||||
| chr2:148676768
|
C | T | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-13446C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676768 | ||||||
| chr2:148676777
|
GCT | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 163 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.154-13414_154-1341 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676777 | |||||
| chr2:148676777
|
GCTCTCT | G | 115 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(112): Show | 115 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.154-13418_154-1341 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676777 | |||||
| chr2:148676777
|
GCTCTCTC others(3): Show |
G | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154-13422_154-1341 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676777 | |||||
| chr2:148676865
|
C | CT | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(130): Show | 133 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.154-13342dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676865 | |||||
| chr2:148676872
|
T | TTG | 26 | a0001c0001t0001g0134a0001c0001t0001g0167a0001c0001t0001g0190others(23): Show | 26 | HG00673.hp2 HG02074.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.154-13342_154-1334 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676872 | ||||||
| chr2:148676872
|
TG | T | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-13332delG | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676872 | |||||
| chr2:148676874
|
G | GC | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-13340_154-1333 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676874 | ||||||
| chr2:148676916
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(127): Show | 130 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.154-13298G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676916 | ||||||
| chr2:148676961
|
A | T | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-13253A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676961 | ||||||
| chr2:148677542
|
G | A | 24 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(21): Show | 24 | HG00673.hp2 HG02074.hp2 HG02647.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-12672G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677542 | ||||||
| chr2:148677591
|
G | A | 4 | a0001c0005t0001g0187a0002c0002t0001g0254a0002c0002t0001g0308others(1): Show | 4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-12623G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677591 | ||||||
| chr2:148677615
|
C | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(117): Show | 120 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.154-12599C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677615 | ||||||
| chr2:148677673
|
G | A | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-12541G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677673 | ||||||
| chr2:148677694
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.154-12520T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677694 | ||||||
| chr2:148677770
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154-12444G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677770 | ||||||
| chr2:148677773
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154-12441C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677773 | ||||||
| chr2:148677802
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.154-12412C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677802 | ||||||
| chr2:148677831
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-12383G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677831 | ||||||
| chr2:148677892
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA19003.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.154-12322T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677892 | ||||||
| chr2:148677896
|
T | A | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-12318T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677896 | ||||||
| chr2:148677927
|
C | G | 1 | a0001c0001t0004g0176 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.154-12287C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677927 | ||||||
| chr2:148678013
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-12201C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678013 | ||||||
| chr2:148678075
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154-12139T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678075 | ||||||
| chr2:148678079
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.154-12135C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678079 | ||||||
| chr2:148678191
|
A | C | 4 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-12023A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678191 | ||||||
| chr2:148678221
|
G | C | 1 | a0001c0006t0001g0006 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154-11993G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678221 | ||||||
| chr2:148678244
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-11970A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678244 | ||||||
| chr2:148678277
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-11937C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678277 | ||||||
| chr2:148678339
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-11875C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678339 | ||||||
| chr2:148678457
|
G | A | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-11757G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678457 | ||||||
| chr2:148678474
|
G | A | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.154-11740G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678474 | ||||||
| chr2:148678478
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11736T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678478 | ||||||
| chr2:148678481
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11733G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678481 | ||||||
| chr2:148678533
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.154-11681C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678533 | ||||||
| chr2:148678547
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11667C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678547 | ||||||
| chr2:148678641
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-11573C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678641 | ||||||
| chr2:148678757
|
A | G | 120 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(117): Show | 120 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.154-11457A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678757 | ||||||
| chr2:148678838
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154-11376A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678838 | ||||||
| chr2:148678848
|
T | C | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-11366T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678848 | ||||||
| chr2:148678860
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-11354C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678860 | ||||||
| chr2:148678894
|
G | C | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-11320G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678894 | ||||||
| chr2:148678902
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11312G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678902 | ||||||
| chr2:148678941
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.154-11273T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678941 | ||||||
| chr2:148679022
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154-11192C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679022 | ||||||
| chr2:148679557
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA18960.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.154-10657C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679557 | ||||||
| chr2:148679719
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.154-10495C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679719 | ||||||
| chr2:148679724
|
C | T | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-10490C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679724 | ||||||
| chr2:148679741
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154-10473G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679741 | ||||||
| chr2:148679768
|
C | G | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154-10446C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679768 | ||||||
| chr2:148679825
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-10389T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679825 | ||||||
| chr2:148679833
|
A | G | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-10381A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679833 | ||||||
| chr2:148679886
|
G | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-10328G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679886 | ||||||
| chr2:148679938
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.154-10276C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679938 | ||||||
| chr2:148680089
|
C | CT | 26 | a0001c0001t0001g0189a0001c0001t0001g0199a0001c0001t0001g0200others(23): Show | 26 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.154-10110dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148680089 | |||||
| chr2:148680089
|
CT | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02040.hp2 HG02132.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.154-10110delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148680089 | |||||
| chr2:148680090
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-10124T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680090 | ||||||
| chr2:148680091
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0028others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-10123T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680091 | ||||||
| chr2:148680092
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.154-10122T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680092 | ||||||
| chr2:148680280
|
T | C | 3 | a0001c0001t0002g0062a0001c0001t0002g0094a0001c0001t0002g0095 | 3 | HG00673.hp1 HG02040.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.154-9934T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680280 | ||||||
| chr2:148680534
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-9680T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680534 | ||||||
| chr2:148680623
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.154-9591A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680623 | ||||||
| chr2:148680642
|
G | A | 123 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(120): Show | 123 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.154-9572G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680642 | ||||||
| chr2:148680669
|
G | A | 1 | a0001c0001t0003g0083 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.154-9545G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680669 | ||||||
| chr2:148681006
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-9208A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681006 | ||||||
| chr2:148681039
|
A | C | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-9175A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681039 | ||||||
| chr2:148681271
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-8943A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681271 | ||||||
| chr2:148681435
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.154-8779T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681435 | ||||||
| chr2:148681624
|
C | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(117): Show | 120 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.154-8590C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681624 | ||||||
| chr2:148681625
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.154-8589G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681625 | ||||||
| chr2:148681697
|
GGTTT | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-8500_154-8497d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148681697 | |||||
| chr2:148681714
|
G | C | 2 | a0001c0001t0001g0194a0001c0001t0002g0103 | 2 | HG02886.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.154-8500G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681714 | ||||||
| chr2:148681718
|
C | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 156 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.154-8496C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681718 | ||||||
| chr2:148681756
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-8458A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681756 | ||||||
| chr2:148681821
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.154-8393T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681821 | ||||||
| chr2:148681868
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154-8346C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681868 | ||||||
| chr2:148681891
|
C | T | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154-8323C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681891 | ||||||
| chr2:148681903
|
G | A | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8311G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681903 | ||||||
| chr2:148681968
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.154-8246G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681968 | ||||||
| chr2:148682027
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8187C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682027 | ||||||
| chr2:148682070
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.154-8144C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682070 | ||||||
| chr2:148682071
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8143G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682071 | ||||||
| chr2:148682112
|
A | G | 110 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.154-8102A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682112 | ||||||
| chr2:148682421
|
C | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-7793C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682421 | ||||||
| chr2:148682960
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-7254A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682960 | ||||||
| chr2:148683021
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.154-7193C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683021 | ||||||
| chr2:148683081
|
T | A | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-7133T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683081 | ||||||
| chr2:148683310
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-6904C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683310 | ||||||
| chr2:148683680
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.154-6534A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683680 | ||||||
| chr2:148683725
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.154-6489T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683725 | ||||||
| chr2:148683750
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-6464T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683750 | ||||||
| chr2:148683835
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.154-6379T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683835 | ||||||
| chr2:148683875
|
G | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-6339G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683875 | ||||||
| chr2:148683906
|
A | C | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-6308A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683906 | ||||||
| chr2:148684035
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-6179T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684035 | ||||||
| chr2:148684096
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.154-6118A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684096 | ||||||
| chr2:148684125
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-6089T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684125 | ||||||
| chr2:148684282
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-5932A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684282 | ||||||
| chr2:148684581
|
C | G | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18939.hp2 NA18945.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-5633C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684581 | ||||||
| chr2:148684665
|
G | A | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-5549G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684665 | ||||||
| chr2:148685250
|
GT | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.154-4954delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148685250 | |||||
| chr2:148685260
|
T | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-4954T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685260 | ||||||
| chr2:148685267
|
T | C | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-4947T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685267 | ||||||
| chr2:148685301
|
C | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-4913C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685301 | ||||||
| chr2:148685343
|
A | G | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-4871A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685343 | ||||||
| chr2:148685499
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-4715G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685499 | ||||||
| chr2:148685557
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-4657G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685557 | ||||||
| chr2:148685624
|
G | C | 1 | a0001c0001t0002g0125 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.154-4590G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685624 | ||||||
| chr2:148685654
|
A | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-4560A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685654 | ||||||
| chr2:148685698
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-4516C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685698 | ||||||
| chr2:148685724
|
G | A | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-4490G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685724 | ||||||
| chr2:148685753
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.154-4461T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685753 | ||||||
| chr2:148685825
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.154-4389A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685825 | ||||||
| chr2:148685991
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.154-4223G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685991 | ||||||
| chr2:148686015
|
G | A | 3 | a0001c0005t0001g0187a0002c0002t0001g0308a0002c0002t0007g0255 | 3 | HG02647.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.154-4199G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686015 | ||||||
| chr2:148686033
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-4181A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686033 | ||||||
| chr2:148686450
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-3764T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686450 | ||||||
| chr2:148686460
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-3754G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686460 | ||||||
| chr2:148687038
|
C | T | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-3176C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687038 | ||||||
| chr2:148687197
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-3017A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687197 | ||||||
| chr2:148687460
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.154-2754T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687460 | ||||||
| chr2:148687622
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.154-2592C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687622 | ||||||
| chr2:148687624
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.154-2590A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687624 | ||||||
| chr2:148687794
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.154-2420G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687794 | ||||||
| chr2:148687831
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-2383C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687831 | ||||||
| chr2:148687906
|
C | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-2308C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687906 | ||||||
| chr2:148688041
|
TATA | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-2168_154-2166d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148688041 | |||||
| chr2:148688086
|
C | G | 1 | a0001c0001t0002g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.154-2128C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688086 | ||||||
| chr2:148688302
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.154-1912T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688302 | ||||||
| chr2:148688419
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.154-1795G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688419 | ||||||
| chr2:148688428
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154-1786G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688428 | ||||||
| chr2:148688459
|
G | C | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-1755G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688459 | ||||||
| chr2:148688712
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.154-1502T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688712 | ||||||
| chr2:148688801
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154-1413G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688801 | ||||||
| chr2:148688959
|
G | A | 5 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-1255G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688959 | ||||||
| chr2:148689035
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.154-1179A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689035 | ||||||
| chr2:148689069
|
G | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(151): Show | 154 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.154-1145G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689069 | ||||||
| chr2:148689240
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-974G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689240 | ||||||
| chr2:148689338
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-876G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689338 | ||||||
| chr2:148689368
|
C | T | 24 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(21): Show | 24 | HG00673.hp2 HG02074.hp2 HG02647.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-846C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689368 | ||||||
| chr2:148689472
|
A | C | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-742A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689472 | ||||||
| chr2:148689893
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-321G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689893 | ||||||
| chr2:148689986
|
T | TA | 113 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.154-222dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148689986 | |||||
| chr2:148689988
|
A | AC | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-226_154-225ins others(1): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689988 | ||||||
| chr2:148690410
|
TA | T | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.313+40delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148690410 | |||||
| chr2:148690523
|
G | T | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313+150G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690523 | ||||||
| chr2:148690565
|
A | T | 13 | a0001c0001t0001g0168a0001c0001t0001g0203a0001c0001t0001g0219others(10): Show | 13 | HG00609.hp1 HG01346.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+192A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690565 | ||||||
| chr2:148690728
|
T | C | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+355T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690728 | ||||||
| chr2:148690729
|
C | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+356C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690729 | ||||||
| chr2:148690734
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.313+361C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690734 | ||||||
| chr2:148690963
|
G | A | 24 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(21): Show | 24 | HG00673.hp2 HG02074.hp2 HG02647.hp2 others(21): Show |
intron_variant | MODIFIER | c.313+590G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690963 | ||||||
| chr2:148691077
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+704G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691077 | ||||||
| chr2:148691146
|
G | A | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+773G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691146 | ||||||
| chr2:148691146
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313+773G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691146 | ||||||
| chr2:148691221
|
C | T | 1 | a0002c0002t0007g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.313+848C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691221 | ||||||
| chr2:148691227
|
A | T | 1 | a0001c0001t0001g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.313+854A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691227 | ||||||
| chr2:148691300
|
G | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.313+927G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691300 | ||||||
| chr2:148691347
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.313+974G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691347 | ||||||
| chr2:148691401
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.313+1028A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691401 | ||||||
| chr2:148691508
|
T | C | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+1135T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691508 | ||||||
| chr2:148691616
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0168others(68): Show | 71 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.313+1243G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691616 | ||||||
| chr2:148691862
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.313+1489C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691862 | ||||||
| chr2:148691980
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.313+1607T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691980 | ||||||
| chr2:148691999
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313+1626A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691999 | ||||||
| chr2:148692156
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+1783T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692156 | ||||||
| chr2:148692167
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+1794A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692167 | ||||||
| chr2:148692282
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+1909A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692282 | ||||||
| chr2:148692624
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+2251A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692624 | ||||||
| chr2:148693148
|
A | T | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00423.hp1 NA18981.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+2775A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693148 | ||||||
| chr2:148693157
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.313+2784A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693157 | ||||||
| chr2:148693272
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+2899A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693272 | ||||||
| chr2:148693295
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.313+2922G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693295 | ||||||
| chr2:148693598
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+3225C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693598 | ||||||
| chr2:148693692
|
C | G | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+3319C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693692 | ||||||
| chr2:148693908
|
T | C | 8 | a0001c0001t0001g0139a0001c0001t0001g0166a0001c0001t0001g0284others(5): Show | 8 | NA18747.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+3535T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693908 | ||||||
| chr2:148693910
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+3537G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693910 | ||||||
| chr2:148693916
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+3543G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693916 | ||||||
| chr2:148693993
|
G | A | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.313+3620G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693993 | ||||||
| chr2:148694020
|
T | C | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+3647T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694020 | ||||||
| chr2:148694224
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+3851G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694224 | ||||||
| chr2:148694270
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0178 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.313+3897C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694270 | ||||||
| chr2:148694304
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.313+3931T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694304 | ||||||
| chr2:148694439
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.313+4066T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694439 | ||||||
| chr2:148694465
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.313+4092A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694465 | ||||||
| chr2:148694626
|
T | C | 2 | a0001c0001t0004g0172a0001c0001t0004g0182 | 2 | HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.313+4253T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694626 | ||||||
| chr2:148694709
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+4336C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694709 | ||||||
| chr2:148694769
|
C | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.313+4396C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694769 | ||||||
| chr2:148694856
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+4483C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694856 | ||||||
| chr2:148695007
|
A | G | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.313+4634A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695007 | ||||||
| chr2:148695067
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.313+4694C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695067 | ||||||
| chr2:148695115
|
C | A | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+4742C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695115 | ||||||
| chr2:148695160
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+4787T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695160 | ||||||
| chr2:148695231
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+4858C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695231 | ||||||
| chr2:148695232
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0214a0001c0001t0001g0224others(2): Show | 5 | HG00738.hp1 HG01070.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+4859G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695232 | ||||||
| chr2:148695263
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+4890G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695263 | ||||||
| chr2:148695727
|
T | TA | 6 | a0001c0001t0002g0040a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG02132.hp2 NA18946.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+5355dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148695727 | |||||
| chr2:148695786
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.313+5413A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695786 | ||||||
| chr2:148695896
|
A | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+5523A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695896 | ||||||
| chr2:148695975
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+5602C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695975 | ||||||
| chr2:148696159
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+5786T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696159 | ||||||
| chr2:148696231
|
T | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+5858T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696231 | ||||||
| chr2:148696385
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+6012G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696385 | ||||||
| chr2:148696403
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+6030C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696403 | ||||||
| chr2:148696647
|
A | G | 127 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(124): Show | 127 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.313+6274A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696647 | ||||||
| chr2:148696652
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+6279G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696652 | ||||||
| chr2:148696676
|
G | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.313+6303G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696676 | ||||||
| chr2:148696731
|
A | G | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.313+6358A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696731 | ||||||
| chr2:148696737
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313+6364A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696737 | ||||||
| chr2:148696769
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.313+6396C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696769 | ||||||
| chr2:148696842
|
T | A | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313+6469T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696842 | ||||||
| chr2:148696891
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.313+6518C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696891 | ||||||
| chr2:148697015
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.313+6642T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697015 | ||||||
| chr2:148697016
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.313+6643G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697016 | ||||||
| chr2:148697038
|
G | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.313+6665G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697038 | ||||||
| chr2:148697127
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.313+6754C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697127 | ||||||
| chr2:148697240
|
A | G | 1 | a0001c0001t0001g0168 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.313+6867A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697240 | ||||||
| chr2:148697263
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.313+6890A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697263 | ||||||
| chr2:148697327
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG00558.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.313+6954A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697327 | ||||||
| chr2:148697399
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+7026A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697399 | ||||||
| chr2:148697498
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.313+7125C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697498 | ||||||
| chr2:148697612
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+7239T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697612 | ||||||
| chr2:148697634
|
A | G | 103 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.313+7261A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697634 | ||||||
| chr2:148697691
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313+7318A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697691 | ||||||
| chr2:148697727
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+7354C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697727 | ||||||
| chr2:148697816
|
A | G | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+7443A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697816 | ||||||
| chr2:148698047
|
A | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+7674A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698047 | ||||||
| chr2:148698067
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+7694T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698067 | ||||||
| chr2:148698351
|
G | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+7978G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698351 | ||||||
| chr2:148698364
|
G | T | 2 | a0001c0004t0001g0022a0001c0004t0001g0025 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.313+7991G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698364 | ||||||
| chr2:148698370
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+7997G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698370 | ||||||
| chr2:148698406
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.313+8033G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698406 | ||||||
| chr2:148698452
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.313+8079A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698452 | ||||||
| chr2:148698465
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(9): Show | 12 | HG02040.hp2 HG02132.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.313+8092A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698465 | ||||||
| chr2:148698467
|
C | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+8094C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698467 | ||||||
| chr2:148698633
|
C | CA | 20 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0018others(17): Show | 20 | HG00423.hp1 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.313+8285dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | |||||
| chr2:148698633
|
C | CAA | 68 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0173others(65): Show | 68 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.313+8284_313+8285d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | |||||
| chr2:148698633
|
C | CAAA | 33 | a0001c0001t0001g0174a0001c0001t0002g0037a0001c0001t0002g0043others(30): Show | 33 | HG00423.hp2 HG00673.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.313+8283_313+8285d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | |||||
| chr2:148698633
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 129 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.313+8285delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | |||||
| chr2:148698633
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.313+8273_313+8285d others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | |||||
| chr2:148698633
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313+8272_313+8285d others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | |||||
| chr2:148698694
|
C | CT | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 76 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.313+8339dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698694
|
C | CTT | 53 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(50): Show | 53 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.313+8338_313+8339d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698694
|
C | CTTT | 12 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(9): Show | 12 | HG00639.hp1 HG02027.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+8337_313+8339d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698694
|
C | CTTTT | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.313+8336_313+8339d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698694
|
C | CTTTTT | 9 | a0001c0001t0002g0050a0001c0001t0002g0058a0001c0001t0002g0080others(6): Show | 9 | HG00642.hp2 HG01175.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+8335_313+8339d others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698694
|
CT | C | 29 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0041others(26): Show | 29 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.313+8339delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698694
|
CTT | C | 14 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0141others(11): Show | 14 | HG02080.hp1 HG02135.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.313+8338_313+8339d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | |||||
| chr2:148698829
|
C | CT | 138 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(135): Show | 138 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.313+8468dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698829 | |||||
| chr2:148698829
|
C | CTT | 110 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0128others(107): Show | 110 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+8467_313+8468d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698829 | |||||
| chr2:148698829
|
C | CTTT | 16 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(13): Show | 16 | HG00544.hp1 HG00558.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.313+8466_313+8468d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698829 | |||||
| chr2:148698841
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+8468T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698841 | ||||||
| chr2:148698841
|
T | TA | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG00673.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+8477dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698841 | |||||
| chr2:148698842
|
A | T | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 15 | HG02040.hp2 HG02074.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.313+8469A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698842 | ||||||
| chr2:148698843
|
A | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+8470A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698843 | ||||||
| chr2:148698859
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.313+8486C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698859 | ||||||
| chr2:148698892
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.313+8519G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698892 | ||||||
| chr2:148698999
|
C | A | 1 | a0001c0001t0002g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.313+8626C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698999 | ||||||
| chr2:148699016
|
C | G | 1 | a0001c0001t0001g0287 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.313+8643C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699016 | ||||||
| chr2:148699212
|
A | G | 1 | a0001c0001t0003g0107 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+8839A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699212 | ||||||
| chr2:148699692
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+9319G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699692 | ||||||
| chr2:148699813
|
G | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+9440G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699813 | ||||||
| chr2:148699816
|
A | G | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.313+9443A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699816 | ||||||
| chr2:148699908
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.313+9535T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699908 | ||||||
| chr2:148699963
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+9590C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699963 | ||||||
| chr2:148700033
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.313+9660G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700033 | ||||||
| chr2:148700122
|
C | T | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313+9749C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700122 | ||||||
| chr2:148700123
|
G | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+9750G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700123 | ||||||
| chr2:148700169
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+9796C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700169 | ||||||
| chr2:148700406
|
A | G | 122 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(119): Show | 122 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.313+10033A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700406 | ||||||
| chr2:148700464
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+10091G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700464 | ||||||
| chr2:148700479
|
C | T | 1 | a0001c0001t0004g0172 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.313+10106C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700479 | ||||||
| chr2:148700482
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.313+10109C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700482 | ||||||
| chr2:148700483
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.313+10110C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700483 | ||||||
| chr2:148700491
|
C | G | 11 | a0001c0001t0002g0062a0001c0001t0002g0075a0001c0001t0002g0078others(8): Show | 11 | HG00673.hp1 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.313+10118C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700491 | ||||||
| chr2:148700494
|
G | C | 1 | a0001c0001t0002g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.313+10121G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700494 | ||||||
| chr2:148700499
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.313+10126G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700499 | ||||||
| chr2:148700499
|
G | T | 1 | a0001c0001t0002g0127 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.313+10126G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700499 | ||||||
| chr2:148700690
|
C | CT | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+10332dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148700690 | |||||
| chr2:148700690
|
CT | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0210a0001c0001t0001g0275others(8): Show | 11 | HG01517.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.313+10332delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148700690 | |||||
| chr2:148700857
|
A | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+10484A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700857 | ||||||
| chr2:148700906
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 289 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.313+10533A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700906 | ||||||
| chr2:148700956
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+10583C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700956 | ||||||
| chr2:148700997
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.313+10624G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700997 | ||||||
| chr2:148701135
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+10762A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701135 | ||||||
| chr2:148701410
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.313+11037T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701410 | ||||||
| chr2:148701470
|
G | T | 1 | a0001c0001t0003g0107 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+11097G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701470 | ||||||
| chr2:148701605
|
T | C | 1 | a0001c0001t0002g0119 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.313+11232T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701605 | ||||||
| chr2:148701678
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.313+11305C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701678 | ||||||
| chr2:148701702
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+11329A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701702 | ||||||
| chr2:148701825
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0026 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.313+11452T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701825 | ||||||
| chr2:148701880
|
T | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0206a0001c0001t0001g0231 | 3 | HG01433.hp1 HG02004.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.313+11507T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701880 | ||||||
| chr2:148702008
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.313+11635A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702008 | ||||||
| chr2:148702067
|
T | A | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.313+11694T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702067 | ||||||
| chr2:148702698
|
G | A | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.313+12325G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702698 | ||||||
| chr2:148702723
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+12350A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702723 | ||||||
| chr2:148702823
|
AT | A | 105 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.313+12462delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148702823 | |||||
| chr2:148702839
|
A | AT | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+12472dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148702839 | |||||
| chr2:148702979
|
C | A | 4 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+12606C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702979 | ||||||
| chr2:148703185
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.313+12812T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703185 | ||||||
| chr2:148703254
|
A | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+12881A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703254 | ||||||
| chr2:148703442
|
GT | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 278 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.313+13078delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148703442 | |||||
| chr2:148703961
|
A | C | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313+13588A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703961 | ||||||
| chr2:148703966
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+13593G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703966 | ||||||
| chr2:148704110
|
G | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+13737G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704110 | ||||||
| chr2:148704186
|
G | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+13813G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704186 | ||||||
| chr2:148704258
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 303 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.313+13885C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704258 | ||||||
| chr2:148704333
|
G | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+13960G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704333 | ||||||
| chr2:148704369
|
T | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+13996T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704369 | ||||||
| chr2:148704452
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.313+14079A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704452 | ||||||
| chr2:148704579
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.313+14206A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704579 | ||||||
| chr2:148704965
|
T | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0110a0001c0001t0002g0132 | 3 | HG00741.hp1 HG01496.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.313+14592T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704965 | ||||||
| chr2:148705220
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+14847C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705220 | ||||||
| chr2:148705297
|
TA | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+14934delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148705297 | |||||
| chr2:148705415
|
C | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+15042C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705415 | ||||||
| chr2:148705611
|
CT | C | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+15239delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705611 | ||||||
| chr2:148705691
|
G | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+15318G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705691 | ||||||
| chr2:148705707
|
C | CAG | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+15334_313+1533 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705707 | ||||||
| chr2:148705754
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+15381G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705754 | ||||||
| chr2:148705874
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.313+15501A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705874 | ||||||
| chr2:148705888
|
G | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.313+15515G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705888 | ||||||
| chr2:148705933
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+15560C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705933 | ||||||
| chr2:148705974
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0283 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.313+15601C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705974 | ||||||
| chr2:148705975
|
G | A | 16 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(13): Show | 16 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.313+15602G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705975 | ||||||
| chr2:148705990
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.313+15617G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705990 | ||||||
| chr2:148706035
|
G | A | 2 | a0001c0004t0001g0022a0001c0004t0001g0025 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.313+15662G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706035 | ||||||
| chr2:148706222
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0267 | 2 | HG02015.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.313+15849C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706222 | ||||||
| chr2:148706425
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313+16052A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706425 | ||||||
| chr2:148706513
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.313+16140A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706513 | ||||||
| chr2:148706515
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+16142C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706515 | ||||||
| chr2:148706664
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.313+16291C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706664 | ||||||
| chr2:148706745
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+16372C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706745 | ||||||
| chr2:148706756
|
A | C | 1 | a0001c0001t0002g0119 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.313+16383A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706756 | ||||||
| chr2:148706783
|
A | C | 1 | a0001c0001t0002g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.313+16410A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706783 | ||||||
| chr2:148706784
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.313+16411G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706784 | ||||||
| chr2:148706809
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+16436G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706809 | ||||||
| chr2:148706827
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+16454G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706827 | ||||||
| chr2:148706962
|
A | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0001g0248 | 3 | NA18954.hp1 NA18970.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.313+16589A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706962 | ||||||
| chr2:148707087
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.313+16714T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707087 | ||||||
| chr2:148707250
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+16877A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707250 | ||||||
| chr2:148707251
|
A | C | 1 | a0001c0001t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.313+16878A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707251 | ||||||
| chr2:148707390
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.313+17017A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707390 | ||||||
| chr2:148707435
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.313+17062T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707435 | ||||||
| chr2:148707459
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+17086G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707459 | ||||||
| chr2:148707572
|
T | C | 4 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+17199T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707572 | ||||||
| chr2:148707613
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+17240G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707613 | ||||||
| chr2:148707622
|
A | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+17249A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707622 | ||||||
| chr2:148707691
|
A | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+17318A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707691 | ||||||
| chr2:148707878
|
A | G | 9 | a0001c0001t0002g0039a0001c0001t0002g0070a0001c0001t0002g0071others(6): Show | 9 | HG02071.hp2 NA18950.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+17505A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707878 | ||||||
| chr2:148707915
|
C | A | 1 | a0001c0001t0008g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.313+17542C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707915 | ||||||
| chr2:148707986
|
ATAACT | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+17617_313+1762 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148707986 | |||||
| chr2:148708097
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.313+17724G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708097 | ||||||
| chr2:148708308
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+17935G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708308 | ||||||
| chr2:148708415
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.313+18042A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708415 | ||||||
| chr2:148708458
|
A | C | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+18085A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708458 | ||||||
| chr2:148708527
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+18154C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708527 | ||||||
| chr2:148708531
|
GAC | G | 4 | a0001c0005t0001g0187a0002c0002t0001g0254a0002c0002t0001g0308others(1): Show | 4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+18162_313+1816 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148708531 | |||||
| chr2:148708577
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0249 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.313+18204T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708577 | ||||||
| chr2:148708647
|
A | G | 1 | a0001c0001t0008g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.313+18274A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708647 | ||||||
| chr2:148708747
|
G | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+18374G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708747 | ||||||
| chr2:148708861
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+18488A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708861 | ||||||
| chr2:148708955
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG01175.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313+18582C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708955 | ||||||
| chr2:148709028
|
C | T | 122 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(119): Show | 122 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.313+18655C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709028 | ||||||
| chr2:148709031
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.313+18658A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709031 | ||||||
| chr2:148709333
|
C | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0275a0001c0001t0001g0276others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+18960C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709333 | ||||||
| chr2:148709371
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+18998C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709371 | ||||||
| chr2:148709444
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+19071C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709444 | ||||||
| chr2:148709446
|
T | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0244 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.313+19073T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709446 | ||||||
| chr2:148709447
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.313+19074C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709447 | ||||||
| chr2:148709459
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0210 | 2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.313+19086A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709459 | ||||||
| chr2:148709505
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+19132A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709505 | ||||||
| chr2:148709672
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+19299A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709672 | ||||||
| chr2:148709931
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.313+19558G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709931 | ||||||
| chr2:148709944
|
A | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.313+19571A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709944 | ||||||
| chr2:148709976
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.313+19603A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709976 | ||||||
| chr2:148709978
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.313+19605A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709978 | ||||||
| chr2:148710002
|
C | G | 1 | a0001c0001t0002g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.313+19629C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710002 | ||||||
| chr2:148710004
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+19631A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710004 | ||||||
| chr2:148710006
|
TTAAAC | T | 9 | a0001c0001t0002g0037a0001c0001t0002g0052a0001c0001t0002g0053others(6): Show | 9 | HG00280.hp2 HG00741.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+19638_313+1964 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148710006 | |||||
| chr2:148710062
|
CCTACAGA others(21): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.313+19694_313+1972 others(32): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148710062 | |||||
| chr2:148710226
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313+19853C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710226 | ||||||
| chr2:148710327
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+19954G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710327 | ||||||
| chr2:148710338
|
G | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+19965G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710338 | ||||||
| chr2:148710397
|
G | T | 6 | a0001c0001t0003g0061a0001c0001t0003g0083a0001c0001t0003g0086others(3): Show | 6 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+20024G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710397 | ||||||
| chr2:148710398
|
G | T | 6 | a0001c0001t0003g0061a0001c0001t0003g0083a0001c0001t0003g0086others(3): Show | 6 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+20025G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710398 | ||||||
| chr2:148710458
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+20085A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710458 | ||||||
| chr2:148710553
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0079a0001c0001t0002g0080 | 3 | NA18975.hp1 NA19077.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.313+20180T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710553 | ||||||
| chr2:148710576
|
G | A | 119 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(116): Show | 119 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.313+20203G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710576 | ||||||
| chr2:148710683
|
T | TC | 119 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(116): Show | 119 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.313+20310_313+2031 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710683 | ||||||
| chr2:148710728
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.313+20355C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710728 | ||||||
| chr2:148710762
|
C | T | 13 | a0001c0001t0001g0041a0001c0001t0001g0170a0001c0001t0001g0190others(10): Show | 13 | HG00639.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+20389C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710762 | ||||||
| chr2:148710852
|
G | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0234a0001c0001t0001g0258 | 3 | HG01515.hp2 HG03831.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.313+20479G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710852 | ||||||
| chr2:148710880
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.313+20507A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710880 | ||||||
| chr2:148710968
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+20595A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710968 | ||||||
| chr2:148710996
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+20623T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710996 | ||||||
| chr2:148711029
|
C | CTT | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+20660_313+2066 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148711029 | |||||
| chr2:148711127
|
T | A | 1 | a0001c0001t0002g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.313+20754T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711127 | ||||||
| chr2:148711231
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+20858G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711231 | ||||||
| chr2:148711374
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+21001T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711374 | ||||||
| chr2:148711438
|
C | G | 1 | a0001c0001t0002g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.313+21065C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711438 | ||||||
| chr2:148711467
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+21094C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711467 | ||||||
| chr2:148711750
|
ATAGT | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0204others(1): Show | 4 | NA18985.hp2 NA19006.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+21379_313+2138 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148711750 | |||||
| chr2:148711777
|
A | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+21404A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711777 | ||||||
| chr2:148711823
|
T | G | 1 | a0001c0001t0002g0085 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.313+21450T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711823 | ||||||
| chr2:148711842
|
T | C | 107 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+21469T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711842 | ||||||
| chr2:148712144
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.313+21771G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712144 | ||||||
| chr2:148712242
|
G | GGT | 5 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG01943.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+21870_313+2187 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148712242 | |||||
| chr2:148712244
|
G | T | 109 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(106): Show | 109 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.313+21871G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712244 | ||||||
| chr2:148712392
|
G | GT | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+22020dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148712392 | |||||
| chr2:148712445
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+22072A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712445 | ||||||
| chr2:148712577
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.313+22204T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712577 | ||||||
| chr2:148712660
|
C | CTGGAAGA others(1): Show |
11 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+22290_313+2229 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148712660 | |||||
| chr2:148712682
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.313+22309G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712682 | ||||||
| chr2:148712712
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+22339G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712712 | ||||||
| chr2:148712753
|
T | C | 10 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01891.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.313+22380T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712753 | ||||||
| chr2:148712835
|
A | C | 1 | a0001c0001t0001g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.313+22462A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712835 | ||||||
| chr2:148712937
|
C | T | 1 | a0001c0006t0001g0006 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.313+22564C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712937 | ||||||
| chr2:148712963
|
C | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+22590C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712963 | ||||||
| chr2:148713007
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.313+22634A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713007 | ||||||
| chr2:148713098
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+22725A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713098 | ||||||
| chr2:148713145
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+22772T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713145 | ||||||
| chr2:148713314
|
C | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+22941C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713314 | ||||||
| chr2:148713316
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313+22943A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713316 | ||||||
| chr2:148713462
|
TAA | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+23092_313+2309 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148713462 | |||||
| chr2:148713518
|
A | T | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.313+23145A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713518 | ||||||
| chr2:148713519
|
T | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+23146T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713519 | ||||||
| chr2:148713630
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.313+23257A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713630 | ||||||
| chr2:148713678
|
A | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.313+23305A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713678 | ||||||
| chr2:148713682
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.313+23309T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713682 | ||||||
| chr2:148713798
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.313+23425C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713798 | ||||||
| chr2:148714092
|
G | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+23719G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714092 | ||||||
| chr2:148714433
|
G | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+24060G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714433 | ||||||
| chr2:148714445
|
G | GTCAAAT | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+24073_313+2407 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148714445 | |||||
| chr2:148714558
|
A | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+24185A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714558 | ||||||
| chr2:148714772
|
A | G | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.313+24399A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714772 | ||||||
| chr2:148714801
|
A | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+24428A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714801 | ||||||
| chr2:148714861
|
T | C | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.313+24488T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714861 | ||||||
| chr2:148715025
|
G | GT | 10 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(7): Show | 10 | HG01891.hp1 HG02132.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+24677dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | |||||
| chr2:148715025
|
GT | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(123): Show | 126 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.313+24677delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | |||||
| chr2:148715025
|
GTT | G | 13 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0247others(10): Show | 13 | HG00673.hp2 HG04184.hp2 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+24676_313+2467 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | |||||
| chr2:148715025
|
GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0002g0074a0001c0001t0002g0089a0001c0001t0002g0126 | 3 | HG02071.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.313+24667_313+2467 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | |||||
| chr2:148715025
|
GTTTTTTT others(5): Show |
G | 92 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(89): Show | 92 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.313+24666_313+2467 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | |||||
| chr2:148715191
|
A | G | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+24818A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715191 | ||||||
| chr2:148715324
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0242 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.313+24951C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715324 | ||||||
| chr2:148715341
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.313+24968C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715341 | ||||||
| chr2:148715342
|
G | A | 19 | a0001c0001t0002g0037a0001c0001t0002g0052a0001c0001t0002g0053others(16): Show | 19 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.313+24969G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715342 | ||||||
| chr2:148715577
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.313+25204G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715577 | ||||||
| chr2:148715604
|
T | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+25231T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715604 | ||||||
| chr2:148715687
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(2): Show | 5 | HG01106.hp2 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+25314G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715687 | ||||||
| chr2:148716064
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.313+25691C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716064 | ||||||
| chr2:148716130
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.313+25757G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716130 | ||||||
| chr2:148716379
|
A | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.313+26006A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716379 | ||||||
| chr2:148716609
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+26236G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716609 | ||||||
| chr2:148716669
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.313+26296C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716669 | ||||||
| chr2:148716728
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.313+26355T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716728 | ||||||
| chr2:148716872
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.313+26499G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716872 | ||||||
| chr2:148716903
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.313+26530G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716903 | ||||||
| chr2:148717074
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.314-26548G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717074 | ||||||
| chr2:148717193
|
A | AT | 7 | a0001c0001t0001g0042a0001c0001t0002g0063a0001c0001t0002g0098others(4): Show | 7 | HG00735.hp1 HG01433.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-26409dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148717193 | |||||
| chr2:148717193
|
AT | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 154 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.314-26409delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148717193 | |||||
| chr2:148717193
|
ATT | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(28): Show | 31 | HG00639.hp1 HG01069.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.314-26410_314-2640 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148717193 | |||||
| chr2:148717395
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-26227G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717395 | ||||||
| chr2:148717425
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.314-26197A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717425 | ||||||
| chr2:148717434
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-26188C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717434 | ||||||
| chr2:148717667
|
G | C | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-25955G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717667 | ||||||
| chr2:148717817
|
A | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-25805A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717817 | ||||||
| chr2:148717827
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.314-25795T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717827 | ||||||
| chr2:148717844
|
G | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0281 | 2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.314-25778G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717844 | ||||||
| chr2:148717996
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.314-25626T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717996 | ||||||
| chr2:148718003
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.314-25619C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718003 | ||||||
| chr2:148718112
|
CTTTAT | C | 4 | a0001c0005t0001g0187a0002c0002t0001g0254a0002c0002t0001g0308others(1): Show | 4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-25506_314-2550 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148718112 | |||||
| chr2:148718168
|
G | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-25454G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718168 | ||||||
| chr2:148718178
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-25444G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718178 | ||||||
| chr2:148718319
|
C | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-25303C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718319 | ||||||
| chr2:148718711
|
T | G | 1 | a0001c0001t0002g0127 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.314-24911T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718711 | ||||||
| chr2:148718959
|
A | G | 119 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(116): Show | 119 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.314-24663A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718959 | ||||||
| chr2:148719099
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314-24523A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719099 | ||||||
| chr2:148719211
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-24411T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719211 | ||||||
| chr2:148719268
|
G | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG02027.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-24354G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719268 | ||||||
| chr2:148719493
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314-24129C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719493 | ||||||
| chr2:148719628
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-23994G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719628 | ||||||
| chr2:148719724
|
C | T | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-23898C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719724 | ||||||
| chr2:148719725
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.314-23897G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719725 | ||||||
| chr2:148719797
|
T | A | 1 | a0001c0001t0008g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314-23825T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719797 | ||||||
| chr2:148719799
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-23823A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719799 | ||||||
| chr2:148719961
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.314-23661G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719961 | ||||||
| chr2:148720135
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-23487G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720135 | ||||||
| chr2:148720282
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-23340C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720282 | ||||||
| chr2:148720420
|
T | C | 123 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(120): Show | 123 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.314-23202T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720420 | ||||||
| chr2:148720454
|
A | C | 123 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(120): Show | 123 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.314-23168A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720454 | ||||||
| chr2:148720454
|
A | G | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-23168A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720454 | ||||||
| chr2:148720462
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0110a0001c0001t0002g0132 | 3 | HG00741.hp1 HG01496.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.314-23160C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720462 | ||||||
| chr2:148720590
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.314-23032C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720590 | ||||||
| chr2:148720768
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.314-22854C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720768 | ||||||
| chr2:148720822
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0267 | 2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.314-22800A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720822 | ||||||
| chr2:148720899
|
C | G | 6 | a0001c0001t0002g0040a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG02132.hp2 NA18946.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-22723C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720899 | ||||||
| chr2:148720967
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.314-22655A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720967 | ||||||
| chr2:148721126
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-22496C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721126 | ||||||
| chr2:148721214
|
G | T | 1 | a0001c0001t0002g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.314-22408G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721214 | ||||||
| chr2:148721250
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-22372T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721250 | ||||||
| chr2:148721328
|
GT | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-22283delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721328 | |||||
| chr2:148721501
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-22121A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721501 | ||||||
| chr2:148721607
|
A | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-22015A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721607 | ||||||
| chr2:148721712
|
C | CT | 94 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(91): Show | 94 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.314-21893dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721712 | |||||
| chr2:148721712
|
CT | C | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG00639.hp2 HG01175.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-21893delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721712 | |||||
| chr2:148721712
|
CTT | C | 90 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(87): Show | 90 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.314-21894_314-2189 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721712 | |||||
| chr2:148721840
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314-21782A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721840 | ||||||
| chr2:148721890
|
C | CT | 32 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0161others(29): Show | 32 | HG00280.hp1 HG00639.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.314-21715dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721890
|
C | CTT | 86 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(83): Show | 86 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.314-21716_314-2171 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721890
|
C | CTTT | 102 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0140others(99): Show | 102 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.314-21717_314-2171 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721890
|
C | CTTTT | 16 | a0001c0001t0001g0256a0001c0001t0001g0294a0001c0001t0001g0300others(13): Show | 16 | HG00735.hp2 HG01106.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.314-21718_314-2171 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721890
|
C | CTTTTT | 18 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(15): Show | 18 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(15): Show |
intron_variant | MODIFIER | c.314-21719_314-2171 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721890
|
C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0032others(6): Show | 9 | HG02040.hp2 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-21722_314-2171 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721890
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.314-21724_314-2171 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | |||||
| chr2:148721891
|
T | TTTC | 10 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(7): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-21729_314-2172 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721891 | |||||
| chr2:148722024
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-21598C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722024 | ||||||
| chr2:148722118
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-21504C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722118 | ||||||
| chr2:148722146
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314-21476G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722146 | ||||||
| chr2:148722166
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-21456G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722166 | ||||||
| chr2:148722267
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.314-21355G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722267 | ||||||
| chr2:148722448
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-21174G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722448 | ||||||
| chr2:148722596
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-21026C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722596 | ||||||
| chr2:148722629
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-20993A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722629 | ||||||
| chr2:148722747
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-20875C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722747 | ||||||
| chr2:148722852
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-20770G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722852 | ||||||
| chr2:148722867
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.314-20755G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722867 | ||||||
| chr2:148723022
|
T | C | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.314-20600T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723022 | ||||||
| chr2:148723180
|
T | C | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0056 | 3 | HG01106.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.314-20442T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723180 | ||||||
| chr2:148723258
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-20364A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723258 | ||||||
| chr2:148723369
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-20253C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723369 | ||||||
| chr2:148723406
|
C | G | 1 | a0001c0001t0002g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.314-20216C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723406 | ||||||
| chr2:148723473
|
C | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-20149C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723473 | ||||||
| chr2:148723493
|
G | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-20129G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723493 | ||||||
| chr2:148723552
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.314-20070C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723552 | ||||||
| chr2:148723657
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-19965T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723657 | ||||||
| chr2:148723756
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-19866G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723756 | ||||||
| chr2:148723814
|
C | T | 4 | a0001c0005t0001g0187a0002c0002t0001g0254a0002c0002t0001g0308others(1): Show | 4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-19808C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723814 | ||||||
| chr2:148723885
|
T | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-19737T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723885 | ||||||
| chr2:148723906
|
T | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.314-19716T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723906 | ||||||
| chr2:148724074
|
G | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-19548G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724074 | ||||||
| chr2:148724101
|
T | TTATAATC others(7): Show |
1 | a0001c0001t0001g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.314-19508_314-1950 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148724101 | |||||
| chr2:148724192
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.314-19430G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724192 | ||||||
| chr2:148724236
|
A | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-19386A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724236 | ||||||
| chr2:148724342
|
G | A | 2 | a0001c0001t0001g0256a0001c0006t0001g0006 | 2 | HG00735.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.314-19280G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724342 | ||||||
| chr2:148724386
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-19236T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724386 | ||||||
| chr2:148724387
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.314-19235G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724387 | ||||||
| chr2:148724621
|
G | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.314-19001G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724621 | ||||||
| chr2:148724767
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.314-18855A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724767 | ||||||
| chr2:148724822
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-18800G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724822 | ||||||
| chr2:148724889
|
C | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-18733C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724889 | ||||||
| chr2:148724920
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314-18702A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724920 | ||||||
| chr2:148725040
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-18582G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725040 | ||||||
| chr2:148725096
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.314-18526C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725096 | ||||||
| chr2:148725293
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-18329G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725293 | ||||||
| chr2:148725615
|
C | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.314-18007C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725615 | ||||||
| chr2:148725764
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-17858C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725764 | ||||||
| chr2:148725884
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18941.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.314-17738A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725884 | ||||||
| chr2:148726098
|
C | A | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-17524C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726098 | ||||||
| chr2:148726136
|
T | G | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-17486T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726136 | ||||||
| chr2:148726187
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.314-17435A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726187 | ||||||
| chr2:148726269
|
G | A | 8 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0272others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-17353G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726269 | ||||||
| chr2:148726299
|
T | C | 1 | a0001c0001t0002g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.314-17323T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726299 | ||||||
| chr2:148726358
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-17264T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726358 | ||||||
| chr2:148726396
|
C | G | 111 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.314-17226C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726396 | ||||||
| chr2:148726556
|
T | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-17066T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726556 | ||||||
| chr2:148726765
|
G | GT | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(99): Show | 102 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.314-16843dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148726765 | |||||
| chr2:148726765
|
G | GTT | 6 | a0001c0001t0001g0168a0001c0001t0001g0201a0001c0001t0001g0217others(3): Show | 6 | HG02004.hp1 HG02647.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-16844_314-1684 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148726765 | |||||
| chr2:148726765
|
G | T | 2 | a0001c0001t0001g0241a0002c0002t0001g0308 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.314-16857G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726765 | ||||||
| chr2:148726767
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-16855T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726767 | ||||||
| chr2:148726841
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.314-16781A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726841 | ||||||
| chr2:148727165
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-16457C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727165 | ||||||
| chr2:148727196
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.314-16426C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727196 | ||||||
| chr2:148727212
|
G | C | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-16410G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727212 | ||||||
| chr2:148727370
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(163): Show | 166 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.314-16252A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727370 | ||||||
| chr2:148727471
|
T | C | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.314-16151T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727471 | ||||||
| chr2:148727546
|
G | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-16076G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727546 | ||||||
| chr2:148727580
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.314-16042G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727580 | ||||||
| chr2:148727706
|
G | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-15916G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727706 | ||||||
| chr2:148727792
|
T | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-15830T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727792 | ||||||
| chr2:148727879
|
T | A | 1 | a0001c0001t0001g0206 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.314-15743T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727879 | ||||||
| chr2:148727880
|
C | CA | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-15741dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148727880 | |||||
| chr2:148728104
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-15518C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728104 | ||||||
| chr2:148728244
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-15378A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728244 | ||||||
| chr2:148728301
|
TTTTG | T | 36 | a0001c0001t0001g0134a0001c0001t0001g0173a0001c0001t0001g0174others(33): Show | 36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.314-15305_314-1530 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728301 | |||||
| chr2:148728365
|
A | G | 15 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(12): Show | 15 | HG00673.hp2 HG02074.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-15257A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728365 | ||||||
| chr2:148728517
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-15105A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728517 | ||||||
| chr2:148728615
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-15007A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728615 | ||||||
| chr2:148728629
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.314-14993C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728629 | ||||||
| chr2:148728675
|
A | AGCCATGA others(2): Show |
95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-14945_314-1493 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728675 | |||||
| chr2:148728729
|
C | CT | 23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(20): Show | 23 | HG00673.hp2 HG02074.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.314-14879dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728729 | |||||
| chr2:148728743
|
TA | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0134a0001c0001t0001g0191others(11): Show | 14 | HG00558.hp2 HG01496.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-14872delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728743 | |||||
| chr2:148728744
|
A | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 278 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.314-14878A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728744 | ||||||
| chr2:148728745
|
A | T | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.314-14877A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728745 | ||||||
| chr2:148728754
|
C | T | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-14868C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728754 | ||||||
| chr2:148728815
|
G | A | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-14807G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728815 | ||||||
| chr2:148728894
|
T | C | 4 | a0001c0005t0001g0187a0002c0002t0001g0254a0002c0002t0001g0308others(1): Show | 4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-14728T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728894 | ||||||
| chr2:148728954
|
C | T | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-14668C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728954 | ||||||
| chr2:148728986
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.314-14636C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728986 | ||||||
| chr2:148728988
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.314-14634C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728988 | ||||||
| chr2:148728992
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-14630A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728992 | ||||||
| chr2:148729011
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.314-14611G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729011 | ||||||
| chr2:148729031
|
C | CA | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(75): Show | 78 | HG00642.hp1 HG00673.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.314-14565dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | |||||
| chr2:148729031
|
C | CAA | 27 | a0001c0001t0001g0168a0001c0001t0001g0183a0001c0001t0001g0188others(24): Show | 27 | HG00280.hp1 HG00609.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.314-14566_314-1456 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | |||||
| chr2:148729031
|
CA | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0179others(3): Show | 6 | HG01106.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-14565delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | |||||
| chr2:148729031
|
CAA | C | 16 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(13): Show | 16 | HG00544.hp2 HG00609.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.314-14566_314-1456 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | |||||
| chr2:148729031
|
CAAAAAA | C | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-14570_314-1456 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | |||||
| chr2:148729031
|
CAAAAAAA others(1): Show |
C | 93 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(90): Show | 93 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.314-14572_314-1456 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | |||||
| chr2:148729076
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-14546C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729076 | ||||||
| chr2:148729140
|
C | T | 3 | a0001c0001t0005g0010a0001c0001t0005g0216a0001c0001t0005g0228 | 3 | HG01943.hp2 HG02273.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.314-14482C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729140 | ||||||
| chr2:148729177
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-14445A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729177 | ||||||
| chr2:148729247
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.314-14375A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729247 | ||||||
| chr2:148729340
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.314-14282C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729340 | ||||||
| chr2:148729348
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-14274T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729348 | ||||||
| chr2:148729481
|
C | G | 1 | a0001c0001t0001g0289 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.314-14141C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729481 | ||||||
| chr2:148729621
|
C | T | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-14001C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729621 | ||||||
| chr2:148729641
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314-13981A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729641 | ||||||
| chr2:148729775
|
A | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-13847A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729775 | ||||||
| chr2:148730142
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314-13480A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730142 | ||||||
| chr2:148730268
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.314-13354T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730268 | ||||||
| chr2:148730363
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.314-13259G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730363 | ||||||
| chr2:148730420
|
A | C | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-13202A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730420 | ||||||
| chr2:148730650
|
G | C | 2 | a0002c0002t0001g0308a0002c0002t0007g0255 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.314-12972G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730650 | ||||||
| chr2:148730699
|
C | A | 4 | a0001c0001t0001g0168a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG01515.hp2 HG03831.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-12923C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730699 | ||||||
| chr2:148730741
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-12881G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730741 | ||||||
| chr2:148730749
|
T | G | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-12873T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730749 | ||||||
| chr2:148730801
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.314-12821A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730801 | ||||||
| chr2:148730809
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.314-12813C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730809 | ||||||
| chr2:148731036
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314-12586G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731036 | ||||||
| chr2:148731272
|
C | T | 12 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-12350C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731272 | ||||||
| chr2:148731319
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.314-12303C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731319 | ||||||
| chr2:148731521
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314-12101G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731521 | ||||||
| chr2:148731697
|
C | T | 2 | a0001c0001t0002g0064a0001c0001t0002g0065 | 2 | HG01884.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.314-11925C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731697 | ||||||
| chr2:148731717
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-11905C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731717 | ||||||
| chr2:148731985
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.314-11637T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731985 | ||||||
| chr2:148732027
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.314-11595G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732027 | ||||||
| chr2:148732030
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-11592A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732030 | ||||||
| chr2:148732131
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.314-11491G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732131 | ||||||
| chr2:148732133
|
A | G | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-11489A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732133 | ||||||
| chr2:148732253
|
C | T | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-11369C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732253 | ||||||
| chr2:148732381
|
C | CT | 13 | a0001c0001t0001g0135a0001c0001t0001g0155a0001c0001t0001g0195others(10): Show | 13 | HG00609.hp1 HG02071.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.314-11224dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732381 | |||||
| chr2:148732381
|
C | CTT | 90 | a0001c0001t0001g0251a0001c0001t0002g0036a0001c0001t0002g0037others(87): Show | 90 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.314-11225_314-1122 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732381 | |||||
| chr2:148732386
|
T | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.314-11236T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732386 | ||||||
| chr2:148732531
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-11091C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732531 | ||||||
| chr2:148732542
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-11080G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732542 | ||||||
| chr2:148732569
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.314-11053T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732569 | ||||||
| chr2:148732863
|
A | G | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-10759A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732863 | ||||||
| chr2:148732919
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.314-10703T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732919 | ||||||
| chr2:148732946
|
C | CT | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(117): Show | 120 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.314-10656dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732946 | |||||
| chr2:148732965
|
TTC | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0028others(8): Show | 11 | HG02040.hp2 HG02132.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-10656_314-1065 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732965 | ||||||
| chr2:148732966
|
TC | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(11): Show | 14 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-10654delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732966 | |||||
| chr2:148732967
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(275): Show | 278 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.314-10655C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732967 | ||||||
| chr2:148733032
|
CTTGAACT others(3): Show |
C | 1 | a0001c0001t0002g0100 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.314-10578_314-1056 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733032 | |||||
| chr2:148733074
|
G | GAAGATTT others(320): Show |
1 | a0001c0001t0002g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | |||||
| chr2:148733074
|
G | GAAGATTT others(320): Show |
1 | a0001c0001t0002g0092 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | |||||
| chr2:148733074
|
G | GAAGATTT others(320): Show |
1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | |||||
| chr2:148733074
|
G | GAAGATTT others(319): Show |
2 | a0001c0001t0002g0106a0001c0001t0003g0107 | 2 | NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.314-10532_314-1053 others(330): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | |||||
| chr2:148733074
|
G | GAAGATTT others(320): Show |
86 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(83): Show | 86 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | |||||
| chr2:148733148
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.314-10474C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733148 | ||||||
| chr2:148733153
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.314-10469G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733153 | ||||||
| chr2:148733164
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-10458A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733164 | ||||||
| chr2:148733186
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0197others(21): Show | 24 | HG01256.hp2 HG01433.hp1 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.314-10436T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733186 | ||||||
| chr2:148733240
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314-10382A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733240 | ||||||
| chr2:148733250
|
T | C | 4 | a0001c0001t0002g0051a0001c0001t0002g0060a0001c0001t0002g0088others(1): Show | 4 | HG03654.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-10372T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733250 | ||||||
| chr2:148733311
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-10311C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733311 | ||||||
| chr2:148733432
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.314-10190T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733432 | ||||||
| chr2:148733473
|
C | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-10149C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733473 | ||||||
| chr2:148733479
|
A | AT | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(23): Show | 26 | HG01123.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.314-10107dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATT | 13 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0144others(10): Show | 13 | HG00558.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.314-10108_314-1010 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTT | 6 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0141others(3): Show | 6 | HG02071.hp1 HG02080.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-10109_314-1010 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.314-10117_314-1010 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG00423.hp1 HG03195.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.314-10118_314-1010 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.314-10119_314-1010 others(17): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.314-10123_314-1010 others(21): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.314-10124_314-1010 others(22): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0217 | 2 | HG02922.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.314-10126_314-1010 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
AT | A | 16 | a0001c0001t0001g0027a0001c0001t0001g0170a0001c0001t0001g0173others(13): Show | 16 | HG00544.hp2 HG00639.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.314-10107delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATT | A | 26 | a0001c0001t0001g0133a0001c0001t0001g0169a0001c0001t0001g0171others(23): Show | 26 | HG00280.hp2 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.314-10108_314-1010 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTT | A | 37 | a0001c0001t0001g0168a0001c0001t0001g0201a0001c0001t0001g0203others(34): Show | 37 | HG00280.hp1 HG00609.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.314-10109_314-1010 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTT | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0202a0001c0001t0001g0210others(7): Show | 10 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-10110_314-1010 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTT | A | 15 | a0001c0001t0001g0234a0001c0001t0002g0060a0001c0001t0002g0064others(12): Show | 15 | HG02004.hp2 HG02027.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-10112_314-1010 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT | A | 54 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(51): Show | 54 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.314-10113_314-1010 others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(3): Show |
A | 18 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(15): Show | 18 | HG01884.hp1 HG02040.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.314-10116_314-1010 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(4): Show |
A | 14 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0035others(11): Show | 14 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-10117_314-1010 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0290a0001c0001t0001g0299 | 2 | NA18949.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.314-10118_314-1010 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(6): Show |
A | 15 | a0001c0001t0001g0016a0001c0001t0001g0186a0001c0001t0001g0257others(12): Show | 15 | HG00673.hp2 HG02074.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-10119_314-1010 others(17): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(7): Show |
A | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG02922.hp1 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-10120_314-1010 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.314-10121_314-1010 others(19): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(12): Show |
A | 3 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.314-10125_314-1010 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0002g0097 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.314-10126_314-1010 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733479
|
ATTTTTTT others(14): Show |
A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-10127_314-1010 others(25): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | |||||
| chr2:148733515
|
T | G | 1 | a0001c0001t0002g0119 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.314-10107T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733515 | ||||||
| chr2:148733613
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.314-10009T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733613 | ||||||
| chr2:148733680
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-9942G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733680 | ||||||
| chr2:148733754
|
T | G | 1 | a0001c0001t0001g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-9868T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733754 | ||||||
| chr2:148733866
|
G | A | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-9756G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733866 | ||||||
| chr2:148733893
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-9729G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733893 | ||||||
| chr2:148734013
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0236 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.314-9609C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734013 | ||||||
| chr2:148734014
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.314-9608A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734014 | ||||||
| chr2:148734043
|
A | G | 5 | a0001c0001t0003g0061a0001c0001t0003g0086a0001c0001t0003g0090others(2): Show | 5 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-9579A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734043 | ||||||
| chr2:148734561
|
G | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-9061G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734561 | ||||||
| chr2:148734648
|
T | C | 1 | a0001c0001t0002g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.314-8974T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734648 | ||||||
| chr2:148734803
|
C | CT | 96 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(93): Show | 96 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.314-8805dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148734803 | |||||
| chr2:148734803
|
CT | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0026others(11): Show | 14 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.314-8805delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148734803 | |||||
| chr2:148735125
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.314-8497T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735125 | ||||||
| chr2:148735170
|
A | G | 36 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(33): Show | 36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.314-8452A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735170 | ||||||
| chr2:148735307
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.314-8315C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735307 | ||||||
| chr2:148735391
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.314-8231C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735391 | ||||||
| chr2:148735471
|
C | G | 7 | a0001c0001t0002g0062a0001c0001t0002g0075a0001c0001t0002g0078others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-8151C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735471 | ||||||
| chr2:148735653
|
A | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.314-7969A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735653 | ||||||
| chr2:148735728
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.314-7894A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735728 | ||||||
| chr2:148735799
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.314-7823T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735799 | ||||||
| chr2:148735830
|
T | TATAAG | 111 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.314-7791_314-7787d others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148735830 | |||||
| chr2:148736059
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.314-7563G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736059 | ||||||
| chr2:148736578
|
T | C | 2 | a0001c0004t0001g0022a0001c0004t0001g0025 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.314-7044T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736578 | ||||||
| chr2:148736655
|
G | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.314-6967G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736655 | ||||||
| chr2:148736836
|
A | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-6786A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736836 | ||||||
| chr2:148736890
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-6732A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736890 | ||||||
| chr2:148736894
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-6728G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736894 | ||||||
| chr2:148736921
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.314-6701G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736921 | ||||||
| chr2:148736936
|
C | CA | 6 | a0001c0001t0001g0142a0001c0001t0001g0196a0001c0001t0001g0287others(3): Show | 6 | HG02922.hp1 HG03098.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-6670dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148736936 | |||||
| chr2:148736936
|
CA | C | 11 | a0001c0001t0001g0239a0001c0001t0002g0037a0001c0001t0002g0052others(8): Show | 11 | HG00280.hp2 HG00609.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-6670delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148736936 | |||||
| chr2:148736997
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-6625G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736997 | ||||||
| chr2:148737078
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-6544G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737078 | ||||||
| chr2:148737108
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.314-6514T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737108 | ||||||
| chr2:148737123
|
GT | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-6492delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148737123 | |||||
| chr2:148737174
|
C | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-6448C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737174 | ||||||
| chr2:148737209
|
A | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-6413A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737209 | ||||||
| chr2:148737291
|
C | T | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.314-6331C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737291 | ||||||
| chr2:148737368
|
G | T | 4 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6254G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737368 | ||||||
| chr2:148737369
|
A | ATATTCTA others(21): Show |
4 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6253_314-6252i others(30): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737369 | ||||||
| chr2:148737370
|
G | A | 4 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6252G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737370 | ||||||
| chr2:148737371
|
G | T | 4 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6251G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737371 | ||||||
| chr2:148737431
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-6191T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737431 | ||||||
| chr2:148737567
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.314-6055G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737567 | ||||||
| chr2:148737687
|
TA | T | 6 | a0001c0001t0004g0172a0001c0001t0004g0175a0001c0001t0004g0176others(3): Show | 6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-5933delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148737687 | |||||
| chr2:148737705
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.314-5917C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737705 | ||||||
| chr2:148737950
|
A | G | 12 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-5672A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737950 | ||||||
| chr2:148738041
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.314-5581A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738041 | ||||||
| chr2:148738084
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.314-5538C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738084 | ||||||
| chr2:148738123
|
A | AAAC | 98 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0041others(95): Show | 98 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.314-5478_314-5476d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148738123 | |||||
| chr2:148738149
|
A | T | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-5473A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738149 | ||||||
| chr2:148738284
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.314-5338T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738284 | ||||||
| chr2:148738528
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-5094T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738528 | ||||||
| chr2:148738609
|
T | C | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-5013T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738609 | ||||||
| chr2:148738913
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.314-4709C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738913 | ||||||
| chr2:148738920
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-4702G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738920 | ||||||
| chr2:148738941
|
C | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-4681C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738941 | ||||||
| chr2:148739138
|
G | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-4484G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739138 | ||||||
| chr2:148739358
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 279 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.314-4264C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739358 | ||||||
| chr2:148739589
|
T | C | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.314-4033T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739589 | ||||||
| chr2:148739750
|
G | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.314-3872G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739750 | ||||||
| chr2:148739813
|
C | T | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-3809C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739813 | ||||||
| chr2:148739830
|
C | CT | 7 | a0001c0001t0001g0251a0001c0001t0002g0036a0001c0001t0002g0046others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-3790dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | |||||
| chr2:148739830
|
C | CTT | 54 | a0001c0001t0002g0040a0001c0001t0002g0044a0001c0001t0002g0045others(51): Show | 54 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.314-3791_314-3790d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | |||||
| chr2:148739830
|
C | CTTT | 22 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0043others(19): Show | 22 | HG00642.hp2 HG00673.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.314-3790_314-3789i others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | |||||
| chr2:148739830
|
C | CTTTT | 6 | a0001c0001t0002g0073a0001c0001t0002g0097a0001c0001t0002g0098others(3): Show | 6 | HG00423.hp2 NA18985.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-3790_314-3789i others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | |||||
| chr2:148739830
|
CTTCTTTT others(2): Show |
C | 7 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG02132.hp1 HG02155.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-3789_314-3781d others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | |||||
| chr2:148739830
|
CTTCTTTT others(3): Show |
C | 2 | a0001c0001t0001g0032a0001c0001t0002g0094 | 2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.314-3789_314-3780d others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | |||||
| chr2:148739833
|
C | T | 90 | a0001c0001t0001g0251a0001c0001t0002g0036a0001c0001t0002g0037others(87): Show | 90 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.314-3789C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739833 | ||||||
| chr2:148739833
|
CT | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG00673.hp2 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-3764delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | |||||
| chr2:148739833
|
CTT | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(39): Show | 42 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.314-3765_314-3764d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | |||||
| chr2:148739833
|
CTTT | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0135others(117): Show | 120 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.314-3766_314-3764d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | |||||
| chr2:148739833
|
CTTTT | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01070.hp1 HG01515.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-3767_314-3764d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | |||||
| chr2:148739833
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0307others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-3772_314-3764d others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | |||||
| chr2:148739836
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-3786T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739836 | ||||||
| chr2:148739916
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.314-3706G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739916 | ||||||
| chr2:148740093
|
G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-3529G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740093 | ||||||
| chr2:148740241
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-3381T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740241 | ||||||
| chr2:148740342
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0236 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.314-3280G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740342 | ||||||
| chr2:148740531
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.314-3091T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740531 | ||||||
| chr2:148741053
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.314-2569T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741053 | ||||||
| chr2:148741433
|
C | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-2189C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741433 | ||||||
| chr2:148741499
|
G | A | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-2123G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741499 | ||||||
| chr2:148741552
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.314-2070A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741552 | ||||||
| chr2:148741653
|
A | G | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-1969A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741653 | ||||||
| chr2:148741745
|
T | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1877T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741745 | ||||||
| chr2:148741930
|
C | T | 2 | a0002c0002t0001g0308a0002c0002t0007g0255 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.314-1692C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741930 | ||||||
| chr2:148741991
|
A | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-1631A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741991 | ||||||
| chr2:148742149
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.314-1473A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742149 | ||||||
| chr2:148742348
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-1274G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742348 | ||||||
| chr2:148742474
|
GGT | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-1142_314-1141d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148742474 | |||||
| chr2:148742532
|
C | G | 13 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0154others(10): Show | 13 | HG02135.hp1 NA18747.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-1090C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742532 | ||||||
| chr2:148742567
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.314-1055G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742567 | ||||||
| chr2:148742707
|
A | G | 2 | a0001c0004t0001g0022a0001c0004t0001g0025 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.314-915A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742707 | ||||||
| chr2:148742736
|
G | A | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-886G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742736 | ||||||
| chr2:148742784
|
C | CA | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 137 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.314-822dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148742784 | |||||
| chr2:148742784
|
CA | C | 93 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(90): Show | 93 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.314-822delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148742784 | |||||
| chr2:148742844
|
A | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-778A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742844 | ||||||
| chr2:148743213
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-409A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743213 | ||||||
| chr2:148743246
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-376A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743246 | ||||||
| chr2:148743375
|
A | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.314-247A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743375 | ||||||
| chr2:148743434
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.314-188T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743434 | ||||||
| chr2:148743566
|
C | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-56C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743566 | ||||||
| chr2:148743861
|
A | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.459+94A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148743861 | ||||||
| chr2:148743981
|
A | T | 1 | a0001c0001t0002g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.459+214A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148743981 | ||||||
| chr2:148744279
|
C | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+512C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744279 | ||||||
| chr2:148744572
|
A | G | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+805A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744572 | ||||||
| chr2:148744587
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+820G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744587 | ||||||
| chr2:148744789
|
AATTGTTA others(5): Show |
A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.459+1026_459+1037d others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744789 | |||||
| chr2:148744813
|
T | TTAGAGA | 111 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.459+1051_459+1052i others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744813 | |||||
| chr2:148744844
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+1077T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744844 | ||||||
| chr2:148744873
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.459+1106A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744873 | ||||||
| chr2:148744977
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.459+1210G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744977 | ||||||
| chr2:148744989
|
G | GC | 64 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0129others(61): Show | 64 | HG00423.hp1 HG00558.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.459+1234dupC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | |||||
| chr2:148744989
|
G | GCC | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0135others(38): Show | 41 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.459+1233_459+1234d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | |||||
| chr2:148744989
|
G | GCCC | 32 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0154others(29): Show | 32 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.459+1232_459+1234d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | |||||
| chr2:148744989
|
G | GCCCC | 33 | a0001c0001t0001g0003a0001c0001t0001g0189a0001c0001t0001g0197others(30): Show | 33 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.459+1231_459+1234d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | |||||
| chr2:148744989
|
GC | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0029others(14): Show | 17 | HG00639.hp1 HG01123.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.459+1234delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | |||||
| chr2:148744994
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.459+1227C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744994 | ||||||
| chr2:148744997
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459+1230C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744997 | ||||||
| chr2:148745147
|
G | C | 6 | a0001c0001t0004g0172a0001c0001t0004g0175a0001c0001t0004g0176others(3): Show | 6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+1380G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745147 | ||||||
| chr2:148745150
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG02258.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.459+1383G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745150 | ||||||
| chr2:148745191
|
A | G | 105 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.459+1424A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745191 | ||||||
| chr2:148745193
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+1426C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745193 | ||||||
| chr2:148745202
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+1435C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745202 | ||||||
| chr2:148745288
|
A | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459+1521A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745288 | ||||||
| chr2:148745421
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.459+1654G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745421 | ||||||
| chr2:148745431
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(162): Show | 165 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.459+1664C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745431 | ||||||
| chr2:148745789
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+2022G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745789 | ||||||
| chr2:148745848
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG02027.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.459+2081C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745848 | ||||||
| chr2:148745862
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+2095C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745862 | ||||||
| chr2:148745925
|
C | G | 1 | a0001c0001t0001g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.459+2158C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745925 | ||||||
| chr2:148745928
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+2161T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745928 | ||||||
| chr2:148745943
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.459+2176A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745943 | ||||||
| chr2:148746033
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.459+2266A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746033 | ||||||
| chr2:148746193
|
G | A | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+2426G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746193 | ||||||
| chr2:148746226
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+2459C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746226 | ||||||
| chr2:148746431
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0249 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.459+2664T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746431 | ||||||
| chr2:148746441
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.459+2674G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746441 | ||||||
| chr2:148746541
|
G | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+2774G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746541 | ||||||
| chr2:148746780
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+3013G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746780 | ||||||
| chr2:148746822
|
T | TAC | 96 | a0001c0001t0001g0027a0001c0001t0001g0128a0001c0001t0001g0129others(93): Show | 96 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.459+3069_459+3070d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148746822 | |||||
| chr2:148747132
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.459+3365T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747132 | ||||||
| chr2:148747317
|
C | A | 5 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+3550C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747317 | ||||||
| chr2:148747344
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+3577C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747344 | ||||||
| chr2:148747363
|
C | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+3596C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747363 | ||||||
| chr2:148747568
|
T | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+3801T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747568 | ||||||
| chr2:148747573
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+3806T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747573 | ||||||
| chr2:148747587
|
C | T | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.459+3820C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747587 | ||||||
| chr2:148747591
|
A | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(162): Show | 165 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.459+3824A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747591 | ||||||
| chr2:148747599
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.459+3832C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747599 | ||||||
| chr2:148747810
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+4043C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747810 | ||||||
| chr2:148747811
|
A | G | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.459+4044A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747811 | ||||||
| chr2:148747919
|
G | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+4152G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747919 | ||||||
| chr2:148748219
|
G | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.459+4452G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748219 | ||||||
| chr2:148748434
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.459+4667G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748434 | ||||||
| chr2:148748484
|
T | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.459+4717T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748484 | ||||||
| chr2:148748609
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.459+4842A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748609 | ||||||
| chr2:148748730
|
CAA | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459+4965_459+4966d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148748730 | |||||
| chr2:148748741
|
C | G | 1 | a0001c0003t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.459+4974C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748741 | ||||||
| chr2:148748759
|
C | A | 1 | a0001c0001t0001g0265 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.459+4992C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748759 | ||||||
| chr2:148748851
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.460-5076A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748851 | ||||||
| chr2:148748914
|
G | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.460-5013G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748914 | ||||||
| chr2:148748973
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.460-4954G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748973 | ||||||
| chr2:148749026
|
T | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-4901T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749026 | ||||||
| chr2:148749223
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02155.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.460-4704T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749223 | ||||||
| chr2:148749472
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.460-4455A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749472 | ||||||
| chr2:148749479
|
G | GT | 14 | a0001c0001t0001g0135a0001c0001t0001g0145a0001c0001t0001g0148others(11): Show | 14 | HG02074.hp2 HG02080.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-4435dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749479 | |||||
| chr2:148749479
|
GT | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0030others(6): Show | 9 | HG00639.hp2 HG01981.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-4435delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749479 | |||||
| chr2:148749479
|
GTT | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0028others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-4436_460-4435d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749479 | |||||
| chr2:148749493
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.460-4434C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749493 | ||||||
| chr2:148749502
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460-4425G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749502 | ||||||
| chr2:148749625
|
G | C | 1 | a0001c0001t0002g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.460-4302G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749625 | ||||||
| chr2:148749649
|
T | A | 1 | a0001c0001t0002g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.460-4278T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749649 | ||||||
| chr2:148749811
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.460-4116G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749811 | ||||||
| chr2:148749828
|
TTA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-4097_460-4096d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749828 | |||||
| chr2:148749955
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.460-3972G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749955 | ||||||
| chr2:148750471
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-3456G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750471 | ||||||
| chr2:148750519
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.460-3408T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750519 | ||||||
| chr2:148750710
|
G | T | 1 | a0001c0001t0001g0278 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.460-3217G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750710 | ||||||
| chr2:148750899
|
G | A | 15 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(12): Show | 15 | HG00673.hp2 HG02074.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-3028G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750899 | ||||||
| chr2:148750976
|
A | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.460-2951A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750976 | ||||||
| chr2:148751245
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.460-2682G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751245 | ||||||
| chr2:148751528
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.460-2399T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751528 | ||||||
| chr2:148751695
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.460-2232G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751695 | ||||||
| chr2:148751763
|
A | G | 11 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-2164A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751763 | ||||||
| chr2:148751884
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-2043A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751884 | ||||||
| chr2:148752092
|
A | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.460-1835A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752092 | ||||||
| chr2:148752099
|
A | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1828A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752099 | ||||||
| chr2:148752163
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-1764A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752163 | ||||||
| chr2:148752384
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-1543G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752384 | ||||||
| chr2:148752416
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-1511C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752416 | ||||||
| chr2:148752418
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1509G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752418 | ||||||
| chr2:148752466
|
T | G | 1 | a0001c0001t0002g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.460-1461T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752466 | ||||||
| chr2:148752592
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.460-1335G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752592 | ||||||
| chr2:148752613
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.460-1314C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752613 | ||||||
| chr2:148752713
|
G | A | 40 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.460-1214G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752713 | ||||||
| chr2:148752733
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-1194A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752733 | ||||||
| chr2:148752909
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.460-1018C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752909 | ||||||
| chr2:148752943
|
T | G | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.460-984T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752943 | ||||||
| chr2:148753113
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.460-814T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753113 | ||||||
| chr2:148753310
|
A | G | 8 | a0001c0001t0001g0290a0001c0001t0001g0292a0001c0001t0001g0298others(5): Show | 8 | HG00673.hp2 NA18949.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-617A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753310 | ||||||
| chr2:148753497
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-430G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753497 | ||||||
| chr2:148753597
|
CAG | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.460-327_460-326del others(2): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148753597 | |||||
| chr2:148753749
|
A | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.460-178A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753749 | ||||||
| chr2:148754142
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.666+9C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754142 | ||||||
| chr2:148754201
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+68A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754201 | ||||||
| chr2:148754448
|
A | T | 111 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.666+315A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754448 | ||||||
| chr2:148754537
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.666+404G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754537 | ||||||
| chr2:148754844
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.666+711T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754844 | ||||||
| chr2:148754888
|
T | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.666+755T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754888 | ||||||
| chr2:148754932
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.666+799C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754932 | ||||||
| chr2:148755317
|
T | C | 98 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(95): Show | 98 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.666+1184T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755317 | ||||||
| chr2:148755510
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.666+1377C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755510 | ||||||
| chr2:148755601
|
T | G | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.666+1468T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755601 | ||||||
| chr2:148755674
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.666+1541A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755674 | ||||||
| chr2:148755761
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01891.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.666+1628C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755761 | ||||||
| chr2:148755910
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666+1777T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755910 | ||||||
| chr2:148755995
|
C | A | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666+1862C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755995 | ||||||
| chr2:148756317
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.666+2184A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756317 | ||||||
| chr2:148756466
|
T | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2333T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756466 | ||||||
| chr2:148756541
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.666+2408C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756541 | ||||||
| chr2:148756791
|
G | A | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.666+2658G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756791 | ||||||
| chr2:148756986
|
A | C | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.666+2853A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756986 | ||||||
| chr2:148757058
|
A | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2925A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757058 | ||||||
| chr2:148757077
|
T | A | 1 | a0001c0001t0002g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.666+2944T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757077 | ||||||
| chr2:148757136
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.666+3003G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757136 | ||||||
| chr2:148757147
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.666+3014C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757147 | ||||||
| chr2:148757239
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666+3106G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757239 | ||||||
| chr2:148757325
|
G | A | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.666+3192G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757325 | ||||||
| chr2:148757352
|
G | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+3219G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757352 | ||||||
| chr2:148757562
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.666+3429G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757562 | ||||||
| chr2:148757791
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.666+3658C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757791 | ||||||
| chr2:148757795
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.666+3662A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757795 | ||||||
| chr2:148757862
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.666+3729A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757862 | ||||||
| chr2:148757945
|
G | T | 1 | a0002c0002t0007g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.666+3812G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757945 | ||||||
| chr2:148757982
|
G | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.667-3800G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757982 | ||||||
| chr2:148758084
|
G | A | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.667-3698G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758084 | ||||||
| chr2:148758154
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.667-3628A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758154 | ||||||
| chr2:148758159
|
T | TGTGG | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-3607_667-3604d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 148758159 | |||||
| chr2:148758162
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.667-3620G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758162 | ||||||
| chr2:148758197
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.667-3585G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758197 | ||||||
| chr2:148758207
|
A | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.667-3575A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758207 | ||||||
| chr2:148758343
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.667-3439A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758343 | ||||||
| chr2:148758398
|
A | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 161 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.667-3384A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758398 | ||||||
| chr2:148758464
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.667-3318C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758464 | ||||||
| chr2:148758527
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-3255C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758527 | ||||||
| chr2:148758642
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-3140C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758642 | ||||||
| chr2:148759252
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-2530C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759252 | ||||||
| chr2:148759284
|
G | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.667-2498G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759284 | ||||||
| chr2:148759386
|
C | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0046a0001c0001t0002g0047 | 3 | HG01069.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.667-2396C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759386 | ||||||
| chr2:148759388
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.667-2394C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759388 | ||||||
| chr2:148759389
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-2393G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759389 | ||||||
| chr2:148759605
|
G | T | 1 | a0001c0001t0002g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.667-2177G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759605 | ||||||
| chr2:148759799
|
T | C | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.667-1983T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759799 | ||||||
| chr2:148759886
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-1896T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759886 | ||||||
| chr2:148759887
|
G | C | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-1895G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759887 | ||||||
| chr2:148759973
|
TGG | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-1808_667-1807d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759973 | ||||||
| chr2:148760072
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.667-1710A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760072 | ||||||
| chr2:148760123
|
A | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-1659A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760123 | ||||||
| chr2:148760171
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0219 | 2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.667-1611C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760171 | ||||||
| chr2:148760183
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-1599G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760183 | ||||||
| chr2:148760307
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA18960.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.667-1475C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760307 | ||||||
| chr2:148760318
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.667-1464C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760318 | ||||||
| chr2:148760371
|
C | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0153 | 3 | NA19005.hp2 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.667-1411C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760371 | ||||||
| chr2:148760483
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.667-1299G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760483 | ||||||
| chr2:148761232
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-550C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761232 | ||||||
| chr2:148761380
|
G | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.667-402G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761380 | ||||||
| chr2:148761392
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-390C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761392 | ||||||
| chr2:148761439
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667-343T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761439 | ||||||
| chr2:148761660
|
C | T | 1 | a0001c0005t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.667-122C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761660 | ||||||
| chr2:148761729
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.667-53G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761729 | ||||||
| chr2:148761998
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.815+68G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148761998 | ||||||
| chr2:148762089
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.815+159T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762089 | ||||||
| chr2:148762443
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-227G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762443 | ||||||
| chr2:148762490
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.816-180G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762490 | ||||||
| chr2:148762617
|
T | C | 40 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.816-53T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762617 | ||||||
| chr2:148762645
|
C | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(122): Show | 125 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.816-25C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762645 | ||||||
| chr2:148762911
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.948+109G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148762911 | ||||||
| chr2:148762969
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.948+167G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148762969 | ||||||
| chr2:148763313
|
T | G | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.948+511T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763313 | ||||||
| chr2:148763510
|
C | CT | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+711dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 148763510 | |||||
| chr2:148763528
|
T | A | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.948+726T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763528 | ||||||
| chr2:148763749
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.948+947C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763749 | ||||||
| chr2:148763811
|
A | G | 1 | a0001c0003t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.948+1009A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763811 | ||||||
| chr2:148764028
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.949-927A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764028 | ||||||
| chr2:148764280
|
C | T | 4 | a0001c0001t0001g0298a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | NA18959.hp2 NA18998.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-675C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764280 | ||||||
| chr2:148764292
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.949-663A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764292 | ||||||
| chr2:148764607
|
ATAG | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.949-346_949-344del others(3): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 148764607 | |||||
| chr2:148764721
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.949-234G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764721 | ||||||
| chr2:148764756
|
CA | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02258.hp2 HG02717.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.949-198delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764756 | ||||||
| chr2:148764794
|
A | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.949-161A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764794 | ||||||
| chr2:148764827
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.949-128C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764827 | ||||||
| chr2:148764828
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0204others(2): Show | 5 | NA18985.hp2 NA19006.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.949-127G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764828 | ||||||
| chr2:148765280
|
G | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140+134G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765280 | ||||||
| chr2:148765380
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1140+234T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765380 | ||||||
| chr2:148765493
|
G | T | 4 | a0001c0001t0001g0272a0001c0003t0001g0250a0001c0003t0001g0270others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+347G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765493 | ||||||
| chr2:148765798
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1140+652G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765798 | ||||||
| chr2:148765823
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.1140+677A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765823 | ||||||
| chr2:148765887
|
TC | T | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1140+742delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765887 | ||||||
| chr2:148765908
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+762C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765908 | ||||||
| chr2:148765918
|
C | T | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+772C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765918 | ||||||
| chr2:148765973
|
T | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1140+827T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765973 | ||||||
| chr2:148766078
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0166 | 2 | NA18941.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1140+932A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766078 | ||||||
| chr2:148766129
|
G | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140+983G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766129 | ||||||
| chr2:148766524
|
T | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1140+1378T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766524 | ||||||
| chr2:148766552
|
T | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140+1406T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766552 | ||||||
| chr2:148766610
|
A | G | 5 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+1464A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766610 | ||||||
| chr2:148766715
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1140+1569C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766715 | ||||||
| chr2:148766757
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1140+1611T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766757 | ||||||
| chr2:148766840
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1140+1694G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766840 | ||||||
| chr2:148766925
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1140+1779T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766925 | ||||||
| chr2:148766950
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(158): Show | 161 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1140+1804G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766950 | ||||||
| chr2:148766976
|
G | T | 1 | a0001c0005t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140+1830G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766976 | ||||||
| chr2:148767038
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1140+1892A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767038 | ||||||
| chr2:148767128
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+1982A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767128 | ||||||
| chr2:148767139
|
T | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.1140+1993T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767139 | ||||||
| chr2:148767197
|
CA | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 162 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1141-1936delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 148767197 | |||||
| chr2:148767197
|
CAA | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(26): Show | 29 | HG00673.hp2 HG02040.hp2 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1141-1937_1141-193 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 148767197 | |||||
| chr2:148767285
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1141-1866A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767285 | ||||||
| chr2:148767383
|
T | C | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1141-1768T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767383 | ||||||
| chr2:148767419
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1141-1732T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767419 | ||||||
| chr2:148767439
|
G | C | 10 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(7): Show | 10 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1141-1712G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767439 | ||||||
| chr2:148767461
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1141-1690C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767461 | ||||||
| chr2:148767592
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1141-1559C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767592 | ||||||
| chr2:148767658
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1141-1493A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767658 | ||||||
| chr2:148768320
|
C | G | 1 | a0002c0002t0007g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1141-831C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768320 | ||||||
| chr2:148768378
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-773C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768378 | ||||||
| chr2:148768426
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1141-725G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768426 | ||||||
| chr2:148768564
|
A | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1141-587A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768564 | ||||||
| chr2:148768645
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1141-506T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768645 | ||||||
| chr2:148768682
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1141-469T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768682 | ||||||
| chr2:148768892
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1141-259T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768892 | ||||||
| chr2:148768986
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1141-165A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768986 | ||||||
| chr2:148769759
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1230+519T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148769759 | ||||||
| chr2:148769895
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0108 | 2 | HG02523.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1230+655G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148769895 | ||||||
| chr2:148769960
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1230+720C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148769960 | ||||||
| chr2:148770293
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-499G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770293 | ||||||
| chr2:148770294
|
C | A | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-498C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770294 | ||||||
| chr2:148770305
|
G | A | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-487G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770305 | ||||||
| chr2:148770332
|
A | C | 1 | a0001c0001t0002g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1231-460A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770332 | ||||||
| chr2:148770395
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-397T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770395 | ||||||
| chr2:148770419
|
AATAT | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231-372_1231-369d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770419 | ||||||
| chr2:148770565
|
T | G | 2 | a0001c0004t0001g0022a0001c0004t0001g0025 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1231-227T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770565 | ||||||
| chr2:148770594
|
G | C | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-198G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770594 | ||||||
| chr2:148770608
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1231-184T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770608 | ||||||
| chr2:148770626
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1231-166T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770626 | ||||||
| chr2:148770651
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1231-141G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770651 | ||||||
| chr2:148771514
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.1720+127T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771514 | ||||||
| chr2:148771526
|
A | G | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1720+139A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771526 | ||||||
| chr2:148771618
|
TC | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+234delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148771618 | |||||
| chr2:148771643
|
C | T | 94 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(91): Show | 94 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1720+256C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771643 | ||||||
| chr2:148771802
|
A | AT | 113 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1720+430dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148771802 | |||||
| chr2:148771922
|
C | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1720+535C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771922 | ||||||
| chr2:148771925
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+538A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771925 | ||||||
| chr2:148772095
|
G | A | 5 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+708G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772095 | ||||||
| chr2:148772373
|
C | A | 13 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0154others(10): Show | 13 | HG02135.hp1 NA18747.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1720+986C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772373 | ||||||
| chr2:148772427
|
G | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(127): Show | 130 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1720+1040G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772427 | ||||||
| chr2:148772808
|
C | A | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1720+1421C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772808 | ||||||
| chr2:148772810
|
A | T | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1720+1423A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772810 | ||||||
| chr2:148772811
|
A | T | 1 | a0001c0001t0009g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1720+1424A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772811 | ||||||
| chr2:148773034
|
C | T | 16 | a0001c0001t0001g0197a0001c0001t0001g0201a0001c0001t0001g0202others(13): Show | 16 | HG01256.hp2 HG01433.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1720+1647C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773034 | ||||||
| chr2:148773092
|
T | C | 35 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(32): Show | 35 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1720+1705T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773092 | ||||||
| chr2:148773101
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1720+1714C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773101 | ||||||
| chr2:148773254
|
A | ATTTAT | 7 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+1871_1720+187 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148773254 | |||||
| chr2:148773271
|
A | AGGC | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720+1886_1720+188 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148773271 | |||||
| chr2:148773275
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+1888G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773275 | ||||||
| chr2:148773621
|
T | C | 1 | a0001c0001t0002g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1720+2234T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773621 | ||||||
| chr2:148773783
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1720+2396T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773783 | ||||||
| chr2:148774246
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1720+2859T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774246 | ||||||
| chr2:148774349
|
G | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | NA19064.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1720+2962G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774349 | ||||||
| chr2:148774438
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1720+3051G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774438 | ||||||
| chr2:148774614
|
A | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02145.hp2 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+3227A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774614 | ||||||
| chr2:148774616
|
A | T | 112 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1720+3229A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774616 | ||||||
| chr2:148774622
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(28): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(32): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(34): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(12): Show |
6 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0056others(3): Show | 6 | HG01106.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(14): Show |
31 | a0001c0001t0002g0043a0001c0001t0002g0052a0001c0001t0002g0055others(28): Show | 31 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(25): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(16): Show |
14 | a0001c0001t0002g0037a0001c0001t0002g0064a0001c0001t0002g0065others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(27): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(18): Show |
17 | a0001c0001t0002g0036a0001c0001t0002g0040a0001c0001t0002g0044others(14): Show | 17 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(29): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(20): Show |
9 | a0001c0001t0002g0048a0001c0001t0002g0059a0001c0001t0002g0062others(6): Show | 9 | HG00558.hp2 HG00673.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(31): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(22): Show |
5 | a0001c0001t0002g0057a0001c0001t0002g0101a0001c0001t0002g0115others(2): Show | 5 | NA18952.hp2 NA18959.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(33): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(24): Show |
3 | a0001c0001t0002g0049a0001c0001t0002g0074a0001c0001t0002g0116 | 3 | HG00423.hp2 HG01943.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(35): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(26): Show |
3 | a0001c0001t0002g0039a0001c0001t0002g0071a0001c0001t0002g0072 | 3 | NA18950.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(37): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTA others(30): Show |
1 | a0001c0001t0002g0118 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(41): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774622
|
T | TTATATTT others(12): Show |
4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | |||||
| chr2:148774623
|
T | TAA | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774623 | ||||||
| chr2:148774624
|
T | A | 100 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(97): Show | 100 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1720+3237T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774624 | ||||||
| chr2:148774624
|
T | TTA | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00673.hp2 HG02074.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1720+3253_1720+325 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774624 | |||||
| chr2:148774640
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1720+3254_1720+325 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774640 | |||||
| chr2:148774853
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3466C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774853 | ||||||
| chr2:148774903
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720+3516C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774903 | ||||||
| chr2:148774961
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1720+3574C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774961 | ||||||
| chr2:148774992
|
G | A | 15 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(12): Show | 15 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1720+3605G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774992 | ||||||
| chr2:148775006
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1720+3619G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775006 | ||||||
| chr2:148775088
|
CA | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.1720+3717delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775088 | |||||
| chr2:148775088
|
CAAA | C | 105 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1720+3715_1720+371 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775088 | |||||
| chr2:148775135
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1720+3748G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775135 | ||||||
| chr2:148775228
|
T | C | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(88): Show | 91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1720+3841T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775228 | ||||||
| chr2:148775340
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3953G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775340 | ||||||
| chr2:148775522
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1720+4135C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775522 | ||||||
| chr2:148775606
|
A | G | 9 | a0001c0001t0001g0188a0001c0001t0001g0195a0001c0001t0001g0232others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+4219A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775606 | ||||||
| chr2:148775650
|
T | TTTAAATA others(28): Show |
102 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(99): Show | 102 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1720+4281_1720+431 others(39): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775650 | |||||
| chr2:148775650
|
T | TTTAAATA others(63): Show |
1 | a0001c0001t0002g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1720+4315_1720+431 others(74): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775650 | |||||
| chr2:148775658
|
A | AAATTAAA others(13): Show |
1 | a0001c0001t0001g0195 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1720+4276_1720+429 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | |||||
| chr2:148775658
|
A | AAATTAAA others(18): Show |
165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 165 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.1720+4290_1720+431 others(29): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | |||||
| chr2:148775658
|
A | AAATTAAA others(53): Show |
1 | a0001c0001t0001g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1720+4315_1720+431 others(64): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | |||||
| chr2:148775658
|
A | AAATTAAA others(43): Show |
20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+4314_1720+431 others(54): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | |||||
| chr2:148775658
|
A | AAATTAAA others(18): Show |
1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1720+4279_1720+428 others(29): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | |||||
| chr2:148775658
|
A | AAATTAAA others(8): Show |
3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720+4279_1720+428 others(19): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | |||||
| chr2:148775700
|
A | ATT | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4314_1720+431 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775700 | |||||
| chr2:148775703
|
T | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4316T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775703 | ||||||
| chr2:148775704
|
C | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4317C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775704 | ||||||
| chr2:148775707
|
T | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4320T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775707 | ||||||
| chr2:148775714
|
TAA | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4332_1720+433 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775714 | |||||
| chr2:148775730
|
T | TTTATTAA others(8): Show |
1 | a0001c0001t0001g0136 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1720+4346_1720+434 others(19): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775730 | |||||
| chr2:148775749
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1720+4362T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775749 | ||||||
| chr2:148775775
|
C | CT | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 129 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.1720+4408dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | |||||
| chr2:148775775
|
C | CTT | 12 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(9): Show | 12 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1720+4407_1720+440 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | |||||
| chr2:148775775
|
C | CTTTTT | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1720+4404_1720+440 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | |||||
| chr2:148775775
|
CT | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0041others(11): Show | 14 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1720+4408delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | |||||
| chr2:148775804
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1720+4417G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775804 | ||||||
| chr2:148775831
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1720+4444A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775831 | ||||||
| chr2:148775840
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1720+4453C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775840 | ||||||
| chr2:148775851
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1720+4464C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775851 | ||||||
| chr2:148775878
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG01891.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1720+4491C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775878 | ||||||
| chr2:148775922
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1720+4535T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775922 | ||||||
| chr2:148775927
|
A | G | 4 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0103others(1): Show | 4 | HG02074.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+4540A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775927 | ||||||
| chr2:148775972
|
A | G | 11 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG00544.hp1 HG00558.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1720+4585A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775972 | ||||||
| chr2:148775982
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1720+4595T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775982 | ||||||
| chr2:148776014
|
C | G | 12 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1720+4627C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776014 | ||||||
| chr2:148776016
|
C | T | 11 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(8): Show | 11 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+4629C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776016 | ||||||
| chr2:148776137
|
G | GAT | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.1720+4750_1720+475 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776137 | ||||||
| chr2:148776195
|
A | C | 5 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4808A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776195 | ||||||
| chr2:148776195
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1720+4808A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776195 | ||||||
| chr2:148776336
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1720+4949A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776336 | ||||||
| chr2:148776531
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-5113T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776531 | ||||||
| chr2:148776833
|
A | G | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1721-4811A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776833 | ||||||
| chr2:148776846
|
G | GTCTC | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131 | 3 | HG00639.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1721-4790_1721-478 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776846 | |||||
| chr2:148776856
|
C | CTCTCTTT others(14): Show |
1 | a0001c0001t0001g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1721-4787_1721-478 others(25): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTCTCTTT others(15): Show |
1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1721-4787_1721-478 others(26): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTCTTTTT others(3): Show |
1 | a0001c0001t0002g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1721-4787_1721-478 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTTTTTTT | 7 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG02155.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-4772_1721-476 others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTTTTTTT others(2): Show |
50 | a0001c0001t0001g0035a0001c0001t0002g0037a0001c0001t0002g0039others(47): Show | 50 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1721-4774_1721-476 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTTTTTTT others(3): Show |
32 | a0001c0001t0001g0041a0001c0001t0002g0036a0001c0001t0002g0040others(29): Show | 32 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1721-4775_1721-476 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0048a0001c0001t0002g0060a0001c0001t0002g0066others(2): Show | 5 | HG01346.hp1 HG03942.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1721-4776_1721-476 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0050others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-4777_1721-476 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
CT | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0272a0001c0001t0001g0273others(14): Show | 17 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1721-4766delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
CTT | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01515.hp2 HG02451.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721-4767_1721-476 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776856
|
CTTT | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(144): Show | 147 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1721-4768_1721-476 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | |||||
| chr2:148776859
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1721-4785T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776859 | ||||||
| chr2:148776860
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1721-4784T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776860 | ||||||
| chr2:148777108
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1721-4536C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777108 | ||||||
| chr2:148777302
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1721-4342T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777302 | ||||||
| chr2:148777368
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1721-4276A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777368 | ||||||
| chr2:148777527
|
AT | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4116delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777527 | ||||||
| chr2:148777529
|
C | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4115C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777529 | ||||||
| chr2:148777530
|
T | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4114T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777530 | ||||||
| chr2:148777532
|
T | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4112T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777532 | ||||||
| chr2:148777533
|
G | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4111G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777533 | ||||||
| chr2:148777534
|
T | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4110T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777534 | ||||||
| chr2:148777535
|
T | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4109T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777535 | ||||||
| chr2:148777586
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1721-4058G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777586 | ||||||
| chr2:148777953
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1721-3691C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777953 | ||||||
| chr2:148778251
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1721-3393C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778251 | ||||||
| chr2:148778381
|
A | G | 5 | a0001c0001t0002g0040a0001c0001t0002g0076a0001c0001t0002g0077others(2): Show | 5 | HG02132.hp2 NA18946.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-3263A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778381 | ||||||
| chr2:148778535
|
G | GC | 13 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG02040.hp2 HG02071.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1721-3102dupC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148778535 | |||||
| chr2:148778543
|
G | A | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0003t0001g0250others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-3101G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778543 | ||||||
| chr2:148778683
|
G | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1721-2961G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778683 | ||||||
| chr2:148778705
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-2939T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778705 | ||||||
| chr2:148778784
|
T | C | 1 | a0001c0001t0008g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1721-2860T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778784 | ||||||
| chr2:148778869
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1721-2775G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778869 | ||||||
| chr2:148779141
|
C | CA | 95 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1721-2497dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148779141 | |||||
| chr2:148779208
|
G | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(104): Show | 107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1721-2436G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779208 | ||||||
| chr2:148779210
|
A | G | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1721-2434A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779210 | ||||||
| chr2:148779356
|
A | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1721-2288A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779356 | ||||||
| chr2:148779821
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1721-1823C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779821 | ||||||
| chr2:148779863
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1721-1781C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779863 | ||||||
| chr2:148779872
|
T | C | 1 | a0002c0002t0001g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1721-1772T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779872 | ||||||
| chr2:148779895
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.1721-1749G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779895 | ||||||
| chr2:148779951
|
T | A | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): Show | 20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.1721-1693T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779951 | ||||||
| chr2:148780415
|
T | A | 82 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(79): Show | 82 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1721-1229T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780415 | ||||||
| chr2:148780589
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1721-1055C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780589 | ||||||
| chr2:148780601
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1721-1043C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780601 | ||||||
| chr2:148780648
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1721-996C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780648 | ||||||
| chr2:148780849
|
A | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0153 | 3 | NA19005.hp2 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1721-795A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780849 | ||||||
| chr2:148781280
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1721-364T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781280 | ||||||
| chr2:148781485
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1721-159G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781485 | ||||||
| chr2:148781491
|
T | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0133others(109): Show | 112 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1721-153T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781491 | ||||||
| chr2:148781562
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1721-82A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781562 | ||||||
| chr2:148781862
|
G | C | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1857+82G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148781862 | ||||||
| chr2:148782018
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1857+238G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782018 | ||||||
| chr2:148782147
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1857+367T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782147 | ||||||
| chr2:148782256
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1857+476A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782256 | ||||||
| chr2:148782351
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1857+571A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782351 | ||||||
| chr2:148782398
|
A | T | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1857+618A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782398 | ||||||
| chr2:148782486
|
A | AT | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1857+706_1857+707i others(3): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782486 | ||||||
| chr2:148782488
|
G | GGACT | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1857+708_1857+709i others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782488 | ||||||
| chr2:148782543
|
AAAC | A | 86 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0039others(83): Show | 86 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1857+766_1857+768d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 148782543 | |||||
| chr2:148782544
|
AAC | A | 20 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 20 | HG00639.hp2 HG02040.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857+766_1857+767d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 148782544 | |||||
| chr2:148782602
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1857+822G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782602 | ||||||
| chr2:148782671
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1857+891G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782671 | ||||||
| chr2:148782692
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-905C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782692 | ||||||
| chr2:148782715
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1858-882A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782715 | ||||||
| chr2:148782761
|
T | TTTCTC | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.1858-834_1858-833i others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 148782761 | |||||
| chr2:148783067
|
G | T | 12 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1858-530G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148783067 | ||||||
| chr2:148783407
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1858-190T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148783407 | ||||||
| chr2:148783541
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1858-56T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148783541 | ||||||
| chr2:148783910
|
A | G | 3 | a0001c0001t0002g0068a0001c0001t0002g0110a0001c0001t0002g0122 | 3 | HG00280.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2017+154A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148783910 | ||||||
| chr2:148783975
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2017+219G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148783975 | ||||||
| chr2:148784250
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2018-418T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784250 | ||||||
| chr2:148784357
|
A | C | 72 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0040others(69): Show | 72 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2018-311A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784357 | ||||||
| chr2:148784410
|
A | G | 1 | a0001c0001t0002g0127 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2018-258A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784410 | ||||||
| chr2:148784490
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2018-178G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784490 | ||||||
| chr2:148785112
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2351+111A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785112 | ||||||
| chr2:148785298
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.2351+297A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785298 | ||||||
| chr2:148785314
|
T | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0226 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2351+313T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785314 | ||||||
| chr2:148785322
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2351+321C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785322 | ||||||
| chr2:148785389
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2351+388G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785389 | ||||||
| chr2:148785458
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2351+457G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785458 | ||||||
| chr2:148785463
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2351+462G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785463 | ||||||
| chr2:148785472
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2351+471C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785472 | ||||||
| chr2:148785669
|
A | G | 6 | a0001c0001t0004g0172a0001c0001t0004g0175a0001c0001t0004g0176others(3): Show | 6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2352-636A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785669 | ||||||
| chr2:148785774
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2352-531C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785774 | ||||||
| chr2:148785892
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2352-413G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785892 | ||||||
| chr2:148785977
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2352-328T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785977 | ||||||
| chr2:148785986
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2352-319A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785986 | ||||||
| chr2:148786136
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2352-169G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148786136 | ||||||
| chr2:148786149
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.2352-156T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148786149 |