| geneid | 1950 |
|---|---|
| ensemblid | ENSG00000138798.13 |
| hgncid | 3229 |
| symbol | EGF |
| name | epidermal growth factor |
| refseq_nuc | NM_001963.6 |
| refseq_prot | NP_001954.2 |
| ensembl_nuc | ENST00000265171.10 |
| ensembl_prot | ENSP00000265171.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 109912883 |
| end | 110013766 |
| strand | + |
| ver | v1.2 |
| region | chr4:109912883-110013766 |
| region5000 | chr4:109907883-110018766 |
| regionname0 | EGF_chr4_109912883_110013766 |
| regionname5000 | EGF_chr4_109907883_110018766 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1207 | 142 | 41 | 25 | 62 | 3 | 11 | 49 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002 | 0/0 | 1207 | 81 | 7 | 17 | 43 | 5 | 9 | 32 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0003 | 0/0 | 1152 | 44 | 0 | 0 | 36 | 0 | 8 | 25 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004 | 0/0 | 1207 | 40 | 1 | 5 | 29 | 1 | 4 | 24 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005 | 0/0 | 1207 | 20 | 16 | 2 | 2 | 0 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0006 | 1/0 | 1207 | 14 | 1 | 5 | 0 | 1 | 6 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0007 | 0/0 | 1207 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0008 | 0/0 | 1207 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0009 | 0/0 | 1207 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0010 | 0/0 | 1207 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0011 | 0/0 | 1207 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0012 | 0/0 | 1207 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0013 | 0/0 | 1152 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0014 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0015 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0016 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0017 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0018 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0019 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0020 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0021 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0022 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0023 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0024 | 0/0 | 1207 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0025 | 0/0 | 1223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0026 | 0/1 | 1207 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0027 | 0/0 | 1207 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3624 | 124 | 39 | 21 | 58 | 0 | 6 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0002 | 0/0 | 3624 | 81 | 7 | 17 | 43 | 5 | 9 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0003 | 0/0 | 3625 | 44 | 0 | 0 | 36 | 0 | 8 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0004 | 0/0 | 3624 | 39 | 1 | 5 | 29 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0005 | 0/0 | 3624 | 20 | 16 | 2 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0006 | 1/0 | 3624 | 14 | 1 | 5 | 0 | 1 | 6 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0007 | 0/0 | 3624 | 8 | 0 | 3 | 0 | 2 | 3 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0008 | 0/0 | 3624 | 7 | 0 | 0 | 7 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0009 | 0/0 | 3624 | 7 | 0 | 0 | 7 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0010 | 0/0 | 3624 | 5 | 4 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0011 | 0/0 | 3624 | 4 | 0 | 0 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0012 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0013 | 0/0 | 3624 | 3 | 0 | 0 | 0 | 1 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0014 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0015 | 0/0 | 3625 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0016 | 0/0 | 3624 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0017 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0018 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0019 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0020 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0021 | 0/1 | 3624 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0022 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0023 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0024 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0025 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0026 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0027 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0028 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0029 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0030 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0031 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0032 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0033 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0034 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| c0035 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2765 | 77 | 6 | 17 | 39 | 4 | 10 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0002 | 0/0 | 2764 | 49 | 6 | 14 | 18 | 3 | 8 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0003 | 0/0 | 2764 | 37 | 1 | 4 | 29 | 1 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0004 | 0/0 | 2764 | 37 | 4 | 8 | 24 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0005 | 0/0 | 2765 | 28 | 0 | 0 | 23 | 0 | 5 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0006 | 0/0 | 2765 | 24 | 4 | 3 | 14 | 0 | 3 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0007 | 0/0 | 2764 | 18 | 18 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0008 | 0/0 | 2766 | 14 | 0 | 0 | 12 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0009 | 0/0 | 2766 | 11 | 1 | 3 | 5 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0010 | 0/0 | 2765 | 8 | 0 | 1 | 6 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0011 | 0/0 | 2764 | 8 | 7 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0012 | 0/0 | 2764 | 6 | 2 | 0 | 3 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0013 | 0/0 | 2765 | 6 | 0 | 1 | 5 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0014 | 0/0 | 2764 | 5 | 5 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0015 | 0/0 | 2764 | 5 | 2 | 0 | 3 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0016 | 0/0 | 2764 | 5 | 3 | 2 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0017 | 0/0 | 2763 | 5 | 5 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0018 | 0/0 | 2765 | 4 | 1 | 0 | 2 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0019 | 0/0 | 2764 | 4 | 4 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0020 | 0/0 | 2764 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0021 | 0/0 | 2766 | 3 | 1 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0022 | 0/0 | 2764 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0023 | 0/0 | 2765 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0024 | 0/0 | 2764 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0025 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0026 | 0/0 | 2765 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0027 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0028 | 0/0 | 2763 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0029 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0030 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0031 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0032 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0033 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0034 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0035 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0036 | 1/0 | 2765 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0037 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0038 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0039 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0040 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0041 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0042 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0043 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0044 | 0/0 | 2765 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0045 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| t0046 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| 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 | 0/0 | 3624 | 124 | 39 | 21 | 58 | 0 | 6 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0007 | 0/0 | 3624 | 8 | 0 | 3 | 0 | 2 | 3 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0013 | 0/0 | 3624 | 3 | 0 | 0 | 0 | 1 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0016 | 0/0 | 3624 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0019 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0026 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0027 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0033 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002 | 0/0 | 3624 | 81 | 7 | 17 | 43 | 5 | 9 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0003c0003 | 0/0 | 3625 | 44 | 0 | 0 | 36 | 0 | 8 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0004 | 0/0 | 3624 | 39 | 1 | 5 | 29 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0032 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005 | 0/0 | 3624 | 20 | 16 | 2 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0006c0006 | 1/0 | 3624 | 14 | 1 | 5 | 0 | 1 | 6 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0007c0009 | 0/0 | 3624 | 7 | 0 | 0 | 7 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0008c0008 | 0/0 | 3624 | 7 | 0 | 0 | 7 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0009c0010 | 0/0 | 3624 | 5 | 4 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0010c0011 | 0/0 | 3624 | 4 | 0 | 0 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0011c0012 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0012c0014 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0013c0015 | 0/0 | 3625 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0014c0017 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0015c0018 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0016c0034 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0017c0023 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0018c0024 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0019c0025 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0020c0022 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0021c0031 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0022c0029 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0023c0028 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0024c0030 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0025c0035 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0026c0021 | 0/1 | 3624 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0027c0020 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6387 | 36 | 6 | 10 | 16 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0003 | 0/0 | 6387 | 3 | 0 | 0 | 3 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0004 | 0/0 | 6387 | 32 | 4 | 8 | 19 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0006 | 0/0 | 6388 | 9 | 1 | 1 | 6 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0007 | 0/0 | 6387 | 6 | 6 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0011 | 0/0 | 6387 | 7 | 7 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0012 | 0/0 | 6387 | 4 | 2 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0013 | 0/0 | 6388 | 5 | 0 | 1 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0014 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0015 | 0/0 | 6387 | 4 | 2 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0018 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0020 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0022 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0025 | 0/0 | 6387 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0027 | 0/0 | 6387 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0028 | 0/0 | 6386 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0029 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0030 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0033 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0034 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0040 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0001t0044 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0007t0002 | 0/0 | 6387 | 8 | 0 | 3 | 0 | 2 | 3 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0013t0002 | 0/0 | 6387 | 2 | 0 | 0 | 0 | 1 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0013t0006 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0016t0002 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0016t0006 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0019t0007 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0019t0017 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0026t0002 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0027t0004 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0001c0033t0004 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0001 | 0/0 | 6388 | 54 | 4 | 13 | 29 | 3 | 5 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0002 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0006 | 0/0 | 6388 | 8 | 0 | 2 | 5 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0009 | 0/0 | 6389 | 8 | 1 | 2 | 4 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0012 | 0/0 | 6387 | 2 | 0 | 0 | 1 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0015 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0021 | 0/0 | 6389 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0023 | 0/0 | 6388 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0035 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0037 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0002c0002t0043 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0003c0003t0005 | 0/0 | 6389 | 26 | 0 | 0 | 21 | 0 | 5 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0003c0003t0008 | 0/0 | 6390 | 14 | 0 | 0 | 12 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0003c0003t0018 | 0/0 | 6389 | 2 | 0 | 0 | 1 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0003c0003t0026 | 0/0 | 6389 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0004t0003 | 0/0 | 6387 | 28 | 1 | 4 | 21 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0004t0004 | 0/0 | 6387 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0004t0006 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0004t0010 | 0/0 | 6388 | 7 | 0 | 1 | 5 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0004t0039 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0004c0032t0003 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0004 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0006 | 0/0 | 6388 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0007 | 0/0 | 6387 | 5 | 5 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0011 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0013 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0017 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0019 | 0/0 | 6387 | 4 | 4 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0024 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0038 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0041 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0005c0005t0046 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0006c0006t0001 | 0/0 | 6388 | 11 | 1 | 4 | 0 | 1 | 5 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0006c0006t0009 | 0/0 | 6389 | 2 | 0 | 1 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0006c0006t0036 | 1/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0007c0009t0001 | 0/0 | 6388 | 6 | 0 | 0 | 6 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0007c0009t0009 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0008c0008t0003 | 0/0 | 6387 | 5 | 0 | 0 | 5 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0008c0008t0006 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0008c0008t0032 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0009c0010t0016 | 0/0 | 6387 | 4 | 3 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0009c0010t0042 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0010c0011t0001 | 0/0 | 6388 | 4 | 0 | 0 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0011c0012t0014 | 0/0 | 6387 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0012c0014t0007 | 0/0 | 6387 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0013c0015t0005 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0013c0015t0018 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0014c0017t0007 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0015c0018t0017 | 0/0 | 6386 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0016c0034t0020 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0017c0023t0045 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0018c0024t0007 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0019c0025t0021 | 0/0 | 6389 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0020c0022t0006 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0021c0031t0005 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0022c0029t0031 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0023c0028t0001 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0024c0030t0016 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0025c0035t0017 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0026c0021t0001 | 0/1 | 6388 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| a0027c0020t0010 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | copy fasta | chr4 | 109907883 | 110018766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0006g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0012g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0012g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0013g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0013g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0013g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0013g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0013g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0014g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0014g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0015g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0015g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0015g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0018g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0020g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0022g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0022g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0025g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0025g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0027g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0027g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0028g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0030g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0033g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0034g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0040g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0001t0044g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0007t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0013t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0013t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0013t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0016t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0016t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0019t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0019t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0026t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0027t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0001c0033t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0006g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0012g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0021g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0021g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0023g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0023g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0035g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0037g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0002c0002t0043g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0008g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0018g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0018g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0026g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0003c0003t0026g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0003g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0010g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0004t0039g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0004c0032t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0011g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0013g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0017g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0019g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0019g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0019g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0024g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0038g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0041g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0005c0005t0046g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0009g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0009g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0006c0006t0036g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0007c0009t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0008c0008t0032g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0009c0010t0016g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0009c0010t0016g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0009c0010t0016g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0009c0010t0016g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0009c0010t0042g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0010c0011t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0010c0011t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0010c0011t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0010c0011t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0011c0012t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0011c0012t0014g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0011c0012t0014g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0012c0014t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0012c0014t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0012c0014t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0013c0015t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0013c0015t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0014c0017t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0014c0017t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0015c0018t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0015c0018t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0016c0034t0020g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0017c0023t0045g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0018c0024t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0019c0025t0021g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0020c0022t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0021c0031t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0022c0029t0031g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0023c0028t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0024c0030t0016g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0025c0035t0017g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0026c0021t0001g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| a0027c0020t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0012 | g0181 | EUR | GBR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00140 | hp2 | a0006 | c0006 | t0001 | g0300 | EUR | GBR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0180 | EUR | FIN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00323 | hp2 | a0001 | c0013 | t0002 | g0067 | EUR | FIN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00408 | hp2 | a0001 | c0001 | t0012 | g0217 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00423 | hp1 | a0003 | c0003 | t0008 | g0053 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00438 | hp2 | a0001 | c0001 | t0013 | g0350 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00558 | hp1 | a0004 | c0004 | t0004 | g0267 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00597 | hp2 | a0004 | c0004 | t0003 | g0277 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0339 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00609 | hp2 | a0003 | c0003 | t0005 | g0037 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00621 | hp1 | a0003 | c0003 | t0008 | g0027 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00673 | hp2 | a0002 | c0002 | t0006 | g0371 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0364 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00735 | hp2 | a0001 | c0001 | t0028 | g0242 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00738 | hp1 | a0024 | c0030 | t0016 | g0310 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01069 | hp1 | a0001 | c0026 | t0002 | g0076 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0358 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0309 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0004 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01081 | hp1 | a0006 | c0006 | t0001 | g0304 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01081 | hp2 | a0002 | c0002 | t0006 | g0004 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01109 | hp1 | a0006 | c0006 | t0001 | g0303 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01109 | hp2 | a0005 | c0005 | t0011 | g0319 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0366 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0365 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01175 | hp1 | a0004 | c0004 | t0003 | g0281 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01175 | hp2 | a0006 | c0006 | t0009 | g0173 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01255 | hp1 | a0005 | c0005 | t0046 | g0305 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01255 | hp2 | a0002 | c0002 | t0009 | g0136 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0359 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01358 | hp1 | a0006 | c0006 | t0001 | g0302 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01515 | hp1 | a0001 | c0007 | t0002 | g0102 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01515 | hp2 | a0002 | c0002 | t0035 | g0137 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0138 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01517 | hp2 | a0001 | c0007 | t0002 | g0108 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01884 | hp1 | a0005 | c0005 | t0006 | g0254 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01884 | hp2 | a0011 | c0012 | t0014 | g0229 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0376 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0362 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01928 | hp2 | a0004 | c0004 | t0003 | g0261 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0367 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01934 | hp2 | a0001 | c0007 | t0002 | g0107 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0360 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01975 | hp2 | a0009 | c0010 | t0016 | g0321 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01978 | hp2 | a0004 | c0004 | t0003 | g0280 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0363 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02004 | hp1 | a0004 | c0004 | t0003 | g0272 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02004 | hp2 | a0006 | c0006 | t0001 | g0170 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02015 | hp1 | a0003 | c0003 | t0005 | g0048 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02027 | hp1 | a0003 | c0003 | t0008 | g0044 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02040 | hp2 | a0003 | c0003 | t0005 | g0043 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02055 | hp1 | a0001 | c0001 | t0022 | g0244 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0142 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02056 | hp1 | a0003 | c0003 | t0008 | g0040 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02056 | hp2 | a0002 | c0002 | t0009 | g0227 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02074 | hp2 | a0003 | c0003 | t0005 | g0014 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02080 | hp2 | a0003 | c0003 | t0008 | g0052 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02083 | hp2 | a0021 | c0031 | t0005 | g0029 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02129 | hp1 | a0002 | c0002 | t0006 | g0083 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02129 | hp2 | a0004 | c0004 | t0003 | g0270 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02148 | hp1 | a0001 | c0007 | t0002 | g0104 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02148 | hp2 | a0004 | c0004 | t0010 | g0287 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02155 | hp1 | a0004 | c0004 | t0006 | g0279 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02155 | hp2 | a0003 | c0003 | t0005 | g0021 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02165 | hp1 | a0004 | c0004 | t0003 | g0132 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02165 | hp2 | a0002 | c0002 | t0012 | g0171 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02257 | hp1 | a0014 | c0017 | t0007 | g0121 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0143 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02258 | hp2 | a0006 | c0006 | t0001 | g0169 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02280 | hp1 | a0002 | c0002 | t0023 | g0218 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02280 | hp2 | a0001 | c0001 | t0022 | g0241 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02293 | hp1 | a0001 | c0001 | t0013 | g0361 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02293 | hp2 | a0002 | c0002 | t0009 | g0204 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02523 | hp1 | a0013 | c0015 | t0005 | g0369 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02572 | hp1 | a0001 | c0001 | t0034 | g0238 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02572 | hp2 | a0005 | c0005 | t0024 | g0001 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02602 | hp1 | a0006 | c0006 | t0009 | g0212 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02615 | hp1 | a0001 | c0001 | t0033 | g0240 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02615 | hp2 | a0001 | c0019 | t0017 | g0140 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0145 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02622 | hp2 | a0012 | c0014 | t0007 | g0120 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02630 | hp1 | a0001 | c0019 | t0007 | g0139 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0239 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0123 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02647 | hp2 | a0005 | c0005 | t0007 | g0246 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0296 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02723 | hp1 | a0001 | c0001 | t0020 | g0233 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02723 | hp2 | a0005 | c0005 | t0007 | g0290 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02735 | hp1 | a0003 | c0003 | t0005 | g0020 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02735 | hp2 | a0006 | c0006 | t0001 | g0299 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02738 | hp1 | a0003 | c0003 | t0005 | g0045 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0088 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02809 | hp1 | a0022 | c0029 | t0031 | g0235 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02809 | hp2 | a0015 | c0018 | t0017 | g0117 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0377 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02886 | hp2 | a0005 | c0005 | t0017 | g0248 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02895 | hp1 | a0009 | c0010 | t0016 | g0323 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02896 | hp2 | a0009 | c0010 | t0016 | g0322 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02922 | hp1 | a0005 | c0005 | t0006 | g0250 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02922 | hp2 | a0012 | c0014 | t0007 | g0119 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02965 | hp1 | a0015 | c0018 | t0017 | g0058 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02965 | hp2 | a0001 | c0001 | t0020 | g0237 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02970 | hp1 | a0019 | c0025 | t0021 | g0291 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02970 | hp2 | a0005 | c0005 | t0019 | g0251 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02976 | hp1 | a0025 | c0035 | t0017 | g0131 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02976 | hp2 | a0005 | c0005 | t0019 | g0249 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03017 | hp2 | a0006 | c0006 | t0001 | g0175 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03098 | hp2 | a0005 | c0005 | t0041 | g0288 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03130 | hp1 | a0018 | c0024 | t0007 | g0292 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0378 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03139 | hp2 | a0001 | c0001 | t0040 | g0127 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0236 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0125 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03209 | hp1 | a0011 | c0012 | t0014 | g0230 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0144 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03239 | hp2 | a0003 | c0003 | t0005 | g0022 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03453 | hp1 | a0001 | c0001 | t0029 | g0243 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03486 | hp2 | a0009 | c0010 | t0042 | g0320 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03490 | hp2 | a0003 | c0003 | t0008 | g0002 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03491 | hp1 | a0006 | c0006 | t0001 | g0006 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03491 | hp2 | a0001 | c0007 | t0002 | g0089 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03492 | hp1 | a0003 | c0003 | t0005 | g0002 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03492 | hp2 | a0006 | c0006 | t0001 | g0006 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03516 | hp1 | a0020 | c0022 | t0006 | g0294 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03516 | hp2 | a0001 | c0001 | t0018 | g0234 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0146 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03669 | hp2 | a0004 | c0004 | t0003 | g0282 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03704 | hp1 | a0002 | c0002 | t0043 | g0346 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03710 | hp1 | a0004 | c0004 | t0003 | g0256 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03710 | hp2 | a0001 | c0013 | t0006 | g0069 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03831 | hp1 | a0003 | c0003 | t0008 | g0025 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03834 | hp1 | a0002 | c0002 | t0037 | g0187 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03942 | hp1 | a0003 | c0003 | t0018 | g0188 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0311 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04115 | hp1 | a0002 | c0002 | t0009 | g0183 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04115 | hp2 | a0004 | c0004 | t0010 | g0259 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04184 | hp2 | a0001 | c0007 | t0002 | g0116 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04199 | hp1 | a0001 | c0007 | t0002 | g0105 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04199 | hp2 | a0006 | c0006 | t0001 | g0182 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04204 | hp1 | a0003 | c0003 | t0005 | g0033 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG04204 | hp2 | a0002 | c0002 | t0006 | g0357 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18522 | hp1 | a0002 | c0002 | t0023 | g0211 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0232 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18612 | hp1 | a0003 | c0003 | t0005 | g0028 | EAS | CHB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18612 | hp2 | a0001 | c0001 | t0015 | g0208 | EAS | CHB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18906 | hp1 | a0005 | c0005 | t0019 | g0007 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18939 | hp1 | a0003 | c0003 | t0005 | g0030 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18939 | hp2 | a0008 | c0008 | t0003 | g0348 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18941 | hp1 | a0002 | c0002 | t0021 | g0342 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18942 | hp2 | a0004 | c0004 | t0004 | g0278 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18945 | hp1 | a0003 | c0003 | t0008 | g0034 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18946 | hp1 | a0007 | c0009 | t0001 | g0163 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18946 | hp2 | a0001 | c0001 | t0027 | g0063 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18947 | hp1 | a0003 | c0003 | t0008 | g0047 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18947 | hp2 | a0008 | c0008 | t0003 | g0349 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18949 | hp1 | a0004 | c0004 | t0010 | g0271 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18949 | hp2 | a0002 | c0002 | t0006 | g0345 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18950 | hp1 | a0007 | c0009 | t0001 | g0162 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18951 | hp1 | a0003 | c0003 | t0005 | g0032 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18951 | hp2 | a0001 | c0001 | t0012 | g0216 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18953 | hp1 | a0003 | c0003 | t0008 | g0373 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18953 | hp2 | a0010 | c0011 | t0001 | g0194 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18954 | hp1 | a0004 | c0004 | t0003 | g0318 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18956 | hp1 | a0004 | c0004 | t0010 | g0057 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18956 | hp2 | a0010 | c0011 | t0001 | g0213 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18959 | hp1 | a0002 | c0002 | t0006 | g0333 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18960 | hp1 | a0001 | c0027 | t0004 | g0351 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18962 | hp1 | a0010 | c0011 | t0001 | g0185 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18962 | hp2 | a0003 | c0003 | t0005 | g0024 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18963 | hp1 | a0002 | c0002 | t0006 | g0372 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18964 | hp2 | a0004 | c0004 | t0003 | g0273 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18965 | hp1 | a0004 | c0004 | t0003 | g0255 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18965 | hp2 | a0003 | c0003 | t0005 | g0026 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18966 | hp1 | a0004 | c0004 | t0003 | g0274 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18967 | hp1 | a0002 | c0002 | t0009 | g0201 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0316 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18968 | hp1 | a0001 | c0016 | t0006 | g0023 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18970 | hp2 | a0007 | c0009 | t0001 | g0055 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18971 | hp2 | a0001 | c0016 | t0002 | g0039 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18973 | hp1 | a0004 | c0004 | t0003 | g0276 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18973 | hp2 | a0002 | c0002 | t0009 | g0149 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18974 | hp1 | a0004 | c0004 | t0003 | g0286 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18974 | hp2 | a0001 | c0033 | t0004 | g0336 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18978 | hp1 | a0003 | c0003 | t0008 | g0046 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18978 | hp2 | a0004 | c0004 | t0003 | g0307 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18979 | hp1 | a0004 | c0004 | t0003 | g0275 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18979 | hp2 | a0003 | c0003 | t0008 | g0051 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18980 | hp1 | a0008 | c0008 | t0003 | g0355 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18981 | hp1 | a0004 | c0004 | t0003 | g0266 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18983 | hp1 | a0004 | c0004 | t0003 | g0264 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18984 | hp1 | a0001 | c0001 | t0015 | g0159 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18985 | hp1 | a0004 | c0004 | t0010 | g0262 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18985 | hp2 | a0001 | c0001 | t0013 | g0327 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18988 | hp2 | a0002 | c0002 | t0015 | g0152 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18989 | hp1 | a0001 | c0001 | t0030 | g0209 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18989 | hp2 | a0004 | c0004 | t0010 | g0268 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18991 | hp1 | a0002 | c0002 | t0009 | g0197 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18991 | hp2 | a0004 | c0004 | t0003 | g0260 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18994 | hp1 | a0004 | c0004 | t0003 | g0008 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18994 | hp2 | a0003 | c0003 | t0026 | g0016 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18995 | hp2 | a0003 | c0003 | t0008 | g0049 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18998 | hp1 | a0003 | c0003 | t0005 | g0036 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA18999 | hp2 | a0003 | c0003 | t0008 | g0054 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19000 | hp1 | a0027 | c0020 | t0010 | g0285 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19001 | hp1 | a0001 | c0001 | t0025 | g0092 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19002 | hp2 | a0003 | c0003 | t0026 | g0015 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0356 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19004 | hp2 | a0003 | c0003 | t0005 | g0031 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19005 | hp1 | a0004 | c0004 | t0003 | g0247 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19006 | hp1 | a0004 | c0004 | t0010 | g0284 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19007 | hp1 | a0004 | c0004 | t0003 | g0257 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19009 | hp1 | a0004 | c0004 | t0003 | g0265 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19009 | hp2 | a0003 | c0003 | t0005 | g0003 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19012 | hp2 | a0008 | c0008 | t0006 | g0090 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19030 | hp1 | a0005 | c0005 | t0007 | g0293 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19043 | hp1 | a0012 | c0014 | t0007 | g0122 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19043 | hp2 | a0005 | c0005 | t0038 | g0289 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19054 | hp1 | a0013 | c0015 | t0018 | g0221 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19054 | hp2 | a0004 | c0004 | t0003 | g0008 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19058 | hp1 | a0003 | c0003 | t0005 | g0017 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19058 | hp2 | a0007 | c0009 | t0001 | g0177 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19060 | hp1 | a0008 | c0008 | t0032 | g0220 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19062 | hp1 | a0003 | c0003 | t0005 | g0018 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0341 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19063 | hp2 | a0001 | c0001 | t0027 | g0077 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19064 | hp1 | a0003 | c0003 | t0005 | g0035 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19065 | hp1 | a0003 | c0003 | t0005 | g0042 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19065 | hp2 | a0001 | c0001 | t0025 | g0101 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19066 | hp1 | a0005 | c0005 | t0013 | g0263 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19066 | hp2 | a0003 | c0003 | t0005 | g0003 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19070 | hp1 | a0003 | c0003 | t0018 | g0228 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19074 | hp1 | a0005 | c0005 | t0004 | g0306 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19074 | hp2 | a0004 | c0004 | t0003 | g0258 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19076 | hp2 | a0003 | c0003 | t0005 | g0038 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19077 | hp1 | a0004 | c0004 | t0003 | g0379 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19077 | hp2 | a0001 | c0001 | t0013 | g0335 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19078 | hp1 | a0002 | c0002 | t0021 | g0354 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19078 | hp2 | a0008 | c0008 | t0003 | g0370 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0368 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19080 | hp2 | a0003 | c0003 | t0005 | g0050 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19081 | hp2 | a0007 | c0009 | t0001 | g0178 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19082 | hp2 | a0008 | c0008 | t0003 | g0374 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19084 | hp1 | a0007 | c0009 | t0009 | g0161 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19087 | hp1 | a0001 | c0001 | t0044 | g0081 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19087 | hp2 | a0007 | c0009 | t0001 | g0056 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19090 | hp1 | a0001 | c0001 | t0013 | g0344 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19090 | hp2 | a0010 | c0011 | t0001 | g0226 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19091 | hp2 | a0003 | c0003 | t0005 | g0041 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19240 | hp1 | a0005 | c0005 | t0019 | g0007 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA19240 | hp2 | a0005 | c0005 | t0024 | g0001 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20129 | hp1 | a0009 | c0010 | t0016 | g0324 | AFR | ASW | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ASW | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20805 | hp1 | a0004 | c0032 | t0003 | g0269 | EUR | TSI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0167 | EUR | TSI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20905 | hp1 | a0001 | c0013 | t0002 | g0070 | SAS | GIH | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20905 | hp2 | a0004 | c0004 | t0039 | g0245 | SAS | GIH | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG01123 | hp2 | a0001 | c0007 | t0002 | g0103 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02486 | hp1 | a0005 | c0005 | t0007 | g0295 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02486 | hp2 | a0014 | c0017 | t0007 | g0118 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02559 | hp1 | a0017 | c0023 | t0045 | g0252 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG02559 | hp2 | a0016 | c0034 | t0020 | g0375 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03471 | hp1 | a0005 | c0005 | t0007 | g0001 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG03471 | hp2 | a0011 | c0012 | t0014 | g0231 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0317 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| HG06807 | hp2 | a0023 | c0028 | t0001 | g0012 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20300 | hp1 | a0004 | c0004 | t0003 | g0283 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| NA20300 | hp2 | a0002 | c0002 | t0009 | g0215 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| homoSapiens_chm13v2 | hp1 | a0026 | c0021 | t0001 | g0301 | REF | REF | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| homoSapiens_grch38 | hp1 | a0006 | c0006 | t0036 | g0196 | REF | REF | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109913381
|
A | C | 1 | a0007 | 7 | NA18946.hp1 NA18950.hp1 NA18970.hp2 others(4): Show |
missense_variant | MODERATE | c.46A>C | p.Ser16Arg | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 499/6388 | 46/3624 | 16/1207 | chr4 | 109913381 | ||
| chr4:109913435
|
G | A | 1 | a0027 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 553/6388 | 100/3624 | 34/1207 | chr4 | 109913435 | ||
| chr4:109943377
|
C | T | 3 | a0012a0014a0015 | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.451C>T | p.His151Tyr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/24 | 904/6388 | 451/3624 | 151/1207 | chr4 | 109943377 | ||
| chr4:109943888
|
G | C | 3 | a0012a0014a0015 | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.556G>C | p.Asp186His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/24 | 1009/6388 | 556/3624 | 186/1207 | chr4 | 109943888 | ||
| chr4:109943994
|
G | C | 1 | a0026 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.662G>C | p.Arg221Thr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/24 | 1115/6388 | 662/3624 | 221/1207 | chr4 | 109943994 | ||
| chr4:109945104
|
G | C | 1 | a0011 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.769G>C | p.Asp257His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/24 | 1222/6388 | 769/3624 | 257/1207 | chr4 | 109945104 | ||
| chr4:109945210
|
T | A | 1 | a0016 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.875T>A | p.Leu292His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/24 | 1328/6388 | 875/3624 | 292/1207 | chr4 | 109945210 | ||
| chr4:109961965
|
G | A | 8 | a0004a0005a0009others(5): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
missense_variant | MODERATE | c.1292G>A | p.Arg431Lys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/24 | 1745/6388 | 1292/3624 | 431/1207 | chr4 | 109961965 | ||
| chr4:109963227
|
C | A | 1 | a0020 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1367C>A | p.Pro456Gln | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/24 | 1820/6388 | 1367/3624 | 456/1207 | chr4 | 109963227 | ||
| chr4:109976096
|
C | G | 1 | a0011 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.1914C>G | p.Ser638Arg | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/24 | 2367/6388 | 1914/3624 | 638/1207 | chr4 | 109976096 | ||
| chr4:109976211
|
C | T | 1 | a0021 | 1 | HG02083.hp2 | stop_gained | HIGH | c.2029C>T | p.Arg677* | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/24 | 2482/6388 | 2029/3624 | 677/1207 | chr4 | 109976211 | ||
| chr4:109980042
|
G | A | 19 | a0001a0003a0004others(16): Show | 277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
missense_variant | MODERATE | c.2124G>A | p.Met708Ile | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/24 | 2577/6388 | 2124/3624 | 708/1207 | chr4 | 109980042 | ||
| chr4:109980955
|
A | T | 3 | a0004a0008a0027 | 48 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(45): Show |
missense_variant | MODERATE | c.2351A>T | p.Asp784Val | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/24 | 2804/6388 | 2351/3624 | 784/1207 | chr4 | 109980955 | ||
| chr4:109987777
|
T | C | 4 | a0015a0016a0024others(1): Show | 5 | HG00738.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.2525T>C | p.Met842Thr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/24 | 2978/6388 | 2525/3624 | 842/1207 | chr4 | 109987777 | ||
| chr4:109988649
|
G | A | 1 | a0023 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2674G>A | p.Glu892Lys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/24 | 3127/6388 | 2674/3624 | 892/1207 | chr4 | 109988649 | ||
| chr4:109993271
|
A | T | 25 | a0001a0002a0003others(22): Show | 373 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(370): Show |
missense_variant | MODERATE | c.2759A>T | p.Glu920Val | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/24 | 3212/6388 | 2759/3624 | 920/1207 | chr4 | 109993271 | ||
| chr4:109999791
|
G | A | 1 | a0010 | 4 | NA18953.hp2 NA18956.hp2 NA18962.hp1 others(1): Show |
missense_variant | MODERATE | c.3118G>A | p.Val1040Met | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/24 | 3571/6388 | 3118/3624 | 1040/1207 | chr4 | 109999791 | ||
| chr4:109999800
|
C | T | 2 | a0009a0024 | 6 | HG00738.hp1 HG01975.hp2 HG02895.hp1 others(3): Show |
missense_variant | MODERATE | c.3127C>T | p.Leu1043Phe | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/24 | 3580/6388 | 3127/3624 | 1043/1207 | chr4 | 109999800 | ||
| chr4:110004582
|
C | G | 2 | a0017a0022 | 2 | HG02559.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.3251C>G | p.Ala1084Gly | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/24 | 3704/6388 | 3251/3624 | 1084/1207 | chr4 | 110004582 | ||
| chr4:110011233
|
G | GC | 3 | a0003a0013a0021 | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
frameshift_variant | HIGH | c.3406dupC | p.Gln1136fs | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 3860/6388 | 3407/3624 | 1136/1207 | INFO_REALIGN_3_PRIME | chr4 | 110011233 | |
| chr4:110011352
|
C | A | 2 | a0014a0018 | 3 | HG02257.hp1 HG02486.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.3521C>A | p.Thr1174Asn | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 3974/6388 | 3521/3624 | 1174/1207 | chr4 | 110011352 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109941082
|
C | T | 3 | a0001c0019a0016c0034a0025c0035 | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.264C>T | p.Ile88Ile | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/24 | 717/6388 | 264/3624 | 88/1207 | chr4 | 109941082 | ||
| chr4:109943379
|
C | T | 1 | a0001c0033 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.453C>T | p.His151His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/24 | 906/6388 | 453/3624 | 151/1207 | chr4 | 109943379 | ||
| chr4:109960895
|
T | C | 1 | a0001c0013 | 3 | HG00323.hp2 HG03710.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.1095T>C | p.His365His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/24 | 1548/6388 | 1095/3624 | 365/1207 | chr4 | 109960895 | ||
| chr4:109960928
|
A | T | 1 | a0004c0032 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1128A>T | p.Gly376Gly | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/24 | 1581/6388 | 1128/3624 | 376/1207 | chr4 | 109960928 | ||
| chr4:109968997
|
G | A | 1 | a0001c0026 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.1602G>A | p.Lys534Lys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/24 | 2055/6388 | 1602/3624 | 534/1207 | chr4 | 109968997 | ||
| chr4:109969105
|
T | C | 1 | a0001c0027 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.1710T>C | p.Tyr570Tyr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/24 | 2163/6388 | 1710/3624 | 570/1207 | chr4 | 109969105 | ||
| chr4:109976159
|
C | T | 1 | a0001c0007 | 8 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
synonymous_variant | LOW | c.1977C>T | p.Cys659Cys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/24 | 2430/6388 | 1977/3624 | 659/1207 | chr4 | 109976159 | ||
| chr4:109979991
|
A | G | 7 | a0001c0016a0003c0003a0015c0018others(4): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
synonymous_variant | LOW | c.2073A>G | p.Ala691Ala | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/24 | 2526/6388 | 2073/3624 | 691/1207 | chr4 | 109979991 | ||
| chr4:109980902
|
G | A | 1 | a0015c0018 | 2 | HG02809.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.2298G>A | p.Ser766Ser | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/24 | 2751/6388 | 2298/3624 | 766/1207 | chr4 | 109980902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109912912
|
G | A | 3 | a0001c0001t0022a0001c0001t0028a0001c0001t0029 | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-424G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 424 | chr4 | 109912912 | |||||
| chr4:109912954
|
A | G | 64 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(61): Show | 267 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(264): Show |
5_prime_UTR_variant | MODIFIER | c.-382A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 382 | chr4 | 109912954 | |||||
| chr4:109912994
|
C | T | 3 | a0005c0005t0019a0005c0005t0046a0017c0023t0045 | 6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-342C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 342 | chr4 | 109912994 | |||||
| chr4:109913258
|
A | G | 2 | a0001c0001t0027a0001c0001t0044 | 3 | NA18946.hp2 NA19063.hp2 NA19087.hp1 |
5_prime_UTR_variant | MODIFIER | c.-78A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 78 | chr4 | 109913258 | |||||
| chr4:110011612
|
G | A | 1 | a0001c0001t0030 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 157 | chr4 | 110011612 | |||||
| chr4:110011848
|
T | C | 11 | a0001c0001t0003a0004c0004t0003a0004c0004t0010others(8): Show | 50 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*393T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 393 | chr4 | 110011848 | |||||
| chr4:110011938
|
C | T | 4 | a0001c0019t0017a0005c0005t0017a0015c0018t0017others(1): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 483 | chr4 | 110011938 | |||||
| chr4:110012367
|
G | GT | 6 | a0002c0002t0009a0002c0002t0021a0003c0003t0008others(3): Show | 28 | HG00423.hp1 HG00621.hp1 HG01175.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*926dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 927 | INFO_REALIGN_3_PRIME | chr4 | 110012367 | ||||
| chr4:110012367
|
GT | G | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(43): Show | 193 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*926delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 926 | INFO_REALIGN_3_PRIME | chr4 | 110012367 | ||||
| chr4:110012367
|
GTT | G | 6 | a0001c0001t0028a0001c0001t0033a0001c0019t0017others(3): Show | 7 | HG00735.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*926delTT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 925 | INFO_REALIGN_3_PRIME | chr4 | 110012367 | ||||
| chr4:110012384
|
G | A | 2 | a0005c0005t0024a0005c0005t0041 | 3 | HG02572.hp2 HG03098.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 929 | chr4 | 110012384 | |||||
| chr4:110012624
|
C | T | 1 | a0002c0002t0043 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1169 | chr4 | 110012624 | |||||
| chr4:110012677
|
A | G | 13 | a0001c0001t0004a0001c0001t0013a0001c0001t0015others(10): Show | 55 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1222A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1222 | chr4 | 110012677 | |||||
| chr4:110012699
|
T | C | 58 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(55): Show | 207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1244T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1244 | chr4 | 110012699 | |||||
| chr4:110012721
|
T | A | 2 | a0001c0001t0011a0005c0005t0011 | 8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1266T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1266 | chr4 | 110012721 | |||||
| chr4:110012738
|
C | T | 1 | a0003c0003t0026 | 2 | NA18994.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1283C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1283 | chr4 | 110012738 | |||||
| chr4:110012890
|
T | C | 2 | a0017c0023t0045a0022c0029t0031 | 2 | HG02559.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1435T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1435 | chr4 | 110012890 | |||||
| chr4:110013029
|
G | A | 1 | a0002c0002t0023 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1574G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1574 | chr4 | 110013029 | |||||
| chr4:110013043
|
G | C | 3 | a0009c0010t0016a0009c0010t0042a0024c0030t0016 | 6 | HG00738.hp1 HG01975.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1588G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1588 | chr4 | 110013043 | |||||
| chr4:110013214
|
T | G | 1 | a0005c0005t0038 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1759 | chr4 | 110013214 | |||||
| chr4:110013278
|
C | A | 4 | a0001c0001t0020a0001c0001t0034a0001c0001t0040others(1): Show | 5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1823C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1823 | chr4 | 110013278 | |||||
| chr4:110013284
|
T | C | 3 | a0001c0001t0022a0001c0001t0029a0005c0005t0019 | 7 | HG02055.hp1 HG02280.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1829T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1829 | chr4 | 110013284 | |||||
| chr4:110013488
|
T | A | 1 | a0004c0004t0039 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2033T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2033 | chr4 | 110013488 | |||||
| chr4:110013496
|
G | C | 8 | a0001c0001t0011a0001c0001t0020a0001c0001t0028others(5): Show | 15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2041 | chr4 | 110013496 | |||||
| chr4:110013614
|
T | C | 1 | a0002c0002t0035 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2159 | chr4 | 110013614 | |||||
| chr4:110013649
|
T | C | 8 | a0001c0001t0011a0001c0001t0020a0001c0001t0028others(5): Show | 15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2194T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2194 | chr4 | 110013649 | |||||
| chr4:110013650
|
C | G | 8 | a0001c0001t0011a0001c0001t0020a0001c0001t0028others(5): Show | 15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2195C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2195 | chr4 | 110013650 | |||||
| chr4:110013667
|
C | T | 92 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(89): Show | 387 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(384): Show |
3_prime_UTR_variant | MODIFIER | c.*2212C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2212 | chr4 | 110013667 | |||||
| chr4:110013691
|
T | A | 1 | a0002c0002t0037 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2236T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2236 | chr4 | 110013691 | |||||
| chr4:110013729
|
C | T | 8 | a0001c0001t0011a0001c0001t0020a0001c0001t0028others(5): Show | 15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2274C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2274 | chr4 | 110013729 | |||||
| chr4:110013731
|
C | A | 1 | a0001c0001t0025 | 2 | NA19001.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2276 | chr4 | 110013731 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109913475
|
A | G | 1 | a0004c0004t0003g0379 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.127+13A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913475 | ||||||
| chr4:109913491
|
G | T | 4 | a0001c0001t0012g0376a0001c0001t0015g0377a0001c0001t0015g0378others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+29G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913491 | ||||||
| chr4:109913560
|
G | A | 5 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0011others(2): Show | 5 | HG02818.hp1 HG03225.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+98G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913560 | ||||||
| chr4:109913569
|
T | C | 44 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+107T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913569 | ||||||
| chr4:109913761
|
G | A | 2 | a0007c0009t0001g0055a0007c0009t0001g0056 | 2 | NA18970.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.127+299G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913761 | ||||||
| chr4:109913764
|
A | G | 58 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0328others(55): Show | 58 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.127+302A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913764 | ||||||
| chr4:109913781
|
T | TG | 44 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+320dupG | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109913781 | |||||
| chr4:109913898
|
A | T | 58 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0328others(55): Show | 58 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.127+436A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913898 | ||||||
| chr4:109914282
|
T | TG | 44 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+820_127+821ins others(1): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914282 | ||||||
| chr4:109914288
|
C | T | 5 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(2): Show | 5 | NA18963.hp2 NA18967.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+826C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914288 | ||||||
| chr4:109914354
|
T | C | 1 | a0004c0004t0010g0057 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.127+892T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914354 | ||||||
| chr4:109914382
|
A | G | 1 | a0002c0002t0001g0311 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.127+920A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914382 | ||||||
| chr4:109914587
|
G | C | 44 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+1125G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914587 | ||||||
| chr4:109914687
|
T | A | 1 | a0015c0018t0017g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127+1225T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914687 | ||||||
| chr4:109914829
|
A | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+1367A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914829 | ||||||
| chr4:109914874
|
A | G | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG00733.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.127+1412A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914874 | ||||||
| chr4:109914892
|
G | A | 64 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(61): Show | 65 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.127+1430G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914892 | ||||||
| chr4:109914925
|
G | T | 1 | a0004c0004t0003g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127+1463G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914925 | ||||||
| chr4:109914926
|
T | G | 1 | a0004c0004t0003g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127+1464T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914926 | ||||||
| chr4:109915099
|
G | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+1637G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915099 | ||||||
| chr4:109915315
|
T | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+1853T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915315 | ||||||
| chr4:109915355
|
C | A | 1 | a0004c0004t0003g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127+1893C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915355 | ||||||
| chr4:109915408
|
G | A | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+1946G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915408 | ||||||
| chr4:109915434
|
A | T | 1 | a0005c0005t0004g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.127+1972A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915434 | ||||||
| chr4:109915444
|
A | G | 1 | a0008c0008t0003g0374 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.127+1982A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915444 | ||||||
| chr4:109915471
|
C | T | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127+2009C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915471 | ||||||
| chr4:109915606
|
C | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+2144C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915606 | ||||||
| chr4:109915733
|
C | T | 6 | a0006c0006t0001g0299a0006c0006t0001g0300a0006c0006t0001g0302others(3): Show | 6 | HG00140.hp2 HG01081.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2271C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915733 | ||||||
| chr4:109915849
|
G | A | 1 | a0004c0004t0003g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127+2387G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915849 | ||||||
| chr4:109916131
|
C | T | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+2669C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916131 | ||||||
| chr4:109916226
|
A | T | 45 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(42): Show | 46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.127+2764A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916226 | ||||||
| chr4:109916333
|
C | T | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+2871C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916333 | ||||||
| chr4:109916364
|
T | C | 6 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(3): Show | 6 | HG00738.hp2 HG01192.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+2902T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916364 | ||||||
| chr4:109916417
|
C | A | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+2955C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916417 | ||||||
| chr4:109916425
|
TGC | T | 5 | a0001c0001t0004g0368a0002c0002t0006g0371a0002c0002t0006g0372others(2): Show | 5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2964_127+2965d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916425 | ||||||
| chr4:109916430
|
C | CCTGGATT others(14): Show |
5 | a0001c0001t0004g0368a0002c0002t0006g0371a0002c0002t0006g0372others(2): Show | 5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2968_127+2969i others(23): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916430 | ||||||
| chr4:109916431
|
T | A | 5 | a0001c0001t0004g0368a0002c0002t0006g0371a0002c0002t0006g0372others(2): Show | 5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2969T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916431 | ||||||
| chr4:109916452
|
T | C | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127+2990T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916452 | ||||||
| chr4:109916511
|
G | A | 216 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(213): Show | 221 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.127+3049G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916511 | ||||||
| chr4:109916574
|
C | T | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127+3112C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916574 | ||||||
| chr4:109916623
|
T | A | 1 | a0004c0004t0039g0245 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127+3161T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916623 | ||||||
| chr4:109916635
|
T | C | 1 | a0005c0005t0007g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127+3173T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916635 | ||||||
| chr4:109916729
|
G | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+3267G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916729 | ||||||
| chr4:109916747
|
G | GT | 278 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(275): Show | 284 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.127+3289dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109916747 | |||||
| chr4:109916784
|
G | A | 1 | a0002c0002t0001g0148 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127+3322G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916784 | ||||||
| chr4:109916839
|
A | G | 10 | a0001c0001t0004g0358a0001c0001t0004g0359a0001c0001t0004g0360others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.127+3377A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916839 | ||||||
| chr4:109916853
|
T | C | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127+3391T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916853 | ||||||
| chr4:109916970
|
G | A | 262 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(259): Show | 268 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.127+3508G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916970 | ||||||
| chr4:109917133
|
G | C | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061 | 3 | HG00735.hp1 HG01358.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.127+3671G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917133 | ||||||
| chr4:109917431
|
A | G | 1 | a0001c0007t0002g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127+3969A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917431 | ||||||
| chr4:109917706
|
C | T | 261 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(258): Show | 267 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.127+4244C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917706 | ||||||
| chr4:109917779
|
C | T | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG02717.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127+4317C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917779 | ||||||
| chr4:109917780
|
C | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+4318C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917780 | ||||||
| chr4:109917794
|
A | AT | 3 | a0001c0001t0012g0376a0001c0001t0015g0377a0001c0001t0015g0378 | 3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+4337dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109917794 | |||||
| chr4:109917799
|
T | C | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+4337T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917799 | ||||||
| chr4:109917835
|
G | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.127+4373G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917835 | ||||||
| chr4:109918255
|
G | GT | 210 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(207): Show | 215 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.127+4809dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109918255 | |||||
| chr4:109918273
|
A | T | 5 | a0001c0001t0004g0368a0002c0002t0006g0371a0002c0002t0006g0372others(2): Show | 5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+4811A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918273 | ||||||
| chr4:109918299
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.127+4837T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918299 | ||||||
| chr4:109918345
|
C | T | 55 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(52): Show | 57 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.127+4883C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918345 | ||||||
| chr4:109918370
|
G | A | 1 | a0004c0004t0003g0318 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.127+4908G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918370 | ||||||
| chr4:109918514
|
C | T | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+5052C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918514 | ||||||
| chr4:109918671
|
C | T | 3 | a0006c0006t0001g0302a0006c0006t0001g0303a0006c0006t0001g0304 | 3 | HG01081.hp1 HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.127+5209C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918671 | ||||||
| chr4:109918676
|
C | A | 1 | a0002c0002t0009g0149 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.127+5214C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918676 | ||||||
| chr4:109918798
|
C | T | 73 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(70): Show | 75 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.127+5336C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918798 | ||||||
| chr4:109918832
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+5370T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918832 | ||||||
| chr4:109918872
|
G | A | 6 | a0001c0001t0002g0066a0001c0001t0002g0068a0001c0001t0002g0071others(3): Show | 6 | HG00323.hp2 HG02300.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+5410G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918872 | ||||||
| chr4:109918923
|
G | A | 9 | a0002c0002t0001g0150a0002c0002t0001g0151a0002c0002t0001g0153others(6): Show | 9 | NA18941.hp2 NA18957.hp1 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+5461G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918923 | ||||||
| chr4:109919250
|
G | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+5788G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919250 | ||||||
| chr4:109919267
|
T | C | 3 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124 | 4 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5805T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919267 | ||||||
| chr4:109919287
|
G | GTC | 27 | a0001c0001t0002g0065a0001c0001t0002g0109a0001c0001t0002g0110others(24): Show | 27 | HG00733.hp1 HG01169.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.127+5878_127+5879d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
G | GTCTC | 19 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0130others(16): Show | 19 | HG00408.hp2 HG01070.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+5876_127+5879d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
G | GTCTCTC | 5 | a0001c0001t0002g0115a0001c0001t0033g0240a0002c0002t0001g0222others(2): Show | 5 | HG00438.hp1 HG00597.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+5874_127+5879d others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
G | GTCTCTCT others(1): Show |
4 | a0001c0001t0002g0312a0002c0002t0001g0224a0002c0002t0001g0225others(1): Show | 4 | NA19006.hp2 NA19086.hp2 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+5872_127+5879d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
G | GTCTCTCT others(3): Show |
1 | a0002c0002t0009g0227 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.127+5870_127+5879d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
G | GTCTCTCT others(13): Show |
1 | a0002c0002t0001g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+5860_127+5879d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
G | GTCTCTGT others(3): Show |
1 | a0001c0001t0015g0378 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127+5830_127+5831i others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTC | G | 37 | a0001c0001t0002g0071a0001c0001t0002g0098a0001c0001t0002g0099others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.127+5878_127+5879d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTC | G | 39 | a0001c0001t0002g0062a0001c0001t0002g0096a0001c0001t0002g0097others(36): Show | 40 | HG00408.hp1 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.127+5876_127+5879d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTC | G | 33 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(30): Show | 34 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.127+5874_127+5879d others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(1): Show |
G | 87 | a0001c0001t0002g0082a0001c0001t0002g0084a0001c0001t0002g0085others(84): Show | 90 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(87): Show |
intron_variant | MODIFIER | c.127+5872_127+5879d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(3): Show |
G | 17 | a0001c0001t0002g0060a0001c0001t0004g0358a0001c0001t0011g0141others(14): Show | 17 | HG00735.hp2 HG01070.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+5870_127+5879d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(5): Show |
G | 10 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0004g0325others(7): Show | 10 | HG01358.hp1 NA18942.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+5868_127+5879d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(7): Show |
G | 12 | a0001c0001t0002g0059a0001c0001t0003g0073a0001c0001t0003g0074others(9): Show | 12 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.127+5866_127+5879d others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(9): Show |
G | 11 | a0001c0001t0007g0317a0003c0003t0005g0050a0003c0003t0008g0049others(8): Show | 11 | HG01109.hp2 HG01975.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+5864_127+5879d others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(11): Show |
G | 40 | a0001c0001t0002g0072a0001c0001t0004g0019a0001c0016t0002g0039others(37): Show | 41 | HG00609.hp2 HG00621.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.127+5862_127+5879d others(20): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(13): Show |
G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+5860_127+5879d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(17): Show |
G | 1 | a0003c0003t0018g0228 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.127+5856_127+5879d others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919287
|
GTCTCTCT others(33): Show |
G | 4 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(1): Show | 5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+5840_127+5879d others(42): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | |||||
| chr4:109919291
|
C | G | 1 | a0002c0002t0001g0158 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.127+5829C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919291 | ||||||
| chr4:109919293
|
C | G | 1 | a0001c0001t0015g0377 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127+5831C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919293 | ||||||
| chr4:109919297
|
C | G | 4 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5835C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919297 | ||||||
| chr4:109919299
|
C | G | 1 | a0001c0001t0012g0376 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127+5837C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919299 | ||||||
| chr4:109919301
|
C | G | 1 | a0001c0001t0022g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.127+5839C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919301 | ||||||
| chr4:109919303
|
C | G | 7 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(4): Show | 7 | HG00735.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+5841C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919303 | ||||||
| chr4:109919323
|
C | T | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+5861C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919323 | ||||||
| chr4:109919428
|
T | C | 1 | a0004c0004t0003g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127+5966T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919428 | ||||||
| chr4:109919429
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+5967T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919429 | ||||||
| chr4:109919450
|
C | A | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127+5988C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919450 | ||||||
| chr4:109919540
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+6078G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919540 | ||||||
| chr4:109919552
|
G | A | 1 | a0003c0003t0005g0014 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.127+6090G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919552 | ||||||
| chr4:109919582
|
AAGAGGAC others(4991): Show |
A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+6123_127+11120 others(3): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919582 | |||||
| chr4:109919592
|
C | T | 271 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(268): Show | 277 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.127+6130C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919592 | ||||||
| chr4:109919629
|
T | C | 3 | a0001c0001t0012g0376a0001c0001t0015g0377a0001c0001t0015g0378 | 3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+6167T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919629 | ||||||
| chr4:109919630
|
G | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+6168G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919630 | ||||||
| chr4:109919635
|
G | T | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+6173G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919635 | ||||||
| chr4:109919655
|
G | A | 1 | a0002c0002t0001g0172 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127+6193G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919655 | ||||||
| chr4:109919711
|
G | A | 135 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(132): Show | 138 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.127+6249G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919711 | ||||||
| chr4:109919790
|
A | G | 255 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(252): Show | 261 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.127+6328A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919790 | ||||||
| chr4:109919858
|
A | G | 1 | a0005c0005t0006g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+6396A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919858 | ||||||
| chr4:109919870
|
C | A | 73 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(70): Show | 75 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.127+6408C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919870 | ||||||
| chr4:109919936
|
T | A | 1 | a0002c0002t0001g0224 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.127+6474T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919936 | ||||||
| chr4:109919981
|
G | A | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+6519G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919981 | ||||||
| chr4:109920274
|
T | C | 11 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(8): Show | 11 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+6812T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920274 | ||||||
| chr4:109920565
|
C | A | 1 | a0001c0007t0002g0089 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.127+7103C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920565 | ||||||
| chr4:109920643
|
A | G | 4 | a0002c0002t0001g0191a0002c0002t0001g0219a0002c0002t0001g0223others(1): Show | 4 | HG00438.hp1 NA18983.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+7181A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920643 | ||||||
| chr4:109920745
|
A | T | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+7283A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920745 | ||||||
| chr4:109920864
|
G | A | 41 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(38): Show | 42 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.127+7402G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920864 | ||||||
| chr4:109921253
|
T | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+7791T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921253 | ||||||
| chr4:109921253
|
T | TAGAAACT others(627): Show |
1 | a0001c0001t0014g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127+7807_127+7808i others(636): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109921253 | |||||
| chr4:109921253
|
T | TAGAAACT others(636): Show |
4 | a0001c0001t0012g0236a0001c0001t0020g0233a0001c0001t0020g0237others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+7807_127+7808i others(645): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109921253 | |||||
| chr4:109921262
|
C | T | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+7800C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921262 | ||||||
| chr4:109921357
|
T | G | 1 | a0002c0002t0001g0134 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.127+7895T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921357 | ||||||
| chr4:109921398
|
T | C | 2 | a0004c0004t0003g0257a0004c0004t0003g0258 | 2 | NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.127+7936T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921398 | ||||||
| chr4:109921399
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+7937T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921399 | ||||||
| chr4:109921625
|
C | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+8163C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921625 | ||||||
| chr4:109921652
|
C | T | 1 | a0003c0003t0005g0048 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.127+8190C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921652 | ||||||
| chr4:109921720
|
A | G | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+8258A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921720 | ||||||
| chr4:109921728
|
A | C | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+8266A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921728 | ||||||
| chr4:109921822
|
T | C | 1 | a0004c0004t0010g0259 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127+8360T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921822 | ||||||
| chr4:109921877
|
G | C | 11 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(8): Show | 11 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+8415G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921877 | ||||||
| chr4:109921984
|
T | C | 136 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(133): Show | 139 | HG00323.hp2 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.127+8522T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921984 | ||||||
| chr4:109921992
|
T | G | 209 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(206): Show | 214 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.127+8530T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921992 | ||||||
| chr4:109922075
|
A | G | 1 | a0002c0002t0021g0354 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.127+8613A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922075 | ||||||
| chr4:109922086
|
A | C | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127+8624A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922086 | ||||||
| chr4:109922104
|
A | G | 271 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(268): Show | 277 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.127+8642A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922104 | ||||||
| chr4:109922143
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+8681C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922143 | ||||||
| chr4:109922182
|
G | T | 3 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147 | 3 | HG02622.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127+8720G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922182 | ||||||
| chr4:109922272
|
C | G | 50 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0328others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.127+8810C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922272 | ||||||
| chr4:109922297
|
T | C | 1 | a0003c0003t0018g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.127+8835T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922297 | ||||||
| chr4:109922687
|
G | A | 1 | a0001c0019t0017g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+9225G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922687 | ||||||
| chr4:109922794
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+9332C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922794 | ||||||
| chr4:109922835
|
T | C | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+9373T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922835 | ||||||
| chr4:109923092
|
C | A | 1 | a0002c0002t0001g0168 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127+9630C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923092 | ||||||
| chr4:109923174
|
T | A | 3 | a0001c0001t0012g0376a0001c0001t0015g0377a0001c0001t0015g0378 | 3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+9712T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923174 | ||||||
| chr4:109923326
|
A | G | 9 | a0001c0001t0012g0236a0001c0001t0014g0232a0001c0001t0014g0239others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+9864A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923326 | ||||||
| chr4:109923659
|
C | T | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+10197C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923659 | ||||||
| chr4:109923827
|
C | A | 1 | a0002c0002t0001g0192 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.127+10365C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923827 | ||||||
| chr4:109923848
|
T | C | 1 | a0001c0001t0004g0347 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.127+10386T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923848 | ||||||
| chr4:109923929
|
T | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+10467T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923929 | ||||||
| chr4:109924056
|
C | T | 1 | a0002c0002t0006g0371 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.127+10594C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924056 | ||||||
| chr4:109924212
|
C | T | 1 | a0005c0005t0007g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127+10750C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924212 | ||||||
| chr4:109924333
|
C | CA | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+10879dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109924333 | |||||
| chr4:109924395
|
T | C | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+10933T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924395 | ||||||
| chr4:109924467
|
C | T | 1 | a0001c0001t0004g0353 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.127+11005C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924467 | ||||||
| chr4:109924508
|
T | C | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127+11046T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924508 | ||||||
| chr4:109924523
|
G | GACATCAC others(6): Show |
4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+11066_127+1107 others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109924523 | |||||
| chr4:109924551
|
T | C | 255 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(252): Show | 261 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.127+11089T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924551 | ||||||
| chr4:109924607
|
A | G | 278 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(275): Show | 284 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.127+11145A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924607 | ||||||
| chr4:109924690
|
G | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+11228G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924690 | ||||||
| chr4:109924730
|
T | G | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+11268T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924730 | ||||||
| chr4:109924807
|
G | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+11345G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924807 | ||||||
| chr4:109924961
|
CCATCAGG others(901): Show |
C | 1 | a0001c0001t0004g0359 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.127+11502_127+1240 others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109924961 | |||||
| chr4:109925223
|
C | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+11761C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925223 | ||||||
| chr4:109925226
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.127+11764C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925226 | ||||||
| chr4:109925361
|
G | A | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+11899G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925361 | ||||||
| chr4:109925481
|
A | T | 1 | a0006c0006t0009g0212 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127+12019A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925481 | ||||||
| chr4:109925640
|
A | G | 120 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(117): Show | 123 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+12178A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925640 | ||||||
| chr4:109925758
|
C | T | 5 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(2): Show | 5 | NA18963.hp2 NA18967.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+12296C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925758 | ||||||
| chr4:109925953
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+12491T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925953 | ||||||
| chr4:109926041
|
A | G | 1 | a0002c0002t0001g0168 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127+12579A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926041 | ||||||
| chr4:109926245
|
C | T | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+12783C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926245 | ||||||
| chr4:109926350
|
C | CT | 32 | a0001c0001t0002g0060a0001c0001t0002g0071a0001c0001t0002g0080others(29): Show | 32 | HG00423.hp2 HG00733.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+12908dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109926350 | |||||
| chr4:109926350
|
CT | C | 116 | a0001c0001t0004g0126a0001c0001t0004g0296a0001c0001t0004g0297others(113): Show | 120 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.127+12908delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109926350 | |||||
| chr4:109926392
|
T | A | 1 | a0005c0005t0019g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+12930T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926392 | ||||||
| chr4:109926430
|
C | T | 3 | a0001c0001t0014g0232a0001c0001t0018g0234a0022c0029t0031g0235 | 3 | HG02809.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.127+12968C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926430 | ||||||
| chr4:109926509
|
C | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+13047C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926509 | ||||||
| chr4:109926512
|
A | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+13050A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926512 | ||||||
| chr4:109926568
|
A | G | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+13106A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926568 | ||||||
| chr4:109926633
|
T | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+13171T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926633 | ||||||
| chr4:109926690
|
G | T | 1 | a0001c0001t0040g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+13228G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926690 | ||||||
| chr4:109926693
|
A | G | 1 | a0020c0022t0006g0294 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127+13231A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926693 | ||||||
| chr4:109926988
|
C | T | 1 | a0003c0003t0005g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.127+13526C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926988 | ||||||
| chr4:109927152
|
G | A | 48 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0328others(45): Show | 48 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.127+13690G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927152 | ||||||
| chr4:109927163
|
T | C | 80 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(77): Show | 81 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.127+13701T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927163 | ||||||
| chr4:109927206
|
C | G | 8 | a0001c0007t0002g0089a0001c0007t0002g0102a0001c0007t0002g0103others(5): Show | 8 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-13740C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927206 | ||||||
| chr4:109927462
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-13484T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927462 | ||||||
| chr4:109927496
|
A | G | 260 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(257): Show | 266 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.128-13450A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927496 | ||||||
| chr4:109927579
|
T | C | 214 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(211): Show | 219 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.128-13367T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927579 | ||||||
| chr4:109927587
|
G | A | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.128-13359G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927587 | ||||||
| chr4:109927596
|
C | T | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-13350C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927596 | ||||||
| chr4:109927638
|
A | G | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-13308A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927638 | ||||||
| chr4:109927641
|
G | T | 1 | a0002c0002t0001g0167 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128-13305G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927641 | ||||||
| chr4:109927642
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.128-13304C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927642 | ||||||
| chr4:109927648
|
C | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-13298C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927648 | ||||||
| chr4:109927719
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.128-13227G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927719 | ||||||
| chr4:109927723
|
C | CA | 32 | a0001c0001t0002g0066a0001c0001t0002g0109a0001c0001t0004g0296others(29): Show | 33 | HG00140.hp2 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.128-13205dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927723 | |||||
| chr4:109927723
|
CA | C | 51 | a0001c0001t0004g0019a0001c0001t0012g0216a0001c0001t0012g0217others(48): Show | 52 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.128-13205delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927723 | |||||
| chr4:109927760
|
T | C | 1 | a0002c0002t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.128-13186T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927760 | ||||||
| chr4:109927806
|
C | CGT | 39 | a0001c0001t0004g0297a0001c0001t0004g0298a0001c0001t0007g0317others(36): Show | 40 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-13098_128-1309 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
C | CGTGT | 19 | a0002c0002t0009g0227a0003c0003t0005g0042a0004c0004t0003g0280others(16): Show | 20 | HG01975.hp2 HG01978.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.128-13100_128-1309 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
C | CGTGTGT | 4 | a0003c0003t0008g0047a0004c0004t0003g0255a0005c0005t0007g0293others(1): Show | 4 | HG02965.hp1 NA18947.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-13102_128-1309 others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGT | C | 163 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0066others(160): Show | 167 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.128-13098_128-1309 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGTGT | C | 65 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(62): Show | 66 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.128-13100_128-1309 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGTGTGT | C | 8 | a0001c0001t0004g0019a0001c0001t0012g0376a0001c0001t0015g0378others(5): Show | 8 | HG00738.hp1 HG01515.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-13102_128-1309 others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGTGTGTG others(3): Show |
C | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-13106_128-1309 others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGTGTGTG others(5): Show |
C | 1 | a0002c0002t0001g0189 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.128-13108_128-1309 others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGTGTGTG others(7): Show |
C | 2 | a0002c0002t0001g0193a0002c0002t0001g0202 | 2 | HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.128-13110_128-1309 others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927806
|
CGTGTGTG others(9): Show |
C | 1 | a0006c0006t0001g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.128-13112_128-1309 others(20): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | |||||
| chr4:109927846
|
T | A | 1 | a0001c0013t0002g0067 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.128-13100T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927846 | ||||||
| chr4:109927848
|
T | A | 127 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(124): Show | 129 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.128-13098T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927848 | ||||||
| chr4:109927848
|
T | TGA | 9 | a0001c0001t0004g0366a0001c0001t0022g0241a0001c0001t0022g0244others(6): Show | 9 | HG00735.hp2 HG01167.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-13097_128-1309 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927848 | |||||
| chr4:109927848
|
T | TGTGTGTG others(1): Show |
3 | a0012c0014t0007g0119a0014c0017t0007g0118a0014c0017t0007g0121 | 3 | HG02257.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.128-13097_128-1309 others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927848 | |||||
| chr4:109927848
|
T | TGTGTGTG others(5): Show |
1 | a0012c0014t0007g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128-13097_128-1309 others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927848 | |||||
| chr4:109928352
|
G | C | 64 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(61): Show | 67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.128-12594G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928352 | ||||||
| chr4:109928399
|
C | A | 2 | a0001c0001t0011g0141a0001c0001t0011g0144 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.128-12547C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928399 | ||||||
| chr4:109928613
|
C | T | 11 | a0005c0005t0007g0001a0005c0005t0007g0246a0005c0005t0007g0290others(8): Show | 12 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-12333C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928613 | ||||||
| chr4:109928706
|
C | T | 6 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(3): Show | 7 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-12240C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928706 | ||||||
| chr4:109928971
|
T | C | 1 | a0001c0026t0002g0076 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.128-11975T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928971 | ||||||
| chr4:109929226
|
T | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-11720T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929226 | ||||||
| chr4:109929307
|
C | G | 3 | a0001c0001t0012g0376a0001c0001t0015g0377a0001c0001t0015g0378 | 3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.128-11639C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929307 | ||||||
| chr4:109929320
|
G | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-11626G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929320 | ||||||
| chr4:109929714
|
A | AT | 65 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(62): Show | 68 | HG00558.hp1 HG00597.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.128-11225dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109929714 | |||||
| chr4:109929912
|
T | C | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-11034T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929912 | ||||||
| chr4:109929980
|
G | A | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-10966G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929980 | ||||||
| chr4:109930017
|
T | G | 3 | a0001c0001t0012g0376a0001c0001t0015g0377a0001c0001t0015g0378 | 3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.128-10929T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930017 | ||||||
| chr4:109930220
|
A | G | 2 | a0002c0002t0001g0195a0002c0002t0001g0214 | 2 | HG04184.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.128-10726A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930220 | ||||||
| chr4:109930234
|
A | G | 1 | a0005c0005t0007g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128-10712A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930234 | ||||||
| chr4:109930815
|
G | A | 5 | a0002c0002t0021g0354a0008c0008t0003g0348a0008c0008t0003g0349others(2): Show | 5 | NA18939.hp2 NA18947.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-10131G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930815 | ||||||
| chr4:109930854
|
A | G | 1 | a0003c0003t0005g0041 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.128-10092A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930854 | ||||||
| chr4:109930899
|
C | G | 1 | a0001c0001t0002g0087 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.128-10047C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930899 | ||||||
| chr4:109930910
|
C | A | 1 | a0004c0004t0003g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.128-10036C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930910 | ||||||
| chr4:109930981
|
AT | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-9964delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930981 | ||||||
| chr4:109931154
|
C | T | 1 | a0002c0002t0001g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.128-9792C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109931154 | ||||||
| chr4:109931303
|
A | G | 146 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(143): Show | 148 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.128-9643A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109931303 | ||||||
| chr4:109931769
|
C | T | 1 | a0010c0011t0001g0185 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.128-9177C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109931769 | ||||||
| chr4:109932057
|
G | A | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-8889G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932057 | ||||||
| chr4:109932075
|
T | A | 67 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(64): Show | 68 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.128-8871T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932075 | ||||||
| chr4:109932081
|
A | C | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8865A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932081 | ||||||
| chr4:109932186
|
C | T | 75 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(72): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-8760C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932186 | ||||||
| chr4:109932187
|
G | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-8759G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932187 | ||||||
| chr4:109932324
|
C | CT | 123 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(120): Show | 124 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.128-8609dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932324 | |||||
| chr4:109932360
|
C | CATATATA others(1): Show |
3 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130 | 3 | HG02895.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.128-8576_128-8569d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(15): Show |
1 | a0001c0001t0015g0377 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(24): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(17): Show |
5 | a0001c0001t0002g0080a0001c0001t0003g0074a0001c0001t0018g0234others(2): Show | 5 | HG00673.hp1 HG02129.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(19): Show |
17 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0002g0065others(14): Show | 17 | HG00673.hp2 HG01928.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(21): Show |
49 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0084others(46): Show | 50 | HG00323.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(30): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(23): Show |
26 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0068others(23): Show | 26 | HG01167.hp1 HG01167.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(32): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(25): Show |
1 | a0001c0001t0002g0091 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(34): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(27): Show |
1 | a0001c0007t0002g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(36): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(61): Show |
1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(70): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932360
|
C | CATATATA others(33): Show |
1 | a0001c0001t0002g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(42): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | |||||
| chr4:109932363
|
A | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-8583A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932363 | ||||||
| chr4:109932376
|
T | TATATA | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(18): Show |
1 | a0001c0001t0011g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(19): Show |
2 | a0001c0001t0004g0328a0001c0001t0013g0335 | 2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(21): Show |
9 | a0001c0001t0004g0325a0001c0001t0004g0329a0001c0001t0004g0330others(6): Show | 9 | HG00408.hp1 HG00438.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(30): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(22): Show |
1 | a0001c0001t0003g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(31): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(23): Show |
7 | a0001c0001t0004g0326a0001c0001t0004g0338a0001c0001t0013g0344others(4): Show | 7 | NA18939.hp2 NA18947.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(32): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(24): Show |
1 | a0008c0008t0003g0355 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(33): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932376
|
T | TATATATA others(25): Show |
3 | a0001c0001t0004g0340a0001c0001t0013g0327a0008c0008t0003g0374 | 3 | NA18985.hp2 NA18998.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(34): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | |||||
| chr4:109932377
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0004g0341a0001c0019t0017g0140 | 2 | HG02615.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(25): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | ||||||
| chr4:109932377
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0004g0298a0024c0030t0016g0310 | 2 | HG00738.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | ||||||
| chr4:109932377
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0002g0093a0001c0001t0006g0094 | 2 | NA18945.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(29): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | ||||||
| chr4:109932377
|
A | ATATATAT others(22): Show |
1 | a0001c0019t0007g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(31): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | ||||||
| chr4:109932377
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0004g0365 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(33): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | ||||||
| chr4:109932377
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0004g0364 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(35): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | ||||||
| chr4:109932378
|
A | T | 47 | a0001c0001t0002g0109a0001c0001t0004g0019a0001c0016t0002g0039others(44): Show | 48 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.128-8568A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932378 | ||||||
| chr4:109932379
|
A | T | 10 | a0001c0001t0003g0075a0001c0001t0011g0145a0008c0008t0003g0355others(7): Show | 10 | HG00621.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-8567A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932379 | ||||||
| chr4:109932379
|
AT | A | 25 | a0005c0005t0006g0250a0005c0005t0006g0254a0005c0005t0007g0001others(22): Show | 27 | HG01109.hp2 HG01255.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.128-8550delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932379 | |||||
| chr4:109932380
|
T | A | 8 | a0001c0001t0002g0093a0001c0001t0004g0298a0001c0001t0004g0341others(5): Show | 8 | HG00738.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-8566T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932380 | ||||||
| chr4:109932380
|
T | TATATATA others(18): Show |
1 | a0003c0003t0005g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-8566_128-8565i others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932380 | ||||||
| chr4:109932380
|
T | TATATATA others(19): Show |
1 | a0001c0001t0002g0109 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.128-8566_128-8565i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932380 | ||||||
| chr4:109932381
|
T | A | 45 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(42): Show | 46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.128-8565T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932381 | ||||||
| chr4:109932382
|
T | A | 1 | a0003c0003t0005g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-8564T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(13): Show |
1 | a0003c0003t0005g0021 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.128-8564_128-8563i others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(15): Show |
5 | a0003c0003t0005g0017a0003c0003t0005g0022a0003c0003t0008g0044others(2): Show | 5 | HG02027.hp1 HG03239.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(24): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(17): Show |
8 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(5): Show | 8 | HG00621.hp1 HG03017.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(19): Show |
17 | a0003c0003t0005g0002a0003c0003t0005g0014a0003c0003t0005g0028others(14): Show | 17 | HG00423.hp1 HG02015.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(21): Show |
7 | a0003c0003t0005g0003a0003c0003t0005g0018a0003c0003t0005g0035others(4): Show | 8 | NA18945.hp1 NA18953.hp1 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(30): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(23): Show |
4 | a0003c0003t0005g0020a0003c0003t0005g0037a0003c0003t0008g0051others(1): Show | 4 | HG00609.hp2 HG02080.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(32): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(25): Show |
1 | a0003c0003t0005g0045 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.128-8564_128-8563i others(34): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932382
|
T | TATATATA others(27): Show |
1 | a0003c0003t0005g0038 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.128-8564_128-8563i others(36): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | ||||||
| chr4:109932383
|
T | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-8563T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932383 | ||||||
| chr4:109932405
|
G | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-8541G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932405 | ||||||
| chr4:109932415
|
G | C | 1 | a0001c0001t0022g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.128-8531G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932415 | ||||||
| chr4:109932519
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.128-8427C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932519 | ||||||
| chr4:109932539
|
T | G | 1 | a0002c0002t0001g0134 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.128-8407T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932539 | ||||||
| chr4:109932546
|
T | G | 2 | a0006c0006t0001g0299a0006c0006t0001g0300 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.128-8400T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932546 | ||||||
| chr4:109932554
|
A | G | 1 | a0003c0003t0005g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.128-8392A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932554 | ||||||
| chr4:109932599
|
C | T | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-8347C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932599 | ||||||
| chr4:109932600
|
G | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-8346G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932600 | ||||||
| chr4:109932621
|
G | A | 138 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(135): Show | 139 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.128-8325G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932621 | ||||||
| chr4:109932659
|
G | A | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.128-8287G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932659 | ||||||
| chr4:109932679
|
G | A | 1 | a0005c0005t0017g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.128-8267G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932679 | ||||||
| chr4:109932857
|
C | A | 1 | a0001c0001t0004g0364 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.128-8089C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932857 | ||||||
| chr4:109933160
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-7786C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933160 | ||||||
| chr4:109933187
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.128-7759C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933187 | ||||||
| chr4:109933275
|
G | A | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-7671G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933275 | ||||||
| chr4:109933379
|
A | G | 1 | a0004c0004t0003g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.128-7567A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933379 | ||||||
| chr4:109933388
|
C | T | 145 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(142): Show | 146 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.128-7558C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933388 | ||||||
| chr4:109933424
|
CT | C | 127 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(124): Show | 129 | HG00323.hp2 HG00423.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.128-7508delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109933424 | |||||
| chr4:109933439
|
A | G | 7 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-7507A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933439 | ||||||
| chr4:109933532
|
C | T | 3 | a0001c0019t0007g0139a0001c0019t0017g0140a0025c0035t0017g0131 | 3 | HG02615.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.128-7414C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933532 | ||||||
| chr4:109933533
|
G | C | 1 | a0002c0002t0001g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.128-7413G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933533 | ||||||
| chr4:109933557
|
C | T | 1 | a0002c0002t0037g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.128-7389C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933557 | ||||||
| chr4:109933596
|
C | T | 2 | a0010c0011t0001g0213a0010c0011t0001g0226 | 2 | NA18956.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.128-7350C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933596 | ||||||
| chr4:109933668
|
C | T | 59 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(56): Show | 59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.128-7278C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933668 | ||||||
| chr4:109933761
|
T | A | 1 | a0004c0004t0004g0267 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.128-7185T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933761 | ||||||
| chr4:109933781
|
C | T | 6 | a0005c0005t0011g0319a0009c0010t0016g0321a0009c0010t0016g0322others(3): Show | 6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-7165C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933781 | ||||||
| chr4:109933783
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.128-7163T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933783 | ||||||
| chr4:109933784
|
G | C | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128-7162G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933784 | ||||||
| chr4:109933893
|
A | G | 194 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(191): Show | 196 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.128-7053A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933893 | ||||||
| chr4:109934023
|
A | G | 1 | a0001c0001t0014g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.128-6923A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934023 | ||||||
| chr4:109934237
|
T | C | 1 | a0002c0002t0001g0148 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128-6709T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934237 | ||||||
| chr4:109934255
|
G | A | 1 | a0002c0002t0001g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.128-6691G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934255 | ||||||
| chr4:109934270
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-6676G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934270 | ||||||
| chr4:109934399
|
T | G | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-6547T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934399 | ||||||
| chr4:109934427
|
ATTTG | A | 4 | a0001c0001t0002g0082a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG00621.hp2 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-6515_128-6512d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109934427 | |||||
| chr4:109934443
|
T | C | 1 | a0001c0001t0011g0142 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.128-6503T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934443 | ||||||
| chr4:109934629
|
C | T | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-6317C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934629 | ||||||
| chr4:109934685
|
A | G | 1 | a0003c0003t0005g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.128-6261A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934685 | ||||||
| chr4:109934719
|
A | G | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-6227A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934719 | ||||||
| chr4:109934781
|
T | G | 194 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(191): Show | 196 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.128-6165T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934781 | ||||||
| chr4:109934795
|
C | T | 67 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(64): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-6151C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934795 | ||||||
| chr4:109934802
|
C | T | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.128-6144C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934802 | ||||||
| chr4:109934837
|
G | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-6109G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934837 | ||||||
| chr4:109934943
|
C | T | 11 | a0005c0005t0007g0001a0005c0005t0007g0246a0005c0005t0007g0290others(8): Show | 12 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-6003C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934943 | ||||||
| chr4:109935036
|
G | T | 59 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(56): Show | 59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.128-5910G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935036 | ||||||
| chr4:109935041
|
A | G | 67 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(64): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-5905A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935041 | ||||||
| chr4:109935169
|
G | T | 1 | a0003c0003t0008g0054 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.128-5777G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935169 | ||||||
| chr4:109935186
|
T | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-5760T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935186 | ||||||
| chr4:109935278
|
TC | T | 3 | a0001c0019t0007g0139a0001c0019t0017g0140a0025c0035t0017g0131 | 3 | HG02615.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.128-5665delC | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109935278 | |||||
| chr4:109935323
|
A | G | 2 | a0006c0006t0001g0299a0006c0006t0001g0300 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.128-5623A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935323 | ||||||
| chr4:109935368
|
A | G | 7 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-5578A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935368 | ||||||
| chr4:109935406
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.128-5540A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935406 | ||||||
| chr4:109935447
|
T | C | 67 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(64): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-5499T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935447 | ||||||
| chr4:109935456
|
G | A | 49 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5490G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935456 | ||||||
| chr4:109935475
|
G | A | 49 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5471G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935475 | ||||||
| chr4:109935476
|
G | A | 49 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5470G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935476 | ||||||
| chr4:109935483
|
A | G | 49 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5463A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935483 | ||||||
| chr4:109935530
|
T | C | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-5416T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935530 | ||||||
| chr4:109935628
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-5318T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935628 | ||||||
| chr4:109935759
|
T | A | 1 | a0002c0002t0001g0174 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.128-5187T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935759 | ||||||
| chr4:109935870
|
C | G | 31 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(28): Show | 32 | HG00558.hp1 HG00597.hp2 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.128-5076C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935870 | ||||||
| chr4:109935900
|
C | T | 55 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(52): Show | 55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.128-5046C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935900 | ||||||
| chr4:109935957
|
T | C | 1 | a0005c0005t0017g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.128-4989T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935957 | ||||||
| chr4:109935970
|
T | C | 1 | a0002c0002t0001g0309 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.128-4976T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935970 | ||||||
| chr4:109936011
|
T | C | 53 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(50): Show | 55 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.128-4935T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936011 | ||||||
| chr4:109936093
|
A | G | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-4853A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936093 | ||||||
| chr4:109936137
|
G | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-4809G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936137 | ||||||
| chr4:109936311
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-4635C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936311 | ||||||
| chr4:109936319
|
G | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-4627G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936319 | ||||||
| chr4:109936372
|
T | A | 7 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0097others(4): Show | 7 | HG01167.hp2 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-4574T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936372 | ||||||
| chr4:109936383
|
G | A | 1 | a0002c0002t0006g0333 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.128-4563G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936383 | ||||||
| chr4:109936613
|
G | A | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128-4333G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936613 | ||||||
| chr4:109936627
|
T | G | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-4319T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936627 | ||||||
| chr4:109936667
|
T | A | 1 | a0003c0003t0005g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.128-4279T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936667 | ||||||
| chr4:109936686
|
C | A | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-4260C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936686 | ||||||
| chr4:109936790
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-4156G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936790 | ||||||
| chr4:109936897
|
C | T | 1 | a0001c0001t0015g0377 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.128-4049C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936897 | ||||||
| chr4:109936959
|
C | T | 2 | a0001c0001t0004g0364a0003c0003t0008g0044 | 2 | HG00733.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.128-3987C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936959 | ||||||
| chr4:109937108
|
G | A | 1 | a0002c0002t0001g0151 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.128-3838G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937108 | ||||||
| chr4:109937137
|
T | C | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-3809T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937137 | ||||||
| chr4:109937144
|
C | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3802C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937144 | ||||||
| chr4:109937318
|
C | G | 270 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(267): Show | 275 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.128-3628C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937318 | ||||||
| chr4:109937359
|
CT | C | 124 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0006g0253others(121): Show | 129 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.128-3572delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109937359 | |||||
| chr4:109937359
|
CTT | C | 147 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(144): Show | 148 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.128-3573_128-3572d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109937359 | |||||
| chr4:109937537
|
A | G | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-3409A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937537 | ||||||
| chr4:109937652
|
G | A | 7 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-3294G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937652 | ||||||
| chr4:109937824
|
A | G | 67 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(64): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-3122A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937824 | ||||||
| chr4:109937893
|
A | G | 67 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(64): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-3053A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937893 | ||||||
| chr4:109937935
|
G | T | 1 | a0018c0024t0007g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.128-3011G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937935 | ||||||
| chr4:109938006
|
C | T | 1 | a0001c0001t0004g0352 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.128-2940C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938006 | ||||||
| chr4:109938020
|
G | A | 4 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(1): Show | 5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2926G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938020 | ||||||
| chr4:109938024
|
G | A | 3 | a0003c0003t0005g0014a0003c0003t0005g0043a0003c0003t0018g0228 | 3 | HG02040.hp2 HG02074.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.128-2922G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938024 | ||||||
| chr4:109938222
|
T | C | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-2724T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938222 | ||||||
| chr4:109938281
|
A | G | 1 | a0004c0032t0003g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.128-2665A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938281 | ||||||
| chr4:109938323
|
C | T | 1 | a0004c0004t0010g0268 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.128-2623C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938323 | ||||||
| chr4:109938419
|
C | T | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-2527C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938419 | ||||||
| chr4:109938538
|
T | C | 1 | a0001c0001t0014g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.128-2408T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938538 | ||||||
| chr4:109938619
|
C | CT | 6 | a0005c0005t0011g0319a0009c0010t0016g0321a0009c0010t0016g0322others(3): Show | 6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2322dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109938619 | |||||
| chr4:109938712
|
T | C | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-2234T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938712 | ||||||
| chr4:109938824
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0061 | 2 | HG00735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.128-2122T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938824 | ||||||
| chr4:109939022
|
G | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-1924G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939022 | ||||||
| chr4:109939067
|
G | T | 1 | a0001c0001t0006g0094 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.128-1879G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939067 | ||||||
| chr4:109939165
|
G | A | 5 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(2): Show | 6 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-1781G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939165 | ||||||
| chr4:109939233
|
A | G | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.128-1713A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939233 | ||||||
| chr4:109939295
|
A | T | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG00621.hp2 HG00673.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.128-1651A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939295 | ||||||
| chr4:109939303
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-1643G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939303 | ||||||
| chr4:109939308
|
C | A | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1638C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939308 | ||||||
| chr4:109939369
|
G | T | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1577G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939369 | ||||||
| chr4:109939389
|
G | A | 6 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(3): Show | 7 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-1557G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939389 | ||||||
| chr4:109939399
|
C | T | 5 | a0006c0006t0001g0170a0011c0012t0014g0229a0011c0012t0014g0230others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-1547C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939399 | ||||||
| chr4:109939458
|
G | C | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-1488G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939458 | ||||||
| chr4:109939513
|
C | T | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1433C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939513 | ||||||
| chr4:109939523
|
C | T | 54 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(51): Show | 54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.128-1423C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939523 | ||||||
| chr4:109939640
|
T | C | 1 | a0002c0002t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.128-1306T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939640 | ||||||
| chr4:109939661
|
C | T | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-1285C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939661 | ||||||
| chr4:109939662
|
G | A | 5 | a0002c0002t0001g0203a0002c0002t0001g0224a0002c0002t0009g0149others(2): Show | 5 | HG02293.hp2 HG02300.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-1284G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939662 | ||||||
| chr4:109939681
|
A | G | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-1265A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939681 | ||||||
| chr4:109939705
|
G | A | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-1241G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939705 | ||||||
| chr4:109939717
|
G | T | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1229G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939717 | ||||||
| chr4:109940071
|
G | A | 1 | a0001c0001t0040g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.128-875G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940071 | ||||||
| chr4:109940236
|
G | A | 1 | a0001c0001t0006g0113 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-710G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940236 | ||||||
| chr4:109940271
|
G | A | 1 | a0002c0002t0012g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.128-675G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940271 | ||||||
| chr4:109940284
|
T | C | 2 | a0005c0005t0007g0290a0005c0005t0007g0293 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.128-662T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940284 | ||||||
| chr4:109940313
|
T | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-633T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940313 | ||||||
| chr4:109940357
|
T | C | 2 | a0001c0001t0011g0141a0001c0001t0011g0144 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.128-589T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940357 | ||||||
| chr4:109940487
|
G | A | 59 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(56): Show | 59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.128-459G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940487 | ||||||
| chr4:109940628
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.128-318A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940628 | ||||||
| chr4:109940760
|
C | T | 2 | a0001c0001t0004g0343a0004c0032t0003g0269 | 2 | NA18975.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.128-186C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940760 | ||||||
| chr4:109940771
|
G | A | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-175G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940771 | ||||||
| chr4:109940785
|
T | G | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-161T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940785 | ||||||
| chr4:109940867
|
G | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-79G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940867 | ||||||
| chr4:109940882
|
G | A | 2 | a0004c0004t0003g0257a0004c0004t0003g0258 | 2 | NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.128-64G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940882 | ||||||
| chr4:109941207
|
C | T | 50 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(47): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.327+62C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941207 | ||||||
| chr4:109941257
|
G | A | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.327+112G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941257 | ||||||
| chr4:109941271
|
T | C | 2 | a0001c0016t0002g0039a0001c0016t0006g0023 | 2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.327+126T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941271 | ||||||
| chr4:109941289
|
A | G | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.327+144A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941289 | ||||||
| chr4:109941480
|
T | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.327+335T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941480 | ||||||
| chr4:109941481
|
G | A | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+336G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941481 | ||||||
| chr4:109941489
|
A | G | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+344A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941489 | ||||||
| chr4:109941526
|
C | T | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.327+381C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941526 | ||||||
| chr4:109941561
|
G | A | 9 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0002g0091others(6): Show | 9 | NA18942.hp1 NA18946.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.327+416G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941561 | ||||||
| chr4:109941575
|
G | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327+430G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941575 | ||||||
| chr4:109941952
|
T | G | 1 | a0003c0003t0005g0024 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.327+807T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941952 | ||||||
| chr4:109942065
|
C | A | 5 | a0002c0002t0001g0150a0002c0002t0001g0154a0002c0002t0001g0155others(2): Show | 5 | NA18941.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+920C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942065 | ||||||
| chr4:109942202
|
T | C | 2 | a0003c0003t0005g0002a0003c0003t0008g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.328-1052T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942202 | ||||||
| chr4:109942257
|
T | C | 6 | a0005c0005t0011g0319a0009c0010t0016g0321a0009c0010t0016g0322others(3): Show | 6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-997T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942257 | ||||||
| chr4:109942513
|
G | A | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-741G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942513 | ||||||
| chr4:109942589
|
C | T | 4 | a0003c0003t0005g0017a0003c0003t0005g0018a0003c0003t0026g0015others(1): Show | 4 | NA18994.hp2 NA19002.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-665C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942589 | ||||||
| chr4:109942663
|
A | G | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-591A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942663 | ||||||
| chr4:109942779
|
G | A | 1 | a0003c0003t0008g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.328-475G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942779 | ||||||
| chr4:109942842
|
A | G | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.328-412A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942842 | ||||||
| chr4:109942852
|
G | T | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-402G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942852 | ||||||
| chr4:109942897
|
T | C | 67 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(64): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.328-357T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942897 | ||||||
| chr4:109943053
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.328-201T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109943053 | ||||||
| chr4:109943567
|
G | A | 9 | a0005c0005t0007g0001a0005c0005t0007g0246a0005c0005t0007g0290others(6): Show | 10 | HG02572.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+132G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943567 | ||||||
| chr4:109943600
|
G | A | 2 | a0001c0016t0002g0039a0001c0016t0006g0023 | 2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.509+165G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943600 | ||||||
| chr4:109943674
|
T | TA | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-168_510-167ins others(1): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943674 | ||||||
| chr4:109943675
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-167G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943675 | ||||||
| chr4:109943702
|
G | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-140G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943702 | ||||||
| chr4:109943773
|
A | T | 1 | a0001c0001t0002g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.510-69A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943773 | ||||||
| chr4:109944115
|
T | G | 138 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(135): Show | 139 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.737+46T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944115 | ||||||
| chr4:109944160
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.737+91G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944160 | ||||||
| chr4:109944168
|
G | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+99G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944168 | ||||||
| chr4:109944169
|
G | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+100G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944169 | ||||||
| chr4:109944210
|
G | A | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+141G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944210 | ||||||
| chr4:109944222
|
G | T | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+153G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944222 | ||||||
| chr4:109944255
|
C | T | 1 | a0005c0005t0006g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+186C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944255 | ||||||
| chr4:109944270
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.737+201T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944270 | ||||||
| chr4:109944276
|
A | G | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.737+207A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944276 | ||||||
| chr4:109944309
|
A | G | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.737+240A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944309 | ||||||
| chr4:109944312
|
A | G | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+243A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944312 | ||||||
| chr4:109944329
|
T | C | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+260T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944329 | ||||||
| chr4:109944331
|
C | T | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+262C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944331 | ||||||
| chr4:109944366
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.737+297G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944366 | ||||||
| chr4:109944390
|
T | G | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+321T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944390 | ||||||
| chr4:109944414
|
G | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.737+345G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944414 | ||||||
| chr4:109944418
|
G | A | 3 | a0004c0004t0003g0270a0004c0004t0010g0262a0005c0005t0004g0306 | 3 | HG02129.hp2 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.737+349G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944418 | ||||||
| chr4:109944429
|
A | C | 1 | a0003c0003t0005g0017 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.737+360A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944429 | ||||||
| chr4:109944442
|
A | G | 1 | a0002c0002t0001g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.737+373A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944442 | ||||||
| chr4:109944552
|
A | G | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+483A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944552 | ||||||
| chr4:109945022
|
A | C | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.738-51A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109945022 | ||||||
| chr4:109945286
|
G | A | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.940+11G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945286 | ||||||
| chr4:109945297
|
G | A | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+22G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945297 | ||||||
| chr4:109945352
|
C | T | 145 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(142): Show | 146 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.940+77C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945352 | ||||||
| chr4:109945370
|
A | T | 72 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(69): Show | 75 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(72): Show |
intron_variant | MODIFIER | c.940+95A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945370 | ||||||
| chr4:109945426
|
A | T | 53 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(50): Show | 55 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.940+151A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945426 | ||||||
| chr4:109945561
|
G | A | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.940+286G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945561 | ||||||
| chr4:109945564
|
C | T | 3 | a0003c0003t0005g0032a0003c0003t0005g0036a0003c0003t0008g0040 | 3 | HG02056.hp1 NA18951.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.940+289C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945564 | ||||||
| chr4:109945565
|
G | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+290G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945565 | ||||||
| chr4:109945579
|
C | CGAAA | 5 | a0005c0005t0019g0007a0005c0005t0019g0249a0005c0005t0019g0251others(2): Show | 6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+321_940+324dup others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109945579 | |||||
| chr4:109945995
|
ATTGT | A | 5 | a0002c0002t0001g0150a0002c0002t0001g0154a0002c0002t0001g0155others(2): Show | 5 | NA18941.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+724_940+727del others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109945995 | |||||
| chr4:109946072
|
C | A | 59 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(56): Show | 59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.940+797C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946072 | ||||||
| chr4:109946194
|
G | T | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.940+919G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946194 | ||||||
| chr4:109946274
|
A | G | 2 | a0005c0005t0006g0250a0005c0005t0006g0254 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.940+999A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946274 | ||||||
| chr4:109946442
|
A | G | 1 | a0004c0004t0003g0286 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.940+1167A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946442 | ||||||
| chr4:109946523
|
A | C | 1 | a0002c0002t0009g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.940+1248A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946523 | ||||||
| chr4:109946780
|
A | G | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.940+1505A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946780 | ||||||
| chr4:109946892
|
A | C | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+1617A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946892 | ||||||
| chr4:109946930
|
C | A | 1 | a0001c0001t0015g0377 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.940+1655C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946930 | ||||||
| chr4:109946931
|
C | T | 1 | a0002c0002t0006g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.940+1656C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946931 | ||||||
| chr4:109946968
|
A | C | 5 | a0005c0005t0019g0007a0005c0005t0019g0249a0005c0005t0019g0251others(2): Show | 6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+1693A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946968 | ||||||
| chr4:109946987
|
C | T | 6 | a0002c0002t0001g0186a0002c0002t0001g0190a0002c0002t0001g0193others(3): Show | 6 | HG01074.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+1712C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946987 | ||||||
| chr4:109947129
|
T | TA | 59 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(56): Show | 59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.940+1865dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109947129 | |||||
| chr4:109947163
|
C | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+1888C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947163 | ||||||
| chr4:109947179
|
G | GA | 275 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(272): Show | 281 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.940+1911dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109947179 | |||||
| chr4:109947195
|
G | A | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940+1920G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947195 | ||||||
| chr4:109947362
|
T | C | 6 | a0005c0005t0011g0319a0009c0010t0016g0321a0009c0010t0016g0322others(3): Show | 6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+2087T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947362 | ||||||
| chr4:109947378
|
C | A | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+2103C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947378 | ||||||
| chr4:109947431
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.940+2156G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947431 | ||||||
| chr4:109947552
|
C | G | 3 | a0002c0002t0001g0189a0002c0002t0009g0197a0002c0002t0009g0201 | 3 | NA18967.hp1 NA18991.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.940+2277C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947552 | ||||||
| chr4:109947628
|
T | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.940+2353T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947628 | ||||||
| chr4:109947712
|
T | C | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+2437T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947712 | ||||||
| chr4:109947787
|
T | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0010 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.940+2512T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947787 | ||||||
| chr4:109947911
|
T | G | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+2636T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947911 | ||||||
| chr4:109947986
|
G | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+2711G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947986 | ||||||
| chr4:109948028
|
C | A | 5 | a0005c0005t0019g0007a0005c0005t0019g0249a0005c0005t0019g0251others(2): Show | 6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+2753C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948028 | ||||||
| chr4:109948043
|
C | T | 1 | a0004c0004t0003g0266 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.940+2768C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948043 | ||||||
| chr4:109948068
|
G | A | 1 | a0005c0005t0013g0263 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.940+2793G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948068 | ||||||
| chr4:109948090
|
G | A | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.940+2815G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948090 | ||||||
| chr4:109948105
|
A | G | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.940+2830A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948105 | ||||||
| chr4:109948106
|
T | A | 1 | a0002c0002t0001g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.940+2831T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948106 | ||||||
| chr4:109948195
|
G | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.940+2920G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948195 | ||||||
| chr4:109948497
|
G | C | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.940+3222G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948497 | ||||||
| chr4:109948497
|
G | T | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.940+3222G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948497 | ||||||
| chr4:109948529
|
G | T | 1 | a0011c0012t0014g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.940+3254G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948529 | ||||||
| chr4:109948547
|
G | A | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.940+3272G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948547 | ||||||
| chr4:109948593
|
C | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.940+3318C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948593 | ||||||
| chr4:109948660
|
G | A | 195 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(192): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.940+3385G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948660 | ||||||
| chr4:109948678
|
G | A | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.940+3403G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948678 | ||||||
| chr4:109948990
|
A | G | 4 | a0004c0004t0003g0281a0004c0004t0003g0282a0004c0004t0003g0283others(1): Show | 4 | HG01175.hp1 HG02148.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3715A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948990 | ||||||
| chr4:109948991
|
T | C | 2 | a0004c0004t0003g0261a0004c0004t0003g0280 | 2 | HG01928.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.940+3716T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948991 | ||||||
| chr4:109949007
|
A | C | 4 | a0002c0002t0001g0184a0002c0002t0001g0192a0002c0002t0001g0210others(1): Show | 4 | HG00597.hp1 HG02040.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3732A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949007 | ||||||
| chr4:109949070
|
T | C | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.940+3795T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949070 | ||||||
| chr4:109949092
|
A | G | 1 | a0002c0002t0012g0181 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.940+3817A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949092 | ||||||
| chr4:109949097
|
C | T | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+3822C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949097 | ||||||
| chr4:109949128
|
G | A | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.940+3853G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949128 | ||||||
| chr4:109949153
|
G | A | 1 | a0004c0004t0003g0008 | 2 | NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.940+3878G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949153 | ||||||
| chr4:109949238
|
T | G | 4 | a0001c0001t0012g0236a0001c0001t0020g0233a0001c0001t0020g0237others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3963T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949238 | ||||||
| chr4:109949255
|
C | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+3980C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949255 | ||||||
| chr4:109949297
|
C | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+4022C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949297 | ||||||
| chr4:109949354
|
G | A | 1 | a0001c0001t0004g0347 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.940+4079G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949354 | ||||||
| chr4:109949609
|
T | C | 81 | a0001c0001t0004g0126a0001c0001t0006g0253a0001c0001t0007g0005others(78): Show | 85 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(82): Show |
intron_variant | MODIFIER | c.940+4334T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949609 | ||||||
| chr4:109949618
|
CT | C | 21 | a0001c0001t0004g0329a0001c0001t0004g0365a0001c0001t0007g0317others(18): Show | 21 | HG00597.hp1 HG01070.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.940+4357delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109949618 | |||||
| chr4:109949648
|
T | A | 1 | a0001c0001t0002g0313 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.940+4373T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949648 | ||||||
| chr4:109949937
|
G | A | 1 | a0002c0002t0006g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.940+4662G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949937 | ||||||
| chr4:109950013
|
C | G | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+4738C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950013 | ||||||
| chr4:109950077
|
C | G | 1 | a0009c0010t0016g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.940+4802C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950077 | ||||||
| chr4:109950164
|
G | A | 3 | a0005c0005t0019g0007a0005c0005t0019g0251a0017c0023t0045g0252 | 4 | HG02559.hp1 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+4889G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950164 | ||||||
| chr4:109950293
|
G | A | 2 | a0001c0001t0004g0328a0001c0001t0013g0335 | 2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.940+5018G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950293 | ||||||
| chr4:109950297
|
C | A | 1 | a0001c0026t0002g0076 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.940+5022C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950297 | ||||||
| chr4:109950355
|
T | C | 198 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(195): Show | 200 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.940+5080T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950355 | ||||||
| chr4:109950380
|
A | G | 8 | a0003c0003t0005g0021a0003c0003t0005g0024a0003c0003t0005g0030others(5): Show | 8 | HG00609.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.940+5105A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950380 | ||||||
| chr4:109950387
|
T | C | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+5112T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950387 | ||||||
| chr4:109950411
|
C | T | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940+5136C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950411 | ||||||
| chr4:109950512
|
A | AT | 6 | a0001c0001t0015g0208a0001c0001t0030g0209a0002c0002t0001g0191others(3): Show | 6 | HG00438.hp1 NA18612.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+5238dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109950512 | |||||
| chr4:109950535
|
A | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+5260A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950535 | ||||||
| chr4:109950670
|
C | T | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+5395C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950670 | ||||||
| chr4:109950786
|
A | G | 1 | a0023c0028t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.940+5511A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950786 | ||||||
| chr4:109950805
|
C | T | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.940+5530C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950805 | ||||||
| chr4:109951034
|
C | T | 5 | a0001c0019t0007g0139a0001c0019t0017g0140a0006c0006t0001g0006others(2): Show | 6 | HG02615.hp2 HG02630.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+5759C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951034 | ||||||
| chr4:109951146
|
A | AAAAAT | 72 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(69): Show | 72 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.940+5922_940+5926d others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
A | AAAAATAA others(3): Show |
15 | a0001c0001t0002g0065a0001c0001t0002g0130a0001c0001t0002g0313others(12): Show | 17 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.940+5917_940+5926d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
A | AAAAATAA others(8): Show |
9 | a0001c0001t0002g0128a0001c0001t0007g0123a0001c0001t0007g0125others(6): Show | 9 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.940+5912_940+5926d others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
A | AAAAATAA others(13): Show |
2 | a0001c0001t0011g0142a0001c0001t0028g0242 | 2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.940+5907_940+5926d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
A | AAAAATAA others(18): Show |
1 | a0001c0001t0002g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.940+5902_940+5926d others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
AAAAAT | A | 118 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0004g0019others(115): Show | 120 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.940+5922_940+5926d others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
AAAAATAA others(3): Show |
A | 59 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(56): Show | 60 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.940+5917_940+5926d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
AAAAATAA others(8): Show |
A | 7 | a0001c0001t0014g0232a0001c0001t0018g0234a0002c0002t0001g0135others(4): Show | 7 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.940+5912_940+5926d others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951146
|
AAAAATAA others(18): Show |
A | 1 | a0003c0003t0005g0024 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.940+5902_940+5926d others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | |||||
| chr4:109951176
|
T | C | 1 | a0009c0010t0016g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.940+5901T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951176 | ||||||
| chr4:109951247
|
A | G | 3 | a0004c0004t0003g0270a0004c0004t0010g0262a0005c0005t0004g0306 | 3 | HG02129.hp2 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.940+5972A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951247 | ||||||
| chr4:109951403
|
G | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+6128G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951403 | ||||||
| chr4:109951470
|
GT | G | 6 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(3): Show | 7 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+6202delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951470 | |||||
| chr4:109951960
|
A | G | 5 | a0005c0005t0019g0007a0005c0005t0019g0249a0005c0005t0019g0251others(2): Show | 6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+6685A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951960 | ||||||
| chr4:109952575
|
G | A | 5 | a0002c0002t0001g0150a0002c0002t0001g0154a0002c0002t0001g0155others(2): Show | 5 | NA18941.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.941-6737G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952575 | ||||||
| chr4:109952575
|
G | T | 1 | a0001c0027t0004g0351 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.941-6737G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952575 | ||||||
| chr4:109952596
|
A | G | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-6716A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952596 | ||||||
| chr4:109952601
|
A | G | 79 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(76): Show | 80 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.941-6711A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952601 | ||||||
| chr4:109952623
|
T | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-6689T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952623 | ||||||
| chr4:109952630
|
A | T | 1 | a0010c0011t0001g0213 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.941-6682A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952630 | ||||||
| chr4:109952638
|
C | A | 1 | a0005c0005t0006g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.941-6674C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952638 | ||||||
| chr4:109952770
|
T | C | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.941-6542T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952770 | ||||||
| chr4:109952910
|
G | C | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-6402G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952910 | ||||||
| chr4:109952954
|
T | C | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-6358T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952954 | ||||||
| chr4:109953141
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.941-6171G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953141 | ||||||
| chr4:109953217
|
T | C | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.941-6095T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953217 | ||||||
| chr4:109953513
|
C | A | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.941-5799C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953513 | ||||||
| chr4:109953513
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.941-5799C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953513 | ||||||
| chr4:109953554
|
A | C | 2 | a0001c0016t0002g0039a0001c0016t0006g0023 | 2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.941-5758A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953554 | ||||||
| chr4:109953617
|
A | T | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941-5695A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953617 | ||||||
| chr4:109953869
|
G | A | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.941-5443G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953869 | ||||||
| chr4:109953957
|
C | T | 55 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(52): Show | 55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.941-5355C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953957 | ||||||
| chr4:109954052
|
T | C | 2 | a0007c0009t0001g0055a0007c0009t0001g0056 | 2 | NA18970.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.941-5260T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954052 | ||||||
| chr4:109954074
|
C | T | 1 | a0005c0005t0006g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.941-5238C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954074 | ||||||
| chr4:109954106
|
C | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-5206C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954106 | ||||||
| chr4:109954124
|
TCACTGCA others(1): Show |
T | 3 | a0004c0004t0003g0270a0004c0004t0010g0262a0005c0005t0004g0306 | 3 | HG02129.hp2 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.941-5186_941-5179d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109954124 | |||||
| chr4:109954194
|
G | A | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-5118G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954194 | ||||||
| chr4:109954222
|
T | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.941-5090T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954222 | ||||||
| chr4:109954434
|
C | G | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.941-4878C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954434 | ||||||
| chr4:109954505
|
C | T | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.941-4807C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954505 | ||||||
| chr4:109954663
|
C | T | 7 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-4649C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954663 | ||||||
| chr4:109954761
|
G | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.941-4551G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954761 | ||||||
| chr4:109954968
|
G | A | 4 | a0001c0001t0012g0376a0001c0001t0014g0239a0001c0001t0015g0377others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-4344G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954968 | ||||||
| chr4:109955086
|
G | T | 1 | a0001c0001t0025g0101 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.941-4226G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955086 | ||||||
| chr4:109955152
|
T | G | 1 | a0001c0001t0006g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.941-4160T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955152 | ||||||
| chr4:109955253
|
G | T | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.941-4059G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955253 | ||||||
| chr4:109955574
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.941-3738G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955574 | ||||||
| chr4:109955611
|
G | A | 1 | a0002c0002t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.941-3701G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955611 | ||||||
| chr4:109955792
|
C | T | 1 | a0010c0011t0001g0185 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.941-3520C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955792 | ||||||
| chr4:109955796
|
G | A | 1 | a0001c0001t0015g0377 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.941-3516G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955796 | ||||||
| chr4:109955891
|
G | A | 4 | a0001c0001t0012g0236a0001c0001t0020g0233a0001c0001t0020g0237others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-3421G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955891 | ||||||
| chr4:109956187
|
A | T | 53 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(50): Show | 54 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.941-3125A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956187 | ||||||
| chr4:109956260
|
A | T | 140 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(137): Show | 141 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.941-3052A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956260 | ||||||
| chr4:109956364
|
C | T | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-2948C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956364 | ||||||
| chr4:109956822
|
G | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-2490G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956822 | ||||||
| chr4:109957109
|
C | G | 1 | a0005c0005t0007g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.941-2203C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109957109 | ||||||
| chr4:109957413
|
A | C | 1 | a0002c0002t0001g0207 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.941-1899A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109957413 | ||||||
| chr4:109957659
|
C | G | 1 | a0001c0001t0004g0330 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.941-1653C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109957659 | ||||||
| chr4:109958135
|
C | T | 4 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0011others(1): Show | 4 | HG02818.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-1177C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958135 | ||||||
| chr4:109958144
|
A | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-1168A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958144 | ||||||
| chr4:109958190
|
G | A | 8 | a0003c0003t0005g0021a0003c0003t0005g0024a0003c0003t0005g0030others(5): Show | 8 | HG00609.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-1122G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958190 | ||||||
| chr4:109958299
|
C | T | 1 | a0008c0008t0032g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.941-1013C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958299 | ||||||
| chr4:109958328
|
T | C | 3 | a0001c0001t0004g0338a0001c0001t0004g0340a0001c0001t0013g0344 | 3 | NA18957.hp2 NA18998.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.941-984T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958328 | ||||||
| chr4:109958566
|
T | C | 1 | a0001c0001t0029g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.941-746T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958566 | ||||||
| chr4:109958725
|
C | T | 5 | a0005c0005t0019g0007a0005c0005t0019g0249a0005c0005t0019g0251others(2): Show | 6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.941-587C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958725 | ||||||
| chr4:109958747
|
G | A | 7 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-565G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958747 | ||||||
| chr4:109958883
|
A | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.941-429A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958883 | ||||||
| chr4:109958900
|
A | G | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941-412A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958900 | ||||||
| chr4:109958917
|
C | CA | 29 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(26): Show | 31 | HG00140.hp2 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.941-374dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109958917 | |||||
| chr4:109958917
|
CA | C | 140 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(137): Show | 142 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.941-374delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109958917 | |||||
| chr4:109958917
|
CAA | C | 63 | a0001c0001t0002g0068a0001c0001t0004g0296a0001c0001t0004g0297others(60): Show | 63 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.941-375_941-374del others(2): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109958917 | |||||
| chr4:109959002
|
C | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.941-310C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959002 | ||||||
| chr4:109959190
|
C | T | 1 | a0003c0003t0005g0018 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.941-122C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959190 | ||||||
| chr4:109959206
|
T | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.941-106T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959206 | ||||||
| chr4:109959208
|
T | C | 193 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(190): Show | 195 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.941-104T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959208 | ||||||
| chr4:109959222
|
A | C | 5 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-90A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959222 | ||||||
| chr4:109959418
|
A | AGACCGGA others(41): Show |
1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1049_1066+30dupACC others(45): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr4 | 109959418 | |||||
| chr4:109959447
|
G | C | 2 | a0003c0003t0005g0042a0003c0003t0008g0047 | 2 | NA18947.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1066+10G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959447 | ||||||
| chr4:109959477
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1066+40C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959477 | ||||||
| chr4:109959631
|
C | T | 3 | a0001c0001t0004g0338a0001c0001t0004g0340a0001c0001t0013g0344 | 3 | NA18957.hp2 NA18998.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1066+194C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959631 | ||||||
| chr4:109959982
|
A | G | 1 | a0002c0002t0001g0158 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1066+545A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959982 | ||||||
| chr4:109960002
|
G | A | 1 | a0001c0001t0020g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1066+565G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960002 | ||||||
| chr4:109960208
|
G | A | 1 | a0002c0002t0006g0004 | 2 | HG01074.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1067-659G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960208 | ||||||
| chr4:109960210
|
T | G | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1067-657T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960210 | ||||||
| chr4:109960338
|
A | G | 151 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(148): Show | 153 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1067-529A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960338 | ||||||
| chr4:109960456
|
G | A | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1067-411G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960456 | ||||||
| chr4:109960645
|
G | A | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1067-222G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960645 | ||||||
| chr4:109960746
|
C | T | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1067-121C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960746 | ||||||
| chr4:109961304
|
G | A | 79 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(76): Show | 80 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.1189+315G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961304 | ||||||
| chr4:109961309
|
C | G | 7 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189+320C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961309 | ||||||
| chr4:109961320
|
C | A | 199 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(196): Show | 202 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1189+331C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961320 | ||||||
| chr4:109961434
|
A | G | 151 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(148): Show | 153 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1190-429A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961434 | ||||||
| chr4:109961753
|
C | A | 1 | a0002c0002t0001g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1190-110C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961753 | ||||||
| chr4:109961824
|
G | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1190-39G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961824 | ||||||
| chr4:109961840
|
T | C | 65 | a0001c0001t0004g0126a0001c0001t0004g0296a0001c0001t0004g0297others(62): Show | 66 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1190-23T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961840 | ||||||
| chr4:109962008
|
C | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1312+23C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962008 | ||||||
| chr4:109962185
|
T | G | 10 | a0001c0001t0015g0159a0002c0002t0001g0160a0002c0002t0001g0164others(7): Show | 10 | HG02165.hp2 HG03704.hp1 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312+200T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962185 | ||||||
| chr4:109962188
|
C | T | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1312+203C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962188 | ||||||
| chr4:109962449
|
A | G | 4 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(1): Show | 5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312+464A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962449 | ||||||
| chr4:109962464
|
G | A | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1312+479G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962464 | ||||||
| chr4:109962580
|
T | C | 1 | a0008c0008t0003g0374 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1313-593T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962580 | ||||||
| chr4:109962731
|
C | T | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-442C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962731 | ||||||
| chr4:109962896
|
G | A | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1313-277G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962896 | ||||||
| chr4:109962998
|
C | A | 10 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(7): Show | 11 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1313-175C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962998 | ||||||
| chr4:109963064
|
C | CA | 7 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(4): Show | 8 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1313-92dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 109963064 | |||||
| chr4:109963064
|
C | CAA | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-93_1313-92dup others(2): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 109963064 | |||||
| chr4:109963064
|
CA | C | 64 | a0001c0001t0002g0112a0001c0001t0002g0314a0001c0001t0006g0253others(61): Show | 65 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.1313-92delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 109963064 | |||||
| chr4:109963140
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1313-33C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109963140 | ||||||
| chr4:109963163
|
G | T | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01192.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1313-10G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109963163 | ||||||
| chr4:109963401
|
G | A | 7 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1438+103G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963401 | ||||||
| chr4:109963587
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1438+289T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963587 | ||||||
| chr4:109963589
|
T | C | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1438+291T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963589 | ||||||
| chr4:109963612
|
A | G | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1438+314A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963612 | ||||||
| chr4:109963785
|
A | G | 3 | a0002c0002t0023g0211a0002c0002t0023g0218a0002c0002t0037g0187 | 3 | HG02280.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1438+487A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963785 | ||||||
| chr4:109963830
|
A | T | 11 | a0005c0005t0007g0001a0005c0005t0007g0246a0005c0005t0007g0290others(8): Show | 12 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1438+532A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963830 | ||||||
| chr4:109963896
|
A | G | 1 | a0002c0002t0035g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1439-505A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963896 | ||||||
| chr4:109963988
|
C | T | 1 | a0002c0002t0037g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1439-413C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963988 | ||||||
| chr4:109964086
|
A | T | 151 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(148): Show | 153 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1439-315A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109964086 | ||||||
| chr4:109964188
|
G | A | 1 | a0006c0006t0001g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1439-213G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109964188 | ||||||
| chr4:109964554
|
T | C | 1 | a0002c0002t0001g0165 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1575+17T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964554 | ||||||
| chr4:109964587
|
A | G | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+50A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964587 | ||||||
| chr4:109964626
|
A | T | 1 | a0008c0008t0003g0374 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1575+89A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964626 | ||||||
| chr4:109964656
|
A | G | 1 | a0002c0002t0009g0197 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1575+119A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964656 | ||||||
| chr4:109964712
|
T | C | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1575+175T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964712 | ||||||
| chr4:109964773
|
C | T | 1 | a0002c0002t0001g0311 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1575+236C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964773 | ||||||
| chr4:109964801
|
G | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1575+264G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964801 | ||||||
| chr4:109964993
|
C | T | 58 | a0001c0019t0007g0139a0001c0019t0017g0140a0004c0004t0003g0008others(55): Show | 60 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+456C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964993 | ||||||
| chr4:109965029
|
G | A | 1 | a0005c0005t0006g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1575+492G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965029 | ||||||
| chr4:109965098
|
G | C | 1 | a0001c0001t0015g0378 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1575+561G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965098 | ||||||
| chr4:109965150
|
G | A | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1575+613G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965150 | ||||||
| chr4:109965187
|
G | C | 271 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(268): Show | 277 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1575+650G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965187 | ||||||
| chr4:109965341
|
C | A | 10 | a0001c0001t0002g0093a0001c0001t0002g0095a0001c0001t0002g0109others(7): Show | 10 | HG02523.hp2 NA18945.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+804C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965341 | ||||||
| chr4:109965648
|
T | C | 78 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(75): Show | 79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1575+1111T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965648 | ||||||
| chr4:109965884
|
T | C | 1 | a0001c0001t0015g0208 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1575+1347T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965884 | ||||||
| chr4:109966036
|
A | AAT | 53 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(50): Show | 55 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.1575+1500_1575+150 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109966036 | |||||
| chr4:109966036
|
A | AATAT | 4 | a0001c0019t0007g0139a0001c0019t0017g0140a0005c0005t0006g0250others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1575+1500_1575+150 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109966036 | |||||
| chr4:109966037
|
A | T | 1 | a0001c0001t0002g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1575+1500A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966037 | ||||||
| chr4:109966038
|
A | T | 58 | a0001c0019t0007g0139a0001c0019t0017g0140a0004c0004t0003g0008others(55): Show | 60 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+1501A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966038 | ||||||
| chr4:109966040
|
T | A | 18 | a0001c0001t0006g0253a0001c0001t0011g0141a0001c0001t0011g0142others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1575+1503T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966040 | ||||||
| chr4:109966076
|
A | G | 1 | a0001c0001t0029g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1575+1539A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966076 | ||||||
| chr4:109966098
|
T | C | 55 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(52): Show | 55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1575+1561T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966098 | ||||||
| chr4:109966299
|
A | G | 1 | a0002c0002t0035g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1575+1762A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966299 | ||||||
| chr4:109966470
|
G | T | 1 | a0002c0002t0001g0184 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1575+1933G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966470 | ||||||
| chr4:109966505
|
C | T | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1575+1968C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966505 | ||||||
| chr4:109966673
|
G | A | 58 | a0001c0019t0007g0139a0001c0019t0017g0140a0004c0004t0003g0008others(55): Show | 60 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+2136G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966673 | ||||||
| chr4:109966833
|
G | A | 277 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(274): Show | 283 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1576-2138G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966833 | ||||||
| chr4:109967310
|
A | G | 1 | a0005c0005t0019g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1576-1661A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967310 | ||||||
| chr4:109967311
|
C | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-1660C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967311 | ||||||
| chr4:109967352
|
G | A | 1 | a0002c0002t0009g0149 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1576-1619G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967352 | ||||||
| chr4:109967371
|
G | C | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1576-1600G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967371 | ||||||
| chr4:109967473
|
G | A | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1576-1498G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967473 | ||||||
| chr4:109967699
|
C | T | 3 | a0001c0001t0029g0243a0016c0034t0020g0375a0025c0035t0017g0131 | 3 | HG02559.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1576-1272C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967699 | ||||||
| chr4:109967848
|
A | G | 1 | a0004c0004t0010g0259 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1576-1123A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967848 | ||||||
| chr4:109967851
|
A | C | 75 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(72): Show | 76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.1576-1120A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967851 | ||||||
| chr4:109967855
|
A | C | 1 | a0001c0001t0006g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1576-1116A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967855 | ||||||
| chr4:109968118
|
A | G | 4 | a0001c0001t0014g0232a0001c0001t0018g0234a0001c0001t0033g0240others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-853A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968118 | ||||||
| chr4:109968145
|
G | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1576-826G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968145 | ||||||
| chr4:109968280
|
T | G | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-691T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968280 | ||||||
| chr4:109968553
|
A | G | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1576-418A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968553 | ||||||
| chr4:109968557
|
A | G | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1576-414A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968557 | ||||||
| chr4:109968673
|
C | CATCT | 14 | a0001c0001t0011g0142a0001c0001t0011g0143a0001c0001t0011g0146others(11): Show | 14 | HG01109.hp2 HG01169.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1576-264_1576-261d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968673
|
C | CATCTATC others(1): Show |
41 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(38): Show | 41 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1576-268_1576-261d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968673
|
C | CATCTATC others(5): Show |
94 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0064others(91): Show | 95 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1576-272_1576-261d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968673
|
C | CATCTATC others(9): Show |
40 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0066others(37): Show | 42 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1576-276_1576-261d others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968673
|
C | CATCTATC others(13): Show |
21 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0087others(18): Show | 21 | HG00597.hp2 HG00609.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1576-280_1576-261d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968673
|
CATCT | C | 92 | a0001c0001t0006g0253a0001c0001t0012g0216a0001c0001t0012g0217others(89): Show | 94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1576-264_1576-261d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968673
|
CATCTATC others(1): Show |
C | 3 | a0002c0002t0001g0172a0002c0002t0001g0176a0002c0002t0001g0179 | 3 | NA18969.hp1 NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1576-268_1576-261d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | |||||
| chr4:109968676
|
C | CTATCTAT others(1): Show |
5 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(2): Show | 6 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-288_1576-287i others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968676 | |||||
| chr4:109968699
|
T | TCTACCTA others(5): Show |
13 | a0003c0003t0005g0003a0003c0003t0005g0014a0003c0003t0005g0026others(10): Show | 14 | HG00609.hp2 HG02015.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1576-269_1576-268i others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968699 | |||||
| chr4:109968703
|
T | C | 13 | a0003c0003t0005g0003a0003c0003t0005g0014a0003c0003t0005g0026others(10): Show | 14 | HG00609.hp2 HG02015.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1576-268T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968703 | ||||||
| chr4:109968703
|
T | TCTACCTA others(9): Show |
26 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(23): Show | 26 | HG00423.hp1 HG02027.hp1 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1576-265_1576-264i others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968703 | |||||
| chr4:109968707
|
T | C | 39 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(36): Show | 40 | HG00423.hp1 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.1576-264T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968707 | ||||||
| chr4:109968707
|
T | TCTACCTA others(5): Show |
10 | a0004c0004t0010g0262a0004c0032t0003g0269a0005c0005t0006g0250others(7): Show | 11 | HG01255.hp1 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1576-252_1576-241d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | |||||
| chr4:109968707
|
T | TCTACCTA others(9): Show |
41 | a0001c0019t0007g0139a0001c0019t0017g0140a0004c0004t0003g0008others(38): Show | 42 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1576-256_1576-241d others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | |||||
| chr4:109968707
|
T | TCTACCTA others(13): Show |
15 | a0003c0003t0005g0042a0003c0003t0008g0027a0003c0003t0008g0034others(12): Show | 15 | HG00621.hp1 HG01109.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1576-260_1576-241d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | |||||
| chr4:109968707
|
T | TCTACCTA others(17): Show |
1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1576-241_1576-240i others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | |||||
| chr4:109968707
|
T | TCTATCTA others(5): Show |
1 | a0001c0001t0015g0378 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1576-261_1576-260i others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | |||||
| chr4:109968707
|
T | TCTATCTA others(13): Show |
1 | a0001c0001t0004g0332 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1576-261_1576-260i others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | |||||
| chr4:109968711
|
C | T | 7 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0002g0091others(4): Show | 7 | NA18942.hp1 NA18946.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-260C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968711 | ||||||
| chr4:109968753
|
T | C | 106 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(103): Show | 109 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1576-218T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968753 | ||||||
| chr4:109968779
|
T | A | 47 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0328others(44): Show | 47 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-192T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968779 | ||||||
| chr4:109968860
|
C | T | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-111C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968860 | ||||||
| chr4:109968887
|
T | C | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1576-84T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968887 | ||||||
| chr4:109968933
|
T | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-38T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968933 | ||||||
| chr4:109968933
|
TA | T | 49 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1576-29delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968933 | |||||
| chr4:109969310
|
C | T | 5 | a0002c0002t0001g0184a0002c0002t0001g0192a0002c0002t0001g0210others(2): Show | 5 | HG00597.hp1 HG02040.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724+191C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969310 | ||||||
| chr4:109969373
|
T | A | 7 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724+254T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969373 | ||||||
| chr4:109969381
|
C | T | 6 | a0001c0001t0004g0338a0001c0001t0004g0340a0001c0001t0004g0343others(3): Show | 6 | HG00438.hp2 NA18957.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1724+262C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969381 | ||||||
| chr4:109969548
|
T | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1724+429T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969548 | ||||||
| chr4:109969606
|
A | C | 2 | a0016c0034t0020g0375a0025c0035t0017g0131 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1724+487A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969606 | ||||||
| chr4:109969744
|
T | C | 46 | a0001c0001t0004g0019a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1724+625T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969744 | ||||||
| chr4:109969780
|
C | A | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1724+661C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969780 | ||||||
| chr4:109969832
|
A | C | 1 | a0004c0004t0003g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1724+713A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969832 | ||||||
| chr4:109970168
|
G | A | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1724+1049G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970168 | ||||||
| chr4:109970186
|
T | A | 4 | a0004c0004t0003g0255a0004c0004t0003g0265a0004c0004t0003g0266others(1): Show | 4 | NA18954.hp1 NA18965.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1724+1067T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970186 | ||||||
| chr4:109970387
|
A | C | 155 | a0001c0001t0004g0019a0001c0001t0004g0325a0001c0001t0004g0326others(152): Show | 158 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.1724+1268A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970387 | ||||||
| chr4:109970517
|
T | C | 279 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(276): Show | 284 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1724+1398T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970517 | ||||||
| chr4:109970602
|
A | G | 1 | a0002c0002t0001g0174 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1724+1483A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970602 | ||||||
| chr4:109970617
|
G | A | 1 | a0002c0002t0037g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1724+1498G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970617 | ||||||
| chr4:109970622
|
C | G | 9 | a0001c0001t0006g0253a0001c0001t0012g0236a0001c0001t0020g0233others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1724+1503C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970622 | ||||||
| chr4:109970629
|
A | C | 2 | a0015c0018t0017g0058a0015c0018t0017g0117 | 2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1724+1510A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970629 | ||||||
| chr4:109970629
|
A | G | 3 | a0004c0004t0003g0307a0004c0004t0010g0057a0005c0005t0013g0263 | 3 | NA18956.hp1 NA18978.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1724+1510A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970629 | ||||||
| chr4:109970631
|
C | T | 1 | a0002c0002t0037g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1724+1512C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970631 | ||||||
| chr4:109970639
|
A | G | 1 | a0002c0002t0009g0197 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1724+1520A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970639 | ||||||
| chr4:109970642
|
T | C | 7 | a0001c0001t0006g0253a0002c0002t0001g0134a0002c0002t0009g0197others(4): Show | 7 | HG02809.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1724+1523T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970642 | ||||||
| chr4:109970643
|
G | A | 1 | a0004c0004t0003g0247 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1724+1524G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970643 | ||||||
| chr4:109970653
|
C | T | 136 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0004g0019others(133): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1724+1534C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970653 | ||||||
| chr4:109970686
|
C | A | 1 | a0003c0003t0008g0054 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1724+1567C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970686 | ||||||
| chr4:109970703
|
T | C | 4 | a0001c0001t0002g0082a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG00621.hp2 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1724+1584T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970703 | ||||||
| chr4:109970742
|
G | T | 1 | a0002c0002t0001g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1724+1623G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970742 | ||||||
| chr4:109970749
|
T | C | 1 | a0001c0001t0011g0142 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1724+1630T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970749 | ||||||
| chr4:109970752
|
A | G | 1 | a0001c0001t0011g0142 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1724+1633A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970752 | ||||||
| chr4:109970773
|
G | C | 2 | a0004c0004t0010g0259a0024c0030t0016g0310 | 2 | HG00738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1724+1654G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970773 | ||||||
| chr4:109970780
|
G | A | 3 | a0001c0007t0002g0102a0001c0007t0002g0104a0001c0007t0002g0108 | 3 | HG01515.hp1 HG01517.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1724+1661G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970780 | ||||||
| chr4:109970812
|
G | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1724+1693G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970812 | ||||||
| chr4:109970824
|
C | CA | 88 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(85): Show | 89 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1724+1727dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAA | 10 | a0001c0001t0002g0064a0001c0001t0002g0078a0001c0001t0002g0114others(7): Show | 10 | HG02486.hp1 HG02615.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1724+1726_1724+172 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(1): Show |
41 | a0004c0004t0003g0008a0004c0004t0003g0132a0004c0004t0003g0247others(38): Show | 42 | HG00558.hp1 HG00597.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1724+1720_1724+172 others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(2): Show |
58 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(55): Show | 60 | HG00621.hp1 HG01109.hp2 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.1724+1719_1724+172 others(13): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(3): Show |
21 | a0001c0001t0011g0142a0001c0019t0017g0140a0003c0003t0005g0026others(18): Show | 21 | HG00423.hp1 HG00609.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1724+1718_1724+172 others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(4): Show |
1 | a0001c0019t0007g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1724+1717_1724+172 others(15): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(6): Show |
3 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375 | 3 | HG02559.hp2 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1724+1715_1724+172 others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0022g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1724+1713_1724+172 others(19): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0022g0244a0001c0001t0028g0242a0001c0001t0029g0243 | 3 | HG00735.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1724+1712_1724+172 others(20): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970824
|
CA | C | 13 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(10): Show | 13 | HG01070.hp2 HG01891.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1724+1727delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | |||||
| chr4:109970856
|
T | G | 285 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(282): Show | 291 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.1724+1737T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970856 | ||||||
| chr4:109971007
|
T | C | 276 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(273): Show | 281 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.1724+1888T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971007 | ||||||
| chr4:109971416
|
C | T | 47 | a0001c0001t0004g0332a0001c0016t0002g0039a0001c0016t0006g0023others(44): Show | 48 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1724+2297C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971416 | ||||||
| chr4:109971469
|
G | A | 67 | a0001c0001t0007g0317a0004c0004t0003g0008a0004c0004t0003g0132others(64): Show | 69 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1724+2350G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971469 | ||||||
| chr4:109971499
|
G | A | 12 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1724+2380G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971499 | ||||||
| chr4:109971578
|
C | A | 1 | a0002c0002t0035g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1724+2459C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971578 | ||||||
| chr4:109972031
|
A | C | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1725-2672A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972031 | ||||||
| chr4:109972045
|
TA | T | 7 | a0007c0009t0001g0055a0007c0009t0001g0056a0007c0009t0001g0162others(4): Show | 7 | NA18946.hp1 NA18950.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1725-2647delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109972045 | |||||
| chr4:109972056
|
A | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1725-2647A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972056 | ||||||
| chr4:109972408
|
CGAAACAG others(13): Show |
C | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1725-2294_1725-227 others(24): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972408 | ||||||
| chr4:109972434
|
C | T | 1 | a0001c0019t0017g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1725-2269C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972434 | ||||||
| chr4:109972463
|
T | G | 49 | a0001c0001t0004g0332a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1725-2240T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972463 | ||||||
| chr4:109972681
|
G | T | 5 | a0001c0001t0015g0159a0002c0002t0001g0160a0002c0002t0001g0165others(2): Show | 5 | HG02165.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-2022G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972681 | ||||||
| chr4:109972821
|
A | C | 47 | a0001c0001t0004g0332a0001c0016t0002g0039a0001c0016t0006g0023others(44): Show | 48 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1725-1882A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972821 | ||||||
| chr4:109972836
|
A | G | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1867A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972836 | ||||||
| chr4:109973127
|
C | T | 1 | a0002c0002t0006g0357 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1725-1576C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973127 | ||||||
| chr4:109973145
|
C | T | 68 | a0001c0001t0006g0253a0001c0001t0007g0317a0004c0004t0003g0008others(65): Show | 70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1725-1558C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973145 | ||||||
| chr4:109973196
|
G | A | 2 | a0003c0003t0005g0050a0003c0003t0008g0049 | 2 | NA18995.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1725-1507G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973196 | ||||||
| chr4:109973246
|
C | G | 46 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1725-1457C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973246 | ||||||
| chr4:109973293
|
A | G | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 75 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1725-1410A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973293 | ||||||
| chr4:109973324
|
C | A | 1 | a0003c0003t0008g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1725-1379C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973324 | ||||||
| chr4:109973329
|
A | C | 3 | a0015c0018t0017g0058a0015c0018t0017g0117a0025c0035t0017g0131 | 3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1725-1374A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973329 | ||||||
| chr4:109973366
|
C | T | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1337C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973366 | ||||||
| chr4:109973470
|
T | C | 3 | a0015c0018t0017g0058a0015c0018t0017g0117a0025c0035t0017g0131 | 3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1725-1233T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973470 | ||||||
| chr4:109973475
|
G | C | 1 | a0002c0002t0001g0168 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1725-1228G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973475 | ||||||
| chr4:109973488
|
A | G | 1 | a0003c0003t0005g0038 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1725-1215A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973488 | ||||||
| chr4:109973529
|
A | C | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1174A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973529 | ||||||
| chr4:109973594
|
A | G | 1 | a0001c0001t0007g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1725-1109A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973594 | ||||||
| chr4:109973626
|
T | TCC | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725-1076_1725-107 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109973626 | |||||
| chr4:109973710
|
G | T | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1725-993G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973710 | ||||||
| chr4:109973902
|
T | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0106 | 2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1725-801T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973902 | ||||||
| chr4:109973957
|
G | A | 269 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(266): Show | 274 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.1725-746G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973957 | ||||||
| chr4:109974102
|
A | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1725-601A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109974102 | ||||||
| chr4:109974277
|
A | G | 12 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1725-426A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109974277 | ||||||
| chr4:109974691
|
C | A | 48 | a0001c0016t0002g0039a0001c0016t0006g0023a0001c0019t0007g0139others(45): Show | 49 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1725-12C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109974691 | ||||||
| chr4:109974894
|
A | C | 65 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(62): Show | 65 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1829+87A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109974894 | ||||||
| chr4:109974932
|
A | T | 1 | a0007c0009t0001g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1829+125A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109974932 | ||||||
| chr4:109975078
|
T | C | 1 | a0002c0002t0001g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1829+271T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975078 | ||||||
| chr4:109975334
|
C | T | 1 | a0001c0001t0014g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1829+527C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975334 | ||||||
| chr4:109975446
|
C | A | 48 | a0001c0016t0002g0039a0001c0016t0006g0023a0001c0019t0007g0139others(45): Show | 49 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1830-566C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975446 | ||||||
| chr4:109975731
|
T | G | 150 | a0001c0001t0004g0126a0001c0001t0006g0253a0001c0001t0007g0005others(147): Show | 154 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.1830-281T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975731 | ||||||
| chr4:109976379
|
G | A | 74 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(71): Show | 75 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.2053+144G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109976379 | ||||||
| chr4:109976429
|
G | A | 6 | a0006c0006t0009g0212a0012c0014t0007g0119a0012c0014t0007g0120others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2053+194G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109976429 | ||||||
| chr4:109976808
|
T | G | 3 | a0003c0003t0005g0024a0003c0003t0005g0030a0003c0003t0005g0031 | 3 | NA18939.hp1 NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2053+573T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109976808 | ||||||
| chr4:109977100
|
A | G | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2053+865A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977100 | ||||||
| chr4:109977139
|
A | G | 2 | a0002c0002t0001g0195a0002c0002t0001g0214 | 2 | HG04184.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2053+904A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977139 | ||||||
| chr4:109977273
|
T | C | 8 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(5): Show | 8 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2053+1038T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977273 | ||||||
| chr4:109977536
|
TA | T | 10 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(7): Show | 11 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2053+1314delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 109977536 | |||||
| chr4:109977659
|
C | A | 46 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2053+1424C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977659 | ||||||
| chr4:109977769
|
T | G | 148 | a0001c0001t0004g0126a0001c0001t0006g0253a0001c0001t0007g0005others(145): Show | 152 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.2053+1534T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977769 | ||||||
| chr4:109977833
|
G | A | 3 | a0001c0019t0007g0139a0001c0019t0017g0140a0002c0002t0001g0191 | 3 | HG02615.hp2 HG02630.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2053+1598G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977833 | ||||||
| chr4:109977880
|
A | G | 1 | a0005c0005t0007g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2053+1645A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977880 | ||||||
| chr4:109977933
|
C | G | 1 | a0002c0002t0009g0215 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2053+1698C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977933 | ||||||
| chr4:109978074
|
T | G | 2 | a0001c0001t0004g0365a0001c0001t0004g0366 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2053+1839T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109978074 | ||||||
| chr4:109978237
|
T | C | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2054-1735T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109978237 | ||||||
| chr4:109978752
|
G | A | 46 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2054-1220G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109978752 | ||||||
| chr4:109979057
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2054-915C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979057 | ||||||
| chr4:109979081
|
C | A | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2054-891C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979081 | ||||||
| chr4:109979187
|
A | G | 10 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(7): Show | 11 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2054-785A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979187 | ||||||
| chr4:109979289
|
T | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2054-683T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979289 | ||||||
| chr4:109979357
|
C | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2054-615C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979357 | ||||||
| chr4:109979444
|
G | A | 20 | a0001c0001t0006g0253a0001c0001t0007g0317a0005c0005t0006g0250others(17): Show | 21 | HG01109.hp2 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.2054-528G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979444 | ||||||
| chr4:109979450
|
G | A | 3 | a0015c0018t0017g0058a0015c0018t0017g0117a0025c0035t0017g0131 | 3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2054-522G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979450 | ||||||
| chr4:109979536
|
G | C | 272 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(269): Show | 277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2054-436G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979536 | ||||||
| chr4:109979635
|
G | A | 272 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(269): Show | 277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2054-337G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979635 | ||||||
| chr4:109979662
|
A | G | 41 | a0001c0001t0004g0019a0001c0001t0004g0325a0001c0001t0004g0326others(38): Show | 41 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.2054-310A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979662 | ||||||
| chr4:109979861
|
A | G | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2054-111A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979861 | ||||||
| chr4:109979879
|
A | G | 1 | a0002c0002t0001g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2054-93A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979879 | ||||||
| chr4:109980221
|
G | T | 1 | a0003c0003t0008g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2221+82G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980221 | ||||||
| chr4:109980264
|
G | T | 9 | a0005c0005t0011g0319a0009c0010t0016g0321a0009c0010t0016g0322others(6): Show | 9 | HG01109.hp2 HG01975.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2221+125G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980264 | ||||||
| chr4:109980285
|
A | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2221+146A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980285 | ||||||
| chr4:109980418
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2221+279G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980418 | ||||||
| chr4:109980464
|
G | A | 3 | a0002c0002t0023g0211a0002c0002t0023g0218a0002c0002t0037g0187 | 3 | HG02280.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2221+325G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980464 | ||||||
| chr4:109980497
|
T | C | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2222-329T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980497 | ||||||
| chr4:109980532
|
G | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2222-294G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980532 | ||||||
| chr4:109980701
|
A | G | 5 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(2): Show | 5 | HG00738.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2222-125A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980701 | ||||||
| chr4:109980741
|
C | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2222-85C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980741 | ||||||
| chr4:109980994
|
T | A | 1 | a0001c0007t0002g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2371+19T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109980994 | ||||||
| chr4:109981010
|
G | A | 3 | a0004c0004t0003g0260a0004c0004t0003g0261a0004c0004t0003g0280 | 3 | HG01928.hp2 HG01978.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2371+35G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981010 | ||||||
| chr4:109981345
|
T | G | 1 | a0001c0001t0044g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2371+370T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981345 | ||||||
| chr4:109981528
|
T | C | 9 | a0001c0001t0002g0061a0001c0007t0002g0089a0001c0007t0002g0102others(6): Show | 9 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.2371+553T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981528 | ||||||
| chr4:109981543
|
T | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2371+568T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981543 | ||||||
| chr4:109981578
|
T | A | 46 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2371+603T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981578 | ||||||
| chr4:109981686
|
A | T | 2 | a0003c0003t0005g0030a0003c0003t0005g0031 | 2 | NA18939.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2371+711A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981686 | ||||||
| chr4:109981856
|
C | G | 79 | a0001c0001t0006g0253a0001c0001t0007g0317a0001c0001t0011g0141others(76): Show | 81 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2371+881C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981856 | ||||||
| chr4:109981913
|
A | G | 66 | a0001c0001t0006g0253a0001c0001t0007g0317a0004c0004t0003g0008others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(65): Show |
intron_variant | MODIFIER | c.2371+938A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981913 | ||||||
| chr4:109982070
|
G | A | 5 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0011others(2): Show | 5 | HG02818.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2371+1095G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982070 | ||||||
| chr4:109982078
|
G | C | 3 | a0015c0018t0017g0058a0015c0018t0017g0117a0025c0035t0017g0131 | 3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2371+1103G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982078 | ||||||
| chr4:109982223
|
G | T | 1 | a0001c0001t0006g0079 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2372-1199G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982223 | ||||||
| chr4:109982387
|
G | T | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2372-1035G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982387 | ||||||
| chr4:109982418
|
C | G | 8 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0002g0091others(5): Show | 8 | NA18942.hp1 NA18946.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.2372-1004C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982418 | ||||||
| chr4:109982460
|
T | C | 51 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(48): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2372-962T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982460 | ||||||
| chr4:109982629
|
TTTTTC | T | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372-773_2372-769d others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 109982629 | |||||
| chr4:109982629
|
TTTTTCTT others(3): Show |
T | 4 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0028g0242others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372-778_2372-769d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 109982629 | |||||
| chr4:109982658
|
T | C | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372-764T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982658 | ||||||
| chr4:109982697
|
G | A | 2 | a0001c0001t0011g0141a0001c0001t0011g0144 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2372-725G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982697 | ||||||
| chr4:109982821
|
G | T | 2 | a0007c0009t0001g0177a0007c0009t0001g0178 | 2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2372-601G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982821 | ||||||
| chr4:109983095
|
C | T | 4 | a0004c0004t0003g0281a0004c0004t0003g0282a0004c0004t0003g0283others(1): Show | 4 | HG01175.hp1 HG02148.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372-327C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983095 | ||||||
| chr4:109983098
|
G | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2372-324G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983098 | ||||||
| chr4:109983216
|
T | C | 1 | a0001c0001t0006g0315 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2372-206T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983216 | ||||||
| chr4:109983288
|
G | A | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2372-134G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983288 | ||||||
| chr4:109983292
|
C | T | 272 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(269): Show | 277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2372-130C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983292 | ||||||
| chr4:109983334
|
C | T | 3 | a0015c0018t0017g0058a0015c0018t0017g0117a0025c0035t0017g0131 | 3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2372-88C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983334 | ||||||
| chr4:109983346
|
G | A | 194 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(191): Show | 198 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.2372-76G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983346 | ||||||
| chr4:109983561
|
C | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+20C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109983561 | ||||||
| chr4:109983817
|
C | T | 269 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(266): Show | 274 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.2491+276C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109983817 | ||||||
| chr4:109984141
|
C | A | 2 | a0006c0006t0001g0302a0006c0006t0001g0303 | 2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2491+600C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984141 | ||||||
| chr4:109984240
|
A | C | 50 | a0001c0001t0033g0240a0001c0016t0002g0039a0001c0016t0006g0023others(47): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2491+699A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984240 | ||||||
| chr4:109984246
|
C | CA | 91 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(88): Show | 93 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.2491+717dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr4 | 109984246 | |||||
| chr4:109984246
|
C | CAA | 42 | a0001c0001t0004g0019a0001c0001t0004g0325a0001c0001t0004g0326others(39): Show | 42 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.2491+716_2491+717d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr4 | 109984246 | |||||
| chr4:109984271
|
A | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+730A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984271 | ||||||
| chr4:109984272
|
A | G | 1 | a0001c0001t0006g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2491+731A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984272 | ||||||
| chr4:109984603
|
C | T | 1 | a0006c0006t0001g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2491+1062C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984603 | ||||||
| chr4:109984647
|
A | G | 1 | a0002c0002t0001g0207 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2491+1106A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984647 | ||||||
| chr4:109984648
|
G | A | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491+1107G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984648 | ||||||
| chr4:109984698
|
A | G | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+1157A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984698 | ||||||
| chr4:109984715
|
C | G | 1 | a0001c0001t0013g0335 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2491+1174C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984715 | ||||||
| chr4:109984775
|
G | A | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+1234G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984775 | ||||||
| chr4:109984820
|
A | C | 50 | a0001c0001t0033g0240a0001c0016t0002g0039a0001c0016t0006g0023others(47): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2491+1279A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984820 | ||||||
| chr4:109984947
|
C | T | 9 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2491+1406C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984947 | ||||||
| chr4:109985213
|
T | C | 1 | a0001c0001t0007g0317 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2491+1672T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985213 | ||||||
| chr4:109985226
|
C | G | 3 | a0001c0001t0014g0232a0001c0001t0018g0234a0022c0029t0031g0235 | 3 | HG02809.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2491+1685C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985226 | ||||||
| chr4:109985301
|
G | A | 67 | a0001c0001t0006g0253a0001c0001t0007g0317a0003c0003t0005g0021others(64): Show | 69 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(66): Show |
intron_variant | MODIFIER | c.2491+1760G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985301 | ||||||
| chr4:109985415
|
G | A | 46 | a0001c0001t0033g0240a0001c0016t0002g0039a0001c0016t0006g0023others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2491+1874G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985415 | ||||||
| chr4:109985453
|
C | T | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2491+1912C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985453 | ||||||
| chr4:109985559
|
G | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+2018G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985559 | ||||||
| chr4:109985599
|
C | A | 380 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(377): Show | 387 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(384): Show |
intron_variant | MODIFIER | c.2491+2058C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985599 | ||||||
| chr4:109985929
|
T | A | 1 | a0001c0001t0012g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2492-1815T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985929 | ||||||
| chr4:109985971
|
A | G | 2 | a0002c0002t0006g0345a0002c0002t0021g0342 | 2 | NA18941.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.2492-1773A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985971 | ||||||
| chr4:109986000
|
T | A | 49 | a0001c0001t0033g0240a0001c0016t0002g0039a0001c0016t0006g0023others(46): Show | 50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.2492-1744T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986000 | ||||||
| chr4:109986006
|
T | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2492-1738T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986006 | ||||||
| chr4:109986330
|
C | T | 2 | a0002c0002t0001g0180a0002c0002t0012g0181 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2492-1414C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986330 | ||||||
| chr4:109986481
|
G | A | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2492-1263G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986481 | ||||||
| chr4:109986555
|
C | A | 45 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(42): Show | 46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2492-1189C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986555 | ||||||
| chr4:109986577
|
C | T | 4 | a0001c0001t0004g0331a0001c0001t0004g0334a0001c0001t0004g0339others(1): Show | 4 | HG00609.hp1 HG02027.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492-1167C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986577 | ||||||
| chr4:109986592
|
G | A | 9 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2492-1152G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986592 | ||||||
| chr4:109986748
|
G | GA | 85 | a0001c0001t0006g0253a0001c0001t0007g0317a0001c0001t0011g0141others(82): Show | 87 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.2492-984dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr4 | 109986748 | |||||
| chr4:109986824
|
T | G | 1 | a0001c0001t0044g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2492-920T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986824 | ||||||
| chr4:109986959
|
T | C | 2 | a0003c0003t0005g0002a0003c0003t0008g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2492-785T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986959 | ||||||
| chr4:109987154
|
C | T | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492-590C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987154 | ||||||
| chr4:109987201
|
G | A | 45 | a0001c0016t0002g0039a0001c0016t0006g0023a0003c0003t0005g0002others(42): Show | 46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2492-543G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987201 | ||||||
| chr4:109987394
|
C | T | 2 | a0001c0001t0011g0142a0001c0001t0011g0143 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2492-350C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987394 | ||||||
| chr4:109987433
|
A | G | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492-311A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987433 | ||||||
| chr4:109987438
|
C | T | 2 | a0005c0005t0006g0250a0005c0005t0006g0254 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2492-306C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987438 | ||||||
| chr4:109987523
|
C | T | 1 | a0002c0002t0037g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2492-221C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987523 | ||||||
| chr4:109987583
|
C | T | 5 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(2): Show | 5 | HG00738.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2492-161C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987583 | ||||||
| chr4:109987638
|
A | C | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2492-106A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987638 | ||||||
| chr4:109987724
|
G | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2492-20G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987724 | ||||||
| chr4:109987725
|
G | A | 12 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(9): Show | 13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2492-19G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987725 | ||||||
| chr4:109987892
|
A | T | 4 | a0015c0018t0017g0058a0015c0018t0017g0117a0016c0034t0020g0375others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608+32A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987892 | ||||||
| chr4:109987893
|
C | A | 3 | a0002c0002t0001g0200a0002c0002t0001g0225a0002c0002t0009g0227 | 3 | HG00423.hp2 HG02056.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2608+33C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987893 | ||||||
| chr4:109987899
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2608+39T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987899 | ||||||
| chr4:109987933
|
C | T | 12 | a0001c0001t0014g0232a0001c0001t0018g0234a0005c0005t0007g0001others(9): Show | 13 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+73C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987933 | ||||||
| chr4:109987953
|
A | G | 1 | a0002c0002t0001g0172 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2608+93A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987953 | ||||||
| chr4:109988013
|
A | C | 3 | a0015c0018t0017g0058a0015c0018t0017g0117a0025c0035t0017g0131 | 3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2608+153A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988013 | ||||||
| chr4:109988092
|
T | C | 1 | a0001c0001t0033g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2608+232T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988092 | ||||||
| chr4:109988141
|
AT | A | 47 | a0001c0001t0004g0019a0001c0001t0004g0296a0001c0001t0004g0297others(44): Show | 47 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.2608+284delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 109988141 | |||||
| chr4:109988192
|
C | CT | 104 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(101): Show | 104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2608+350dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 109988192 | |||||
| chr4:109988192
|
CT | C | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2608+350delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 109988192 | |||||
| chr4:109988254
|
T | C | 12 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(9): Show | 13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2609-330T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988254 | ||||||
| chr4:109988546
|
T | A | 3 | a0005c0005t0006g0250a0005c0005t0006g0254a0005c0005t0017g0248 | 3 | HG01884.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2609-38T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988546 | ||||||
| chr4:109988579
|
C | A | 2 | a0001c0019t0007g0139a0001c0019t0017g0140 | 2 | HG02615.hp2 HG02630.hp1 |
splice_region_variant&intron_variant | LOW | c.2609-5C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988579 | ||||||
| chr4:109988860
|
G | A | 272 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(269): Show | 277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2734+151G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109988860 | ||||||
| chr4:109988886
|
A | C | 1 | a0001c0001t0004g0337 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2734+177A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109988886 | ||||||
| chr4:109989184
|
A | C | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2734+475A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989184 | ||||||
| chr4:109989247
|
G | A | 1 | a0001c0001t0002g0313 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2734+538G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989247 | ||||||
| chr4:109989375
|
G | A | 1 | a0004c0004t0003g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2734+666G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989375 | ||||||
| chr4:109989415
|
G | A | 3 | a0005c0005t0019g0007a0005c0005t0019g0251a0017c0023t0045g0252 | 4 | HG02559.hp1 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2734+706G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989415 | ||||||
| chr4:109989594
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2734+885G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989594 | ||||||
| chr4:109989664
|
G | A | 1 | a0016c0034t0020g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2734+955G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989664 | ||||||
| chr4:109989701
|
C | A | 3 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122 | 3 | HG02622.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2734+992C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989701 | ||||||
| chr4:109989785
|
A | G | 48 | a0001c0001t0004g0019a0001c0001t0004g0296a0001c0001t0004g0297others(45): Show | 48 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2734+1076A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989785 | ||||||
| chr4:109989859
|
G | A | 65 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(62): Show | 65 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.2734+1150G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989859 | ||||||
| chr4:109989869
|
A | G | 274 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(271): Show | 279 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.2734+1160A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989869 | ||||||
| chr4:109989924
|
T | C | 273 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(270): Show | 278 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.2734+1215T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989924 | ||||||
| chr4:109990033
|
T | A | 135 | a0001c0001t0004g0019a0001c0001t0004g0296a0001c0001t0004g0297others(132): Show | 137 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2734+1324T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990033 | ||||||
| chr4:109990153
|
T | C | 379 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(376): Show | 386 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(383): Show |
intron_variant | MODIFIER | c.2734+1444T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990153 | ||||||
| chr4:109990223
|
C | G | 3 | a0001c0001t0040g0127a0016c0034t0020g0375a0024c0030t0016g0310 | 3 | HG00738.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2734+1514C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990223 | ||||||
| chr4:109990271
|
C | T | 13 | a0001c0001t0004g0126a0001c0001t0007g0005a0001c0001t0007g0123others(10): Show | 14 | HG00738.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2734+1562C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990271 | ||||||
| chr4:109990359
|
T | C | 4 | a0001c0001t0002g0082a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG00621.hp2 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.2734+1650T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990359 | ||||||
| chr4:109990383
|
T | C | 22 | a0001c0001t0004g0126a0001c0001t0012g0236a0001c0001t0014g0232others(19): Show | 23 | HG01884.hp1 HG02486.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.2734+1674T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990383 | ||||||
| chr4:109990411
|
A | G | 273 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(270): Show | 278 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.2734+1702A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990411 | ||||||
| chr4:109990746
|
T | G | 1 | a0010c0011t0001g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2734+2037T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990746 | ||||||
| chr4:109990751
|
T | C | 285 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(282): Show | 291 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.2734+2042T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990751 | ||||||
| chr4:109990789
|
G | A | 6 | a0001c0001t0007g0317a0001c0001t0033g0240a0005c0005t0017g0248others(3): Show | 6 | HG02615.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2734+2080G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990789 | ||||||
| chr4:109991220
|
T | TATATA | 151 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(148): Show | 155 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.2735-2025_2735-202 others(9): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109991220 | |||||
| chr4:109991370
|
G | A | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-1877G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991370 | ||||||
| chr4:109991401
|
G | A | 1 | a0002c0002t0006g0345 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2735-1846G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991401 | ||||||
| chr4:109991426
|
AGTG | A | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-1817_2735-181 others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109991426 | |||||
| chr4:109991500
|
G | A | 1 | a0004c0004t0003g0275 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2735-1747G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991500 | ||||||
| chr4:109991531
|
G | T | 26 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(23): Show | 28 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2735-1716G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991531 | ||||||
| chr4:109991544
|
TAATGTAA others(10): Show |
T | 1 | a0001c0001t0027g0077 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2735-1700_2735-168 others(21): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109991544 | |||||
| chr4:109991546
|
A | T | 1 | a0006c0006t0001g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2735-1701A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991546 | ||||||
| chr4:109991549
|
T | C | 1 | a0001c0001t0014g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2735-1698T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991549 | ||||||
| chr4:109991568
|
G | A | 1 | a0005c0005t0017g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2735-1679G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991568 | ||||||
| chr4:109991720
|
A | T | 26 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(23): Show | 28 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2735-1527A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991720 | ||||||
| chr4:109991784
|
T | C | 26 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(23): Show | 28 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2735-1463T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991784 | ||||||
| chr4:109992037
|
A | G | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-1210A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992037 | ||||||
| chr4:109992170
|
T | TA | 26 | a0001c0001t0015g0377a0002c0002t0001g0148a0002c0002t0001g0164others(23): Show | 27 | HG00323.hp1 HG00558.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2735-1047dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
T | TAA | 14 | a0001c0001t0004g0297a0001c0001t0004g0298a0001c0001t0015g0159others(11): Show | 14 | HG00423.hp2 HG00738.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.2735-1048_2735-104 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
T | TAAA | 42 | a0001c0001t0004g0296a0001c0001t0004g0328a0001c0001t0004g0329others(39): Show | 42 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2735-1049_2735-104 others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
T | TAAAA | 35 | a0001c0001t0004g0325a0001c0001t0004g0330a0001c0001t0004g0339others(32): Show | 36 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2735-1050_2735-104 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
T | TAAAAA | 28 | a0001c0001t0004g0019a0001c0001t0004g0326a0001c0001t0004g0331others(25): Show | 28 | HG02027.hp1 HG02027.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.2735-1051_2735-104 others(9): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
T | TAAAAAA | 24 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(21): Show | 24 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.2735-1052_2735-104 others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
T | TAAAAAAA | 12 | a0001c0001t0028g0242a0004c0004t0003g0008a0004c0004t0003g0272others(9): Show | 13 | HG00735.hp2 HG02004.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.2735-1053_2735-104 others(11): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TA | T | 33 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0144others(30): Show | 34 | HG01069.hp2 HG01070.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2735-1047delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TAA | T | 13 | a0001c0001t0007g0317a0001c0001t0022g0241a0001c0001t0022g0244others(10): Show | 14 | HG02055.hp1 HG02280.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.2735-1048_2735-104 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TAAA | T | 6 | a0001c0019t0017g0140a0011c0012t0014g0229a0011c0012t0014g0230others(3): Show | 6 | HG01884.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2735-1049_2735-104 others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(1): Show | 5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2735-1056_2735-104 others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TAAAAAAA others(4): Show |
T | 2 | a0014c0017t0007g0118a0014c0017t0007g0121 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2735-1057_2735-104 others(15): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TAAAAAAA others(6): Show |
T | 62 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(59): Show | 62 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2735-1059_2735-104 others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992170
|
TAAAAAAA others(7): Show |
T | 3 | a0001c0001t0002g0130a0001c0001t0006g0113a0001c0007t0002g0089 | 3 | HG02895.hp2 HG03491.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2735-1060_2735-104 others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | |||||
| chr4:109992191
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0040g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2735-1054_2735-104 others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992191 | |||||
| chr4:109992205
|
G | A | 1 | a0005c0005t0038g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2735-1042G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992205 | ||||||
| chr4:109992207
|
G | C | 1 | a0005c0005t0046g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2735-1040G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992207 | ||||||
| chr4:109992242
|
C | T | 1 | a0022c0029t0031g0235 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2735-1005C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992242 | ||||||
| chr4:109992257
|
G | A | 1 | a0002c0002t0001g0191 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2735-990G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992257 | ||||||
| chr4:109992331
|
G | A | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2735-916G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992331 | ||||||
| chr4:109992691
|
C | T | 6 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(3): Show | 7 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2735-556C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992691 | ||||||
| chr4:109992827
|
C | G | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-420C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992827 | ||||||
| chr4:109992847
|
A | C | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-400A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992847 | ||||||
| chr4:109992954
|
G | A | 8 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2735-293G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992954 | ||||||
| chr4:109992954
|
G | C | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-293G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992954 | ||||||
| chr4:109992963
|
G | A | 379 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(376): Show | 386 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(383): Show |
intron_variant | MODIFIER | c.2735-284G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992963 | ||||||
| chr4:109992986
|
C | T | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-261C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992986 | ||||||
| chr4:109992992
|
A | AT | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-255_2735-254i others(3): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992992 | ||||||
| chr4:109992993
|
A | G | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-254A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992993 | ||||||
| chr4:109992994
|
A | T | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-253A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992994 | ||||||
| chr4:109993034
|
CATGTATA others(3): Show |
C | 10 | a0001c0001t0004g0338a0001c0001t0004g0340a0001c0001t0004g0343others(7): Show | 10 | HG00438.hp2 NA18942.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.2735-207_2735-198d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109993034 | |||||
| chr4:109993062
|
C | G | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-185C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109993062 | ||||||
| chr4:109993067
|
G | A | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2735-180G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109993067 | ||||||
| chr4:109993110
|
TA | T | 8 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2735-130delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109993110 | |||||
| chr4:109993125
|
G | C | 11 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2735-122G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109993125 | ||||||
| chr4:109993564
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2857+195G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993564 | ||||||
| chr4:109993595
|
A | G | 25 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(22): Show | 27 | HG00735.hp2 HG01884.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.2857+226A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993595 | ||||||
| chr4:109993684
|
TGCAGGGC others(3): Show |
T | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2857+321_2857+330d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109993684 | |||||
| chr4:109993864
|
A | G | 6 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0011others(3): Show | 6 | HG02818.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2857+495A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993864 | ||||||
| chr4:109993954
|
A | G | 1 | a0001c0001t0014g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2857+585A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993954 | ||||||
| chr4:109994031
|
G | GT | 69 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(66): Show | 71 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2857+675dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109994031 | |||||
| chr4:109994031
|
G | GTT | 103 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(100): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2857+674_2857+675d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109994031 | |||||
| chr4:109994031
|
GT | G | 10 | a0001c0001t0002g0064a0001c0001t0011g0141a0001c0001t0011g0142others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2857+675delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109994031 | |||||
| chr4:109994352
|
C | A | 1 | a0003c0003t0008g0051 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2858-381C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994352 | ||||||
| chr4:109994402
|
A | C | 2 | a0002c0002t0006g0345a0002c0002t0021g0342 | 2 | NA18941.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.2858-331A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994402 | ||||||
| chr4:109994460
|
A | T | 1 | a0024c0030t0016g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2858-273A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994460 | ||||||
| chr4:109994549
|
G | A | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2858-184G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994549 | ||||||
| chr4:109994592
|
A | T | 1 | a0004c0004t0010g0057 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2858-141A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994592 | ||||||
| chr4:109995024
|
G | A | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3005+144G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995024 | ||||||
| chr4:109995079
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3005+199C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995079 | ||||||
| chr4:109995193
|
G | A | 11 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3005+313G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995193 | ||||||
| chr4:109995480
|
G | A | 12 | a0002c0002t0001g0203a0002c0002t0001g0224a0002c0002t0006g0083others(9): Show | 12 | HG00673.hp2 HG02129.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.3005+600G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995480 | ||||||
| chr4:109995680
|
G | A | 1 | a0001c0001t0027g0063 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3005+800G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995680 | ||||||
| chr4:109995866
|
G | C | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3005+986G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995866 | ||||||
| chr4:109995961
|
T | G | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3005+1081T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995961 | ||||||
| chr4:109996071
|
G | A | 3 | a0003c0003t0005g0042a0003c0003t0008g0044a0003c0003t0008g0047 | 3 | HG02027.hp1 NA18947.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.3005+1191G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996071 | ||||||
| chr4:109996080
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3005+1200C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996080 | ||||||
| chr4:109996331
|
T | C | 48 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(45): Show | 49 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.3005+1451T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996331 | ||||||
| chr4:109996369
|
G | T | 20 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(17): Show | 22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3005+1489G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996369 | ||||||
| chr4:109996470
|
A | C | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3005+1590A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996470 | ||||||
| chr4:109996918
|
C | A | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3005+2038C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996918 | ||||||
| chr4:109997001
|
A | AT | 8 | a0002c0002t0001g0164a0002c0002t0001g0172a0002c0002t0001g0176others(5): Show | 9 | HG01074.hp2 HG01081.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.3005+2132dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 109997001 | |||||
| chr4:109997158
|
C | T | 1 | a0002c0002t0002g0111 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3005+2278C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997158 | ||||||
| chr4:109997231
|
G | T | 5 | a0009c0010t0016g0321a0009c0010t0016g0322a0009c0010t0016g0323others(2): Show | 5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3005+2351G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997231 | ||||||
| chr4:109997302
|
G | C | 1 | a0001c0001t0011g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3006-2377G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997302 | ||||||
| chr4:109997488
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3006-2191G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997488 | ||||||
| chr4:109997531
|
A | G | 270 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(267): Show | 275 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.3006-2148A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997531 | ||||||
| chr4:109997663
|
G | A | 1 | a0004c0032t0003g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3006-2016G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997663 | ||||||
| chr4:109997777
|
C | G | 1 | a0002c0002t0001g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3006-1902C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997777 | ||||||
| chr4:109997818
|
G | A | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006-1861G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997818 | ||||||
| chr4:109997820
|
A | G | 50 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3006-1859A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997820 | ||||||
| chr4:109997935
|
C | T | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3006-1744C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997935 | ||||||
| chr4:109998038
|
T | A | 1 | a0001c0001t0018g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3006-1641T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998038 | ||||||
| chr4:109998203
|
T | C | 5 | a0009c0010t0016g0321a0009c0010t0016g0322a0009c0010t0016g0323others(2): Show | 5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006-1476T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998203 | ||||||
| chr4:109998244
|
C | T | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3006-1435C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998244 | ||||||
| chr4:109998312
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3006-1367C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998312 | ||||||
| chr4:109998738
|
G | A | 1 | a0005c0005t0017g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3006-941G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998738 | ||||||
| chr4:109998740
|
G | C | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006-939G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998740 | ||||||
| chr4:109998903
|
A | G | 1 | a0002c0002t0001g0134 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3006-776A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998903 | ||||||
| chr4:109998943
|
A | G | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006-736A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998943 | ||||||
| chr4:109999015
|
GAC | G | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3006-662_3006-661d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 109999015 | |||||
| chr4:109999075
|
T | C | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3006-604T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999075 | ||||||
| chr4:109999095
|
G | A | 1 | a0001c0001t0018g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3006-584G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999095 | ||||||
| chr4:109999143
|
A | G | 50 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3006-536A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999143 | ||||||
| chr4:109999175
|
A | C | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006-504A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999175 | ||||||
| chr4:109999217
|
G | A | 1 | a0003c0003t0005g0032 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3006-462G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999217 | ||||||
| chr4:109999291
|
A | G | 3 | a0007c0009t0001g0162a0007c0009t0001g0163a0007c0009t0009g0161 | 3 | NA18946.hp1 NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3006-388A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999291 | ||||||
| chr4:109999297
|
T | G | 1 | a0001c0001t0014g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3006-382T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999297 | ||||||
| chr4:109999314
|
T | C | 1 | a0002c0002t0001g0172 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3006-365T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999314 | ||||||
| chr4:109999568
|
G | A | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3006-111G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999568 | ||||||
| chr4:109999665
|
G | A | 1 | a0012c0014t0007g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3006-14G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999665 | ||||||
| chr4:109999972
|
C | G | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3173+126C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 109999972 | ||||||
| chr4:110000049
|
C | T | 1 | a0001c0001t0011g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3173+203C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000049 | ||||||
| chr4:110000112
|
G | A | 1 | a0025c0035t0017g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3173+266G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000112 | ||||||
| chr4:110000131
|
A | G | 1 | a0001c0001t0013g0350 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3173+285A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000131 | ||||||
| chr4:110000218
|
T | C | 66 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3173+372T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000218 | ||||||
| chr4:110000250
|
C | CA | 34 | a0001c0001t0014g0232a0001c0001t0014g0239a0001c0001t0018g0234others(31): Show | 36 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.3173+424dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | |||||
| chr4:110000250
|
CA | C | 18 | a0001c0001t0002g0312a0001c0001t0004g0126a0001c0001t0006g0079others(15): Show | 18 | HG00738.hp1 HG01975.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.3173+424delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | |||||
| chr4:110000250
|
CAA | C | 100 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(97): Show | 101 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3173+423_3173+424d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | |||||
| chr4:110000250
|
CAAA | C | 9 | a0001c0001t0002g0100a0003c0003t0008g0027a0003c0003t0008g0034others(6): Show | 9 | HG00423.hp1 HG00621.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3173+422_3173+424d others(5): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | |||||
| chr4:110000259
|
A | G | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3173+413A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000259 | ||||||
| chr4:110000420
|
G | A | 2 | a0001c0001t0022g0241a0001c0001t0022g0244 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3173+574G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000420 | ||||||
| chr4:110000832
|
A | G | 1 | a0002c0002t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3173+986A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000832 | ||||||
| chr4:110001038
|
T | C | 56 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(53): Show | 56 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.3173+1192T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001038 | ||||||
| chr4:110001340
|
T | C | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3173+1494T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001340 | ||||||
| chr4:110001423
|
A | G | 66 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3173+1577A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001423 | ||||||
| chr4:110001524
|
G | A | 115 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(112): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.3173+1678G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001524 | ||||||
| chr4:110001530
|
GA | G | 50 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(47): Show | 51 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.3173+1693delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110001530 | |||||
| chr4:110001565
|
C | T | 1 | a0004c0004t0010g0259 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3173+1719C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001565 | ||||||
| chr4:110001722
|
A | G | 1 | a0001c0001t0006g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3173+1876A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001722 | ||||||
| chr4:110001740
|
A | G | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3173+1894A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001740 | ||||||
| chr4:110002040
|
G | A | 1 | a0003c0003t0008g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3173+2194G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002040 | ||||||
| chr4:110002047
|
C | T | 3 | a0002c0002t0023g0211a0002c0002t0023g0218a0002c0002t0037g0187 | 3 | HG02280.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3173+2201C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002047 | ||||||
| chr4:110002088
|
A | G | 1 | a0002c0002t0021g0354 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3173+2242A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002088 | ||||||
| chr4:110002172
|
G | A | 110 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(107): Show | 111 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.3173+2326G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002172 | ||||||
| chr4:110002287
|
G | A | 1 | a0002c0002t0037g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3174-2218G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002287 | ||||||
| chr4:110002380
|
C | T | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3174-2125C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002380 | ||||||
| chr4:110002436
|
T | C | 66 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3174-2069T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002436 | ||||||
| chr4:110002537
|
T | G | 50 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3174-1968T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002537 | ||||||
| chr4:110002542
|
T | G | 13 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0028g0242others(10): Show | 13 | HG00735.hp2 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.3174-1963T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002542 | ||||||
| chr4:110002559
|
C | A | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3174-1946C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002559 | ||||||
| chr4:110002635
|
G | C | 109 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(106): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.3174-1870G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002635 | ||||||
| chr4:110002667
|
A | T | 1 | a0002c0002t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3174-1838A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002667 | ||||||
| chr4:110002774
|
A | G | 1 | a0005c0005t0007g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3174-1731A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002774 | ||||||
| chr4:110002783
|
C | T | 142 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(139): Show | 145 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.3174-1722C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002783 | ||||||
| chr4:110002875
|
C | T | 5 | a0009c0010t0016g0321a0009c0010t0016g0322a0009c0010t0016g0323others(2): Show | 5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3174-1630C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002875 | ||||||
| chr4:110003056
|
G | A | 78 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(75): Show | 81 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.3174-1449G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003056 | ||||||
| chr4:110003069
|
G | A | 11 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3174-1436G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003069 | ||||||
| chr4:110003178
|
C | G | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3174-1327C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003178 | ||||||
| chr4:110003204
|
G | T | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3174-1301G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003204 | ||||||
| chr4:110003401
|
T | C | 1 | a0002c0002t0006g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3174-1104T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003401 | ||||||
| chr4:110003486
|
G | C | 198 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(195): Show | 203 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.3174-1019G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003486 | ||||||
| chr4:110003553
|
G | C | 27 | a0001c0001t0014g0232a0001c0001t0014g0239a0001c0001t0018g0234others(24): Show | 29 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3174-952G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003553 | ||||||
| chr4:110003585
|
A | T | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3174-920A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003585 | ||||||
| chr4:110003616
|
C | T | 203 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(200): Show | 208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3174-889C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003616 | ||||||
| chr4:110003672
|
G | A | 1 | a0004c0004t0003g0247 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3174-833G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003672 | ||||||
| chr4:110003719
|
A | T | 8 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3174-786A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003719 | ||||||
| chr4:110003999
|
A | G | 1 | a0004c0004t0003g0260 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3174-506A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003999 | ||||||
| chr4:110004092
|
T | C | 8 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3174-413T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004092 | ||||||
| chr4:110004191
|
C | A | 2 | a0001c0001t0004g0328a0001c0001t0013g0335 | 2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3174-314C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004191 | ||||||
| chr4:110004198
|
A | G | 1 | a0002c0002t0001g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3174-307A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004198 | ||||||
| chr4:110004208
|
G | GCATA | 8 | a0001c0001t0004g0126a0001c0001t0004g0296a0001c0001t0004g0297others(5): Show | 8 | HG00558.hp1 HG00609.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.3174-290_3174-287d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004208 | |||||
| chr4:110004208
|
GCATA | G | 5 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3174-290_3174-287d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004208 | |||||
| chr4:110004211
|
T | TACAC | 18 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(15): Show | 19 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.3174-291_3174-290i others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | |||||
| chr4:110004211
|
T | TACACAC | 12 | a0004c0004t0003g0255a0004c0004t0003g0265a0004c0004t0003g0266others(9): Show | 12 | NA18939.hp2 NA18947.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.3174-291_3174-290i others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | |||||
| chr4:110004211
|
TACATACA others(3): Show |
T | 27 | a0001c0001t0007g0317a0001c0001t0014g0239a0001c0001t0018g0234others(24): Show | 29 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3174-290_3174-281d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | |||||
| chr4:110004211
|
TACATACA others(5): Show |
T | 2 | a0017c0023t0045g0252a0022c0029t0031g0235 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3174-290_3174-279d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | |||||
| chr4:110004213
|
CAT | C | 8 | a0001c0001t0011g0145a0001c0001t0011g0146a0001c0001t0011g0147others(5): Show | 8 | HG01109.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3174-290_3174-289d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004213 | |||||
| chr4:110004215
|
T | C | 53 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(50): Show | 55 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.3174-290T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004215 | ||||||
| chr4:110004215
|
T | TAC | 56 | a0001c0001t0002g0064a0001c0001t0002g0072a0001c0001t0025g0092others(53): Show | 57 | HG00609.hp2 HG00673.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3174-254_3174-253d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
T | TACAC | 15 | a0001c0001t0006g0253a0001c0007t0002g0116a0002c0002t0001g0010others(12): Show | 16 | HG00323.hp1 HG02015.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.3174-256_3174-253d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
T | TACACAC | 6 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(3): Show | 6 | HG02074.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3174-258_3174-253d others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
T | TACACACA others(13): Show |
1 | a0002c0002t0006g0345 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3174-272_3174-253d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
T | TACACACA others(19): Show |
2 | a0002c0002t0001g0155a0002c0002t0021g0342 | 2 | NA18941.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.3174-278_3174-253d others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
T | TACATAC | 21 | a0001c0001t0004g0331a0001c0001t0004g0332a0001c0001t0004g0334others(18): Show | 21 | HG00733.hp2 HG01070.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.3174-287_3174-286i others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
T | TACATACA others(1): Show |
27 | a0001c0001t0004g0019a0001c0001t0004g0325a0001c0001t0004g0326others(24): Show | 27 | HG00408.hp1 HG00438.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.3174-287_3174-286i others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
TACAC | T | 6 | a0001c0001t0002g0087a0001c0001t0002g0091a0002c0002t0001g0011others(3): Show | 6 | HG01070.hp2 HG02155.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3174-256_3174-253d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004215
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0006g0316 | 3 | NA18967.hp2 NA18969.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3174-260_3174-253d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | |||||
| chr4:110004253
|
A | C | 1 | a0001c0027t0004g0351 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3174-252A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004253 | ||||||
| chr4:110004303
|
G | A | 107 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(104): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.3174-202G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004303 | ||||||
| chr4:110004313
|
C | T | 107 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(104): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.3174-192C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004313 | ||||||
| chr4:110004336
|
C | A | 200 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(197): Show | 205 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.3174-169C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004336 | ||||||
| chr4:110004375
|
A | G | 1 | a0002c0002t0001g0148 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3174-130A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004375 | ||||||
| chr4:110004672
|
C | T | 1 | a0002c0002t0006g0357 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3291+50C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110004672 | ||||||
| chr4:110004750
|
C | A | 1 | a0001c0001t0013g0361 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3291+128C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110004750 | ||||||
| chr4:110004768
|
G | A | 1 | a0001c0001t0012g0376 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3291+146G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110004768 | ||||||
| chr4:110005036
|
C | CT | 115 | a0001c0001t0002g0061a0001c0001t0002g0072a0001c0001t0002g0085others(112): Show | 117 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.3291+438dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | |||||
| chr4:110005036
|
C | CTT | 28 | a0001c0001t0002g0128a0001c0001t0003g0075a0001c0007t0002g0104others(25): Show | 28 | HG00423.hp1 HG00621.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.3291+437_3291+438d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | |||||
| chr4:110005036
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3291+429_3291+438d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | |||||
| chr4:110005036
|
CTTTTTTT others(4): Show |
C | 15 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(12): Show | 16 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.3291+428_3291+438d others(13): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | |||||
| chr4:110005036
|
CTTTTTTT others(5): Show |
C | 1 | a0019c0025t0021g0291 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3291+427_3291+438d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | |||||
| chr4:110005036
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3291+426_3291+438d others(15): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | |||||
| chr4:110005353
|
T | C | 4 | a0002c0002t0001g0160a0002c0002t0001g0165a0002c0002t0002g0111others(1): Show | 4 | HG02165.hp2 NA18954.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3291+731T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005353 | ||||||
| chr4:110005371
|
A | G | 140 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(137): Show | 145 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.3291+749A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005371 | ||||||
| chr4:110005377
|
C | T | 49 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0297others(46): Show | 49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.3291+755C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005377 | ||||||
| chr4:110005525
|
T | C | 1 | a0003c0003t0005g0045 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3291+903T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005525 | ||||||
| chr4:110005574
|
G | A | 201 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(198): Show | 206 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.3291+952G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005574 | ||||||
| chr4:110006047
|
GA | G | 89 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(86): Show | 93 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.3291+1432delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110006047 | |||||
| chr4:110006071
|
T | G | 1 | a0002c0002t0035g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3291+1449T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006071 | ||||||
| chr4:110006183
|
TA | T | 201 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(198): Show | 206 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.3291+1572delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110006183 | |||||
| chr4:110006236
|
TCAAGAGA others(25): Show |
T | 10 | a0001c0001t0002g0061a0001c0007t0002g0089a0001c0007t0002g0102others(7): Show | 10 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3291+1621_3291+165 others(36): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110006236 | |||||
| chr4:110006373
|
G | A | 3 | a0001c0001t0002g0065a0001c0001t0012g0216a0001c0001t0012g0217 | 3 | HG00408.hp2 NA18951.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3291+1751G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006373 | ||||||
| chr4:110006377
|
T | C | 8 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3291+1755T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006377 | ||||||
| chr4:110006407
|
G | C | 290 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(287): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.3292-1745G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006407 | ||||||
| chr4:110006477
|
T | A | 2 | a0017c0023t0045g0252a0022c0029t0031g0235 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3292-1675T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006477 | ||||||
| chr4:110006648
|
G | A | 1 | a0005c0005t0017g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3292-1504G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006648 | ||||||
| chr4:110006709
|
A | T | 203 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(200): Show | 208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3292-1443A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006709 | ||||||
| chr4:110006772
|
G | A | 203 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(200): Show | 208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3292-1380G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006772 | ||||||
| chr4:110006851
|
G | A | 6 | a0001c0001t0022g0241a0001c0001t0022g0244a0001c0001t0029g0243others(3): Show | 7 | HG02055.hp1 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3292-1301G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006851 | ||||||
| chr4:110007060
|
C | T | 3 | a0012c0014t0007g0119a0012c0014t0007g0120a0012c0014t0007g0122 | 3 | HG02622.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3292-1092C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007060 | ||||||
| chr4:110007300
|
T | A | 1 | a0004c0004t0003g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3292-852T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007300 | ||||||
| chr4:110007482
|
A | G | 2 | a0003c0003t0005g0002a0003c0003t0008g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3292-670A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007482 | ||||||
| chr4:110007646
|
A | G | 1 | a0002c0002t0009g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3292-506A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007646 | ||||||
| chr4:110007659
|
A | T | 27 | a0001c0001t0007g0317a0001c0001t0014g0232a0001c0001t0014g0239others(24): Show | 29 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.3292-493A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007659 | ||||||
| chr4:110007730
|
A | G | 2 | a0001c0001t0028g0242a0001c0001t0033g0240 | 2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3292-422A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007730 | ||||||
| chr4:110007735
|
G | A | 1 | a0001c0001t0040g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3292-417G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007735 | ||||||
| chr4:110007756
|
G | A | 2 | a0017c0023t0045g0252a0022c0029t0031g0235 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3292-396G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007756 | ||||||
| chr4:110007793
|
T | G | 203 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(200): Show | 208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3292-359T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007793 | ||||||
| chr4:110007807
|
C | G | 5 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3292-345C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007807 | ||||||
| chr4:110007820
|
A | C | 1 | a0005c0005t0007g0290 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3292-332A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007820 | ||||||
| chr4:110007972
|
G | A | 74 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(71): Show | 77 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.3292-180G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007972 | ||||||
| chr4:110008353
|
C | G | 5 | a0001c0001t0020g0233a0001c0001t0020g0237a0001c0001t0034g0238others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3370+123C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008353 | ||||||
| chr4:110008382
|
G | A | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+152G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008382 | ||||||
| chr4:110008476
|
T | C | 1 | a0002c0002t0009g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3370+246T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008476 | ||||||
| chr4:110008497
|
G | A | 47 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(44): Show | 48 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.3370+267G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008497 | ||||||
| chr4:110008573
|
C | T | 44 | a0001c0001t0004g0019a0001c0001t0004g0325a0001c0001t0004g0326others(41): Show | 44 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.3370+343C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008573 | ||||||
| chr4:110008601
|
A | G | 5 | a0009c0010t0016g0321a0009c0010t0016g0322a0009c0010t0016g0323others(2): Show | 5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+371A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008601 | ||||||
| chr4:110008657
|
C | G | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+427C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008657 | ||||||
| chr4:110008928
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3370+698G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008928 | ||||||
| chr4:110008938
|
A | G | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3370+708A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008938 | ||||||
| chr4:110008970
|
G | A | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3370+740G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008970 | ||||||
| chr4:110009057
|
A | G | 50 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3370+827A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009057 | ||||||
| chr4:110009186
|
C | G | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+956C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009186 | ||||||
| chr4:110009235
|
T | A | 50 | a0001c0001t0004g0019a0001c0001t0004g0126a0001c0001t0004g0296others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3370+1005T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009235 | ||||||
| chr4:110009520
|
A | G | 5 | a0001c0019t0017g0140a0005c0005t0017g0248a0015c0018t0017g0058others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+1290A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009520 | ||||||
| chr4:110009638
|
A | G | 202 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(199): Show | 207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3370+1408A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009638 | ||||||
| chr4:110009834
|
A | G | 1 | a0002c0002t0001g0311 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3371-1368A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009834 | ||||||
| chr4:110009949
|
T | C | 202 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(199): Show | 207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3371-1253T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009949 | ||||||
| chr4:110010064
|
G | A | 7 | a0001c0001t0007g0005a0001c0001t0007g0123a0001c0001t0007g0124others(4): Show | 8 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3371-1138G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010064 | ||||||
| chr4:110010074
|
A | G | 1 | a0001c0001t0002g0314 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3371-1128A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010074 | ||||||
| chr4:110010084
|
G | A | 1 | a0001c0001t0015g0208 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3371-1118G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010084 | ||||||
| chr4:110010246
|
A | C | 2 | a0001c0001t0002g0110a0001c0001t0002g0112 | 2 | NA18959.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.3371-956A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010246 | ||||||
| chr4:110010279
|
A | T | 3 | a0011c0012t0014g0229a0011c0012t0014g0230a0011c0012t0014g0231 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3371-923A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010279 | ||||||
| chr4:110010295
|
CTCTA | C | 3 | a0006c0006t0001g0006a0006c0006t0001g0175a0006c0006t0001g0182 | 4 | HG03017.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3371-902_3371-899d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr4 | 110010295 | |||||
| chr4:110010403
|
T | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3371-799T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010403 | ||||||
| chr4:110010407
|
A | AT | 25 | a0001c0001t0011g0141a0001c0001t0011g0142a0001c0001t0011g0143others(22): Show | 26 | HG01109.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3371-788dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr4 | 110010407 | |||||
| chr4:110010413
|
T | TA | 3 | a0001c0001t0004g0343a0003c0003t0026g0015a0005c0005t0038g0289 | 3 | NA18975.hp1 NA19002.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3371-789_3371-788i others(3): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010413 | ||||||
| chr4:110010414
|
T | A | 3 | a0001c0001t0004g0343a0003c0003t0026g0015a0005c0005t0038g0289 | 3 | NA18975.hp1 NA19002.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3371-788T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010414 | ||||||
| chr4:110010414
|
T | TA | 172 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(169): Show | 176 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.3371-781dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr4 | 110010414 | |||||
| chr4:110010630
|
A | G | 202 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(199): Show | 207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3371-572A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010630 | ||||||
| chr4:110010662
|
G | A | 1 | a0001c0001t0040g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3371-540G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010662 | ||||||
| chr4:110010783
|
G | T | 46 | a0003c0003t0005g0002a0003c0003t0005g0003a0003c0003t0005g0014others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3371-419G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010783 | ||||||
| chr4:110010790
|
G | T | 2 | a0017c0023t0045g0252a0022c0029t0031g0235 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3371-412G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010790 | ||||||
| chr4:110010985
|
G | A | 3 | a0006c0006t0001g0006a0006c0006t0001g0175a0006c0006t0001g0182 | 4 | HG03017.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3371-217G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010985 | ||||||
| chr4:110011048
|
A | G | 1 | a0005c0005t0019g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3371-154A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110011048 |