Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9413 |
|---|---|
| ensemblid | ENSG00000135063.20 |
| hgncid | 24820 |
| symbol | ENTREP1 |
| name | endosomal transmembrane epsin interactor 1 |
| refseq_nuc | NM_001347995.2 |
| refseq_prot | NP_001334924.1 |
| ensembl_nuc | ENST00000303068.14 |
| ensembl_prot | ENSP00000304435.8 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 69325215 |
| end | 69392456 |
| strand | + |
| ver | v1.2 |
| region | chr9:69325215-69392456 |
| region5000 | chr9:69320215-69397456 |
| regionname0 | ENTREP1_chr9_69325215_69392456 |
| regionname5000 | ENTREP1_chr9_69320215_69397456 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 603 | 330 | 77 | 55 | 141 | 14 | 41 | 111 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0002 | 0/0 | 603 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0003 | 0/0 | 603 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0004 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0005 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0006 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0007 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1812 | 327 | 75 | 54 | 141 | 14 | 41 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0002 | 0/0 | 1812 | 6 | 5 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0003 | 0/0 | 1812 | 3 | 2 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0004 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0005 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0006 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0007 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0008 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| c0009 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 738 | 186 | 77 | 21 | 55 | 8 | 25 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0002 | 0/1 | 739 | 98 | 8 | 25 | 47 | 6 | 11 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0003 | 1/0 | 748 | 44 | 0 | 7 | 32 | 0 | 4 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0004 | 0/0 | 749 | 10 | 0 | 1 | 8 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0005 | 0/0 | 749 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0006 | 0/0 | 738 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0007 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| t0008 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1812 | 327 | 75 | 54 | 141 | 14 | 41 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0003 | 0/0 | 1812 | 3 | 2 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0002c0002 | 0/0 | 1812 | 6 | 5 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0003c0006 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0003c0008 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0004c0007 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0005c0009 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0006c0005 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0007c0004 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2549 | 171 | 66 | 19 | 54 | 8 | 24 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0002 | 0/1 | 2550 | 98 | 8 | 25 | 47 | 6 | 11 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0003 | 1/0 | 2559 | 44 | 0 | 7 | 32 | 0 | 4 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0004 | 0/0 | 2560 | 10 | 0 | 1 | 8 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0005 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0006 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0007 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0001t0008 | 0/0 | 2550 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0001c0003t0001 | 0/0 | 2549 | 3 | 2 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0002c0002t0001 | 0/0 | 2549 | 6 | 5 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0003c0006t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0003c0008t0001 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0004c0007t0001 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0005c0009t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0006c0005t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| a0007c0004t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | copy fasta | chr9 | 69320215 | 69397456 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0003c0006t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0003c0008t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0004c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0005c0009t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0006c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0007c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0199 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0288 | EUR | FIN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0271 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0181 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0318 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0317 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0101 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0268 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | CDX | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02886 | hp2 | a0007 | c0004 | t0001 | g0219 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03098 | hp1 | a0006 | c0005 | t0001 | g0222 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03516 | hp1 | a0003 | c0006 | t0001 | g0210 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03927 | hp2 | a0003 | c0008 | t0001 | g0278 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0126 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | CHB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18992 | hp1 | a0004 | c0007 | t0001 | g0028 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ASW | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA21309 | hp2 | a0005 | c0009 | t0001 | g0110 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0068 | REF | REF | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0264 | REF | REF | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69325403
|
G | A | 1 | a0007 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.94G>A | p.Ala32Thr | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 189/2559 | 94/1812 | 32/603 | chr9 | 69325403 | ||
| chr9:69325484
|
G | A | 2 | a0002a0006 | 7 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
missense_variant | MODERATE | c.175G>A | p.Ala59Thr | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 270/2559 | 175/1812 | 59/603 | chr9 | 69325484 | ||
| chr9:69377647
|
C | T | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.856C>T | p.His286Tyr | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/11 | 951/2559 | 856/1812 | 286/603 | chr9 | 69377647 | ||
| chr9:69384020
|
C | T | 2 | a0003a0006 | 3 | HG03098.hp1 HG03516.hp1 HG03927.hp2 |
missense_variant | MODERATE | c.1157C>T | p.Thr386Ile | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/11 | 1252/2559 | 1157/1812 | 386/603 | chr9 | 69384020 | ||
| chr9:69391650
|
C | T | 1 | a0004 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.1658C>T | p.Ser553Leu | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 1753/2559 | 1658/1812 | 553/603 | chr9 | 69391650 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69371606
|
T | C | 2 | a0003c0006a0006c0005 | 2 | HG03098.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.579T>C | p.Asp193Asp | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/11 | 674/2559 | 579/1812 | 193/603 | chr9 | 69371606 | ||
| chr9:69391687
|
C | T | 1 | a0001c0003 | 3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.1695C>T | p.Cys565Cys | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 1790/2559 | 1695/1812 | 565/603 | chr9 | 69391687 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69325273
|
GCCGGCCG others(3): Show |
G | 13 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
5_prime_UTR_variant | MODIFIER | c.-24_-15delGGCCGCAC others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 15 | INFO_REALIGN_3_PRIME | chr9 | 69325273 | ||||
| chr9:69325290
|
G | T | 1 | a0001c0001t0008 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 20 | chr9 | 69325290 | |||||
| chr9:69391887
|
C | CA | 4 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(1): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*91dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 92 | INFO_REALIGN_3_PRIME | chr9 | 69391887 | ||||
| chr9:69392248
|
G | A | 1 | a0001c0001t0005 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 444 | chr9 | 69392248 | |||||
| chr9:69392407
|
C | T | 1 | a0001c0001t0007 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 603 | chr9 | 69392407 | |||||
| chr9:69392416
|
C | A | 1 | a0001c0001t0006 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*612C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 612 | chr9 | 69392416 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69325730
|
A | G | 2 | a0001c0003t0001g0317a0001c0003t0001g0318 | 2 | HG01243.hp2 HG01891.hp1 |
splice_region_variant&intron_variant | LOW | c.414+7A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69325730 | ||||||
| chr9:69325875
|
C | T | 35 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0292others(32): Show | 37 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+152C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69325875 | ||||||
| chr9:69325923
|
CTGTT | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG00621.hp2 HG00673.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+201_414+204del others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69325923 | ||||||
| chr9:69325974
|
T | TAAAC | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.414+254_414+255ins others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69325974 | |||||
| chr9:69326040
|
A | C | 1 | a0001c0001t0003g0283 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.414+317A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326040 | ||||||
| chr9:69326041
|
T | A | 1 | a0001c0001t0003g0283 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.414+318T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326041 | ||||||
| chr9:69326051
|
T | C | 1 | a0001c0001t0003g0283 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.414+328T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326051 | ||||||
| chr9:69326097
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.414+374G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326097 | ||||||
| chr9:69326155
|
G | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(21): Show | 29 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.414+432G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326155 | ||||||
| chr9:69326163
|
A | G | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+440A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326163 | ||||||
| chr9:69326226
|
G | A | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+503G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326226 | ||||||
| chr9:69326301
|
C | A | 1 | a0002c0002t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.414+578C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326301 | ||||||
| chr9:69326342
|
G | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 26 | HG01123.hp1 HG01175.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+619G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326342 | ||||||
| chr9:69326572
|
G | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 37 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+849G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326572 | ||||||
| chr9:69326593
|
A | G | 4 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(1): Show | 4 | HG01243.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+870A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326593 | ||||||
| chr9:69326726
|
A | T | 1 | a0003c0006t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414+1003A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326726 | ||||||
| chr9:69326738
|
T | C | 1 | a0002c0002t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.414+1015T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326738 | ||||||
| chr9:69326826
|
A | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 37 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+1103A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326826 | ||||||
| chr9:69326826
|
AGT | A | 175 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(172): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.414+1107_414+1108d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69326826 | |||||
| chr9:69326841
|
G | A | 75 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0021others(72): Show | 79 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.414+1118G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326841 | ||||||
| chr9:69326922
|
G | T | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.414+1199G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326922 | ||||||
| chr9:69326978
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.414+1255G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326978 | ||||||
| chr9:69327010
|
GA | G | 258 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(255): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.414+1301delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327010 | |||||
| chr9:69327098
|
T | A | 1 | a0001c0001t0002g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414+1375T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327098 | ||||||
| chr9:69327099
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.414+1376C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327099 | ||||||
| chr9:69327176
|
G | A | 27 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0292others(24): Show | 29 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.414+1453G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327176 | ||||||
| chr9:69327370
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0220others(1): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+1647G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327370 | ||||||
| chr9:69327414
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.414+1691G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327414 | ||||||
| chr9:69327619
|
C | CAAAAG | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 70 | HG00597.hp2 HG01123.hp1 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.414+1911_414+1915d others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327619 | |||||
| chr9:69327634
|
G | GAAAAGA | 48 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(45): Show | 50 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.414+1915_414+1916i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327634 | |||||
| chr9:69327634
|
G | GAAAAGAA others(4): Show |
158 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(155): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.414+1915_414+1916i others(13): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327634 | |||||
| chr9:69327926
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0220others(1): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+2203C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327926 | ||||||
| chr9:69327929
|
T | TTAAC | 210 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(207): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.414+2209_414+2210i others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327929 | |||||
| chr9:69327988
|
A | G | 2 | a0001c0003t0001g0317a0001c0003t0001g0318 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.414+2265A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327988 | ||||||
| chr9:69328044
|
A | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+2321A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328044 | ||||||
| chr9:69328086
|
C | T | 210 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(207): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.414+2363C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328086 | ||||||
| chr9:69328227
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414+2504C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328227 | ||||||
| chr9:69328295
|
T | C | 1 | a0001c0001t0006g0126 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.414+2572T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328295 | ||||||
| chr9:69328455
|
C | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0220others(8): Show | 15 | HG01123.hp1 HG01175.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.414+2732C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328455 | ||||||
| chr9:69328546
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.414+2823G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328546 | ||||||
| chr9:69328635
|
C | A | 1 | a0003c0006t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414+2912C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328635 | ||||||
| chr9:69328661
|
T | TA | 162 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.414+2948dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69328661 | |||||
| chr9:69328831
|
A | G | 39 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(36): Show | 41 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.414+3108A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328831 | ||||||
| chr9:69328935
|
T | A | 1 | a0001c0001t0003g0236 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414+3212T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328935 | ||||||
| chr9:69329214
|
C | A | 1 | a0001c0001t0002g0062 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.414+3491C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329214 | ||||||
| chr9:69329351
|
A | G | 6 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(3): Show | 6 | HG01993.hp1 HG02071.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+3628A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329351 | ||||||
| chr9:69329378
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414+3655C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329378 | ||||||
| chr9:69329559
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0197a0001c0001t0002g0198others(1): Show | 5 | HG00140.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+3836C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329559 | ||||||
| chr9:69329763
|
G | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.414+4040G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329763 | ||||||
| chr9:69329800
|
G | A | 221 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.414+4077G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329800 | ||||||
| chr9:69329805
|
AGTTAACG others(27): Show |
A | 9 | a0001c0001t0001g0016a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+4089_414+4122d others(36): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69329805 | |||||
| chr9:69329812
|
G | T | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4089G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329812 | ||||||
| chr9:69329828
|
A | G | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4105A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329828 | ||||||
| chr9:69329832
|
GCGTTAA | G | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4110_414+4115d others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329832 | ||||||
| chr9:69329839
|
T | A | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4116T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329839 | ||||||
| chr9:69329846
|
T | G | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4123T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329846 | ||||||
| chr9:69329862
|
A | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+4139A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329862 | ||||||
| chr9:69329867
|
A | C | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4144A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329867 | ||||||
| chr9:69329872
|
ACTAGGTT others(4): Show |
A | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4150_414+4160d others(13): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329872 | ||||||
| chr9:69329885
|
GGGT | G | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4163_414+4165d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329885 | ||||||
| chr9:69329893
|
T | C | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4170T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329893 | ||||||
| chr9:69329893
|
TTAGATTC others(75): Show |
T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 66 | HG00597.hp2 HG01123.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.414+4349_414+4430d others(84): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69329893 | |||||
| chr9:69329941
|
TTAGATTC others(27): Show |
T | 212 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.414+4246_414+4279d others(36): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69329941 | |||||
| chr9:69329994
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 16 | HG00597.hp2 HG02132.hp1 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+4271G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329994 | ||||||
| chr9:69330084
|
A | G | 1 | a0001c0001t0003g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.414+4361A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330084 | ||||||
| chr9:69330198
|
G | C | 221 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.414+4475G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330198 | ||||||
| chr9:69330200
|
G | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 39 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.414+4477G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330200 | ||||||
| chr9:69330584
|
G | A | 1 | a0001c0001t0002g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.414+4861G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330584 | ||||||
| chr9:69330960
|
A | G | 232 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(229): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.414+5237A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330960 | ||||||
| chr9:69331004
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(2): Show | 5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-5209G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331004 | ||||||
| chr9:69331044
|
GT | G | 217 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.415-5161delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69331044 | |||||
| chr9:69331048
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.415-5165T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331048 | ||||||
| chr9:69331080
|
G | A | 217 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.415-5133G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331080 | ||||||
| chr9:69331083
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.415-5130A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331083 | ||||||
| chr9:69331109
|
T | A | 34 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0292others(31): Show | 36 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.415-5104T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331109 | ||||||
| chr9:69331247
|
G | A | 162 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.415-4966G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331247 | ||||||
| chr9:69331359
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.415-4854G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331359 | ||||||
| chr9:69331409
|
TC | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0220others(1): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-4801delC | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69331409 | |||||
| chr9:69331442
|
C | A | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.415-4771C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331442 | ||||||
| chr9:69331518
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.415-4695G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331518 | ||||||
| chr9:69331668
|
G | A | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | NA18970.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.415-4545G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331668 | ||||||
| chr9:69331815
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0002g0195 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-4398C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331815 | ||||||
| chr9:69332030
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.415-4183C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332030 | ||||||
| chr9:69332030
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.415-4183C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332030 | ||||||
| chr9:69332048
|
A | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-4165A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332048 | ||||||
| chr9:69332289
|
C | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0120a0001c0001t0001g0183others(13): Show | 17 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.415-3924C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332289 | ||||||
| chr9:69332345
|
G | A | 7 | a0001c0001t0002g0221a0002c0002t0001g0003a0002c0002t0001g0215others(4): Show | 9 | HG01123.hp1 HG01175.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-3868G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332345 | ||||||
| chr9:69332418
|
G | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-3795G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332418 | ||||||
| chr9:69332749
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.415-3464C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332749 | ||||||
| chr9:69332952
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.415-3261C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332952 | ||||||
| chr9:69333123
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.415-3090T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333123 | ||||||
| chr9:69333236
|
G | C | 1 | a0001c0001t0003g0239 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.415-2977G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333236 | ||||||
| chr9:69333313
|
T | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-2900T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333313 | ||||||
| chr9:69333317
|
T | A | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2896T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333317 | ||||||
| chr9:69333318
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-2895A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333318 | ||||||
| chr9:69333321
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.415-2892T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333321 | ||||||
| chr9:69333327
|
T | G | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2886T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333327 | ||||||
| chr9:69333350
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.415-2863G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333350 | ||||||
| chr9:69333468
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.415-2745C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333468 | ||||||
| chr9:69333630
|
T | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-2583T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333630 | ||||||
| chr9:69333694
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0220others(1): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-2519C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333694 | ||||||
| chr9:69333743
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.415-2470G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333743 | ||||||
| chr9:69333825
|
G | A | 34 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0292others(31): Show | 36 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.415-2388G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333825 | ||||||
| chr9:69333977
|
A | G | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2236A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333977 | ||||||
| chr9:69334189
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 40 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.415-2024A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334189 | ||||||
| chr9:69334195
|
G | A | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2018G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334195 | ||||||
| chr9:69334291
|
C | T | 221 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.415-1922C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334291 | ||||||
| chr9:69334417
|
A | T | 217 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.415-1796A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334417 | ||||||
| chr9:69334440
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.415-1773G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334440 | ||||||
| chr9:69334552
|
A | G | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.415-1661A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334552 | ||||||
| chr9:69334645
|
A | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1568A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334645 | ||||||
| chr9:69334659
|
T | A | 2 | a0001c0001t0001g0209a0003c0006t0001g0210 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.415-1554T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334659 | ||||||
| chr9:69334774
|
T | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1439T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334774 | ||||||
| chr9:69334775
|
C | CT | 11 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0205others(8): Show | 11 | HG02074.hp2 HG02258.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-1419dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | |||||
| chr9:69334775
|
CT | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(55): Show | 64 | HG00280.hp2 HG00597.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.415-1419delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | |||||
| chr9:69334775
|
CTT | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0040others(5): Show | 9 | HG01167.hp1 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-1420_415-1419d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | |||||
| chr9:69334775
|
CTTTT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1422_415-1419d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | |||||
| chr9:69334908
|
C | T | 1 | a0001c0001t0003g0275 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.415-1305C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334908 | ||||||
| chr9:69335011
|
C | T | 1 | a0001c0001t0004g0274 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.415-1202C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335011 | ||||||
| chr9:69335090
|
G | GT | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0220others(1): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-1117dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335090 | |||||
| chr9:69335373
|
G | T | 70 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0131others(67): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.415-840G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335373 | ||||||
| chr9:69335415
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0120others(13): Show | 17 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.415-798G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335415 | ||||||
| chr9:69335576
|
A | G | 180 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.415-637A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335576 | ||||||
| chr9:69335617
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.415-596A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335617 | ||||||
| chr9:69335638
|
G | A | 1 | a0001c0001t0004g0240 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415-575G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335638 | ||||||
| chr9:69335834
|
A | ATGCGCCT others(12): Show |
70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(67): Show | 75 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.415-363_415-345dup others(19): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335834 | |||||
| chr9:69335834
|
A | ATGCGCCT others(31): Show |
116 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.415-345_415-344ins others(38): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335834 | |||||
| chr9:69335834
|
A | ATGCGCCT others(69): Show |
1 | a0002c0002t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.415-345_415-344ins others(76): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335834 | |||||
| chr9:69335852
|
C | CGTGCGCC others(69): Show |
3 | a0002c0002t0001g0003a0002c0002t0001g0223a0002c0002t0001g0224 | 5 | HG02809.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-345_415-344ins others(76): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335852 | |||||
| chr9:69335857
|
G | GCCTGTAG others(31): Show |
2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | NA18971.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.415-345_415-344ins others(38): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335857 | |||||
| chr9:69335939
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0002g0195 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-274G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335939 | ||||||
| chr9:69335992
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.415-221A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335992 | ||||||
| chr9:69336537
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.471+268T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336537 | ||||||
| chr9:69336662
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+393C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336662 | ||||||
| chr9:69336889
|
G | A | 113 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(110): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.471+620G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336889 | ||||||
| chr9:69336931
|
C | T | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+662C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336931 | ||||||
| chr9:69336944
|
C | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.471+675C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336944 | ||||||
| chr9:69336981
|
A | G | 3 | a0001c0001t0001g0209a0003c0006t0001g0210a0006c0005t0001g0222 | 3 | HG01884.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.471+712A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336981 | ||||||
| chr9:69337005
|
C | CT | 10 | a0001c0001t0003g0208a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 10 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.471+765dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | |||||
| chr9:69337005
|
CTT | C | 10 | a0001c0001t0001g0056a0001c0001t0001g0094a0001c0001t0002g0062others(7): Show | 10 | HG01123.hp1 HG02723.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.471+764_471+765del others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | |||||
| chr9:69337005
|
CTTT | C | 95 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(92): Show | 99 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.471+763_471+765del others(3): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | |||||
| chr9:69337005
|
CTTTT | C | 152 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(149): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.471+762_471+765del others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | |||||
| chr9:69337023
|
T | G | 1 | a0001c0001t0003g0279 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.471+754T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337023 | ||||||
| chr9:69337251
|
G | T | 2 | a0001c0003t0001g0317a0001c0003t0001g0318 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.471+982G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337251 | ||||||
| chr9:69337398
|
A | G | 1 | a0001c0001t0003g0265 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.471+1129A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337398 | ||||||
| chr9:69337425
|
T | C | 1 | a0001c0001t0002g0287 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.471+1156T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337425 | ||||||
| chr9:69337528
|
A | G | 1 | a0001c0001t0002g0009 | 2 | HG00438.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.471+1259A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337528 | ||||||
| chr9:69337551
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.471+1282A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337551 | ||||||
| chr9:69337693
|
G | A | 317 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.471+1424G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337693 | ||||||
| chr9:69337775
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+1506T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337775 | ||||||
| chr9:69337904
|
T | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(2): Show | 5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+1635T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337904 | ||||||
| chr9:69337931
|
A | T | 4 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(1): Show | 4 | HG01243.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+1662A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337931 | ||||||
| chr9:69338210
|
A | AT | 5 | a0001c0001t0001g0016a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1942dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69338210 | |||||
| chr9:69338212
|
A | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1943A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338212 | ||||||
| chr9:69338214
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1945C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338214 | ||||||
| chr9:69338215
|
C | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1946C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338215 | ||||||
| chr9:69338279
|
A | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(71): Show | 79 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.471+2010A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338279 | ||||||
| chr9:69338476
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.471+2207T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338476 | ||||||
| chr9:69338587
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.471+2318C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338587 | ||||||
| chr9:69338703
|
A | G | 114 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(111): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.471+2434A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338703 | ||||||
| chr9:69338730
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0037others(11): Show | 16 | HG00423.hp2 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.471+2461A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338730 | ||||||
| chr9:69338732
|
G | A | 9 | a0001c0001t0002g0008a0001c0001t0002g0057a0001c0001t0002g0059others(6): Show | 10 | HG00099.hp2 HG01106.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+2463G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338732 | ||||||
| chr9:69338776
|
T | C | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+2507T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338776 | ||||||
| chr9:69338803
|
A | G | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.471+2534A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338803 | ||||||
| chr9:69339060
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0188a0001c0001t0001g0190others(2): Show | 6 | HG01496.hp2 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+2791C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339060 | ||||||
| chr9:69339144
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0003g0241others(1): Show | 4 | NA18942.hp1 NA18994.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+2875T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339144 | ||||||
| chr9:69339588
|
G | A | 9 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(6): Show | 11 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+3319G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339588 | ||||||
| chr9:69339698
|
A | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+3429A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339698 | ||||||
| chr9:69339743
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.471+3474C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339743 | ||||||
| chr9:69339769
|
C | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.471+3500C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339769 | ||||||
| chr9:69339942
|
A | C | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+3673A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339942 | ||||||
| chr9:69339961
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.471+3692A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339961 | ||||||
| chr9:69340259
|
G | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+3990G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340259 | ||||||
| chr9:69340282
|
C | G | 1 | a0001c0001t0002g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.471+4013C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340282 | ||||||
| chr9:69340334
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(2): Show | 5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+4065G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340334 | ||||||
| chr9:69340436
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0188a0001c0001t0001g0190others(2): Show | 6 | HG01496.hp2 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+4167C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340436 | ||||||
| chr9:69340475
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.471+4206T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340475 | ||||||
| chr9:69340585
|
G | T | 1 | a0001c0001t0002g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.471+4316G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340585 | ||||||
| chr9:69340595
|
A | ATGCGTGT others(3): Show |
1 | a0001c0001t0001g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+4329_471+4330i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340595 | |||||
| chr9:69340595
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.471+4326A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340595 | ||||||
| chr9:69340595
|
ATGCATGT others(35): Show |
A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4341_471+4382d others(44): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340595 | |||||
| chr9:69340598
|
CATGT | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 110 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.471+4330_471+4333d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340598 | ||||||
| chr9:69340599
|
A | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0225others(11): Show | 15 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+4330A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340599 | ||||||
| chr9:69340613
|
A | ATG | 15 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 15 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+4353_471+4354d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340613 | |||||
| chr9:69340625
|
A | ATGCATG | 7 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(4): Show | 7 | HG02074.hp2 HG02698.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+4358_471+4359i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340625 | |||||
| chr9:69340625
|
ATGTGTGT others(17): Show |
A | 2 | a0001c0001t0001g0005a0001c0001t0001g0053 | 3 | HG02809.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.471+4359_471+4382d others(26): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340625 | |||||
| chr9:69340627
|
G | GCA | 233 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(230): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.471+4358_471+4359i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340627 | ||||||
| chr9:69340628
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0192 | 2 | HG02818.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.471+4359T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340628 | ||||||
| chr9:69340629
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0192 | 2 | HG02818.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.471+4360G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340629 | ||||||
| chr9:69340636
|
C | CATGCATG others(3): Show |
1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4367_471+4368i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340636 | ||||||
| chr9:69340636
|
C | CATGTGTG others(1): Show |
7 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(4): Show | 7 | HG02074.hp2 HG02698.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+4367_471+4368i others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340636 | ||||||
| chr9:69340636
|
C | T | 235 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.471+4367C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340636 | ||||||
| chr9:69340637
|
G | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0039others(15): Show | 19 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+4368G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340637 | ||||||
| chr9:69340641
|
ATGTGTGT others(19): Show |
A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4387_471+4412d others(28): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340641 | |||||
| chr9:69340652
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4383C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340652 | ||||||
| chr9:69340653
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4384A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340653 | ||||||
| chr9:69340653
|
ATG | A | 14 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.471+4395_471+4396d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340653 | |||||
| chr9:69340654
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4385T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340654 | ||||||
| chr9:69340655
|
G | A | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4386G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340655 | ||||||
| chr9:69340655
|
G | GTGTGTGT others(3): Show |
16 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0055others(13): Show | 17 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.471+4394_471+4395i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340655 | |||||
| chr9:69340655
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0001g0015a0007c0004t0001g0219 | 3 | HG02886.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.471+4397_471+4398i others(14): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340655 | |||||
| chr9:69340664
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0111others(2): Show | 5 | HG02055.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4395T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340664 | ||||||
| chr9:69340665
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0111others(2): Show | 5 | HG02055.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4396G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340665 | ||||||
| chr9:69340666
|
C | CAT | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(85): Show | 94 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.471+4397_471+4398i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | ||||||
| chr9:69340666
|
C | CATGTGTG others(7): Show |
102 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(99): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.471+4397_471+4398i others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | ||||||
| chr9:69340666
|
C | CATGTGTG others(9): Show |
37 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0047others(34): Show | 39 | HG01074.hp1 HG01106.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.471+4397_471+4398i others(18): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | ||||||
| chr9:69340666
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0111others(2): Show | 5 | HG02055.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4397C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | ||||||
| chr9:69340667
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 15 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.471+4398G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340667 | ||||||
| chr9:69340668
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+4399T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340668 | ||||||
| chr9:69340677
|
GCA | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 13 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+4409_471+4410d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340677 | ||||||
| chr9:69340679
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0008g0101 | 3 | HG00099.hp2 HG01943.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.471+4412_471+4413i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340679 | |||||
| chr9:69340686
|
T | C | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+4417T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340686 | ||||||
| chr9:69340687
|
G | A | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+4418G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340687 | ||||||
| chr9:69340694
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.471+4425T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340694 | ||||||
| chr9:69340695
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 14 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.471+4426A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340695 | ||||||
| chr9:69340695
|
ATG | A | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+4436_471+4437d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340695 | |||||
| chr9:69340696
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4427T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340696 | ||||||
| chr9:69340697
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4428G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340697 | ||||||
| chr9:69340697
|
G | GTGTGTGT others(29): Show |
2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+4435_471+4436i others(38): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340697 | |||||
| chr9:69340700
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4431T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340700 | ||||||
| chr9:69340701
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4432G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340701 | ||||||
| chr9:69340702
|
T | TGTATGTG others(7): Show |
14 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0225others(11): Show | 15 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+4435_471+4436i others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340702 | |||||
| chr9:69340718
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.471+4449C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340718 | ||||||
| chr9:69340723
|
ATG | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0021others(63): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.471+4464_471+4465d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340723 | |||||
| chr9:69340733
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(172): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.471+4464G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340733 | ||||||
| chr9:69340733
|
GTA | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0233a0001c0001t0002g0234 | 4 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+4466_471+4467d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340733 | |||||
| chr9:69340735
|
A | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(172): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.471+4466A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340735 | ||||||
| chr9:69340737
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.471+4468G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340737 | ||||||
| chr9:69340747
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.471+4478T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340747 | ||||||
| chr9:69340747
|
TTGTG | T | 6 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0205others(3): Show | 6 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+4485_471+4488d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340747 | |||||
| chr9:69340749
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.471+4480G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340749 | ||||||
| chr9:69340758
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4489C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340758 | ||||||
| chr9:69340763
|
ATG | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(48): Show | 55 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.471+4506_471+4507d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340763 | |||||
| chr9:69340763
|
ATGTG | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+4504_471+4507d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340763 | |||||
| chr9:69340765
|
G | GTGTGTA | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0038others(16): Show | 21 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.471+4501_471+4502i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340765 | |||||
| chr9:69340765
|
G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0209a0001c0001t0001g0225a0001c0001t0002g0057others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4503_471+4504i others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340765 | |||||
| chr9:69340765
|
G | GTGTGTGT others(3): Show |
179 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(176): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.471+4505_471+4506i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340765 | |||||
| chr9:69340788
|
C | T | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(57): Show | 65 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.471+4519C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340788 | ||||||
| chr9:69340789
|
A | ATG | 177 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.471+4529_471+4530d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340789 | |||||
| chr9:69340797
|
GTGCA | G | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0225others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+4531_471+4534d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340797 | |||||
| chr9:69340801
|
A | G | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+4532A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340801 | ||||||
| chr9:69340804
|
T | C | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.471+4535T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340804 | ||||||
| chr9:69340805
|
G | A | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.471+4536G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340805 | ||||||
| chr9:69340805
|
G | GTGTGTGT others(3): Show |
49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0025others(46): Show | 53 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+4543_471+4544i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340805 | |||||
| chr9:69340806
|
T | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0225others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+4537T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340806 | ||||||
| chr9:69340807
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4538G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340807 | ||||||
| chr9:69340808
|
T | TGTGTGC | 9 | a0001c0001t0001g0016a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+4543_471+4544i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340808 | |||||
| chr9:69340813
|
A | G | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(65): Show | 73 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.471+4544A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340813 | ||||||
| chr9:69340813
|
ATG | A | 178 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(175): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.471+4558_471+4559d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340813 | |||||
| chr9:69340815
|
G | A | 1 | a0002c0002t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.471+4546G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340815 | ||||||
| chr9:69340963
|
G | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+4694G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340963 | ||||||
| chr9:69341450
|
T | C | 316 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.471+5181T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341450 | ||||||
| chr9:69341484
|
AT | A | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.471+5227delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69341484 | |||||
| chr9:69341793
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.471+5524A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341793 | ||||||
| chr9:69341909
|
A | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.471+5640A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341909 | ||||||
| chr9:69341970
|
A | C | 4 | a0002c0002t0001g0003a0002c0002t0001g0215a0002c0002t0001g0223others(1): Show | 6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+5701A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341970 | ||||||
| chr9:69342504
|
A | G | 4 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(1): Show | 4 | HG01243.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+6235A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342504 | ||||||
| chr9:69342556
|
A | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.471+6287A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342556 | ||||||
| chr9:69342710
|
G | A | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+6441G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342710 | ||||||
| chr9:69342735
|
T | C | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(312): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.471+6466T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342735 | ||||||
| chr9:69342887
|
T | G | 1 | a0001c0001t0003g0242 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.471+6618T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342887 | ||||||
| chr9:69343340
|
G | A | 2 | a0001c0003t0001g0317a0001c0003t0001g0318 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.471+7071G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343340 | ||||||
| chr9:69343437
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.471+7168G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343437 | ||||||
| chr9:69343448
|
G | T | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+7179G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343448 | ||||||
| chr9:69343807
|
GTTGGGAG others(4): Show |
G | 1 | a0001c0001t0003g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.471+7539_471+7549d others(13): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343807 | ||||||
| chr9:69343892
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+7623T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343892 | ||||||
| chr9:69344250
|
C | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+7981C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344250 | ||||||
| chr9:69344264
|
T | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0038others(15): Show | 20 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.471+7995T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344264 | ||||||
| chr9:69344307
|
A | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(2): Show | 5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+8038A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344307 | ||||||
| chr9:69344311
|
A | C | 51 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(48): Show | 53 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+8042A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344311 | ||||||
| chr9:69344340
|
C | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0038others(15): Show | 20 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.471+8071C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344340 | ||||||
| chr9:69344478
|
GT | G | 3 | a0001c0001t0001g0047a0001c0001t0002g0051a0001c0001t0002g0052 | 3 | HG02572.hp1 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.471+8212delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69344478 | |||||
| chr9:69344573
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.471+8304G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344573 | ||||||
| chr9:69344590
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.471+8321T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344590 | ||||||
| chr9:69344666
|
C | G | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+8397C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344666 | ||||||
| chr9:69344755
|
A | C | 1 | a0001c0001t0002g0170 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.471+8486A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344755 | ||||||
| chr9:69344862
|
T | G | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+8593T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344862 | ||||||
| chr9:69344951
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+8682G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344951 | ||||||
| chr9:69345036
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+8767T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345036 | ||||||
| chr9:69345049
|
A | T | 124 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.471+8780A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345049 | ||||||
| chr9:69345471
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.471+9202A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345471 | ||||||
| chr9:69345482
|
A | G | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(97): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.471+9213A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345482 | ||||||
| chr9:69345485
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.471+9216C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345485 | ||||||
| chr9:69345539
|
C | A | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+9270C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345539 | ||||||
| chr9:69346107
|
C | T | 4 | a0002c0002t0001g0003a0002c0002t0001g0215a0002c0002t0001g0223others(1): Show | 6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+9838C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346107 | ||||||
| chr9:69346344
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0002g0220 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.471+10075A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346344 | ||||||
| chr9:69346365
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.471+10096G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346365 | ||||||
| chr9:69346397
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.471+10128T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346397 | ||||||
| chr9:69346452
|
T | A | 22 | a0001c0001t0001g0131a0001c0001t0001g0140a0001c0001t0001g0142others(19): Show | 22 | HG00140.hp2 HG01261.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.471+10183T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346452 | ||||||
| chr9:69346604
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.471+10335C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346604 | ||||||
| chr9:69346612
|
T | A | 1 | a0001c0001t0002g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.471+10343T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346612 | ||||||
| chr9:69346679
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+10410C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346679 | ||||||
| chr9:69346816
|
C | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(2): Show | 5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+10547C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346816 | ||||||
| chr9:69346841
|
C | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.471+10572C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346841 | ||||||
| chr9:69346991
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.471+10722C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346991 | ||||||
| chr9:69346998
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.471+10729G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346998 | ||||||
| chr9:69347007
|
T | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+10738T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347007 | ||||||
| chr9:69347014
|
G | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+10745G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347014 | ||||||
| chr9:69347045
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.471+10776G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347045 | ||||||
| chr9:69347053
|
A | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+10784A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347053 | ||||||
| chr9:69347107
|
T | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 111 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.471+10838T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347107 | ||||||
| chr9:69347392
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+11123G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347392 | ||||||
| chr9:69347465
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+11196A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347465 | ||||||
| chr9:69347612
|
T | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 111 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.471+11343T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347612 | ||||||
| chr9:69347619
|
A | G | 1 | a0001c0001t0003g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.471+11350A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347619 | ||||||
| chr9:69347637
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.471+11368G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347637 | ||||||
| chr9:69347704
|
C | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+11435C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347704 | ||||||
| chr9:69347735
|
G | A | 14 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0225others(11): Show | 15 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+11466G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347735 | ||||||
| chr9:69347799
|
C | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+11530C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347799 | ||||||
| chr9:69347840
|
G | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 111 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.471+11571G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347840 | ||||||
| chr9:69348098
|
A | G | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+11829A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348098 | ||||||
| chr9:69348448
|
G | C | 6 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0313others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+12179G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348448 | ||||||
| chr9:69348476
|
A | G | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+12207A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348476 | ||||||
| chr9:69348509
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0002g0035 | 2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.471+12240C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348509 | ||||||
| chr9:69348566
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.471+12297A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348566 | ||||||
| chr9:69348738
|
T | A | 1 | a0001c0001t0002g0081 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.471+12469T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348738 | ||||||
| chr9:69348761
|
A | G | 270 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.471+12492A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348761 | ||||||
| chr9:69348953
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.471+12684G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348953 | ||||||
| chr9:69348955
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0053 | 3 | HG02809.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.471+12686G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348955 | ||||||
| chr9:69349085
|
G | C | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+12816G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349085 | ||||||
| chr9:69349099
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.471+12830G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349099 | ||||||
| chr9:69349184
|
C | CA | 11 | a0001c0001t0001g0098a0001c0001t0003g0235a0001c0001t0003g0242others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+12942dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | |||||
| chr9:69349184
|
CAAAAAA | C | 23 | a0001c0001t0001g0047a0001c0001t0001g0058a0001c0001t0001g0140others(20): Show | 23 | HG00280.hp2 HG01175.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.471+12937_471+1294 others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | |||||
| chr9:69349184
|
CAAAAAAA | C | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.471+12936_471+1294 others(11): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | |||||
| chr9:69349184
|
CAAAAAAA others(12): Show |
C | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+12924_471+1294 others(23): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | |||||
| chr9:69349191
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.471+12922A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349191 | ||||||
| chr9:69349511
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.471+13242T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349511 | ||||||
| chr9:69349536
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+13267T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349536 | ||||||
| chr9:69349721
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+13452C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349721 | ||||||
| chr9:69349722
|
G | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+13453G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349722 | ||||||
| chr9:69349784
|
C | T | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+13515C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349784 | ||||||
| chr9:69349797
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.471+13528A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349797 | ||||||
| chr9:69349856
|
T | C | 3 | a0001c0001t0002g0221a0001c0003t0001g0317a0003c0008t0001g0278 | 3 | HG01123.hp1 HG01891.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+13587T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349856 | ||||||
| chr9:69350138
|
A | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(46): Show | 53 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+13869A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350138 | ||||||
| chr9:69350167
|
C | T | 7 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(4): Show | 7 | HG02135.hp2 NA18939.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+13898C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350167 | ||||||
| chr9:69350181
|
A | C | 1 | a0001c0001t0002g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.471+13912A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350181 | ||||||
| chr9:69350307
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.471+14038C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350307 | ||||||
| chr9:69350335
|
T | TC | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+14066_471+1406 others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350335 | ||||||
| chr9:69350360
|
C | T | 1 | a0001c0001t0004g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.471+14091C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350360 | ||||||
| chr9:69350556
|
CTTAAA | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+14294_471+1429 others(9): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69350556 | |||||
| chr9:69350697
|
A | G | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+14428A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350697 | ||||||
| chr9:69350773
|
CA | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+14510delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69350773 | |||||
| chr9:69351060
|
T | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+14791T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351060 | ||||||
| chr9:69351088
|
C | T | 2 | a0001c0001t0002g0168a0001c0001t0002g0182 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.471+14819C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351088 | ||||||
| chr9:69351129
|
A | G | 5 | a0001c0001t0001g0299a0001c0001t0002g0018a0001c0001t0002g0286others(2): Show | 6 | NA18951.hp2 NA18978.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+14860A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351129 | ||||||
| chr9:69351388
|
T | TTGA | 16 | a0001c0001t0001g0131a0001c0001t0001g0205a0001c0001t0001g0206others(13): Show | 18 | HG01109.hp1 HG01175.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+15148_471+1515 others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | |||||
| chr9:69351388
|
T | TTGATGA | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0007c0004t0001g0219 | 5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+15145_471+1515 others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | |||||
| chr9:69351388
|
T | TTGATGAT others(5): Show |
6 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0002g0221others(3): Show | 6 | HG01123.hp1 HG01243.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+15139_471+1515 others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | |||||
| chr9:69351388
|
T | TTGATGAT others(8): Show |
9 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.471+15136_471+1515 others(19): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | |||||
| chr9:69351490
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.471+15221C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351490 | ||||||
| chr9:69351502
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.471+15233C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351502 | ||||||
| chr9:69351503
|
A | G | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+15234A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351503 | ||||||
| chr9:69351551
|
G | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+15282G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351551 | ||||||
| chr9:69351554
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.471+15285C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351554 | ||||||
| chr9:69351610
|
G | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+15341G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351610 | ||||||
| chr9:69351629
|
C | T | 1 | a0005c0009t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.471+15360C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351629 | ||||||
| chr9:69351666
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.471+15397C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351666 | ||||||
| chr9:69351679
|
T | G | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+15410T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351679 | ||||||
| chr9:69351981
|
T | C | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+15712T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351981 | ||||||
| chr9:69352082
|
T | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+15813T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352082 | ||||||
| chr9:69352178
|
A | G | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+15909A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352178 | ||||||
| chr9:69352293
|
AT | A | 7 | a0001c0001t0001g0056a0001c0001t0001g0094a0001c0001t0001g0300others(4): Show | 7 | HG01943.hp2 NA18966.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+16029delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69352293 | |||||
| chr9:69352421
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+16152G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352421 | ||||||
| chr9:69352437
|
A | G | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+16168A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352437 | ||||||
| chr9:69352448
|
T | A | 1 | a0001c0001t0003g0277 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.471+16179T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352448 | ||||||
| chr9:69352544
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0001g0143others(2): Show | 6 | HG01123.hp2 HG01255.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+16275C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352544 | ||||||
| chr9:69352554
|
C | T | 9 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(6): Show | 11 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+16285C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352554 | ||||||
| chr9:69352571
|
A | G | 5 | a0001c0001t0003g0242a0001c0001t0003g0260a0001c0001t0003g0262others(2): Show | 5 | HG00438.hp2 HG00621.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+16302A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352571 | ||||||
| chr9:69352609
|
G | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.471+16340G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352609 | ||||||
| chr9:69352966
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.471+16697A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352966 | ||||||
| chr9:69352998
|
A | G | 1 | a0001c0001t0003g0282 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+16729A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352998 | ||||||
| chr9:69353008
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.471+16739A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353008 | ||||||
| chr9:69353027
|
T | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+16758T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353027 | ||||||
| chr9:69353032
|
G | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0002g0121others(2): Show | 5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+16763G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353032 | ||||||
| chr9:69353082
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.471+16813A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353082 | ||||||
| chr9:69353086
|
G | A | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+16817G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353086 | ||||||
| chr9:69353091
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.471+16822C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353091 | ||||||
| chr9:69353135
|
T | C | 1 | a0001c0001t0003g0247 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.471+16866T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353135 | ||||||
| chr9:69353285
|
C | T | 1 | a0001c0001t0004g0246 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.471+17016C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353285 | ||||||
| chr9:69353310
|
G | A | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.471+17041G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353310 | ||||||
| chr9:69353418
|
A | G | 3 | a0001c0001t0001g0047a0001c0001t0002g0051a0001c0001t0002g0052 | 3 | HG02572.hp1 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.471+17149A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353418 | ||||||
| chr9:69353595
|
C | T | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.471+17326C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353595 | ||||||
| chr9:69353688
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.471+17419G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353688 | ||||||
| chr9:69353739
|
A | G | 270 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.471+17470A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353739 | ||||||
| chr9:69353814
|
A | G | 123 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(120): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.471+17545A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353814 | ||||||
| chr9:69353867
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.471+17598T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353867 | ||||||
| chr9:69353909
|
C | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.472-17590C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353909 | ||||||
| chr9:69353968
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.472-17531A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353968 | ||||||
| chr9:69354030
|
T | G | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-17469T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354030 | ||||||
| chr9:69354098
|
T | G | 1 | a0001c0001t0003g0283 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.472-17401T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354098 | ||||||
| chr9:69354137
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.472-17362C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354137 | ||||||
| chr9:69354254
|
A | AT | 7 | a0001c0001t0001g0060a0001c0001t0001g0214a0001c0001t0001g0294others(4): Show | 7 | HG02451.hp2 HG03490.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-17225dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354254
|
A | ATT | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 106 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.472-17226_472-1722 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354254
|
A | ATTT | 40 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0034others(37): Show | 46 | HG00140.hp1 HG01109.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.472-17227_472-1722 others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354254
|
A | ATTTT | 90 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(87): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.472-17228_472-1722 others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354254
|
A | ATTTTT | 14 | a0001c0001t0001g0055a0001c0001t0001g0063a0001c0001t0001g0163others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-17229_472-1722 others(9): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354254
|
AT | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0038others(1): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-17225delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354254
|
ATT | A | 13 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.472-17226_472-1722 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | |||||
| chr9:69354566
|
T | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.472-16933T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354566 | ||||||
| chr9:69354650
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0002g0293 | 2 | NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.472-16849C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354650 | ||||||
| chr9:69354801
|
A | G | 2 | a0001c0001t0002g0221a0003c0008t0001g0278 | 2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.472-16698A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354801 | ||||||
| chr9:69354929
|
T | G | 2 | a0001c0001t0001g0091a0001c0001t0002g0002 | 4 | HG01346.hp2 HG01952.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-16570T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354929 | ||||||
| chr9:69355004
|
T | G | 1 | a0001c0001t0002g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.472-16495T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355004 | ||||||
| chr9:69355066
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.472-16433T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355066 | ||||||
| chr9:69355089
|
A | G | 3 | a0001c0001t0001g0226a0001c0003t0001g0317a0001c0003t0001g0318 | 3 | HG01243.hp2 HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.472-16410A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355089 | ||||||
| chr9:69355164
|
A | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.472-16335A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355164 | ||||||
| chr9:69355224
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.472-16275C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355224 | ||||||
| chr9:69355233
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.472-16266T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355233 | ||||||
| chr9:69355526
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0225 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.472-15973G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355526 | ||||||
| chr9:69355546
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.472-15953G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355546 | ||||||
| chr9:69355746
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0029 | 2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.472-15753G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355746 | ||||||
| chr9:69355830
|
G | A | 8 | a0001c0001t0002g0008a0001c0001t0002g0057a0001c0001t0002g0059others(5): Show | 9 | HG00280.hp2 HG01106.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.472-15669G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355830 | ||||||
| chr9:69355835
|
C | T | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-15664C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355835 | ||||||
| chr9:69355850
|
T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0084 | 2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.472-15649T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355850 | ||||||
| chr9:69355885
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.472-15614T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355885 | ||||||
| chr9:69355918
|
T | C | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-15581T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355918 | ||||||
| chr9:69356041
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.472-15458G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356041 | ||||||
| chr9:69356052
|
G | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(184): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.472-15447G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356052 | ||||||
| chr9:69356087
|
T | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 31 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.472-15412T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356087 | ||||||
| chr9:69356099
|
G | A | 12 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211others(9): Show | 14 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-15400G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356099 | ||||||
| chr9:69356290
|
C | T | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-15209C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356290 | ||||||
| chr9:69356348
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.472-15151A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356348 | ||||||
| chr9:69356494
|
C | CAT | 237 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.472-15004_472-1500 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69356494 | |||||
| chr9:69356734
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.472-14765G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356734 | ||||||
| chr9:69356885
|
T | G | 4 | a0002c0002t0001g0003a0002c0002t0001g0215a0002c0002t0001g0223others(1): Show | 6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-14614T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356885 | ||||||
| chr9:69357095
|
C | CA | 9 | a0001c0001t0001g0094a0001c0001t0001g0302a0001c0001t0001g0311others(6): Show | 9 | HG00621.hp1 HG02300.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-14382dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | |||||
| chr9:69357095
|
CA | C | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(169): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.472-14382delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | |||||
| chr9:69357095
|
CAA | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(12): Show | 17 | HG01167.hp2 HG01243.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.472-14383_472-1438 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | |||||
| chr9:69357095
|
CAAA | C | 11 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(8): Show | 13 | HG01175.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.472-14384_472-1438 others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | |||||
| chr9:69357473
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.472-14026A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357473 | ||||||
| chr9:69357586
|
T | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0032others(42): Show | 49 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.472-13913T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357586 | ||||||
| chr9:69357687
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.472-13812A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357687 | ||||||
| chr9:69357911
|
C | A | 1 | a0001c0001t0003g0266 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.472-13588C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357911 | ||||||
| chr9:69358015
|
T | G | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.472-13484T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358015 | ||||||
| chr9:69358081
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.472-13418A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358081 | ||||||
| chr9:69358149
|
C | A | 1 | a0001c0001t0001g0314 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.472-13350C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358149 | ||||||
| chr9:69358287
|
T | C | 32 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0033others(29): Show | 34 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.472-13212T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358287 | ||||||
| chr9:69358365
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.472-13134T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358365 | ||||||
| chr9:69358510
|
C | A | 1 | a0001c0001t0002g0175 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.472-12989C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358510 | ||||||
| chr9:69358519
|
G | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-12980G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358519 | ||||||
| chr9:69358535
|
G | A | 4 | a0002c0002t0001g0003a0002c0002t0001g0215a0002c0002t0001g0223others(1): Show | 6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-12964G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358535 | ||||||
| chr9:69358601
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0053others(7): Show | 11 | HG01255.hp2 HG02055.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.472-12898A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358601 | ||||||
| chr9:69358621
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.472-12878G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358621 | ||||||
| chr9:69358749
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0064others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-12750A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358749 | ||||||
| chr9:69358750
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.472-12749C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358750 | ||||||
| chr9:69358828
|
G | T | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-12671G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358828 | ||||||
| chr9:69358884
|
T | A | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(109): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.472-12615T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358884 | ||||||
| chr9:69358902
|
CT | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0164a0001c0001t0001g0233others(3): Show | 6 | HG01256.hp1 HG02738.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-12578delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69358902 | |||||
| chr9:69358902
|
CTT | C | 239 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.472-12579_472-1257 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69358902 | |||||
| chr9:69358909
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.472-12590T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358909 | ||||||
| chr9:69358925
|
A | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-12574A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358925 | ||||||
| chr9:69359048
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.472-12451G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359048 | ||||||
| chr9:69359051
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-12448G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359051 | ||||||
| chr9:69359061
|
G | A | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(109): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.472-12438G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359061 | ||||||
| chr9:69359146
|
C | G | 1 | a0001c0001t0003g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472-12353C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359146 | ||||||
| chr9:69359153
|
G | A | 1 | a0001c0001t0003g0237 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.472-12346G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359153 | ||||||
| chr9:69359185
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472-12314C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359185 | ||||||
| chr9:69359428
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472-12071A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359428 | ||||||
| chr9:69359525
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 31 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.472-11974A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359525 | ||||||
| chr9:69359553
|
G | T | 1 | a0001c0003t0001g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.472-11946G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359553 | ||||||
| chr9:69359784
|
T | G | 246 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.472-11715T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359784 | ||||||
| chr9:69359970
|
C | CT | 6 | a0001c0001t0001g0056a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 6 | HG00597.hp1 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-11514dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69359970 | |||||
| chr9:69360115
|
A | C | 95 | a0001c0001t0001g0091a0001c0001t0002g0002a0001c0001t0002g0007others(92): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.472-11384A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360115 | ||||||
| chr9:69360395
|
A | G | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-11104A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360395 | ||||||
| chr9:69360480
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.472-11019T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360480 | ||||||
| chr9:69360557
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0191 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.472-10942G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360557 | ||||||
| chr9:69360640
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.472-10859A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360640 | ||||||
| chr9:69360682
|
T | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(311): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.472-10817T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360682 | ||||||
| chr9:69360819
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.472-10680T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360819 | ||||||
| chr9:69360898
|
CA | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.472-10590delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69360898 | |||||
| chr9:69360963
|
G | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-10536G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360963 | ||||||
| chr9:69360994
|
T | A | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-10505T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360994 | ||||||
| chr9:69361100
|
GA | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-10397delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69361100 | |||||
| chr9:69361163
|
G | A | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.472-10336G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361163 | ||||||
| chr9:69361255
|
G | A | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(109): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.472-10244G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361255 | ||||||
| chr9:69361282
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18944.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.472-10217T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361282 | ||||||
| chr9:69361418
|
T | C | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(109): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.472-10081T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361418 | ||||||
| chr9:69361600
|
T | A | 1 | a0001c0001t0003g0252 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.472-9899T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361600 | ||||||
| chr9:69361787
|
T | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0003g0255 | 3 | HG03927.hp1 NA18981.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.472-9712T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361787 | ||||||
| chr9:69361802
|
G | T | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | NA18978.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.472-9697G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361802 | ||||||
| chr9:69362044
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.472-9455A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362044 | ||||||
| chr9:69362143
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-9356C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362143 | ||||||
| chr9:69362269
|
A | G | 3 | a0001c0003t0001g0049a0001c0003t0001g0317a0001c0003t0001g0318 | 3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.472-9230A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362269 | ||||||
| chr9:69362487
|
G | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0190others(6): Show | 11 | HG01496.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.472-9012G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362487 | ||||||
| chr9:69362564
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 31 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.472-8935A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362564 | ||||||
| chr9:69362575
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(311): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.472-8924A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362575 | ||||||
| chr9:69362618
|
G | A | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-8881G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362618 | ||||||
| chr9:69362681
|
G | T | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-8818G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362681 | ||||||
| chr9:69362713
|
G | A | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(109): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.472-8786G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362713 | ||||||
| chr9:69362873
|
C | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(82): Show | 90 | HG00423.hp2 HG00642.hp2 HG01123.hp2 others(87): Show |
intron_variant | MODIFIER | c.472-8626C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362873 | ||||||
| chr9:69363042
|
A | G | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-8457A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363042 | ||||||
| chr9:69363062
|
A | T | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-8437A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363062 | ||||||
| chr9:69363088
|
T | G | 95 | a0001c0001t0001g0091a0001c0001t0002g0002a0001c0001t0002g0007others(92): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.472-8411T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363088 | ||||||
| chr9:69363146
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.472-8353A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363146 | ||||||
| chr9:69363395
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0027others(9): Show | 13 | NA18944.hp2 NA18960.hp1 NA18964.hp1 others(10): Show |
intron_variant | MODIFIER | c.472-8104A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363395 | ||||||
| chr9:69363439
|
A | T | 1 | a0001c0001t0003g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472-8060A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363439 | ||||||
| chr9:69363550
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0225 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.472-7949C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363550 | ||||||
| chr9:69363680
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.472-7819G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363680 | ||||||
| chr9:69363921
|
T | C | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-7578T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363921 | ||||||
| chr9:69363932
|
A | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-7567A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363932 | ||||||
| chr9:69364124
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.472-7375A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364124 | ||||||
| chr9:69364379
|
C | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.472-7120C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364379 | ||||||
| chr9:69364389
|
A | AT | 110 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(107): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.472-7097dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69364389 | |||||
| chr9:69364389
|
AT | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 138 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.472-7097delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69364389 | |||||
| chr9:69364512
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.472-6987C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364512 | ||||||
| chr9:69364583
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472-6916T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364583 | ||||||
| chr9:69364788
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.472-6711A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364788 | ||||||
| chr9:69364795
|
G | A | 1 | a0001c0001t0002g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.472-6704G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364795 | ||||||
| chr9:69364854
|
A | T | 95 | a0001c0001t0001g0091a0001c0001t0002g0002a0001c0001t0002g0007others(92): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.472-6645A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364854 | ||||||
| chr9:69364876
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.472-6623T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364876 | ||||||
| chr9:69364915
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0003g0255 | 2 | NA18981.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.472-6584G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364915 | ||||||
| chr9:69364991
|
T | C | 1 | a0001c0001t0004g0271 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.472-6508T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364991 | ||||||
| chr9:69364994
|
CTG | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0309a0001c0001t0003g0241 | 3 | NA18985.hp2 NA18994.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.472-6503_472-6502d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69364994 | |||||
| chr9:69365035
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0030 | 2 | NA18987.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.472-6464G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365035 | ||||||
| chr9:69365051
|
C | T | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | NA18970.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.472-6448C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365051 | ||||||
| chr9:69365271
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-6228C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365271 | ||||||
| chr9:69365305
|
C | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.472-6194C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365305 | ||||||
| chr9:69365437
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0002g0020 | 2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.472-6062G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365437 | ||||||
| chr9:69365461
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.472-6038G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365461 | ||||||
| chr9:69365561
|
A | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-5938A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365561 | ||||||
| chr9:69365724
|
C | CTA | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 138 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.472-5774_472-5773i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69365724 | |||||
| chr9:69365831
|
C | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.472-5668C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365831 | ||||||
| chr9:69365952
|
C | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0031others(25): Show | 28 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.472-5547C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365952 | ||||||
| chr9:69366107
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-5392G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366107 | ||||||
| chr9:69366347
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472-5152A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366347 | ||||||
| chr9:69366349
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472-5150C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366349 | ||||||
| chr9:69366384
|
G | GT | 4 | a0001c0001t0001g0211a0001c0001t0002g0195a0001c0001t0002g0198others(1): Show | 4 | HG00140.hp2 HG01261.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(3): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366384
|
G | GTT | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0006c0005t0001g0222 | 3 | HG02559.hp2 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.472-5115_472-5114i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366384
|
G | GTTT | 19 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(16): Show | 19 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366384
|
G | GTTTT | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(72): Show | 79 | HG00423.hp2 HG00642.hp2 HG01168.hp1 others(76): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366384
|
G | GTTTTT | 7 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG02055.hp1 HG02135.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366384
|
G | GTTTTTT | 25 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366384
|
G | GTTTTTTT | 5 | a0001c0001t0001g0060a0001c0001t0001g0213a0001c0001t0001g0311others(2): Show | 5 | HG02622.hp1 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(9): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | ||||||
| chr9:69366385
|
G | GT | 94 | a0001c0001t0001g0048a0001c0001t0001g0091a0001c0001t0001g0180others(91): Show | 102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.472-5099dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69366385 | |||||
| chr9:69366385
|
G | GTT | 9 | a0001c0001t0002g0033a0001c0001t0002g0051a0001c0001t0002g0062others(6): Show | 9 | HG00140.hp1 HG00597.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.472-5100_472-5099d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69366385 | |||||
| chr9:69366385
|
G | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 146 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.472-5114G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366385 | ||||||
| chr9:69366574
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.472-4925G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366574 | ||||||
| chr9:69366638
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472-4861C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366638 | ||||||
| chr9:69366755
|
T | C | 18 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 18 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.472-4744T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366755 | ||||||
| chr9:69366817
|
T | C | 1 | a0001c0001t0003g0260 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.472-4682T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366817 | ||||||
| chr9:69366870
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0107 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.472-4629G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366870 | ||||||
| chr9:69367005
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-4494T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367005 | ||||||
| chr9:69367016
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-4483A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367016 | ||||||
| chr9:69367091
|
A | AT | 6 | a0001c0001t0001g0176a0001c0001t0001g0304a0001c0001t0003g0245others(3): Show | 6 | HG02071.hp2 NA18943.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-4386dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367091 | |||||
| chr9:69367091
|
ATTT | A | 12 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0137others(9): Show | 12 | HG01516.hp2 HG02055.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.472-4388_472-4386d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367091 | |||||
| chr9:69367091
|
ATTTT | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.472-4389_472-4386d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367091 | |||||
| chr9:69367183
|
G | C | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-4316G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367183 | ||||||
| chr9:69367422
|
G | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-4077G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367422 | ||||||
| chr9:69367455
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.472-4044A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367455 | ||||||
| chr9:69367467
|
T | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-4032T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367467 | ||||||
| chr9:69367484
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0190others(10): Show | 17 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.472-4015T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367484 | ||||||
| chr9:69367601
|
A | T | 1 | a0001c0001t0003g0239 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.472-3898A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367601 | ||||||
| chr9:69367614
|
T | C | 1 | a0001c0001t0003g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.472-3885T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367614 | ||||||
| chr9:69367668
|
CACACATA others(15): Show |
C | 5 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0086others(2): Show | 5 | HG00099.hp2 HG02135.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-3819_472-3798d others(24): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367668 | |||||
| chr9:69367672
|
C | CAT | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.472-3821_472-3820d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | |||||
| chr9:69367672
|
C | CATATATA others(21): Show |
8 | a0001c0001t0001g0031a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 10 | HG01175.hp1 HG02132.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-3820_472-3819i others(30): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | |||||
| chr9:69367672
|
C | CATATATA others(47): Show |
1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-3820_472-3819i others(56): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | |||||
| chr9:69367672
|
C | CATATATA others(19): Show |
3 | a0001c0003t0001g0049a0001c0003t0001g0317a0001c0003t0001g0318 | 3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.472-3820_472-3819i others(28): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | |||||
| chr9:69367696
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.472-3803T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367696 | ||||||
| chr9:69367704
|
A | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0190a0001c0001t0001g0192others(9): Show | 15 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.472-3795A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367704 | ||||||
| chr9:69367706
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.472-3793T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367706 | ||||||
| chr9:69367708
|
TATATATA others(15): Show |
T | 86 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(83): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.472-3783_472-3762d others(24): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367708 | |||||
| chr9:69367716
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3783C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367716 | ||||||
| chr9:69367720
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3779T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367720 | ||||||
| chr9:69367728
|
A | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.472-3771A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367728 | ||||||
| chr9:69367730
|
A | T | 10 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0086others(7): Show | 10 | HG00099.hp2 HG01975.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-3769A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367730 | ||||||
| chr9:69367740
|
T | C | 3 | a0001c0001t0002g0179a0003c0006t0001g0210a0006c0005t0001g0222 | 3 | HG01975.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-3759T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367740 | ||||||
| chr9:69367740
|
TAC | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(104): Show | 112 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.472-3755_472-3754d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367740 | |||||
| chr9:69367744
|
C | T | 3 | a0001c0001t0002g0179a0003c0006t0001g0210a0006c0005t0001g0222 | 3 | HG01975.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-3755C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367744 | ||||||
| chr9:69367750
|
T | TAAATATA others(17): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0190others(10): Show | 17 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.472-3726_472-3725i others(26): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367750 | |||||
| chr9:69367752
|
A | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3747A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367752 | ||||||
| chr9:69367754
|
T | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3745T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367754 | ||||||
| chr9:69367762
|
T | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.472-3737T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367762 | ||||||
| chr9:69367764
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3735C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367764 | ||||||
| chr9:69367768
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3731T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367768 | ||||||
| chr9:69367786
|
C | T | 239 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.472-3713C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367786 | ||||||
| chr9:69367790
|
CAT | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.472-3701_472-3700d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367790 | |||||
| chr9:69367798
|
T | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3701T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367798 | ||||||
| chr9:69367800
|
A | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3699A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367800 | ||||||
| chr9:69367810
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(11): Show | 14 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-3689C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367810 | ||||||
| chr9:69367814
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3685C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367814 | ||||||
| chr9:69367814
|
CAT | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.472-3677_472-3676d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367814 | |||||
| chr9:69367816
|
T | TATATAAA others(13): Show |
1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.472-3678_472-3677i others(22): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | |||||
| chr9:69367816
|
T | TATATATA others(179): Show |
1 | a0001c0001t0001g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.472-3666_472-3665i others(188): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | |||||
| chr9:69367816
|
T | TATATATA others(179): Show |
1 | a0001c0001t0003g0252 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.472-3652_472-3651i others(188): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | |||||
| chr9:69367816
|
T | TATATATA others(203): Show |
5 | a0001c0001t0003g0235a0001c0001t0003g0251a0001c0001t0003g0253others(2): Show | 5 | HG00423.hp1 HG02155.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-3652_472-3651i others(212): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | |||||
| chr9:69367824
|
AATAT | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3667_472-3664d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367824 | |||||
| chr9:69367834
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3665T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367834 | ||||||
| chr9:69367838
|
CAT | C | 98 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211others(95): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.472-3651_472-3650d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367838 | |||||
| chr9:69367840
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3659T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367840 | ||||||
| chr9:69367848
|
T | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG00621.hp2 HG00673.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-3651T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367848 | ||||||
| chr9:69367850
|
A | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG00621.hp2 HG00673.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-3649A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367850 | ||||||
| chr9:69367852
|
TATATACA others(3): Show |
T | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089 | 3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3641_472-3632d others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367852 | |||||
| chr9:69367858
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3641C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367858 | ||||||
| chr9:69367864
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-3635T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367864 | ||||||
| chr9:69367872
|
A | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089others(1): Show | 4 | HG01361.hp1 HG01975.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-3627A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367872 | ||||||
| chr9:69367874
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0089others(1): Show | 4 | HG01361.hp1 HG01975.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-3625T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367874 | ||||||
| chr9:69367874
|
T | TATATATA others(215): Show |
5 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG00621.hp2 HG00673.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-3618_472-3617i others(224): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367874 | |||||
| chr9:69367874
|
T | TATATATA others(5): Show |
209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(206): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.472-3615_472-3604d others(14): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367874 | |||||
| chr9:69367888
|
T | TATATATA others(3): Show |
31 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 32 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.472-3604_472-3603i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367888 | |||||
| chr9:69367888
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0074a0001c0001t0002g0076 | 2 | NA19002.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.472-3603_472-3594d others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367888 | |||||
| chr9:69367933
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.472-3566G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367933 | ||||||
| chr9:69368037
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0310a0001c0001t0001g0311others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-3462C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368037 | ||||||
| chr9:69368058
|
C | CTT | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.472-3440_472-3439i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69368058 | |||||
| chr9:69368468
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-3031A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368468 | ||||||
| chr9:69368475
|
T | A | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.472-3024T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368475 | ||||||
| chr9:69368581
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.472-2918A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368581 | ||||||
| chr9:69368739
|
A | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-2760A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368739 | ||||||
| chr9:69368846
|
A | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(107): Show | 115 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.472-2653A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368846 | ||||||
| chr9:69369033
|
A | G | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-2466A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369033 | ||||||
| chr9:69369062
|
T | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-2437T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369062 | ||||||
| chr9:69369292
|
C | T | 1 | a0001c0001t0003g0239 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.472-2207C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369292 | ||||||
| chr9:69369422
|
T | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 149 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.472-2077T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369422 | ||||||
| chr9:69369456
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.472-2043A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369456 | ||||||
| chr9:69369594
|
C | CTT | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(32): Show | 40 | HG00597.hp2 HG01175.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.472-1893_472-1892d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69369594 | |||||
| chr9:69369594
|
C | CTTT | 75 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.472-1894_472-1892d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69369594 | |||||
| chr9:69369747
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-1752G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369747 | ||||||
| chr9:69369824
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472-1675G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369824 | ||||||
| chr9:69369863
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472-1636A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369863 | ||||||
| chr9:69369971
|
A | C | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.472-1528A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369971 | ||||||
| chr9:69370056
|
AGTGAAGA others(7): Show |
A | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0003c0006t0001g0210others(1): Show | 4 | HG02559.hp2 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-1441_472-1428d others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69370056 | |||||
| chr9:69370112
|
T | G | 1 | a0001c0001t0002g0298 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.472-1387T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370112 | ||||||
| chr9:69370157
|
A | G | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.472-1342A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370157 | ||||||
| chr9:69370181
|
T | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 150 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.472-1318T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370181 | ||||||
| chr9:69370188
|
G | A | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-1311G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370188 | ||||||
| chr9:69370235
|
A | G | 23 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(20): Show | 24 | HG00423.hp1 HG00621.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.472-1264A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370235 | ||||||
| chr9:69370253
|
T | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-1246T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370253 | ||||||
| chr9:69370424
|
C | T | 3 | a0001c0001t0002g0062a0001c0001t0002g0093a0001c0001t0002g0194 | 3 | NA18985.hp1 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.472-1075C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370424 | ||||||
| chr9:69370720
|
G | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.472-779G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370720 | ||||||
| chr9:69370795
|
TCTTTTAT others(5): Show |
T | 31 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 32 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.472-690_472-679del others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69370795 | |||||
| chr9:69370967
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.472-532T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370967 | ||||||
| chr9:69371100
|
C | G | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.472-399C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371100 | ||||||
| chr9:69371360
|
G | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(25): Show | 29 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.472-139G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371360 | ||||||
| chr9:69371399
|
T | C | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.472-100T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371399 | ||||||
| chr9:69371400
|
G | A | 114 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(111): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.472-99G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371400 | ||||||
| chr9:69371480
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.472-19C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371480 | ||||||
| chr9:69371672
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211 | 3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.582+63C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371672 | ||||||
| chr9:69371689
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.582+80A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371689 | ||||||
| chr9:69371872
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211 | 3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.582+263A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371872 | ||||||
| chr9:69371889
|
A | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.582+280A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371889 | ||||||
| chr9:69372090
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.582+481C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372090 | ||||||
| chr9:69372189
|
G | A | 98 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(95): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.582+580G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372189 | ||||||
| chr9:69372674
|
T | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0001g0169others(3): Show | 6 | HG02738.hp2 HG04199.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+1065T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372674 | ||||||
| chr9:69372798
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.582+1189G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372798 | ||||||
| chr9:69372849
|
CT | C | 118 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(115): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.582+1251delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 69372849 | |||||
| chr9:69373028
|
TTA | T | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(109): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.582+1421_582+1422d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 69373028 | |||||
| chr9:69373030
|
ATT | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.582+1431_582+1432d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 69373030 | |||||
| chr9:69373332
|
G | A | 118 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(115): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.582+1723G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69373332 | ||||||
| chr9:69373441
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.582+1832C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69373441 | ||||||
| chr9:69374019
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.583-1717C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374019 | ||||||
| chr9:69374130
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.583-1606T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374130 | ||||||
| chr9:69374185
|
A | G | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.583-1551A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374185 | ||||||
| chr9:69374250
|
T | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 150 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.583-1486T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374250 | ||||||
| chr9:69374274
|
A | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 150 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.583-1462A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374274 | ||||||
| chr9:69374521
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.583-1215C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374521 | ||||||
| chr9:69374684
|
A | G | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.583-1052A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374684 | ||||||
| chr9:69374947
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(5): Show | 10 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.583-789C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374947 | ||||||
| chr9:69375376
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.583-360G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69375376 | ||||||
| chr9:69375729
|
C | T | 98 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(95): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
splice_region_variant&intron_variant | LOW | c.583-7C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69375729 | ||||||
| chr9:69375895
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0118 | 2 | HG02083.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.711+31A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69375895 | ||||||
| chr9:69375906
|
G | A | 3 | a0001c0003t0001g0049a0001c0003t0001g0317a0001c0003t0001g0318 | 3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.711+42G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69375906 | ||||||
| chr9:69376018
|
A | C | 1 | a0001c0001t0001g0309 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.711+154A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376018 | ||||||
| chr9:69376112
|
C | T | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.711+248C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376112 | ||||||
| chr9:69376223
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211 | 3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.711+359A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376223 | ||||||
| chr9:69376234
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0002g0177 | 2 | HG00673.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.711+370C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376234 | ||||||
| chr9:69376402
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0310a0001c0001t0001g0311others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+538A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376402 | ||||||
| chr9:69376574
|
G | A | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.711+710G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376574 | ||||||
| chr9:69376883
|
T | G | 240 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.712-487T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376883 | ||||||
| chr9:69376972
|
G | A | 113 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(110): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.712-398G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376972 | ||||||
| chr9:69377026
|
C | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0155 | 2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.712-344C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69377026 | ||||||
| chr9:69377049
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.712-321C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69377049 | ||||||
| chr9:69377283
|
C | T | 4 | a0001c0003t0001g0049a0001c0003t0001g0317a0001c0003t0001g0318others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-87C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69377283 | ||||||
| chr9:69377487
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(12): Show | 19 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.819+10T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 5/10 | chr9 | 69377487 | ||||||
| chr9:69377527
|
T | C | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.819+50T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 5/10 | chr9 | 69377527 | ||||||
| chr9:69377772
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.953+28T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69377772 | ||||||
| chr9:69377789
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.953+45G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69377789 | ||||||
| chr9:69377829
|
A | G | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.953+85A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69377829 | ||||||
| chr9:69378008
|
CTCTG | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0027others(8): Show | 12 | NA18944.hp2 NA18960.hp1 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.953+268_953+271del others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378008 | |||||
| chr9:69378012
|
G | GTC | 100 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.953+280_953+281dup others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378012 | |||||
| chr9:69378123
|
G | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.953+379G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378123 | ||||||
| chr9:69378159
|
G | C | 1 | a0001c0001t0001g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.953+415G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378159 | ||||||
| chr9:69378171
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.953+427C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378171 | ||||||
| chr9:69378177
|
T | TGA | 9 | a0001c0001t0002g0073a0001c0001t0002g0134a0001c0001t0002g0139others(6): Show | 9 | HG01261.hp1 HG01261.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.953+437_953+438dup others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378177 | |||||
| chr9:69378222
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(12): Show | 19 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.953+478G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378222 | ||||||
| chr9:69378489
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.953+745G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378489 | ||||||
| chr9:69378510
|
G | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(14): Show | 21 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.953+766G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378510 | ||||||
| chr9:69378756
|
C | CA | 25 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(22): Show | 30 | HG00140.hp1 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.953+1026dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378756 | |||||
| chr9:69378756
|
CA | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.953+1026delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378756 | |||||
| chr9:69378840
|
T | G | 1 | a0006c0005t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.953+1096T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378840 | ||||||
| chr9:69378941
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.953+1197G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378941 | ||||||
| chr9:69379025
|
T | TAAAGGAT others(318): Show |
1 | a0001c0001t0001g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.953+1294_953+1295i others(327): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69379025 | |||||
| chr9:69379086
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 149 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.953+1342A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379086 | ||||||
| chr9:69379116
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.953+1372C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379116 | ||||||
| chr9:69379127
|
T | C | 1 | a0001c0001t0004g0240 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.953+1383T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379127 | ||||||
| chr9:69379424
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.953+1680G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379424 | ||||||
| chr9:69379606
|
A | G | 260 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(257): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.953+1862A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379606 | ||||||
| chr9:69379618
|
G | A | 1 | a0001c0001t0003g0272 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.953+1874G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379618 | ||||||
| chr9:69379621
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953+1877G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379621 | ||||||
| chr9:69379707
|
T | C | 99 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(96): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.953+1963T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379707 | ||||||
| chr9:69379776
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.953+2032A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379776 | ||||||
| chr9:69379906
|
A | G | 1 | a0001c0001t0005g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.953+2162A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379906 | ||||||
| chr9:69379948
|
C | G | 4 | a0001c0001t0001g0316a0001c0003t0001g0049a0001c0003t0001g0317others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+2204C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379948 | ||||||
| chr9:69379966
|
T | C | 99 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(96): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.953+2222T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379966 | ||||||
| chr9:69380109
|
A | T | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.953+2365A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380109 | ||||||
| chr9:69380135
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.953+2391C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380135 | ||||||
| chr9:69380448
|
C | A | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.953+2704C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380448 | ||||||
| chr9:69380550
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.953+2806C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380550 | ||||||
| chr9:69380571
|
A | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 142 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.953+2827A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380571 | ||||||
| chr9:69380699
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.954-2931T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380699 | ||||||
| chr9:69380828
|
A | G | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.954-2802A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380828 | ||||||
| chr9:69380918
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0209 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.954-2712T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380918 | ||||||
| chr9:69380958
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.954-2672G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380958 | ||||||
| chr9:69381154
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.954-2476T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381154 | ||||||
| chr9:69381454
|
A | G | 7 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(4): Show | 9 | HG01175.hp1 HG02258.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.954-2176A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381454 | ||||||
| chr9:69381520
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.954-2110G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381520 | ||||||
| chr9:69381645
|
T | TAAAAAC | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211 | 3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.954-1961_954-1956d others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69381645 | |||||
| chr9:69381907
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.954-1723G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381907 | ||||||
| chr9:69381929
|
T | A | 1 | a0001c0001t0002g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.954-1701T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381929 | ||||||
| chr9:69381999
|
G | A | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.954-1631G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381999 | ||||||
| chr9:69382051
|
G | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 134 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.954-1579G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382051 | ||||||
| chr9:69382187
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.954-1443T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382187 | ||||||
| chr9:69382423
|
G | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(12): Show | 19 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.954-1207G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382423 | ||||||
| chr9:69382567
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211 | 3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.954-1063C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382567 | ||||||
| chr9:69382902
|
A | G | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(18): Show | 25 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.954-728A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382902 | ||||||
| chr9:69383165
|
A | T | 104 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0211others(101): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.954-465A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383165 | ||||||
| chr9:69383411
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.954-219T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383411 | ||||||
| chr9:69383475
|
T | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(78): Show | 86 | HG00423.hp2 HG00642.hp2 HG01123.hp2 others(83): Show |
intron_variant | MODIFIER | c.954-155T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383475 | ||||||
| chr9:69383573
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.954-57G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383573 | ||||||
| chr9:69383855
|
G | A | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1084-92G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 7/10 | chr9 | 69383855 | ||||||
| chr9:69384048
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0189 | 3 | HG03130.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1162+23A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384048 | ||||||
| chr9:69384049
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1162+24T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384049 | ||||||
| chr9:69384202
|
GA | G | 132 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0032others(129): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1162+187delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69384202 | |||||
| chr9:69384299
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0156a0004c0007t0001g0028 | 3 | NA18964.hp1 NA18992.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1162+274T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384299 | ||||||
| chr9:69384352
|
T | G | 3 | a0001c0003t0001g0049a0001c0003t0001g0317a0001c0003t0001g0318 | 3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1162+327T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384352 | ||||||
| chr9:69384598
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1162+573A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384598 | ||||||
| chr9:69384785
|
A | C | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1162+760A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384785 | ||||||
| chr9:69384848
|
GAATT | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1162+829_1162+832d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69384848 | |||||
| chr9:69384900
|
A | AT | 9 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0048others(6): Show | 10 | HG02109.hp1 HG02717.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163-882dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69384900 | |||||
| chr9:69384907
|
T | A | 248 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1162+882T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384907 | ||||||
| chr9:69384924
|
T | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(15): Show | 22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1163-871T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384924 | ||||||
| chr9:69384971
|
G | A | 101 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1163-824G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384971 | ||||||
| chr9:69385153
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1163-642T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385153 | ||||||
| chr9:69385248
|
T | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1163-547T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385248 | ||||||
| chr9:69385256
|
C | G | 2 | a0001c0001t0003g0242a0001c0001t0003g0272 | 2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1163-539C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385256 | ||||||
| chr9:69385271
|
G | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1163-524G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385271 | ||||||
| chr9:69385300
|
A | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1163-495A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385300 | ||||||
| chr9:69385429
|
T | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1163-366T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385429 | ||||||
| chr9:69385512
|
AC | A | 243 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1163-279delC | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385512 | |||||
| chr9:69385513
|
C | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0209a0003c0006t0001g0210others(2): Show | 5 | HG01884.hp1 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-282C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385513 | ||||||
| chr9:69385541
|
T | G | 1 | a0001c0001t0001g0309 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1163-254T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385541 | ||||||
| chr9:69385690
|
G | T | 1 | a0006c0005t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1163-105G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385690 | ||||||
| chr9:69385702
|
T | C | 1 | a0001c0001t0003g0277 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1163-93T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385702 | ||||||
| chr9:69385758
|
C | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1163-37C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385758 | ||||||
| chr9:69385763
|
CT | C | 10 | a0001c0001t0001g0227a0001c0001t0001g0309a0001c0001t0003g0247others(7): Show | 10 | HG02040.hp1 HG02155.hp2 HG02897.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1163-8delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | |||||
| chr9:69385763
|
CTT | C | 28 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(25): Show | 33 | HG00280.hp2 HG00735.hp2 HG01106.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.1163-9_1163-8delTT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | |||||
| chr9:69385763
|
CTTT | C | 83 | a0001c0001t0001g0193a0001c0001t0001g0205a0001c0001t0002g0002others(80): Show | 90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
splice_region_variant&intron_variant | LOW | c.1163-10_1163-8delT others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | |||||
| chr9:69385763
|
CTTTT | C | 8 | a0001c0001t0002g0097a0001c0001t0002g0168a0001c0001t0002g0179others(5): Show | 8 | HG01074.hp2 HG01169.hp2 HG01943.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1163-11_1163-8delT others(3): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | |||||
| chr9:69385764
|
T | A | 1 | a0001c0001t0001g0006 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1163-31T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385764 | ||||||
| chr9:69385785
|
TTTA | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0079others(8): Show | 11 | HG01167.hp1 HG01943.hp1 HG02451.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1163-9_1163-7delTT others(1): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385785 | ||||||
| chr9:69385786
|
TTA | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 106 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.1163-8_1163-7delTA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385786 | ||||||
| chr9:69385787
|
TA | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0047others(11): Show | 14 | HG01515.hp1 HG01516.hp1 HG01891.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1163-5delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385787 | |||||
| chr9:69385788
|
A | T | 1 | a0001c0003t0001g0049 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.1163-7A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385788 | ||||||
| chr9:69386100
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0291a0001c0001t0004g0248 | 3 | HG02698.hp1 HG03239.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1315+153C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386100 | ||||||
| chr9:69386148
|
G | GT | 4 | a0001c0001t0002g0035a0001c0003t0001g0049a0001c0003t0001g0317others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315+208dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69386148 | |||||
| chr9:69386238
|
C | A | 119 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(116): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1315+291C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386238 | ||||||
| chr9:69386317
|
A | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1315+370A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386317 | ||||||
| chr9:69386318
|
C | A | 101 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1315+371C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386318 | ||||||
| chr9:69386359
|
T | TATCTACT others(1): Show |
3 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0234 | 3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1315+413_1315+414i others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69386359 | |||||
| chr9:69386361
|
G | T | 3 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0234 | 3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1315+414G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386361 | ||||||
| chr9:69386362
|
A | C | 3 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0234 | 3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1315+415A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386362 | ||||||
| chr9:69386420
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1315+473C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386420 | ||||||
| chr9:69386452
|
T | TGA | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1315+506_1315+507i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69386452 | |||||
| chr9:69386457
|
G | C | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1315+510G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386457 | ||||||
| chr9:69386507
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1315+560T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386507 | ||||||
| chr9:69386601
|
T | C | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1315+654T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386601 | ||||||
| chr9:69386750
|
A | G | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1315+803A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386750 | ||||||
| chr9:69386882
|
C | T | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(15): Show | 22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1315+935C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386882 | ||||||
| chr9:69386905
|
A | G | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1315+958A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386905 | ||||||
| chr9:69387076
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1316-1082C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387076 | ||||||
| chr9:69387271
|
A | G | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1316-887A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387271 | ||||||
| chr9:69387307
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0231others(2): Show | 6 | HG02717.hp2 HG02896.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-851C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387307 | ||||||
| chr9:69387358
|
C | A | 2 | a0001c0001t0003g0260a0001c0001t0006g0126 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1316-800C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387358 | ||||||
| chr9:69387638
|
G | A | 101 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1316-520G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387638 | ||||||
| chr9:69387773
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0084 | 2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1316-385C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387773 | ||||||
| chr9:69387995
|
T | TGTTATA | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1316-160_1316-159i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69387995 | |||||
| chr9:69388039
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0291 | 2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1316-119G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69388039 | ||||||
| chr9:69388043
|
A | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(15): Show | 22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1316-115A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69388043 | ||||||
| chr9:69388120
|
T | C | 119 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(116): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1316-38T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69388120 | ||||||
| chr9:69388512
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1608+62G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388512 | ||||||
| chr9:69388613
|
G | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+163G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388613 | ||||||
| chr9:69388669
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0048others(7): Show | 11 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1608+219C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388669 | ||||||
| chr9:69388807
|
G | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+357G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388807 | ||||||
| chr9:69388873
|
GTTCACAT others(2): Show |
G | 4 | a0001c0001t0001g0053a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+424_1608+432d others(11): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388873 | ||||||
| chr9:69388878
|
C | T | 23 | a0001c0001t0002g0020a0001c0001t0002g0073a0001c0001t0002g0096others(20): Show | 23 | HG00140.hp2 HG00621.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1608+428C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388878 | ||||||
| chr9:69388886
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0053others(9): Show | 13 | HG01255.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1608+436T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388886 | ||||||
| chr9:69388975
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1608+525C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388975 | ||||||
| chr9:69389001
|
A | G | 1 | a0005c0009t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1608+551A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389001 | ||||||
| chr9:69389077
|
C | G | 3 | a0001c0001t0004g0248a0001c0001t0004g0250a0001c0001t0004g0259 | 3 | HG02040.hp2 NA18960.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1608+627C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389077 | ||||||
| chr9:69389105
|
A | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+655A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389105 | ||||||
| chr9:69389113
|
T | C | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1608+663T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389113 | ||||||
| chr9:69389130
|
C | T | 52 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(49): Show | 57 | HG00280.hp2 HG00438.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1608+680C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389130 | ||||||
| chr9:69389201
|
T | C | 248 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1608+751T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389201 | ||||||
| chr9:69389233
|
T | A | 251 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1608+783T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389233 | ||||||
| chr9:69389359
|
C | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+909C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389359 | ||||||
| chr9:69389466
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1608+1016T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389466 | ||||||
| chr9:69389551
|
G | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0031others(16): Show | 19 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1608+1101G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389551 | ||||||
| chr9:69389573
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1608+1123C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389573 | ||||||
| chr9:69389889
|
G | GT | 14 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1608+1440dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69389889 | |||||
| chr9:69390142
|
T | TGAACTTT others(9): Show |
1 | a0001c0001t0002g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1609-1458_1609-144 others(20): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69390142 | |||||
| chr9:69390160
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0189others(5): Show | 10 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-1441C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390160 | ||||||
| chr9:69390199
|
T | C | 1 | a0003c0008t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1609-1402T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390199 | ||||||
| chr9:69390672
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0312 | 2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1609-929G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390672 | ||||||
| chr9:69390683
|
A | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1609-918A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390683 | ||||||
| chr9:69390797
|
G | T | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0104others(15): Show | 22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1609-804G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390797 | ||||||
| chr9:69390854
|
T | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG02451.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1609-747T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390854 | ||||||
| chr9:69390946
|
ATTT | A | 240 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1609-639_1609-637d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69390946 | |||||
| chr9:69391032
|
A | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1609-569A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391032 | ||||||
| chr9:69391131
|
G | C | 1 | a0001c0001t0002g0002 | 3 | HG01952.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1609-470G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391131 | ||||||
| chr9:69391224
|
T | C | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1609-377T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391224 | ||||||
| chr9:69391260
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 52 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1609-341C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391260 | ||||||
| chr9:69391357
|
A | T | 12 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609-244A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391357 | ||||||
| chr9:69391360
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0140 | 2 | NA19065.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1609-241T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391360 | ||||||
| chr9:69391466
|
T | G | 4 | a0001c0001t0001g0316a0001c0003t0001g0049a0001c0003t0001g0317others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-135T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391466 | ||||||
| chr9:69391477
|
C | CT | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 136 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.1609-114dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69391477 | |||||
| chr9:69391539
|
G | C | 2 | a0003c0006t0001g0210a0006c0005t0001g0222 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1609-62G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391539 |