| geneid | 51705 |
|---|---|
| ensemblid | ENSG00000164035.10 |
| hgncid | 16041 |
| symbol | EMCN |
| name | endomucin |
| refseq_nuc | NM_016242.4 |
| refseq_prot | NP_057326.2 |
| ensembl_nuc | ENST00000296420.9 |
| ensembl_prot | ENSP00000296420.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 100395341 |
| end | 100518022 |
| strand | - |
| ver | v1.2 |
| region | chr4:100395341-100518022 |
| region5000 | chr4:100390341-100523022 |
| regionname0 | EMCN_chr4_100395341_100518022 |
| regionname5000 | EMCN_chr4_100390341_100523022 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 261 | 166 | 63 | 40 | 31 | 7 | 23 | 20 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002 | 0/0 | 260 | 89 | 18 | 24 | 35 | 0 | 12 | 26 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0003 | 0/0 | 261 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0004 | 0/0 | 261 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0005 | 0/0 | 261 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 786 | 163 | 60 | 40 | 31 | 7 | 23 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0002 | 0/0 | 783 | 88 | 17 | 24 | 35 | 0 | 12 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0003 | 0/0 | 786 | 4 | 3 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0004 | 0/0 | 786 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0005 | 0/0 | 786 | 2 | 0 | 1 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0006 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0007 | 0/0 | 786 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| c0008 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3183 | 68 | 7 | 18 | 33 | 0 | 10 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0002 | 0/0 | 3182 | 67 | 8 | 25 | 15 | 6 | 13 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0003 | 1/0 | 3181 | 21 | 6 | 6 | 7 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0004 | 0/0 | 3183 | 15 | 14 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0005 | 0/0 | 3182 | 15 | 14 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0006 | 0/0 | 3181 | 13 | 2 | 2 | 3 | 0 | 6 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0007 | 0/0 | 3180 | 10 | 7 | 3 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0008 | 0/0 | 3180 | 5 | 4 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0009 | 0/0 | 3181 | 5 | 5 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0010 | 0/0 | 3184 | 4 | 0 | 2 | 1 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0011 | 0/0 | 3183 | 4 | 4 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0012 | 0/0 | 3183 | 3 | 0 | 2 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0013 | 0/1 | 3182 | 3 | 0 | 1 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0014 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0015 | 0/0 | 3184 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0016 | 0/0 | 3184 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0017 | 0/0 | 3181 | 2 | 0 | 1 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0018 | 0/0 | 3181 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0019 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0020 | 0/0 | 3182 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0021 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0022 | 0/0 | 3184 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0023 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0024 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0025 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0026 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0027 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0028 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0029 | 0/0 | 3181 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0030 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0031 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0032 | 0/0 | 3182 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0033 | 0/0 | 3182 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0034 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0035 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0036 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0037 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| t0038 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 786 | 163 | 60 | 40 | 31 | 7 | 23 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0004 | 0/0 | 786 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0008 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002 | 0/0 | 783 | 88 | 17 | 24 | 35 | 0 | 12 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0006 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0003c0003 | 0/0 | 786 | 4 | 3 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0004c0005 | 0/0 | 786 | 2 | 0 | 1 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0005c0007 | 0/0 | 786 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3968 | 7 | 0 | 0 | 6 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0002 | 0/0 | 3967 | 65 | 8 | 24 | 15 | 6 | 12 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0003 | 1/0 | 3966 | 18 | 6 | 5 | 5 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0004 | 0/0 | 3968 | 10 | 9 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0005 | 0/0 | 3967 | 14 | 13 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0006 | 0/0 | 3966 | 12 | 2 | 2 | 3 | 0 | 5 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0007 | 0/0 | 3965 | 4 | 3 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0008 | 0/0 | 3965 | 5 | 4 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0009 | 0/0 | 3966 | 4 | 4 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0011 | 0/0 | 3968 | 4 | 4 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0012 | 0/0 | 3968 | 3 | 0 | 2 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0013 | 0/1 | 3967 | 3 | 0 | 1 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0015 | 0/0 | 3969 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0018 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0019 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0020 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0023 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0027 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0028 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0029 | 0/0 | 3966 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0030 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0032 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0033 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0034 | 0/0 | 3965 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0001t0038 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0004t0004 | 0/0 | 3968 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0001c0008t0005 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0001 | 0/0 | 3965 | 61 | 7 | 18 | 27 | 0 | 9 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0003 | 0/0 | 3963 | 3 | 0 | 1 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0004 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0006 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0007 | 0/0 | 3962 | 6 | 4 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0009 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0010 | 0/0 | 3966 | 4 | 0 | 2 | 1 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0014 | 0/0 | 3965 | 2 | 0 | 0 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0016 | 0/0 | 3966 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0021 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0022 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0024 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0025 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0026 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0031 | 0/0 | 3965 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0002t0037 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0002c0006t0004 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0003c0003t0002 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0003c0003t0004 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0003c0003t0035 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0003c0003t0036 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0004c0005t0017 | 0/0 | 3966 | 2 | 0 | 1 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| a0005c0007t0002 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | copy fasta | chr4 | 100390341 | 100523022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0012g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0012g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0013g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0013g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0013g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0018g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0019g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0027g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0028g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0029g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0030g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0032g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0033g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0034g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0038g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0004t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0004t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0008t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0014g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0016g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0021g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0022g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0024g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0025g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0031g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0037g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0006t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0035g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0036g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0004c0005t0017g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0004c0005t0017g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0005c0007t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00673 | hp1 | a0001 | c0001 | t0033 | g0141 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00735 | hp1 | a0004 | c0005 | t0017 | g0020 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00741 | hp1 | a0001 | c0001 | t0027 | g0247 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01070 | hp1 | a0002 | c0002 | t0007 | g0163 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01071 | hp1 | a0002 | c0002 | t0007 | g0164 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0047 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01106 | hp1 | a0001 | c0001 | t0012 | g0026 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01167 | hp1 | a0003 | c0003 | t0002 | g0172 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0117 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0143 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01361 | hp1 | a0001 | c0001 | t0013 | g0246 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01496 | hp2 | a0002 | c0002 | t0010 | g0148 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01515 | hp2 | a0004 | c0005 | t0017 | g0019 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01975 | hp2 | a0001 | c0001 | t0029 | g0159 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01981 | hp1 | a0002 | c0002 | t0010 | g0145 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02027 | hp1 | a0001 | c0001 | t0023 | g0005 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02071 | hp1 | a0002 | c0002 | t0010 | g0089 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02145 | hp1 | a0001 | c0001 | t0019 | g0155 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0116 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0180 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02257 | hp2 | a0002 | c0006 | t0004 | g0048 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0121 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02615 | hp2 | a0003 | c0003 | t0036 | g0160 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02630 | hp2 | a0001 | c0004 | t0004 | g0249 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02717 | hp2 | a0002 | c0002 | t0007 | g0168 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0133 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02809 | hp2 | a0001 | c0004 | t0004 | g0248 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02818 | hp1 | a0003 | c0003 | t0004 | g0158 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02896 | hp1 | a0003 | c0003 | t0035 | g0198 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02896 | hp2 | a0001 | c0001 | t0028 | g0175 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0124 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02922 | hp2 | a0002 | c0002 | t0016 | g0111 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02970 | hp1 | a0002 | c0002 | t0016 | g0110 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02970 | hp2 | a0002 | c0002 | t0007 | g0165 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02976 | hp1 | a0002 | c0002 | t0007 | g0167 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0151 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0112 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03139 | hp1 | a0002 | c0002 | t0037 | g0123 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03139 | hp2 | a0001 | c0001 | t0030 | g0190 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03209 | hp2 | a0002 | c0002 | t0009 | g0171 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03486 | hp2 | a0002 | c0002 | t0026 | g0049 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03491 | hp1 | a0005 | c0007 | t0002 | g0209 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0120 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03669 | hp1 | a0001 | c0001 | t0032 | g0254 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03669 | hp2 | a0001 | c0001 | t0018 | g0219 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0055 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0147 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0152 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03831 | hp2 | a0002 | c0002 | t0010 | g0090 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03942 | hp1 | a0001 | c0001 | t0034 | g0140 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04115 | hp2 | a0002 | c0002 | t0022 | g0234 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0134 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04204 | hp1 | a0002 | c0002 | t0006 | g0053 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04204 | hp2 | a0001 | c0001 | t0013 | g0008 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0242 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | CHB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18906 | hp1 | a0001 | c0008 | t0005 | g0197 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18946 | hp1 | a0002 | c0002 | t0025 | g0057 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18973 | hp2 | a0002 | c0002 | t0024 | g0097 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18980 | hp1 | a0002 | c0002 | t0014 | g0094 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0162 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19060 | hp1 | a0002 | c0002 | t0014 | g0137 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19084 | hp2 | a0002 | c0002 | t0021 | g0061 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20129 | hp1 | a0002 | c0002 | t0007 | g0166 | AFR | ASW | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ASW | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0238 | EUR | TSI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | GIH | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | GIH | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01123 | hp1 | a0002 | c0002 | t0031 | g0138 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02486 | hp1 | a0001 | c0001 | t0038 | g0211 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0114 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0119 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0118 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0009 | REF | REF | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0213 | REF | REF | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100410282
|
G | A | 1 | a0002 | 1 | HG03139.hp1 | splice_region_variant | LOW | c.*39C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/12 | chr4 | 100410282 | ||||||
| chr4:100465486
|
C | T | 1 | a0003 | 4 | HG01167.hp1 HG02615.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.313G>A | p.Val105Ile | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/12 | 421/3966 | 313/786 | 105/261 | chr4 | 100465486 | ||
| chr4:100465500
|
G | A | 1 | a0004 | 2 | HG00735.hp1 HG01515.hp2 |
missense_variant | MODERATE | c.299C>T | p.Ser100Phe | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/12 | 407/3966 | 299/786 | 100/261 | chr4 | 100465500 | ||
| chr4:100479949
|
A | G | 1 | a0005 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.155T>C | p.Val52Ala | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/12 | 263/3966 | 155/786 | 52/261 | chr4 | 100479949 | ||
| chr4:100480004
|
TAAC | T | 1 | a0002 | 89 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(86): Show |
conservative_inframe_deletion | MODERATE | c.97_99delGTT | p.Val33del | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/12 | 207/3966 | 97/786 | 33/261 | chr4 | 100480004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100415923
|
G | A | 1 | a0001c0008 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.726C>T | p.Thr242Thr | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/12 | 834/3966 | 726/786 | 242/261 | chr4 | 100415923 | ||
| chr4:100465487
|
G | A | 2 | a0001c0004a0002c0006 | 3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.312C>T | p.Asn104Asn | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/12 | 420/3966 | 312/786 | 104/261 | chr4 | 100465487 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100395441
|
A | G | 2 | a0001c0001t0013a0001c0001t0027 | 4 | HG00741.hp1 HG01361.hp1 HG04204.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2972T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14880 | chr4 | 100395441 | |||||
| chr4:100395693
|
G | A | 3 | a0001c0001t0007a0001c0001t0008a0002c0002t0007 | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2720C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14628 | chr4 | 100395693 | |||||
| chr4:100395723
|
G | T | 1 | a0002c0002t0024 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2690C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14598 | chr4 | 100395723 | |||||
| chr4:100395742
|
C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2671G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14579 | chr4 | 100395742 | |||||
| chr4:100396017
|
A | T | 10 | a0001c0001t0004a0001c0001t0011a0001c0001t0015others(7): Show | 25 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2396T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14304 | chr4 | 100396017 | |||||
| chr4:100396027
|
C | G | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2386G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14294 | chr4 | 100396027 | |||||
| chr4:100396052
|
T | A | 1 | a0002c0002t0025 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14269 | chr4 | 100396052 | |||||
| chr4:100396332
|
T | G | 16 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(13): Show | 44 | HG01070.hp2 HG01109.hp2 HG01884.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2081A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13989 | chr4 | 100396332 | |||||
| chr4:100396363
|
C | A | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(40): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2050G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13958 | chr4 | 100396363 | |||||
| chr4:100396486
|
A | G | 1 | a0001c0001t0018 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13835 | chr4 | 100396486 | |||||
| chr4:100396538
|
T | C | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1875A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13783 | chr4 | 100396538 | |||||
| chr4:100396539
|
C | CT | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1873_*1874insA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13781 | chr4 | 100396539 | |||||
| chr4:100396540
|
C | CT | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(17): Show | 166 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*1872dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13780 | chr4 | 100396540 | |||||
| chr4:100396540
|
C | CTT | 11 | a0001c0001t0004a0001c0001t0012a0001c0001t0015others(8): Show | 28 | HG00741.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1871_*1872dupAA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13780 | chr4 | 100396540 | |||||
| chr4:100396540
|
C | T | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1873G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13781 | chr4 | 100396540 | |||||
| chr4:100396540
|
CT | C | 5 | a0001c0001t0007a0001c0001t0008a0001c0001t0034others(2): Show | 17 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1872delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13780 | chr4 | 100396540 | |||||
| chr4:100396604
|
G | A | 1 | a0002c0002t0026 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1809C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13717 | chr4 | 100396604 | |||||
| chr4:100396637
|
G | A | 1 | a0002c0002t0037 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1776C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13684 | chr4 | 100396637 | |||||
| chr4:100396653
|
G | T | 5 | a0001c0001t0006a0001c0001t0033a0001c0001t0034others(2): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1760C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13668 | chr4 | 100396653 | |||||
| chr4:100396692
|
G | A | 3 | a0001c0001t0007a0001c0001t0008a0002c0002t0007 | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1721C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13629 | chr4 | 100396692 | |||||
| chr4:100396771
|
A | AT | 11 | a0001c0001t0004a0001c0001t0011a0001c0001t0015others(8): Show | 26 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1641dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13549 | chr4 | 100396771 | |||||
| chr4:100396806
|
T | G | 10 | a0001c0001t0004a0001c0001t0011a0001c0001t0015others(7): Show | 25 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1607A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13515 | chr4 | 100396806 | |||||
| chr4:100396807
|
G | T | 1 | a0002c0002t0021 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1606C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13514 | chr4 | 100396807 | |||||
| chr4:100396891
|
A | G | 11 | a0001c0001t0001a0001c0001t0023a0002c0002t0001others(8): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1522T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13430 | chr4 | 100396891 | |||||
| chr4:100396942
|
C | CT | 11 | a0001c0001t0001a0001c0001t0023a0002c0002t0001others(8): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1470dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13378 | chr4 | 100396942 | |||||
| chr4:100396942
|
CT | C | 8 | a0001c0001t0004a0001c0001t0019a0001c0001t0020others(5): Show | 18 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1470delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13378 | chr4 | 100396942 | |||||
| chr4:100397015
|
T | G | 6 | a0001c0001t0005a0001c0001t0028a0001c0001t0029others(3): Show | 19 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1398A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13306 | chr4 | 100397015 | |||||
| chr4:100397108
|
C | T | 11 | a0001c0001t0001a0001c0001t0023a0002c0002t0001others(8): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1305G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13213 | chr4 | 100397108 | |||||
| chr4:100397205
|
T | C | 1 | a0003c0003t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13116 | chr4 | 100397205 | |||||
| chr4:100397480
|
G | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 237 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*933C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12841 | chr4 | 100397480 | |||||
| chr4:100397695
|
G | C | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 237 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12626 | chr4 | 100397695 | |||||
| chr4:100397768
|
T | C | 1 | a0002c0002t0031 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12553 | chr4 | 100397768 | |||||
| chr4:100397946
|
C | G | 8 | a0001c0001t0004a0001c0001t0019a0001c0001t0020others(5): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*467G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12375 | chr4 | 100397946 | |||||
| chr4:100398008
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(35): Show | 216 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12313 | chr4 | 100398008 | |||||
| chr4:100398009
|
G | A | 1 | a0002c0002t0016 | 2 | HG02922.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*404C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12312 | chr4 | 100398009 | |||||
| chr4:100398044
|
T | C | 1 | a0002c0002t0016 | 2 | HG02922.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*369A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12277 | chr4 | 100398044 | |||||
| chr4:100398051
|
G | A | 1 | a0001c0001t0032 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12270 | chr4 | 100398051 | |||||
| chr4:100398130
|
T | A | 1 | a0004c0005t0017 | 2 | HG00735.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12191 | chr4 | 100398130 | |||||
| chr4:100398137
|
C | T | 1 | a0001c0001t0008 | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*276G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12184 | chr4 | 100398137 | |||||
| chr4:100398170
|
A | G | 3 | a0001c0001t0007a0001c0001t0008a0002c0002t0007 | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*243T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12151 | chr4 | 100398170 | |||||
| chr4:100398175
|
G | A | 5 | a0001c0001t0006a0001c0001t0033a0001c0001t0034others(2): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12146 | chr4 | 100398175 | |||||
| chr4:100398242
|
T | C | 1 | a0003c0003t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12079 | chr4 | 100398242 | |||||
| chr4:100398298
|
A | G | 1 | a0002c0002t0014 | 2 | NA18980.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12023 | chr4 | 100398298 | |||||
| chr4:100398345
|
G | A | 1 | a0003c0003t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 11976 | chr4 | 100398345 | |||||
| chr4:100410300
|
T | C | 1 | a0001c0001t0038 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/12 | 21 | chr4 | 100410300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100398380
|
G | GCAA | 65 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0127others(62): Show | 66 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(63): Show |
splice_region_variant&intron_variant | LOW | c.*40-10_*40-8dupTTG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398380 | ||||||
| chr4:100398380
|
G | GCAACAA | 3 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0227 | 3 | HG00597.hp1 HG02027.hp2 HG02132.hp1 |
splice_region_variant&intron_variant | LOW | c.*40-13_*40-8dupTTG others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398380 | ||||||
| chr4:100398516
|
A | G | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-143T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398516 | ||||||
| chr4:100398629
|
T | C | 11 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.*40-256A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398629 | ||||||
| chr4:100398692
|
C | T | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.*40-319G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398692 | ||||||
| chr4:100398714
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.*40-341T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398714 | ||||||
| chr4:100398792
|
A | G | 19 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(16): Show | 20 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.*40-419T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398792 | ||||||
| chr4:100399124
|
C | G | 5 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.*40-751G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399124 | ||||||
| chr4:100399127
|
C | T | 1 | a0002c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.*40-754G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399127 | ||||||
| chr4:100399195
|
C | T | 1 | a0001c0001t0032g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*40-822G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399195 | ||||||
| chr4:100399255
|
T | C | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.*40-882A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399255 | ||||||
| chr4:100399381
|
G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-1008C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399381 | ||||||
| chr4:100399421
|
G | C | 1 | a0001c0001t0003g0212 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*40-1048C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399421 | ||||||
| chr4:100399585
|
G | A | 2 | a0002c0002t0001g0054a0002c0002t0001g0064 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.*40-1212C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399585 | ||||||
| chr4:100399649
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-1276T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399649 | ||||||
| chr4:100399680
|
C | T | 211 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(208): Show | 215 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.*40-1307G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399680 | ||||||
| chr4:100399836
|
G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-1463C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399836 | ||||||
| chr4:100399855
|
G | A | 7 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.*40-1482C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399855 | ||||||
| chr4:100399885
|
T | C | 21 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(18): Show | 21 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.*40-1512A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399885 | ||||||
| chr4:100399941
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*40-1568A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399941 | ||||||
| chr4:100400043
|
T | C | 212 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(209): Show | 216 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(213): Show |
intron_variant | MODIFIER | c.*40-1670A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400043 | ||||||
| chr4:100400066
|
G | A | 15 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*40-1693C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400066 | ||||||
| chr4:100400224
|
C | T | 1 | a0002c0002t0016g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*40-1851G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400224 | ||||||
| chr4:100400238
|
A | C | 1 | a0001c0001t0004g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*40-1865T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400238 | ||||||
| chr4:100400285
|
AT | A | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.*40-1913delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400285 | ||||||
| chr4:100400353
|
A | AT | 54 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(51): Show | 55 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.*40-1981dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400353 | ||||||
| chr4:100400353
|
AT | A | 98 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.*40-1981delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400353 | ||||||
| chr4:100400360
|
T | G | 59 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(56): Show | 60 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.*40-1987A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400360 | ||||||
| chr4:100400442
|
T | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-2069A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400442 | ||||||
| chr4:100400498
|
T | C | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-2125A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400498 | ||||||
| chr4:100400607
|
C | T | 212 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(209): Show | 216 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(213): Show |
intron_variant | MODIFIER | c.*40-2234G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400607 | ||||||
| chr4:100400745
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0185a0002c0002t0001g0075 | 3 | HG00408.hp2 NA19012.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.*40-2372T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400745 | ||||||
| chr4:100400944
|
T | C | 102 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(99): Show | 103 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.*40-2571A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400944 | ||||||
| chr4:100401139
|
G | T | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-2766C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401139 | ||||||
| chr4:100401146
|
G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-2773C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401146 | ||||||
| chr4:100401521
|
G | C | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.*40-3148C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401521 | ||||||
| chr4:100401528
|
T | C | 3 | a0002c0002t0016g0110a0002c0002t0016g0111a0003c0003t0035g0198 | 3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*40-3155A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401528 | ||||||
| chr4:100401663
|
A | T | 212 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(209): Show | 216 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(213): Show |
intron_variant | MODIFIER | c.*40-3290T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401663 | ||||||
| chr4:100401720
|
C | A | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-3347G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401720 | ||||||
| chr4:100401775
|
T | C | 3 | a0002c0002t0001g0042a0002c0002t0001g0070a0002c0002t0001g0108 | 3 | HG01261.hp2 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.*40-3402A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401775 | ||||||
| chr4:100401846
|
G | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*40-3473C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401846 | ||||||
| chr4:100401974
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*40-3601G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401974 | ||||||
| chr4:100402055
|
C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-3682G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402055 | ||||||
| chr4:100402099
|
A | T | 1 | a0002c0002t0025g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.*40-3726T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402099 | ||||||
| chr4:100402116
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-3743C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402116 | ||||||
| chr4:100402185
|
A | C | 1 | a0002c0002t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*40-3812T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402185 | ||||||
| chr4:100402214
|
C | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-3841G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402214 | ||||||
| chr4:100402223
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.*40-3850G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402223 | ||||||
| chr4:100402252
|
T | G | 139 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(136): Show | 141 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.*40-3879A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402252 | ||||||
| chr4:100402655
|
A | C | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.*40-4282T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402655 | ||||||
| chr4:100402767
|
G | C | 1 | a0002c0002t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*40-4394C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402767 | ||||||
| chr4:100402771
|
C | T | 23 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(20): Show | 23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.*40-4398G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402771 | ||||||
| chr4:100402772
|
G | A | 15 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*40-4399C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402772 | ||||||
| chr4:100402972
|
A | G | 15 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*40-4599T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402972 | ||||||
| chr4:100402972
|
A | T | 44 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0127others(41): Show | 45 | HG00597.hp1 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.*40-4599T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402972 | ||||||
| chr4:100403012
|
C | G | 3 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0019g0155 | 3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*40-4639G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403012 | ||||||
| chr4:100403157
|
G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-4784C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403157 | ||||||
| chr4:100403243
|
C | T | 3 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0026g0049 | 3 | HG02451.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*40-4870G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403243 | ||||||
| chr4:100403256
|
T | C | 104 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(101): Show | 105 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.*40-4883A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403256 | ||||||
| chr4:100403257
|
A | G | 5 | a0002c0002t0001g0046a0002c0002t0001g0062a0002c0002t0001g0063others(2): Show | 5 | HG01346.hp1 HG01934.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.*40-4884T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403257 | ||||||
| chr4:100403282
|
C | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-4909G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403282 | ||||||
| chr4:100403414
|
C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-5041G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403414 | ||||||
| chr4:100403447
|
A | ATGGGCAT others(9): Show |
22 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(19): Show | 22 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.*40-5090_*40-5075d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403447 | ||||||
| chr4:100403447
|
A | ATGGGCAT others(25): Show |
1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-5106_*40-5075d others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403447 | ||||||
| chr4:100403447
|
ATGGGCAT others(9): Show |
A | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-5090_*40-5075d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403447 | ||||||
| chr4:100403543
|
C | T | 73 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0007others(70): Show | 75 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.*40-5170G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403543 | ||||||
| chr4:100403650
|
G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-5277C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403650 | ||||||
| chr4:100403721
|
C | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*40-5348G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403721 | ||||||
| chr4:100403748
|
T | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.*40-5375A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403748 | ||||||
| chr4:100403779
|
G | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-5406C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403779 | ||||||
| chr4:100404021
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.*40-5648C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404021 | ||||||
| chr4:100404119
|
T | A | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*40-5746A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404119 | ||||||
| chr4:100404242
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-5869C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404242 | ||||||
| chr4:100404355
|
G | C | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*39+5927C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404355 | ||||||
| chr4:100404476
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.*39+5806T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404476 | ||||||
| chr4:100404487
|
G | A | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.*39+5795C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404487 | ||||||
| chr4:100404500
|
T | C | 4 | a0001c0001t0005g0183a0001c0001t0005g0191a0001c0001t0005g0192others(1): Show | 4 | HG02615.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.*39+5782A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404500 | ||||||
| chr4:100404606
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*39+5676A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404606 | ||||||
| chr4:100404663
|
C | A | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*39+5619G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404663 | ||||||
| chr4:100405145
|
A | T | 124 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(121): Show | 126 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.*39+5137T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405145 | ||||||
| chr4:100405163
|
C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+5119G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405163 | ||||||
| chr4:100405173
|
A | G | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.*39+5109T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405173 | ||||||
| chr4:100405234
|
T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+5048A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405234 | ||||||
| chr4:100405371
|
T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+4911A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405371 | ||||||
| chr4:100405758
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*39+4524C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405758 | ||||||
| chr4:100405874
|
G | GT | 7 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.*39+4407dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405874 | ||||||
| chr4:100405913
|
G | A | 1 | a0001c0001t0002g0179 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.*39+4369C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405913 | ||||||
| chr4:100405949
|
T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*39+4333A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405949 | ||||||
| chr4:100406146
|
C | A | 1 | a0002c0002t0007g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*39+4136G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406146 | ||||||
| chr4:100406508
|
A | G | 6 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0091others(3): Show | 6 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.*39+3774T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406508 | ||||||
| chr4:100406521
|
A | T | 15 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*39+3761T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406521 | ||||||
| chr4:100406545
|
T | A | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.*39+3737A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406545 | ||||||
| chr4:100406591
|
G | A | 19 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(16): Show | 19 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.*39+3691C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406591 | ||||||
| chr4:100406591
|
G | T | 81 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(78): Show | 82 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.*39+3691C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406591 | ||||||
| chr4:100407287
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+2995C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407287 | ||||||
| chr4:100407314
|
A | G | 83 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(80): Show | 84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*39+2968T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407314 | ||||||
| chr4:100407478
|
A | G | 239 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(236): Show | 243 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(240): Show |
intron_variant | MODIFIER | c.*39+2804T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407478 | ||||||
| chr4:100407491
|
C | T | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*39+2791G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407491 | ||||||
| chr4:100407502
|
A | G | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+2780T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407502 | ||||||
| chr4:100407568
|
A | G | 6 | a0002c0002t0007g0163a0002c0002t0007g0164a0002c0002t0007g0165others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*39+2714T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407568 | ||||||
| chr4:100407606
|
T | G | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.*39+2676A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407606 | ||||||
| chr4:100407631
|
T | C | 3 | a0002c0002t0016g0110a0002c0002t0016g0111a0003c0003t0035g0198 | 3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+2651A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407631 | ||||||
| chr4:100407772
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*39+2510G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407772 | ||||||
| chr4:100407909
|
A | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+2373T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407909 | ||||||
| chr4:100408001
|
C | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*39+2281G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408001 | ||||||
| chr4:100408017
|
G | A | 5 | a0001c0001t0009g0121a0001c0001t0009g0153a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.*39+2265C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408017 | ||||||
| chr4:100408096
|
T | C | 3 | a0002c0002t0016g0110a0002c0002t0016g0111a0003c0003t0035g0198 | 3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+2186A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408096 | ||||||
| chr4:100408147
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.*39+2135G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408147 | ||||||
| chr4:100408151
|
G | A | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+2131C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408151 | ||||||
| chr4:100408175
|
T | C | 83 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(80): Show | 84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*39+2107A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408175 | ||||||
| chr4:100408284
|
A | C | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+1998T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408284 | ||||||
| chr4:100408392
|
G | A | 1 | a0001c0004t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*39+1890C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408392 | ||||||
| chr4:100408617
|
T | C | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.*39+1665A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408617 | ||||||
| chr4:100408633
|
A | G | 3 | a0002c0002t0016g0110a0002c0002t0016g0111a0003c0003t0035g0198 | 3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+1649T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408633 | ||||||
| chr4:100408655
|
T | C | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.*39+1627A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408655 | ||||||
| chr4:100408729
|
T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*39+1553A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408729 | ||||||
| chr4:100408782
|
C | T | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+1500G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408782 | ||||||
| chr4:100408788
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*39+1494G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408788 | ||||||
| chr4:100408832
|
C | T | 29 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(26): Show | 30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.*39+1450G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408832 | ||||||
| chr4:100408844
|
A | G | 83 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(80): Show | 84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*39+1438T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408844 | ||||||
| chr4:100408853
|
T | A | 73 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0007others(70): Show | 75 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.*39+1429A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408853 | ||||||
| chr4:100408865
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*39+1417T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408865 | ||||||
| chr4:100408896
|
C | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*39+1386G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408896 | ||||||
| chr4:100408904
|
T | C | 2 | a0002c0002t0001g0065a0002c0002t0001g0081 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*39+1378A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408904 | ||||||
| chr4:100409159
|
C | T | 5 | a0001c0001t0009g0121a0001c0001t0009g0153a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.*39+1123G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409159 | ||||||
| chr4:100409215
|
A | ATTTAT | 81 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(78): Show | 82 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.*39+1062_*39+1066d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409215 | ||||||
| chr4:100409215
|
A | ATTTATTT others(3): Show |
1 | a0002c0002t0026g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*39+1066_*39+1067i others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409215 | ||||||
| chr4:100409215
|
A | ATTTATTT others(3): Show |
1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+1057_*39+1066d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409215 | ||||||
| chr4:100409242
|
T | G | 3 | a0002c0002t0016g0110a0002c0002t0016g0111a0003c0003t0035g0198 | 3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+1040A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409242 | ||||||
| chr4:100409303
|
C | T | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.*39+979G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409303 | ||||||
| chr4:100409320
|
T | G | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+962A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409320 | ||||||
| chr4:100409345
|
A | G | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+937T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409345 | ||||||
| chr4:100409380
|
A | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*39+902T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409380 | ||||||
| chr4:100409395
|
C | G | 15 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*39+887G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409395 | ||||||
| chr4:100409429
|
C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*39+853G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409429 | ||||||
| chr4:100409430
|
G | A | 29 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(26): Show | 30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.*39+852C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409430 | ||||||
| chr4:100409588
|
G | A | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.*39+694C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409588 | ||||||
| chr4:100409599
|
T | C | 124 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(121): Show | 126 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.*39+683A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409599 | ||||||
| chr4:100409820
|
T | C | 4 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(1): Show | 4 | HG01975.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.*39+462A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409820 | ||||||
| chr4:100409826
|
A | G | 1 | a0001c0001t0003g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*39+456T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409826 | ||||||
| chr4:100409914
|
G | A | 1 | a0005c0007t0002g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.*39+368C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409914 | ||||||
| chr4:100410102
|
C | A | 3 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126 | 3 | HG01975.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*39+180G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410102 | ||||||
| chr4:100410131
|
T | C | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.*39+151A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410131 | ||||||
| chr4:100410186
|
C | T | 106 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(103): Show | 107 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.*39+96G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410186 | ||||||
| chr4:100410218
|
G | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+64C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410218 | ||||||
| chr4:100410489
|
G | A | 1 | a0001c0001t0005g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.752-134C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410489 | ||||||
| chr4:100410606
|
T | C | 25 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(22): Show | 25 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.752-251A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410606 | ||||||
| chr4:100410613
|
G | A | 2 | a0001c0001t0009g0121a0001c0001t0009g0153 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.752-258C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410613 | ||||||
| chr4:100410697
|
C | T | 1 | a0002c0002t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.752-342G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410697 | ||||||
| chr4:100410711
|
T | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-356A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410711 | ||||||
| chr4:100410716
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.752-361A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410716 | ||||||
| chr4:100410719
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-364C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410719 | ||||||
| chr4:100410757
|
C | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.752-402G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410757 | ||||||
| chr4:100411154
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.752-799G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411154 | ||||||
| chr4:100411160
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-805G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411160 | ||||||
| chr4:100411230
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-875C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411230 | ||||||
| chr4:100411259
|
A | C | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.752-904T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411259 | ||||||
| chr4:100411314
|
C | T | 1 | a0002c0002t0016g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.752-959G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411314 | ||||||
| chr4:100411333
|
C | T | 2 | a0001c0001t0020g0023a0003c0003t0004g0158 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.752-978G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411333 | ||||||
| chr4:100411350
|
C | T | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.752-995G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411350 | ||||||
| chr4:100411395
|
G | T | 104 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(101): Show | 105 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.752-1040C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411395 | ||||||
| chr4:100411429
|
G | A | 3 | a0002c0002t0007g0166a0002c0002t0007g0167a0002c0002t0007g0168 | 3 | HG02717.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.752-1074C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411429 | ||||||
| chr4:100411456
|
G | T | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.752-1101C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411456 | ||||||
| chr4:100411601
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1246T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411601 | ||||||
| chr4:100411643
|
T | C | 73 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0007others(70): Show | 75 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.752-1288A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411643 | ||||||
| chr4:100411678
|
C | A | 1 | a0002c0002t0006g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.752-1323G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411678 | ||||||
| chr4:100411754
|
T | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-1399A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411754 | ||||||
| chr4:100411775
|
T | C | 23 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(20): Show | 23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.752-1420A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411775 | ||||||
| chr4:100411800
|
A | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-1445T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411800 | ||||||
| chr4:100411876
|
C | T | 2 | a0001c0001t0006g0142a0001c0001t0006g0143 | 2 | HG00639.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.752-1521G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411876 | ||||||
| chr4:100411883
|
C | T | 7 | a0001c0001t0029g0159a0002c0002t0007g0163a0002c0002t0007g0164others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.752-1528G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411883 | ||||||
| chr4:100411937
|
T | C | 1 | a0001c0001t0006g0157 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.752-1582A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411937 | ||||||
| chr4:100411952
|
T | TC | 3 | a0002c0002t0016g0110a0002c0002t0016g0111a0003c0003t0035g0198 | 3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-1598_752-1597i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411952 | ||||||
| chr4:100411970
|
A | G | 1 | a0001c0001t0006g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.752-1615T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411970 | ||||||
| chr4:100412011
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1656T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412011 | ||||||
| chr4:100412044
|
ATTAG | A | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1693_752-1690d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412044 | ||||||
| chr4:100412051
|
AGTTT | A | 3 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0227 | 3 | HG00597.hp1 HG02027.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.752-1700_752-1697d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412051 | ||||||
| chr4:100412172
|
A | G | 6 | a0002c0002t0007g0163a0002c0002t0007g0164a0002c0002t0007g0165others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.752-1817T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412172 | ||||||
| chr4:100412201
|
G | A | 29 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(26): Show | 30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.752-1846C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412201 | ||||||
| chr4:100412274
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-1919C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412274 | ||||||
| chr4:100412309
|
C | T | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.752-1954G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412309 | ||||||
| chr4:100412625
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.752-2270G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412625 | ||||||
| chr4:100412798
|
A | G | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.752-2443T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412798 | ||||||
| chr4:100412836
|
A | C | 108 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(105): Show | 109 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.752-2481T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412836 | ||||||
| chr4:100412845
|
T | C | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.752-2490A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412845 | ||||||
| chr4:100412849
|
T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.752-2494A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412849 | ||||||
| chr4:100412904
|
T | TG | 139 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(136): Show | 141 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.752-2550dupC | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412904 | ||||||
| chr4:100412965
|
G | A | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.752-2610C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412965 | ||||||
| chr4:100412995
|
C | A | 233 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(230): Show | 237 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(234): Show |
intron_variant | MODIFIER | c.752-2640G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412995 | ||||||
| chr4:100413113
|
A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.752-2758T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413113 | ||||||
| chr4:100413296
|
A | T | 1 | a0002c0002t0001g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.751+2602T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413296 | ||||||
| chr4:100413298
|
A | G | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.751+2600T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413298 | ||||||
| chr4:100413565
|
T | G | 1 | a0002c0002t0001g0237 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.751+2333A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413565 | ||||||
| chr4:100413612
|
G | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.751+2286C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413612 | ||||||
| chr4:100413704
|
A | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.751+2194T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413704 | ||||||
| chr4:100413707
|
G | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.751+2191C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413707 | ||||||
| chr4:100413801
|
A | G | 44 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0127others(41): Show | 45 | HG00597.hp1 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.751+2097T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413801 | ||||||
| chr4:100413843
|
A | C | 5 | a0002c0002t0001g0093a0002c0002t0001g0095a0002c0002t0001g0096others(2): Show | 5 | HG00597.hp2 HG01361.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+2055T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413843 | ||||||
| chr4:100413919
|
C | T | 2 | a0001c0001t0002g0189a0001c0001t0002g0216 | 2 | HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.751+1979G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413919 | ||||||
| chr4:100414086
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.751+1812C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414086 | ||||||
| chr4:100414228
|
G | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.751+1670C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414228 | ||||||
| chr4:100414348
|
C | CT | 53 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0011others(50): Show | 55 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.751+1549dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414348
|
C | CTT | 16 | a0001c0001t0002g0184a0001c0001t0002g0232a0001c0001t0004g0018others(13): Show | 16 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.751+1548_751+1549d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414348
|
CT | C | 16 | a0001c0001t0002g0012a0001c0001t0002g0040a0001c0001t0003g0235others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.751+1549delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414348
|
CTTTTTTT others(2): Show |
C | 77 | a0001c0001t0001g0043a0001c0001t0001g0101a0001c0001t0001g0182others(74): Show | 78 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.751+1541_751+1549d others(11): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414348
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.751+1540_751+1549d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414348
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.751+1538_751+1549d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414348
|
CTTTTTTT others(7): Show |
C | 6 | a0002c0002t0007g0163a0002c0002t0007g0164a0002c0002t0007g0165others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+1536_751+1549d others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | ||||||
| chr4:100414381
|
C | T | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.751+1517G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414381 | ||||||
| chr4:100414563
|
G | A | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.751+1335C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414563 | ||||||
| chr4:100414653
|
C | T | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.751+1245G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414653 | ||||||
| chr4:100414720
|
A | T | 74 | a0001c0001t0001g0043a0001c0001t0001g0101a0001c0001t0001g0182others(71): Show | 75 | HG00408.hp1 HG00597.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.751+1178T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414720 | ||||||
| chr4:100414931
|
C | A | 1 | a0002c0002t0007g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.751+967G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414931 | ||||||
| chr4:100414931
|
C | T | 20 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(17): Show | 21 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.751+967G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414931 | ||||||
| chr4:100414952
|
G | C | 73 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0007others(70): Show | 75 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.751+946C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414952 | ||||||
| chr4:100414960
|
G | A | 23 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(20): Show | 23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+938C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414960 | ||||||
| chr4:100414988
|
C | G | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.751+910G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414988 | ||||||
| chr4:100414988
|
C | T | 23 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(20): Show | 23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+910G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414988 | ||||||
| chr4:100414999
|
A | G | 1 | a0001c0001t0023g0005 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.751+899T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414999 | ||||||
| chr4:100415210
|
A | C | 3 | a0001c0001t0003g0218a0001c0001t0003g0220a0002c0002t0003g0047 | 3 | HG01074.hp2 HG01934.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.751+688T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415210 | ||||||
| chr4:100415228
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.751+670A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415228 | ||||||
| chr4:100415243
|
G | A | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.751+655C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415243 | ||||||
| chr4:100415264
|
T | A | 1 | a0001c0001t0003g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.751+634A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415264 | ||||||
| chr4:100415366
|
T | C | 1 | a0001c0001t0002g0193 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.751+532A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415366 | ||||||
| chr4:100415481
|
T | C | 1 | a0001c0001t0008g0120 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.751+417A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415481 | ||||||
| chr4:100415660
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.751+238T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415660 | ||||||
| chr4:100415681
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.751+217A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415681 | ||||||
| chr4:100415730
|
G | A | 23 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(20): Show | 23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+168C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415730 | ||||||
| chr4:100415792
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.751+106T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415792 | ||||||
| chr4:100415973
|
A | T | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.690-14T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415973 | ||||||
| chr4:100415976
|
A | C | 3 | a0001c0001t0003g0235a0001c0001t0003g0258a0001c0001t0018g0219 | 3 | HG00642.hp1 HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.690-17T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415976 | ||||||
| chr4:100415986
|
A | G | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.690-27T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415986 | ||||||
| chr4:100415993
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(40): Show | 44 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.690-34G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415993 | ||||||
| chr4:100416058
|
C | CAT | 5 | a0001c0004t0004g0248a0001c0004t0004g0249a0002c0002t0016g0110others(2): Show | 5 | HG02257.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-101_690-100dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416058 | ||||||
| chr4:100416091
|
C | CAT | 21 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(18): Show | 21 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.690-133_690-132ins others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416091 | ||||||
| chr4:100416091
|
C | CGT | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-134_690-133dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416091 | ||||||
| chr4:100416113
|
C | CAT | 19 | a0001c0001t0002g0189a0001c0001t0002g0203a0001c0001t0002g0216others(16): Show | 19 | HG00639.hp1 HG00673.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.690-156_690-155dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416113 | ||||||
| chr4:100416130
|
A | C | 2 | a0001c0001t0002g0224a0001c0001t0002g0228 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.690-171T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416130 | ||||||
| chr4:100416148
|
T | C | 1 | a0001c0001t0003g0103 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.690-189A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416148 | ||||||
| chr4:100416229
|
T | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.690-270A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416229 | ||||||
| chr4:100416280
|
G | T | 6 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0019g0155others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-321C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416280 | ||||||
| chr4:100416373
|
G | T | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.690-414C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416373 | ||||||
| chr4:100416492
|
T | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690-533A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416492 | ||||||
| chr4:100416554
|
G | A | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.689+563C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416554 | ||||||
| chr4:100416777
|
A | G | 5 | a0001c0001t0009g0121a0001c0001t0009g0153a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+340T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416777 | ||||||
| chr4:100416870
|
A | C | 80 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(77): Show | 81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.689+247T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416870 | ||||||
| chr4:100416903
|
A | T | 1 | a0001c0001t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.689+214T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416903 | ||||||
| chr4:100416949
|
A | G | 3 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+168T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416949 | ||||||
| chr4:100417035
|
CA | C | 35 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(32): Show | 35 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.689+81delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100417035 | ||||||
| chr4:100417060
|
T | C | 73 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0007others(70): Show | 75 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.689+57A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100417060 | ||||||
| chr4:100417378
|
G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.665-237C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417378 | ||||||
| chr4:100417476
|
T | C | 2 | a0001c0001t0011g0112a0001c0001t0011g0114 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.665-335A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417476 | ||||||
| chr4:100417577
|
GTGTTTGT others(12): Show |
G | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-455_665-437del others(19): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417577 | ||||||
| chr4:100417658
|
C | T | 1 | a0002c0002t0010g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.665-517G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417658 | ||||||
| chr4:100417741
|
C | G | 1 | a0002c0002t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.665-600G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417741 | ||||||
| chr4:100417756
|
A | C | 1 | a0001c0001t0002g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.665-615T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417756 | ||||||
| chr4:100417781
|
C | T | 119 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(116): Show | 120 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.665-640G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417781 | ||||||
| chr4:100417842
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665-701T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417842 | ||||||
| chr4:100417944
|
T | G | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.665-803A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417944 | ||||||
| chr4:100417952
|
C | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.665-811G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417952 | ||||||
| chr4:100417977
|
T | C | 2 | a0001c0001t0003g0186a0001c0001t0003g0188 | 2 | HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.665-836A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417977 | ||||||
| chr4:100418078
|
AT | A | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.665-938delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418078 | ||||||
| chr4:100418153
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.665-1012T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418153 | ||||||
| chr4:100418590
|
A | G | 4 | a0002c0002t0001g0046a0002c0002t0001g0071a0002c0002t0001g0074others(1): Show | 4 | HG01255.hp1 HG01346.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-1449T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418590 | ||||||
| chr4:100418825
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.665-1684T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418825 | ||||||
| chr4:100418913
|
G | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-1772C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418913 | ||||||
| chr4:100419012
|
C | T | 208 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(205): Show | 211 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.665-1871G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419012 | ||||||
| chr4:100419016
|
C | T | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.665-1875G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419016 | ||||||
| chr4:100419096
|
G | A | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.665-1955C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419096 | ||||||
| chr4:100419097
|
G | A | 3 | a0001c0001t0002g0189a0001c0001t0002g0203a0001c0001t0002g0216 | 3 | HG00738.hp2 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.665-1956C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419097 | ||||||
| chr4:100419226
|
G | A | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.664+2056C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419226 | ||||||
| chr4:100419360
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.664+1922C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419360 | ||||||
| chr4:100419506
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.664+1776C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419506 | ||||||
| chr4:100419539
|
A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.664+1743T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419539 | ||||||
| chr4:100419571
|
T | G | 15 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.664+1711A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419571 | ||||||
| chr4:100419611
|
T | A | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.664+1671A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419611 | ||||||
| chr4:100419627
|
T | A | 208 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(205): Show | 211 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.664+1655A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419627 | ||||||
| chr4:100419844
|
T | C | 36 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(33): Show | 37 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.664+1438A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419844 | ||||||
| chr4:100419845
|
G | A | 34 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(31): Show | 35 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.664+1437C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419845 | ||||||
| chr4:100419853
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1429G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419853 | ||||||
| chr4:100419952
|
G | A | 36 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(33): Show | 37 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.664+1330C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419952 | ||||||
| chr4:100419956
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.664+1326G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419956 | ||||||
| chr4:100420105
|
C | A | 34 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(31): Show | 35 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.664+1177G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420105 | ||||||
| chr4:100420131
|
A | G | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.664+1151T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420131 | ||||||
| chr4:100420168
|
G | A | 76 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(73): Show | 77 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.664+1114C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420168 | ||||||
| chr4:100420228
|
A | G | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.664+1054T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420228 | ||||||
| chr4:100420280
|
T | G | 1 | a0001c0001t0009g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.664+1002A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420280 | ||||||
| chr4:100420334
|
T | TA | 35 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(32): Show | 36 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.664+947dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420334 | ||||||
| chr4:100420345
|
A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.664+937T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420345 | ||||||
| chr4:100420478
|
C | T | 1 | a0001c0001t0006g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664+804G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420478 | ||||||
| chr4:100420483
|
A | G | 70 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(67): Show | 72 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.664+799T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420483 | ||||||
| chr4:100420521
|
C | A | 204 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(201): Show | 207 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(204): Show |
intron_variant | MODIFIER | c.664+761G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420521 | ||||||
| chr4:100420562
|
T | A | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.664+720A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420562 | ||||||
| chr4:100420613
|
C | T | 5 | a0001c0001t0009g0121a0001c0001t0009g0153a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+669G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420613 | ||||||
| chr4:100420672
|
A | G | 16 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(13): Show | 17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.664+610T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420672 | ||||||
| chr4:100420690
|
A | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.664+592T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420690 | ||||||
| chr4:100420844
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+438C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420844 | ||||||
| chr4:100420928
|
C | T | 29 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(26): Show | 30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.664+354G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420928 | ||||||
| chr4:100421055
|
G | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.664+227C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100421055 | ||||||
| chr4:100421095
|
G | A | 43 | a0001c0001t0002g0122a0001c0001t0005g0173a0001c0001t0005g0174others(40): Show | 43 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.664+187C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100421095 | ||||||
| chr4:100421449
|
C | A | 19 | a0001c0001t0002g0122a0001c0001t0004g0004a0001c0001t0004g0018others(16): Show | 20 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.569-72G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421449 | ||||||
| chr4:100421482
|
T | C | 17 | a0001c0001t0002g0122a0001c0001t0003g0207a0001c0001t0003g0210others(14): Show | 17 | HG00735.hp2 HG01975.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.569-105A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421482 | ||||||
| chr4:100421507
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-130C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421507 | ||||||
| chr4:100421541
|
G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.569-164C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421541 | ||||||
| chr4:100421652
|
G | A | 1 | a0001c0001t0009g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.569-275C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421652 | ||||||
| chr4:100421765
|
G | T | 190 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(187): Show | 193 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.569-388C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421765 | ||||||
| chr4:100421901
|
G | T | 29 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(26): Show | 30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-524C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421901 | ||||||
| chr4:100421929
|
G | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.569-552C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421929 | ||||||
| chr4:100421961
|
G | A | 15 | a0001c0001t0002g0021a0001c0001t0002g0024a0001c0001t0002g0025others(12): Show | 15 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.569-584C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421961 | ||||||
| chr4:100422004
|
G | GCCTT | 4 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(1): Show | 4 | HG01975.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-631_569-628dup others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422004 | ||||||
| chr4:100422004
|
G | T | 18 | a0001c0001t0002g0122a0001c0001t0003g0207a0001c0001t0003g0210others(15): Show | 18 | HG00735.hp2 HG02145.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.569-627C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422004 | ||||||
| chr4:100422060
|
G | C | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.569-683C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422060 | ||||||
| chr4:100422260
|
G | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+761C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422260 | ||||||
| chr4:100422749
|
A | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0091 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.568+272T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422749 | ||||||
| chr4:100422798
|
T | A | 1 | a0001c0001t0005g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568+223A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422798 | ||||||
| chr4:100422801
|
C | CTTTCTTT others(5): Show |
1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.568+219_568+220ins others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422801 | ||||||
| chr4:100422813
|
C | T | 193 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(190): Show | 196 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(193): Show |
intron_variant | MODIFIER | c.568+208G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422813 | ||||||
| chr4:100422817
|
C | CTTTCTTT others(4): Show |
16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.568+203_568+204ins others(11): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422817 | ||||||
| chr4:100422817
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.568+204G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422817 | ||||||
| chr4:100422822
|
CT | C | 145 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(142): Show | 148 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.568+198delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422822 | ||||||
| chr4:100422822
|
CTT | C | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.568+197_568+198del others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422822 | ||||||
| chr4:100422823
|
T | TTTTC | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0133others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.568+197_568+198ins others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422823 | ||||||
| chr4:100422853
|
T | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.568+168A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422853 | ||||||
| chr4:100423128
|
T | A | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.509-48A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 6/11 | chr4 | 100423128 | ||||||
| chr4:100423193
|
G | A | 6 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0091others(3): Show | 6 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-113C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 6/11 | chr4 | 100423193 | ||||||
| chr4:100423573
|
C | A | 9 | a0001c0001t0003g0207a0001c0001t0003g0210a0001c0001t0003g0255others(6): Show | 9 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-169G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423573 | ||||||
| chr4:100423653
|
G | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-249C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423653 | ||||||
| chr4:100423724
|
C | T | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.416-320G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423724 | ||||||
| chr4:100423730
|
C | T | 29 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(26): Show | 30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.416-326G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423730 | ||||||
| chr4:100423971
|
C | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-567G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423971 | ||||||
| chr4:100423973
|
A | G | 2 | a0002c0002t0014g0094a0002c0002t0014g0137 | 2 | NA18980.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.416-569T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423973 | ||||||
| chr4:100424016
|
C | T | 2 | a0002c0002t0001g0058a0002c0002t0025g0057 | 2 | NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.416-612G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424016 | ||||||
| chr4:100424127
|
A | C | 1 | a0001c0001t0005g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.416-723T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424127 | ||||||
| chr4:100424137
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-733G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424137 | ||||||
| chr4:100424169
|
ATAAT | A | 3 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-769_416-766del others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424169 | ||||||
| chr4:100424173
|
T | C | 3 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0019g0155 | 3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.416-769A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424173 | ||||||
| chr4:100424277
|
A | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.416-873T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424277 | ||||||
| chr4:100424308
|
G | T | 46 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(43): Show | 47 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.416-904C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424308 | ||||||
| chr4:100424386
|
G | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-982C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424386 | ||||||
| chr4:100424424
|
A | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-1020T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424424 | ||||||
| chr4:100424454
|
C | T | 1 | a0001c0001t0007g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.416-1050G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424454 | ||||||
| chr4:100424737
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-1333T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424737 | ||||||
| chr4:100424897
|
C | A | 1 | a0001c0001t0002g0003 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.416-1493G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424897 | ||||||
| chr4:100424965
|
C | A | 1 | a0001c0001t0002g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.416-1561G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424965 | ||||||
| chr4:100425149
|
G | GCACA | 48 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(45): Show | 49 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.416-1749_416-1746d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACA | 26 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(23): Show | 27 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-1751_416-1746d others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACAC others(1): Show |
19 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0033others(16): Show | 19 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.416-1753_416-1746d others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACAC others(3): Show |
29 | a0001c0001t0002g0010a0001c0001t0002g0236a0001c0001t0004g0253others(26): Show | 29 | HG00741.hp2 HG01099.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-1755_416-1746d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACAC others(5): Show |
73 | a0001c0001t0001g0043a0001c0001t0001g0195a0001c0001t0001g0196others(70): Show | 75 | HG00408.hp1 HG00597.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.416-1757_416-1746d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACAC others(7): Show |
23 | a0001c0001t0001g0182a0001c0001t0004g0154a0001c0001t0004g0156others(20): Show | 23 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-1759_416-1746d others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACAC others(9): Show |
5 | a0001c0001t0004g0018a0001c0001t0004g0131a0001c0001t0006g0134others(2): Show | 5 | HG02132.hp2 HG02572.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1761_416-1746d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425149
|
G | GCACACAC others(11): Show |
2 | a0001c0001t0005g0187a0001c0001t0006g0151 | 2 | HG02109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.416-1763_416-1746d others(20): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | ||||||
| chr4:100425203
|
A | G | 3 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0019g0155 | 3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.416-1799T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425203 | ||||||
| chr4:100425234
|
C | T | 2 | a0001c0001t0004g0251a0001c0001t0004g0252 | 2 | HG01109.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.416-1830G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425234 | ||||||
| chr4:100425351
|
GC | G | 194 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(191): Show | 197 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(194): Show |
intron_variant | MODIFIER | c.416-1948delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425351 | ||||||
| chr4:100425367
|
A | C | 3 | a0001c0001t0003g0235a0001c0001t0003g0258a0001c0001t0018g0219 | 3 | HG00642.hp1 HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.416-1963T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425367 | ||||||
| chr4:100425390
|
C | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.416-1986G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425390 | ||||||
| chr4:100425537
|
C | T | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-2133G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425537 | ||||||
| chr4:100425655
|
T | C | 26 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(23): Show | 27 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-2251A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425655 | ||||||
| chr4:100425984
|
G | A | 83 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(80): Show | 84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.416-2580C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425984 | ||||||
| chr4:100426016
|
A | G | 2 | a0001c0001t0002g0122a0002c0002t0004g0162 | 2 | HG00735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.416-2612T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426016 | ||||||
| chr4:100426035
|
T | C | 2 | a0002c0002t0001g0058a0002c0002t0025g0057 | 2 | NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.416-2631A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426035 | ||||||
| chr4:100426174
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-2770A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426174 | ||||||
| chr4:100426242
|
G | A | 3 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0019g0155 | 3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.416-2838C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426242 | ||||||
| chr4:100426337
|
C | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.416-2933G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426337 | ||||||
| chr4:100426506
|
C | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-3102G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426506 | ||||||
| chr4:100426584
|
G | C | 43 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(40): Show | 44 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.416-3180C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426584 | ||||||
| chr4:100426588
|
C | A | 9 | a0001c0001t0003g0207a0001c0001t0003g0210a0001c0001t0003g0255others(6): Show | 9 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-3184G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426588 | ||||||
| chr4:100426938
|
A | G | 1 | a0002c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-3534T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426938 | ||||||
| chr4:100427001
|
T | A | 1 | a0002c0002t0001g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.416-3597A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427001 | ||||||
| chr4:100427046
|
G | C | 1 | a0001c0001t0002g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.416-3642C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427046 | ||||||
| chr4:100427210
|
T | A | 1 | a0002c0006t0004g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.416-3806A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427210 | ||||||
| chr4:100427255
|
T | G | 35 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(32): Show | 35 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.416-3851A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427255 | ||||||
| chr4:100427451
|
C | CT | 7 | a0001c0001t0001g0196a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-4048dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427451 | ||||||
| chr4:100427452
|
TC | T | 57 | a0001c0001t0002g0122a0001c0001t0004g0004a0001c0001t0004g0018others(54): Show | 58 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.416-4049delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427452 | ||||||
| chr4:100427453
|
C | T | 105 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(102): Show | 106 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.416-4049G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427453 | ||||||
| chr4:100427600
|
T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-4196A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427600 | ||||||
| chr4:100427767
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-4363A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427767 | ||||||
| chr4:100427847
|
C | G | 1 | a0001c0001t0027g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.416-4443G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427847 | ||||||
| chr4:100428063
|
C | CAGCTGAC others(7): Show |
194 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(191): Show | 197 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(194): Show |
intron_variant | MODIFIER | c.416-4660_416-4659i others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428063 | ||||||
| chr4:100428064
|
C | G | 194 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(191): Show | 197 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(194): Show |
intron_variant | MODIFIER | c.416-4660G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428064 | ||||||
| chr4:100428115
|
A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-4711T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428115 | ||||||
| chr4:100428247
|
C | T | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.416-4843G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428247 | ||||||
| chr4:100428399
|
C | T | 57 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(54): Show | 58 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.416-4995G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428399 | ||||||
| chr4:100428566
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.416-5162G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428566 | ||||||
| chr4:100428848
|
G | A | 8 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0007g0163others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.416-5444C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428848 | ||||||
| chr4:100428969
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-5565T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428969 | ||||||
| chr4:100429026
|
G | C | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.416-5622C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429026 | ||||||
| chr4:100429110
|
C | T | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-5706G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429110 | ||||||
| chr4:100429147
|
G | A | 2 | a0001c0001t0002g0122a0002c0002t0004g0162 | 2 | HG00735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.416-5743C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429147 | ||||||
| chr4:100429397
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.416-5993C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429397 | ||||||
| chr4:100429409
|
A | C | 1 | a0001c0001t0013g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.416-6005T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429409 | ||||||
| chr4:100429528
|
C | T | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.416-6124G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429528 | ||||||
| chr4:100429573
|
G | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-6169C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429573 | ||||||
| chr4:100429722
|
A | ATAG | 256 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(253): Show | 260 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(257): Show |
intron_variant | MODIFIER | c.416-6321_416-6319d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429722 | ||||||
| chr4:100429743
|
A | C | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-6339T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429743 | ||||||
| chr4:100429792
|
T | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(1): Show | 5 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-6388A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429792 | ||||||
| chr4:100429801
|
T | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-6397A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429801 | ||||||
| chr4:100429876
|
T | G | 1 | a0001c0001t0002g0226 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.416-6472A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429876 | ||||||
| chr4:100429900
|
C | T | 2 | a0004c0005t0017g0019a0004c0005t0017g0020 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.416-6496G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429900 | ||||||
| chr4:100430240
|
G | A | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.416-6836C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430240 | ||||||
| chr4:100430259
|
G | A | 1 | a0002c0002t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.416-6855C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430259 | ||||||
| chr4:100430527
|
A | G | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.416-7123T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430527 | ||||||
| chr4:100430793
|
G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416-7389C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430793 | ||||||
| chr4:100430799
|
A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-7395T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430799 | ||||||
| chr4:100430891
|
A | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.416-7487T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430891 | ||||||
| chr4:100430956
|
A | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-7552T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430956 | ||||||
| chr4:100431190
|
C | A | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(126): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.416-7786G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431190 | ||||||
| chr4:100431212
|
AAC | A | 3 | a0001c0001t0002g0184a0001c0001t0002g0226a0001c0001t0002g0232 | 3 | HG03831.hp1 HG03942.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.416-7810_416-7809d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431212 | ||||||
| chr4:100431243
|
A | G | 1 | a0001c0001t0011g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416-7839T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431243 | ||||||
| chr4:100431281
|
A | G | 10 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(7): Show | 11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-7877T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431281 | ||||||
| chr4:100431664
|
G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416-8260C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431664 | ||||||
| chr4:100431694
|
T | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-8290A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431694 | ||||||
| chr4:100431721
|
A | ATC | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(224): Show | 231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.416-8319_416-8318d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431721 | ||||||
| chr4:100431747
|
CTGCTCTC others(11): Show |
C | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.416-8361_416-8344d others(20): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431747 | ||||||
| chr4:100431809
|
C | T | 5 | a0001c0001t0009g0121a0001c0001t0009g0153a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-8405G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431809 | ||||||
| chr4:100431830
|
G | A | 5 | a0001c0001t0009g0121a0001c0001t0009g0153a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-8426C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431830 | ||||||
| chr4:100431932
|
G | C | 1 | a0001c0001t0033g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.416-8528C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431932 | ||||||
| chr4:100431965
|
G | A | 63 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(60): Show | 64 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.416-8561C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431965 | ||||||
| chr4:100432017
|
G | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-8613C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432017 | ||||||
| chr4:100432080
|
T | C | 1 | a0002c0002t0010g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.416-8676A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432080 | ||||||
| chr4:100432144
|
T | G | 1 | a0001c0001t0006g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.416-8740A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432144 | ||||||
| chr4:100432163
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-8759G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432163 | ||||||
| chr4:100432383
|
T | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-8979A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432383 | ||||||
| chr4:100432426
|
A | G | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.416-9022T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432426 | ||||||
| chr4:100432679
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-9275T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432679 | ||||||
| chr4:100433306
|
A | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.416-9902T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433306 | ||||||
| chr4:100433543
|
C | CT | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-10140dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433543 | ||||||
| chr4:100433588
|
T | C | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-10184A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433588 | ||||||
| chr4:100433878
|
G | A | 1 | a0002c0002t0010g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.416-10474C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433878 | ||||||
| chr4:100433962
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-10558T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433962 | ||||||
| chr4:100433974
|
C | T | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416-10570G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433974 | ||||||
| chr4:100434155
|
T | C | 2 | a0001c0001t0038g0211a0003c0003t0036g0160 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.416-10751A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434155 | ||||||
| chr4:100434271
|
A | G | 94 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(91): Show | 95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.416-10867T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434271 | ||||||
| chr4:100434378
|
CCAAGCAA others(10): Show |
C | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.416-10991_416-1097 others(21): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434378 | ||||||
| chr4:100434383
|
C | CA | 48 | a0001c0001t0002g0122a0001c0001t0003g0186a0001c0001t0003g0188others(45): Show | 49 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.416-10980dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434383 | ||||||
| chr4:100434383
|
C | CAA | 38 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(35): Show | 39 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.416-10981_416-1098 others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434383 | ||||||
| chr4:100434383
|
C | CAAA | 5 | a0001c0001t0002g0181a0001c0001t0002g0194a0001c0001t0002g0233others(2): Show | 5 | HG01192.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-10982_416-1098 others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434383 | ||||||
| chr4:100434397
|
A | G | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.416-10993T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434397 | ||||||
| chr4:100434424
|
A | T | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-11020T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434424 | ||||||
| chr4:100434585
|
C | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.416-11181G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434585 | ||||||
| chr4:100434644
|
G | A | 1 | a0002c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.416-11240C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434644 | ||||||
| chr4:100434660
|
C | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(38): Show | 42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.416-11256G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434660 | ||||||
| chr4:100434689
|
G | A | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.416-11285C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434689 | ||||||
| chr4:100434834
|
G | A | 6 | a0001c0001t0005g0183a0001c0001t0005g0191a0001c0001t0005g0192others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-11430C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434834 | ||||||
| chr4:100434862
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.416-11458C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434862 | ||||||
| chr4:100434970
|
C | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416-11566G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434970 | ||||||
| chr4:100435034
|
G | C | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.416-11630C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435034 | ||||||
| chr4:100435143
|
A | G | 2 | a0001c0001t0038g0211a0003c0003t0036g0160 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.416-11739T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435143 | ||||||
| chr4:100435418
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-12014T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435418 | ||||||
| chr4:100435431
|
G | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-12027C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435431 | ||||||
| chr4:100435438
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416-12034A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435438 | ||||||
| chr4:100435442
|
C | A | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-12038G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435442 | ||||||
| chr4:100435443
|
A | T | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-12039T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435443 | ||||||
| chr4:100435730
|
T | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+11803A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435730 | ||||||
| chr4:100435849
|
C | T | 44 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(41): Show | 45 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.415+11684G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435849 | ||||||
| chr4:100436174
|
G | GA | 8 | a0001c0001t0005g0201a0001c0001t0038g0211a0002c0002t0016g0110others(5): Show | 8 | HG00735.hp1 HG01070.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+11358dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436174 | ||||||
| chr4:100436178
|
A | T | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+11355T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436178 | ||||||
| chr4:100436457
|
T | C | 2 | a0004c0005t0017g0019a0004c0005t0017g0020 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.415+11076A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436457 | ||||||
| chr4:100436652
|
A | G | 2 | a0001c0001t0002g0122a0002c0002t0004g0162 | 2 | HG00735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.415+10881T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436652 | ||||||
| chr4:100436751
|
G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+10782C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436751 | ||||||
| chr4:100436798
|
C | T | 8 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0067others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+10735G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436798 | ||||||
| chr4:100436850
|
C | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+10683G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436850 | ||||||
| chr4:100436945
|
C | T | 11 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(8): Show | 12 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10588G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436945 | ||||||
| chr4:100437115
|
A | C | 257 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(254): Show | 261 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(258): Show |
intron_variant | MODIFIER | c.415+10418T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437115 | ||||||
| chr4:100437149
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10384T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437149 | ||||||
| chr4:100437237
|
T | A | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415+10296A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437237 | ||||||
| chr4:100437318
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+10215T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437318 | ||||||
| chr4:100437351
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10182T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437351 | ||||||
| chr4:100437460
|
T | TA | 27 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(24): Show | 27 | HG00642.hp1 HG01258.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.415+10072dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437460 | ||||||
| chr4:100437460
|
T | TAA | 217 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(214): Show | 220 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.415+10071_415+1007 others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437460 | ||||||
| chr4:100437460
|
T | TCA | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10072_415+1007 others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437460 | ||||||
| chr4:100437486
|
A | G | 133 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(130): Show | 135 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.415+10047T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437486 | ||||||
| chr4:100437496
|
G | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415+10037C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437496 | ||||||
| chr4:100437654
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+9879T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437654 | ||||||
| chr4:100437767
|
C | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(38): Show | 42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+9766G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437767 | ||||||
| chr4:100437807
|
G | T | 10 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(7): Show | 11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+9726C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437807 | ||||||
| chr4:100437914
|
TG | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0185a0004c0005t0017g0019others(1): Show | 4 | HG00735.hp1 HG01515.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+9618delC | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437914 | ||||||
| chr4:100438025
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+9508T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438025 | ||||||
| chr4:100438112
|
C | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+9421G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438112 | ||||||
| chr4:100438290
|
C | T | 1 | a0001c0004t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.415+9243G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438290 | ||||||
| chr4:100438333
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.415+9200A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438333 | ||||||
| chr4:100438378
|
A | T | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415+9155T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438378 | ||||||
| chr4:100438552
|
T | C | 1 | a0002c0002t0001g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.415+8981A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438552 | ||||||
| chr4:100438845
|
G | A | 1 | a0002c0002t0021g0061 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.415+8688C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438845 | ||||||
| chr4:100438976
|
T | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+8557A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438976 | ||||||
| chr4:100439010
|
C | T | 1 | a0005c0007t0002g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.415+8523G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439010 | ||||||
| chr4:100439086
|
C | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.415+8447G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439086 | ||||||
| chr4:100439424
|
G | A | 1 | a0002c0002t0001g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.415+8109C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439424 | ||||||
| chr4:100439456
|
G | T | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+8077C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439456 | ||||||
| chr4:100439553
|
T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+7980A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439553 | ||||||
| chr4:100439558
|
AT | A | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+7974delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439558 | ||||||
| chr4:100439562
|
T | A | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+7971A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439562 | ||||||
| chr4:100439654
|
C | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.415+7879G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439654 | ||||||
| chr4:100439712
|
A | G | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415+7821T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439712 | ||||||
| chr4:100439842
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(40): Show | 44 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+7691G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439842 | ||||||
| chr4:100439845
|
A | G | 2 | a0001c0001t0038g0211a0003c0003t0036g0160 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.415+7688T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439845 | ||||||
| chr4:100440053
|
T | TGTGAA | 56 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7479_415+7480i others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440053 | ||||||
| chr4:100440054
|
C | A | 1 | a0002c0002t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.415+7479G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440054 | ||||||
| chr4:100440055
|
C | A | 1 | a0002c0002t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.415+7478G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440055 | ||||||
| chr4:100440055
|
C | T | 56 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7478G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440055 | ||||||
| chr4:100440056
|
C | A | 56 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7477G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440056 | ||||||
| chr4:100440057
|
A | T | 56 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7476T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440057 | ||||||
| chr4:100440062
|
A | G | 1 | a0002c0002t0001g0088 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.415+7471T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440062 | ||||||
| chr4:100440086
|
A | G | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+7447T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440086 | ||||||
| chr4:100440199
|
A | T | 2 | a0001c0001t0038g0211a0003c0003t0036g0160 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.415+7334T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440199 | ||||||
| chr4:100440203
|
A | G | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+7330T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440203 | ||||||
| chr4:100440237
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.415+7296C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440237 | ||||||
| chr4:100440322
|
T | C | 1 | a0002c0002t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.415+7211A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440322 | ||||||
| chr4:100440343
|
G | A | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+7190C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440343 | ||||||
| chr4:100440394
|
C | T | 43 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(40): Show | 44 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+7139G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440394 | ||||||
| chr4:100440395
|
G | A | 2 | a0002c0002t0001g0054a0002c0002t0001g0064 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.415+7138C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440395 | ||||||
| chr4:100440439
|
G | A | 3 | a0001c0004t0004g0248a0001c0004t0004g0249a0002c0006t0004g0048 | 3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.415+7094C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440439 | ||||||
| chr4:100440568
|
T | C | 1 | a0004c0005t0017g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415+6965A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440568 | ||||||
| chr4:100440607
|
G | A | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.415+6926C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440607 | ||||||
| chr4:100440630
|
A | G | 2 | a0001c0001t0004g0251a0001c0001t0004g0252 | 2 | HG01109.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.415+6903T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440630 | ||||||
| chr4:100440812
|
C | T | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+6721G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440812 | ||||||
| chr4:100440837
|
G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+6696C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440837 | ||||||
| chr4:100440872
|
T | G | 1 | a0001c0001t0006g0157 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.415+6661A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440872 | ||||||
| chr4:100441094
|
A | C | 31 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(28): Show | 32 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.415+6439T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441094 | ||||||
| chr4:100441121
|
A | T | 2 | a0001c0001t0009g0121a0001c0001t0009g0153 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.415+6412T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441121 | ||||||
| chr4:100441124
|
A | G | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.415+6409T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441124 | ||||||
| chr4:100441245
|
C | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.415+6288G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441245 | ||||||
| chr4:100441306
|
T | C | 5 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(2): Show | 6 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+6227A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441306 | ||||||
| chr4:100441322
|
A | G | 5 | a0002c0002t0001g0046a0002c0002t0001g0071a0002c0002t0001g0074others(2): Show | 5 | HG01074.hp2 HG01255.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+6211T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441322 | ||||||
| chr4:100441465
|
A | G | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+6068T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441465 | ||||||
| chr4:100441495
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.415+6038A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441495 | ||||||
| chr4:100441602
|
T | A | 10 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(7): Show | 11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+5931A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441602 | ||||||
| chr4:100441649
|
A | T | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+5884T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441649 | ||||||
| chr4:100441743
|
T | G | 1 | a0002c0002t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.415+5790A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441743 | ||||||
| chr4:100441750
|
C | A | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+5783G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441750 | ||||||
| chr4:100441760
|
C | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+5773G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441760 | ||||||
| chr4:100441857
|
G | A | 79 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(76): Show | 80 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.415+5676C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441857 | ||||||
| chr4:100441908
|
CAT | C | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+5623_415+5624d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441908 | ||||||
| chr4:100441954
|
A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415+5579T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441954 | ||||||
| chr4:100442124
|
T | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+5409A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442124 | ||||||
| chr4:100442288
|
T | C | 41 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(38): Show | 42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+5245A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442288 | ||||||
| chr4:100442359
|
C | T | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+5174G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442359 | ||||||
| chr4:100442509
|
T | C | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.415+5024A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442509 | ||||||
| chr4:100442558
|
TC | T | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+4974delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442558 | ||||||
| chr4:100442586
|
T | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+4947A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442586 | ||||||
| chr4:100442814
|
T | TC | 41 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(38): Show | 42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+4718dupG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442814 | ||||||
| chr4:100443377
|
C | T | 1 | a0004c0005t0017g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415+4156G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443377 | ||||||
| chr4:100443378
|
G | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.415+4155C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443378 | ||||||
| chr4:100443420
|
G | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+4113C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443420 | ||||||
| chr4:100443478
|
G | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+4055C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443478 | ||||||
| chr4:100443532
|
T | C | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+4001A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443532 | ||||||
| chr4:100443753
|
G | C | 1 | a0001c0001t0001g0044 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.415+3780C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443753 | ||||||
| chr4:100443784
|
C | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+3749G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443784 | ||||||
| chr4:100444089
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415+3444C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444089 | ||||||
| chr4:100444220
|
C | T | 1 | a0002c0002t0010g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.415+3313G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444220 | ||||||
| chr4:100444269
|
A | G | 3 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0019g0155 | 3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.415+3264T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444269 | ||||||
| chr4:100444313
|
G | A | 1 | a0001c0001t0012g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.415+3220C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444313 | ||||||
| chr4:100444338
|
A | G | 231 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(228): Show | 235 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(232): Show |
intron_variant | MODIFIER | c.415+3195T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444338 | ||||||
| chr4:100444388
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+3145T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444388 | ||||||
| chr4:100444430
|
C | G | 19 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(16): Show | 19 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.415+3103G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444430 | ||||||
| chr4:100444432
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(40): Show | 44 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+3101T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444432 | ||||||
| chr4:100444733
|
C | T | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+2800G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444733 | ||||||
| chr4:100444959
|
C | T | 228 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(225): Show | 232 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(229): Show |
intron_variant | MODIFIER | c.415+2574G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444959 | ||||||
| chr4:100445001
|
A | T | 45 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(42): Show | 46 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.415+2532T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445001 | ||||||
| chr4:100445124
|
T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+2409A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445124 | ||||||
| chr4:100445161
|
A | T | 1 | a0002c0002t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.415+2372T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445161 | ||||||
| chr4:100445243
|
T | C | 1 | a0002c0002t0001g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.415+2290A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445243 | ||||||
| chr4:100445418
|
C | T | 230 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(227): Show | 234 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(231): Show |
intron_variant | MODIFIER | c.415+2115G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445418 | ||||||
| chr4:100445503
|
C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+2030G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445503 | ||||||
| chr4:100445728
|
G | A | 37 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(34): Show | 38 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.415+1805C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445728 | ||||||
| chr4:100445813
|
C | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+1720G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445813 | ||||||
| chr4:100445896
|
A | C | 35 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(32): Show | 35 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.415+1637T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445896 | ||||||
| chr4:100445989
|
A | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(38): Show | 42 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.415+1544T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445989 | ||||||
| chr4:100446206
|
C | T | 226 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(223): Show | 230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.415+1327G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446206 | ||||||
| chr4:100446331
|
T | TA | 39 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(36): Show | 40 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.415+1201dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446331 | ||||||
| chr4:100446501
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415+1032A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446501 | ||||||
| chr4:100446514
|
T | C | 1 | a0001c0001t0007g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.415+1019A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446514 | ||||||
| chr4:100446519
|
T | A | 137 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(134): Show | 139 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.415+1014A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446519 | ||||||
| chr4:100446544
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415+989A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446544 | ||||||
| chr4:100446696
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.415+837T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446696 | ||||||
| chr4:100446997
|
G | T | 39 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(36): Show | 40 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.415+536C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446997 | ||||||
| chr4:100447058
|
C | G | 1 | a0001c0001t0003g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.415+475G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447058 | ||||||
| chr4:100447125
|
A | G | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(224): Show | 231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.415+408T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447125 | ||||||
| chr4:100447127
|
T | C | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+406A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447127 | ||||||
| chr4:100447130
|
T | C | 1 | a0001c0001t0038g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415+403A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447130 | ||||||
| chr4:100447171
|
C | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+362G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447171 | ||||||
| chr4:100447172
|
A | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+361T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447172 | ||||||
| chr4:100447205
|
T | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+328A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447205 | ||||||
| chr4:100447344
|
A | G | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+189T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447344 | ||||||
| chr4:100447360
|
T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+173A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447360 | ||||||
| chr4:100447402
|
T | C | 19 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(16): Show | 19 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.415+131A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447402 | ||||||
| chr4:100447409
|
T | C | 6 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(3): Show | 6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+124A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447409 | ||||||
| chr4:100447476
|
T | G | 17 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+57A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447476 | ||||||
| chr4:100447504
|
A | G | 41 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(38): Show | 42 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.415+29T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447504 | ||||||
| chr4:100447822
|
C | T | 2 | a0001c0001t0005g0256a0001c0001t0005g0257 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.377-251G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100447822 | ||||||
| chr4:100447834
|
C | T | 1 | a0002c0002t0009g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377-263G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100447834 | ||||||
| chr4:100447893
|
G | A | 1 | a0002c0006t0004g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.377-322C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100447893 | ||||||
| chr4:100448016
|
T | C | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-445A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448016 | ||||||
| chr4:100448021
|
A | G | 2 | a0001c0001t0002g0021a0001c0001t0002g0041 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.377-450T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448021 | ||||||
| chr4:100448468
|
T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.377-897A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448468 | ||||||
| chr4:100448557
|
C | A | 6 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(3): Show | 6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-986G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448557 | ||||||
| chr4:100448698
|
C | T | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.377-1127G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448698 | ||||||
| chr4:100448730
|
G | A | 6 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(3): Show | 6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-1159C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448730 | ||||||
| chr4:100448795
|
T | TTTTC | 23 | a0001c0001t0002g0003a0001c0001t0002g0181a0001c0001t0002g0184others(20): Show | 24 | HG00639.hp1 HG00673.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(1): Show |
13 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0002g0203others(10): Show | 14 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(5): Show |
4 | a0001c0001t0002g0178a0001c0001t0002g0230a0001c0001t0012g0180others(1): Show | 4 | HG02148.hp1 HG02486.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(9): Show |
56 | a0001c0001t0001g0182a0001c0001t0002g0007a0001c0001t0002g0010others(53): Show | 56 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(13): Show |
70 | a0001c0001t0001g0185a0001c0001t0001g0195a0001c0001t0001g0196others(67): Show | 71 | HG00597.hp2 HG00735.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(22): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(17): Show |
9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0004g0253others(6): Show | 9 | HG00408.hp1 HG00408.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(26): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(21): Show |
4 | a0001c0001t0004g0004a0001c0001t0004g0251a0002c0002t0001g0042others(1): Show | 5 | HG01109.hp2 HG02148.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(30): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(25): Show |
1 | a0002c0002t0001g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.377-1225_377-1224i others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(29): Show |
2 | a0001c0001t0004g0252a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.377-1225_377-1224i others(38): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(9): Show |
1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.377-1225_377-1224i others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(17): Show |
10 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0191others(7): Show | 10 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(26): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(21): Show |
7 | a0001c0001t0005g0183a0001c0001t0005g0187a0001c0001t0005g0244others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(30): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448795
|
T | TTTTCTTT others(25): Show |
4 | a0001c0001t0005g0202a0001c0001t0005g0257a0001c0001t0011g0112others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | ||||||
| chr4:100448796
|
C | T | 46 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(43): Show | 47 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.377-1225G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448796 | ||||||
| chr4:100448800
|
C | T | 23 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0194others(20): Show | 23 | HG00673.hp1 HG00741.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.377-1229G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448800 | ||||||
| chr4:100448820
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.377-1249G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448820 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(33): Show |
1 | a0001c0001t0003g0212 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(42): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(33): Show |
5 | a0001c0001t0003g0207a0001c0001t0003g0255a0001c0001t0009g0242others(2): Show | 5 | HG02559.hp2 HG03209.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-1252_377-1251i others(42): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(37): Show |
5 | a0001c0001t0001g0101a0001c0001t0003g0186a0001c0001t0003g0206others(2): Show | 5 | HG00642.hp1 HG01258.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-1252_377-1251i others(46): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(33): Show |
1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.377-1252_377-1251i others(42): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(37): Show |
2 | a0001c0001t0003g0210a0001c0001t0009g0121 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.377-1252_377-1251i others(46): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(41): Show |
12 | a0001c0001t0002g0189a0001c0001t0002g0216a0001c0001t0003g0102others(9): Show | 12 | HG01516.hp1 HG01934.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.377-1252_377-1251i others(50): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(41): Show |
1 | a0001c0001t0009g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(50): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(45): Show |
1 | a0001c0001t0003g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.377-1252_377-1251i others(54): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(49): Show |
1 | a0001c0001t0003g0085 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(58): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
T | TCCTTCCT others(53): Show |
1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(62): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448822
|
TCCTC | T | 9 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0133others(6): Show | 9 | HG00673.hp1 HG02056.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1255_377-1252d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | ||||||
| chr4:100448824
|
C | T | 127 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(124): Show | 129 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.377-1253G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448824 | ||||||
| chr4:100448826
|
C | T | 218 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(215): Show | 222 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(219): Show |
intron_variant | MODIFIER | c.377-1255G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448826 | ||||||
| chr4:100448830
|
C | T | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(224): Show | 231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.377-1259G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448830 | ||||||
| chr4:100448834
|
C | T | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(224): Show | 231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.377-1263G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448834 | ||||||
| chr4:100448838
|
C | T | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(224): Show | 231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.377-1267G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448838 | ||||||
| chr4:100448839
|
C | A | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.377-1268G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448839 | ||||||
| chr4:100448842
|
C | T | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(224): Show | 231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.377-1271G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448842 | ||||||
| chr4:100448990
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.377-1419G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448990 | ||||||
| chr4:100449050
|
A | G | 6 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(3): Show | 6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-1479T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449050 | ||||||
| chr4:100449252
|
G | A | 1 | a0002c0002t0001g0099 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.377-1681C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449252 | ||||||
| chr4:100449345
|
A | G | 1 | a0002c0002t0001g0063 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.377-1774T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449345 | ||||||
| chr4:100449470
|
C | T | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.377-1899G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449470 | ||||||
| chr4:100449519
|
A | G | 1 | a0002c0002t0022g0234 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.377-1948T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449519 | ||||||
| chr4:100449930
|
A | C | 1 | a0001c0001t0004g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.377-2359T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449930 | ||||||
| chr4:100450184
|
G | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-2613C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450184 | ||||||
| chr4:100450335
|
C | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-2764G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450335 | ||||||
| chr4:100450346
|
C | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-2775G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450346 | ||||||
| chr4:100450660
|
T | G | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-3089A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450660 | ||||||
| chr4:100450835
|
T | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-3264A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450835 | ||||||
| chr4:100451227
|
T | TAAG | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-3659_377-3657d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451227 | ||||||
| chr4:100451307
|
T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-3736A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451307 | ||||||
| chr4:100451308
|
G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-3737C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451308 | ||||||
| chr4:100451384
|
T | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-3813A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451384 | ||||||
| chr4:100451449
|
T | A | 4 | a0001c0001t0015g0022a0001c0001t0015g0115a0002c0002t0016g0110others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-3878A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451449 | ||||||
| chr4:100451653
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.377-4082A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451653 | ||||||
| chr4:100451800
|
A | G | 13 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0133others(10): Show | 13 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-4229T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451800 | ||||||
| chr4:100451936
|
T | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-4365A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451936 | ||||||
| chr4:100452156
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.377-4585C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452156 | ||||||
| chr4:100452248
|
T | C | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.377-4677A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452248 | ||||||
| chr4:100452469
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.377-4898C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452469 | ||||||
| chr4:100452530
|
C | T | 9 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0007g0163others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-4959G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452530 | ||||||
| chr4:100452570
|
G | T | 58 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(55): Show | 59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.377-4999C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452570 | ||||||
| chr4:100452573
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-5002T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452573 | ||||||
| chr4:100452673
|
G | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-5102C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452673 | ||||||
| chr4:100452894
|
C | G | 10 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(7): Show | 11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.377-5323G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452894 | ||||||
| chr4:100453066
|
A | G | 1 | a0001c0001t0034g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.377-5495T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453066 | ||||||
| chr4:100453081
|
G | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-5510C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453081 | ||||||
| chr4:100453117
|
A | T | 1 | a0001c0001t0002g0189 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.377-5546T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453117 | ||||||
| chr4:100453151
|
A | C | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-5580T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453151 | ||||||
| chr4:100453187
|
A | C | 3 | a0001c0001t0003g0210a0001c0001t0015g0022a0001c0001t0015g0115 | 3 | HG02965.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-5616T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453187 | ||||||
| chr4:100453302
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.377-5731T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453302 | ||||||
| chr4:100453719
|
A | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6148T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453719 | ||||||
| chr4:100453847
|
A | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6276T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453847 | ||||||
| chr4:100453870
|
T | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6299A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453870 | ||||||
| chr4:100453915
|
C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-6344G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453915 | ||||||
| chr4:100453940
|
G | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6369C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453940 | ||||||
| chr4:100454060
|
T | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-6489A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454060 | ||||||
| chr4:100454061
|
A | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-6490T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454061 | ||||||
| chr4:100454179
|
TA | T | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-6609delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454179 | ||||||
| chr4:100454188
|
T | A | 11 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.377-6617A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454188 | ||||||
| chr4:100454238
|
C | CA | 34 | a0001c0001t0002g0036a0001c0001t0002g0189a0001c0001t0002g0193others(31): Show | 34 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.377-6668dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | ||||||
| chr4:100454238
|
C | CAA | 64 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(61): Show | 65 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.377-6669_377-6668d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | ||||||
| chr4:100454238
|
C | CAAA | 21 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0007g0130others(18): Show | 21 | HG01123.hp1 HG01169.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.377-6670_377-6668d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | ||||||
| chr4:100454238
|
CA | C | 38 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(35): Show | 40 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.377-6668delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | ||||||
| chr4:100454540
|
T | A | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.377-6969A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454540 | ||||||
| chr4:100454679
|
T | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-7108A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454679 | ||||||
| chr4:100454710
|
A | G | 1 | a0002c0002t0001g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.377-7139T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454710 | ||||||
| chr4:100454852
|
T | C | 3 | a0001c0001t0028g0175a0001c0001t0038g0211a0003c0003t0036g0160 | 3 | HG02486.hp1 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.377-7281A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454852 | ||||||
| chr4:100455148
|
C | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-7577G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455148 | ||||||
| chr4:100455197
|
G | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-7626C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455197 | ||||||
| chr4:100455476
|
T | C | 95 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(92): Show | 96 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.377-7905A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455476 | ||||||
| chr4:100455509
|
G | GT | 61 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(58): Show | 62 | HG00597.hp1 HG00673.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.377-7939dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455509 | ||||||
| chr4:100455509
|
GT | G | 6 | a0001c0001t0005g0174a0001c0001t0007g0130a0001c0001t0038g0211others(3): Show | 6 | HG02148.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-7939delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455509 | ||||||
| chr4:100455530
|
A | C | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-7959T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455530 | ||||||
| chr4:100455540
|
A | AT | 236 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(233): Show | 240 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(237): Show |
intron_variant | MODIFIER | c.377-7970_377-7969i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455540 | ||||||
| chr4:100455561
|
C | T | 1 | a0001c0001t0005g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.377-7990G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455561 | ||||||
| chr4:100455607
|
C | T | 2 | a0004c0005t0017g0019a0004c0005t0017g0020 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.377-8036G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455607 | ||||||
| chr4:100455676
|
A | G | 2 | a0002c0002t0001g0065a0002c0002t0001g0081 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.377-8105T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455676 | ||||||
| chr4:100455685
|
T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.377-8114A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455685 | ||||||
| chr4:100456010
|
G | C | 1 | a0002c0002t0001g0042 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.377-8439C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456010 | ||||||
| chr4:100456173
|
G | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.377-8602C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456173 | ||||||
| chr4:100456327
|
T | G | 2 | a0002c0002t0001g0059a0002c0002t0001g0066 | 2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.377-8756A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456327 | ||||||
| chr4:100456436
|
T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.377-8865A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456436 | ||||||
| chr4:100456479
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.377-8908G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456479 | ||||||
| chr4:100456543
|
C | A | 222 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(219): Show | 226 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(223): Show |
intron_variant | MODIFIER | c.376+8880G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456543 | ||||||
| chr4:100456594
|
T | A | 2 | a0002c0002t0001g0065a0002c0002t0001g0081 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.376+8829A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456594 | ||||||
| chr4:100456990
|
C | T | 57 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(54): Show | 58 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.376+8433G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456990 | ||||||
| chr4:100457038
|
G | A | 10 | a0001c0001t0004g0004a0001c0001t0004g0018a0001c0001t0004g0131others(7): Show | 11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.376+8385C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457038 | ||||||
| chr4:100457071
|
G | GT | 5 | a0001c0001t0002g0122a0001c0001t0003g0220a0002c0002t0001g0017others(2): Show | 5 | HG00735.hp2 HG01934.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+8351dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457071 | ||||||
| chr4:100457190
|
T | TTG | 17 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(14): Show | 17 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.376+8231_376+8232d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457190 | ||||||
| chr4:100457190
|
T | TTGTG | 3 | a0001c0001t0027g0247a0004c0005t0017g0019a0004c0005t0017g0020 | 3 | HG00735.hp1 HG00741.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.376+8229_376+8232d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457190 | ||||||
| chr4:100457190
|
TTGTG | T | 6 | a0001c0001t0002g0122a0001c0001t0011g0109a0001c0001t0011g0112others(3): Show | 6 | HG00735.hp2 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+8229_376+8232d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457190 | ||||||
| chr4:100457205
|
TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+8206_376+8217d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457205 | ||||||
| chr4:100457213
|
TGTGC | T | 136 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(133): Show | 139 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.376+8206_376+8209d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457213 | ||||||
| chr4:100457215
|
TGC | T | 28 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(25): Show | 28 | HG00639.hp1 HG00673.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.376+8206_376+8207d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457215 | ||||||
| chr4:100457217
|
C | T | 58 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(55): Show | 59 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.376+8206G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457217 | ||||||
| chr4:100457241
|
A | T | 4 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0013g0246others(1): Show | 4 | HG00741.hp1 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+8182T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457241 | ||||||
| chr4:100457470
|
T | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+7953A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457470 | ||||||
| chr4:100457629
|
C | T | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+7794G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457629 | ||||||
| chr4:100457865
|
T | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+7558A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457865 | ||||||
| chr4:100457945
|
C | T | 1 | a0001c0001t0008g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.376+7478G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457945 | ||||||
| chr4:100457946
|
G | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+7477C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457946 | ||||||
| chr4:100457974
|
G | A | 1 | a0002c0002t0006g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.376+7449C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457974 | ||||||
| chr4:100458122
|
A | C | 1 | a0001c0001t0005g0201 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.376+7301T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458122 | ||||||
| chr4:100458690
|
C | T | 3 | a0001c0001t0028g0175a0001c0001t0038g0211a0003c0003t0036g0160 | 3 | HG02486.hp1 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.376+6733G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458690 | ||||||
| chr4:100458784
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376+6639G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458784 | ||||||
| chr4:100458944
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.376+6479C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458944 | ||||||
| chr4:100458991
|
G | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.376+6432C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458991 | ||||||
| chr4:100459016
|
G | GA | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+6406dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459016 | ||||||
| chr4:100459054
|
G | A | 16 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(13): Show | 16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+6369C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459054 | ||||||
| chr4:100459055
|
G | A | 2 | a0002c0002t0001g0054a0002c0002t0001g0064 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.376+6368C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459055 | ||||||
| chr4:100459168
|
GCTCT | G | 6 | a0001c0001t0001g0101a0001c0001t0003g0206a0001c0001t0003g0215others(3): Show | 6 | HG00642.hp1 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+6251_376+6254d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCT | G | 6 | a0001c0001t0002g0216a0001c0001t0003g0102a0001c0001t0003g0186others(3): Show | 6 | HG01258.hp2 HG01943.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+6249_376+6254d others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(1): Show |
G | 5 | a0001c0001t0002g0225a0001c0001t0003g0212a0001c0001t0004g0018others(2): Show | 5 | HG01123.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+6247_376+6254d others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(3): Show |
G | 6 | a0001c0001t0002g0181a0001c0001t0003g0207a0001c0001t0003g0210others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+6245_376+6254d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(5): Show |
G | 13 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(10): Show | 14 | HG01109.hp2 HG01167.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.376+6243_376+6254d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(7): Show |
G | 3 | a0001c0001t0002g0230a0001c0001t0002g0236a0001c0001t0011g0114 | 3 | HG01099.hp1 HG02486.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.376+6241_376+6254d others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(9): Show |
G | 7 | a0001c0001t0002g0228a0001c0001t0003g0235a0001c0001t0003g0255others(4): Show | 7 | HG02602.hp2 HG03041.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+6239_376+6254d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(11): Show |
G | 25 | a0001c0001t0002g0003a0001c0001t0002g0127a0001c0001t0002g0129others(22): Show | 26 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.376+6237_376+6254d others(20): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(13): Show |
G | 5 | a0001c0001t0002g0224a0001c0001t0011g0109a0001c0001t0011g0113others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+6235_376+6254d others(22): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(15): Show |
G | 3 | a0001c0001t0002g0122a0001c0001t0032g0254a0002c0002t0004g0162 | 3 | HG00735.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.376+6233_376+6254d others(24): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(17): Show |
G | 1 | a0001c0004t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376+6231_376+6254d others(26): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(19): Show |
G | 3 | a0003c0003t0004g0158a0004c0005t0017g0019a0004c0005t0017g0020 | 3 | HG00735.hp1 HG01515.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.376+6229_376+6254d others(28): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(21): Show |
G | 2 | a0001c0001t0002g0013a0001c0001t0029g0159 | 2 | HG01975.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.376+6227_376+6254d others(30): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(23): Show |
G | 6 | a0001c0001t0002g0161a0001c0001t0028g0175a0001c0001t0038g0211others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+6225_376+6254d others(32): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(25): Show |
G | 146 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.376+6223_376+6254d others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459168
|
GCTCTCTC others(27): Show |
G | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+6221_376+6254d others(36): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | ||||||
| chr4:100459226
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.376+6197A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459226 | ||||||
| chr4:100459304
|
C | CAT | 223 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(220): Show | 227 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(224): Show |
intron_variant | MODIFIER | c.376+6117_376+6118d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459304 | ||||||
| chr4:100459538
|
T | C | 222 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(219): Show | 226 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(223): Show |
intron_variant | MODIFIER | c.376+5885A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459538 | ||||||
| chr4:100459632
|
G | A | 3 | a0001c0001t0028g0175a0001c0001t0038g0211a0003c0003t0036g0160 | 3 | HG02486.hp1 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.376+5791C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459632 | ||||||
| chr4:100459734
|
G | A | 215 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(212): Show | 219 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(216): Show |
intron_variant | MODIFIER | c.376+5689C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459734 | ||||||
| chr4:100460064
|
T | C | 1 | a0002c0002t0026g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.376+5359A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460064 | ||||||
| chr4:100460139
|
C | G | 1 | a0001c0001t0012g0238 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.376+5284G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460139 | ||||||
| chr4:100460139
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.376+5284G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460139 | ||||||
| chr4:100460160
|
A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+5263T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460160 | ||||||
| chr4:100460370
|
A | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+5053T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460370 | ||||||
| chr4:100460519
|
G | A | 2 | a0002c0002t0001g0054a0002c0002t0001g0064 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.376+4904C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460519 | ||||||
| chr4:100460542
|
G | C | 121 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(118): Show | 123 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.376+4881C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460542 | ||||||
| chr4:100460613
|
G | A | 237 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(234): Show | 241 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(238): Show |
intron_variant | MODIFIER | c.376+4810C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460613 | ||||||
| chr4:100460705
|
G | A | 1 | a0002c0002t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.376+4718C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460705 | ||||||
| chr4:100460796
|
T | C | 2 | a0001c0001t0038g0211a0003c0003t0036g0160 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.376+4627A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460796 | ||||||
| chr4:100460962
|
T | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.376+4461A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460962 | ||||||
| chr4:100461457
|
A | G | 135 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(132): Show | 137 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.376+3966T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461457 | ||||||
| chr4:100461682
|
A | C | 125 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(122): Show | 127 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.376+3741T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461682 | ||||||
| chr4:100461746
|
C | T | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.376+3677G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461746 | ||||||
| chr4:100461935
|
C | T | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.376+3488G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461935 | ||||||
| chr4:100462021
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.376+3402T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462021 | ||||||
| chr4:100462051
|
T | C | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.376+3372A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462051 | ||||||
| chr4:100462055
|
A | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+3368T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462055 | ||||||
| chr4:100462211
|
C | T | 1 | a0001c0001t0015g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.376+3212G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462211 | ||||||
| chr4:100462337
|
T | C | 19 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0088others(16): Show | 19 | HG00597.hp2 HG01192.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.376+3086A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462337 | ||||||
| chr4:100462357
|
A | G | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.376+3066T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462357 | ||||||
| chr4:100462475
|
T | C | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.376+2948A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462475 | ||||||
| chr4:100462559
|
C | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.376+2864G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462559 | ||||||
| chr4:100462578
|
T | C | 2 | a0001c0001t0006g0133a0001c0001t0006g0134 | 2 | HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.376+2845A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462578 | ||||||
| chr4:100462619
|
C | T | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+2804G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462619 | ||||||
| chr4:100463053
|
T | C | 1 | a0001c0001t0011g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.376+2370A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463053 | ||||||
| chr4:100463334
|
T | G | 127 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(124): Show | 129 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.376+2089A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463334 | ||||||
| chr4:100463384
|
C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.376+2039G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463384 | ||||||
| chr4:100463403
|
G | T | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+2020C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463403 | ||||||
| chr4:100463511
|
C | T | 5 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(2): Show | 5 | HG01975.hp1 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+1912G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463511 | ||||||
| chr4:100463514
|
C | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.376+1909G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463514 | ||||||
| chr4:100463689
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.376+1734G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463689 | ||||||
| chr4:100463705
|
A | T | 3 | a0001c0001t0009g0121a0001c0001t0009g0242a0001c0001t0009g0243 | 3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.376+1718T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463705 | ||||||
| chr4:100463810
|
C | T | 122 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(119): Show | 124 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.376+1613G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463810 | ||||||
| chr4:100463864
|
T | C | 2 | a0004c0005t0017g0019a0004c0005t0017g0020 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.376+1559A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463864 | ||||||
| chr4:100463918
|
C | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+1505G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463918 | ||||||
| chr4:100464151
|
AC | A | 9 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(6): Show | 10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+1271delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464151 | ||||||
| chr4:100464252
|
C | A | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.376+1171G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464252 | ||||||
| chr4:100464312
|
C | T | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.376+1111G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464312 | ||||||
| chr4:100464346
|
C | T | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.376+1077G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464346 | ||||||
| chr4:100464423
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.376+1000T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464423 | ||||||
| chr4:100464872
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.376+551T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464872 | ||||||
| chr4:100465137
|
A | C | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+286T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100465137 | ||||||
| chr4:100465629
|
G | T | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-90C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100465629 | ||||||
| chr4:100465788
|
C | T | 3 | a0003c0003t0004g0158a0003c0003t0035g0198a0003c0003t0036g0160 | 3 | HG02615.hp2 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-249G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100465788 | ||||||
| chr4:100465976
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-437C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100465976 | ||||||
| chr4:100466052
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.260-513T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466052 | ||||||
| chr4:100466067
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-528A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466067 | ||||||
| chr4:100466096
|
GA | G | 126 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(123): Show | 128 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.260-558delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466096 | ||||||
| chr4:100466214
|
G | GT | 11 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(8): Show | 12 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-676dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466214 | ||||||
| chr4:100466215
|
T | C | 1 | a0001c0001t0002g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.260-676A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466215 | ||||||
| chr4:100466268
|
C | G | 3 | a0003c0003t0004g0158a0003c0003t0035g0198a0003c0003t0036g0160 | 3 | HG02615.hp2 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-729G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466268 | ||||||
| chr4:100466631
|
A | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.260-1092T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466631 | ||||||
| chr4:100466800
|
G | A | 2 | a0003c0003t0004g0158a0003c0003t0035g0198 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-1261C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466800 | ||||||
| chr4:100466808
|
T | G | 2 | a0001c0001t0003g0210a0001c0001t0038g0211 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.260-1269A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466808 | ||||||
| chr4:100466991
|
G | A | 122 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(119): Show | 124 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.260-1452C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466991 | ||||||
| chr4:100467170
|
T | A | 1 | a0002c0002t0010g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.260-1631A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467170 | ||||||
| chr4:100467303
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1764T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467303 | ||||||
| chr4:100467454
|
G | A | 38 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0176others(35): Show | 39 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.260-1915C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467454 | ||||||
| chr4:100467460
|
C | T | 89 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(86): Show | 90 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.260-1921G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467460 | ||||||
| chr4:100467540
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.260-2001C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467540 | ||||||
| chr4:100467635
|
T | C | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.260-2096A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467635 | ||||||
| chr4:100467638
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.260-2099G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467638 | ||||||
| chr4:100467681
|
C | CA | 70 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0002g0003others(67): Show | 72 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.260-2143dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467681 | ||||||
| chr4:100467681
|
C | CAA | 21 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0181others(18): Show | 21 | HG00639.hp1 HG01192.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-2144_260-2143d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467681 | ||||||
| chr4:100468073
|
G | T | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.260-2534C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468073 | ||||||
| chr4:100468153
|
G | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0012g0026 | 3 | HG00738.hp1 HG01106.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.260-2614C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468153 | ||||||
| chr4:100468217
|
G | A | 1 | a0001c0001t0006g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.260-2678C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468217 | ||||||
| chr4:100468296
|
G | A | 2 | a0003c0003t0004g0158a0003c0003t0035g0198 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-2757C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468296 | ||||||
| chr4:100468297
|
T | A | 1 | a0002c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.260-2758A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468297 | ||||||
| chr4:100468372
|
T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260-2833A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468372 | ||||||
| chr4:100468414
|
T | G | 3 | a0001c0001t0009g0121a0001c0001t0009g0242a0001c0001t0009g0243 | 3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.260-2875A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468414 | ||||||
| chr4:100468443
|
A | T | 1 | a0001c0001t0002g0245 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.260-2904T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468443 | ||||||
| chr4:100468674
|
T | A | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.260-3135A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468674 | ||||||
| chr4:100468708
|
C | G | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.260-3169G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468708 | ||||||
| chr4:100469169
|
C | A | 40 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0176others(37): Show | 41 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.260-3630G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469169 | ||||||
| chr4:100469213
|
C | T | 59 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(56): Show | 60 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.260-3674G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469213 | ||||||
| chr4:100469314
|
T | C | 7 | a0002c0002t0001g0139a0002c0002t0001g0144a0002c0002t0001g0146others(4): Show | 7 | HG01109.hp1 HG01123.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-3775A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469314 | ||||||
| chr4:100469358
|
G | C | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.260-3819C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469358 | ||||||
| chr4:100469418
|
T | A | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.260-3879A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469418 | ||||||
| chr4:100469477
|
AAAATGAA others(171): Show |
A | 58 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0127others(55): Show | 59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-4116_260-3939d others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469477 | ||||||
| chr4:100469781
|
T | G | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.260-4242A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469781 | ||||||
| chr4:100469786
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-4247T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469786 | ||||||
| chr4:100469856
|
C | T | 200 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(197): Show | 204 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(201): Show |
intron_variant | MODIFIER | c.260-4317G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469856 | ||||||
| chr4:100469894
|
C | T | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.260-4355G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469894 | ||||||
| chr4:100469948
|
T | G | 58 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0127others(55): Show | 59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-4409A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469948 | ||||||
| chr4:100469959
|
A | G | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.260-4420T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469959 | ||||||
| chr4:100470076
|
C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-4537G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470076 | ||||||
| chr4:100470103
|
G | C | 1 | a0002c0002t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.260-4564C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470103 | ||||||
| chr4:100470214
|
TAACA | T | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-4679_260-4676d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470214 | ||||||
| chr4:100470263
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-4724A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470263 | ||||||
| chr4:100470313
|
C | A | 199 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(196): Show | 203 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(200): Show |
intron_variant | MODIFIER | c.259+4725G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470313 | ||||||
| chr4:100470322
|
C | G | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0222others(3): Show | 6 | HG00597.hp1 HG00673.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+4716G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470322 | ||||||
| chr4:100470378
|
T | TAAAA | 180 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(177): Show | 183 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(180): Show |
intron_variant | MODIFIER | c.259+4656_259+4659d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470378 | ||||||
| chr4:100470378
|
T | TAAAAA | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+4655_259+4659d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470378 | ||||||
| chr4:100470391
|
A | T | 1 | a0001c0001t0002g0230 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.259+4647T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470391 | ||||||
| chr4:100470403
|
G | T | 1 | a0002c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.259+4635C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470403 | ||||||
| chr4:100470439
|
T | C | 196 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(193): Show | 200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.259+4599A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470439 | ||||||
| chr4:100470593
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+4445A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470593 | ||||||
| chr4:100470897
|
G | A | 122 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(119): Show | 124 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.259+4141C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470897 | ||||||
| chr4:100470943
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.259+4095G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470943 | ||||||
| chr4:100470999
|
G | T | 14 | a0001c0001t0002g0021a0001c0001t0002g0024a0001c0001t0002g0025others(11): Show | 14 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+4039C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470999 | ||||||
| chr4:100471082
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+3956T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471082 | ||||||
| chr4:100471100
|
C | A | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.259+3938G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471100 | ||||||
| chr4:100471325
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259+3713G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471325 | ||||||
| chr4:100471335
|
G | A | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+3703C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471335 | ||||||
| chr4:100471424
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+3614T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471424 | ||||||
| chr4:100471505
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+3533T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471505 | ||||||
| chr4:100471507
|
A | G | 3 | a0001c0001t0006g0128a0001c0001t0006g0149a0001c0001t0033g0141 | 3 | HG00673.hp1 HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.259+3531T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471507 | ||||||
| chr4:100471564
|
A | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259+3474T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471564 | ||||||
| chr4:100471580
|
C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+3458G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471580 | ||||||
| chr4:100471622
|
C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+3416G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471622 | ||||||
| chr4:100471844
|
A | G | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.259+3194T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471844 | ||||||
| chr4:100471860
|
C | A | 2 | a0003c0003t0004g0158a0003c0003t0035g0198 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.259+3178G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471860 | ||||||
| chr4:100471903
|
C | T | 1 | a0002c0002t0007g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259+3135G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471903 | ||||||
| chr4:100471904
|
G | A | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.259+3134C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471904 | ||||||
| chr4:100472091
|
A | G | 197 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(194): Show | 201 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.259+2947T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472091 | ||||||
| chr4:100472191
|
T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+2847A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472191 | ||||||
| chr4:100472285
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259+2753A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472285 | ||||||
| chr4:100472349
|
T | A | 15 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(12): Show | 15 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+2689A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472349 | ||||||
| chr4:100472543
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.259+2495A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472543 | ||||||
| chr4:100472587
|
C | A | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+2451G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472587 | ||||||
| chr4:100472783
|
T | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259+2255A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472783 | ||||||
| chr4:100472892
|
C | T | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+2146G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472892 | ||||||
| chr4:100472919
|
TATAG | T | 4 | a0002c0002t0001g0060a0003c0003t0004g0158a0003c0003t0035g0198others(1): Show | 4 | HG02129.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+2115_259+2118d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472919 | ||||||
| chr4:100473009
|
T | TTA | 9 | a0001c0001t0002g0029a0001c0001t0034g0140a0002c0002t0001g0086others(6): Show | 9 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+2027_259+2028d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473009 | ||||||
| chr4:100473012
|
T | G | 1 | a0001c0001t0009g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.259+2026A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473012 | ||||||
| chr4:100473015
|
A | G | 1 | a0002c0002t0001g0062 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.259+2023T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473015 | ||||||
| chr4:100473019
|
A | AT | 9 | a0001c0001t0002g0205a0001c0001t0002g0225a0001c0001t0002g0236others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.259+2018dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473019 | ||||||
| chr4:100473021
|
A | AT | 114 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(111): Show | 116 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.259+2016dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473021 | ||||||
| chr4:100473021
|
A | T | 16 | a0001c0001t0002g0205a0001c0001t0002g0225a0001c0001t0002g0236others(13): Show | 16 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.259+2017T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473021 | ||||||
| chr4:100473022
|
T | TA | 46 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(43): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.259+2015_259+2016i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473022 | ||||||
| chr4:100473023
|
T | A | 11 | a0001c0001t0002g0122a0001c0001t0003g0210a0001c0001t0003g0255others(8): Show | 11 | HG00735.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.259+2015A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473023 | ||||||
| chr4:100473024
|
T | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+2014A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473024 | ||||||
| chr4:100473025
|
T | A | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+2013A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473025 | ||||||
| chr4:100473054
|
G | A | 16 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.259+1984C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473054 | ||||||
| chr4:100473168
|
C | T | 9 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(6): Show | 10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1870G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473168 | ||||||
| chr4:100473365
|
G | GTTTT | 12 | a0002c0002t0001g0002a0002c0002t0001g0050a0002c0002t0001g0051others(9): Show | 13 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.259+1669_259+1672d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTT | 17 | a0001c0001t0001g0196a0001c0001t0002g0032a0002c0002t0001g0017others(14): Show | 17 | HG00408.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.259+1668_259+1672d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTT | 17 | a0001c0001t0001g0195a0001c0001t0002g0024a0001c0001t0002g0028others(14): Show | 17 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.259+1667_259+1672d others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT | 12 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(9): Show | 12 | HG00408.hp1 HG00738.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+1666_259+1672d others(9): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT others(1): Show |
11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(8): Show | 11 | HG00642.hp2 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+1672_259+1673i others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT others(2): Show |
6 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0033others(3): Show | 7 | HG00741.hp2 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+1672_259+1673i others(11): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0023g0005 | 3 | HG02027.hp1 HG03927.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.259+1672_259+1673i others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0015 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259+1672_259+1673i others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0002g0014a0001c0001t0013g0008 | 2 | HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.259+1672_259+1673i others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
G | GTTTTTTT others(6): Show |
1 | a0002c0002t0001g0016 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.259+1672_259+1673i others(15): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+1663_259+1672d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.259+1662_259+1672d others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
GTTTTTTT others(5): Show |
G | 2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.259+1661_259+1672d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473365
|
GTTTTTTT others(6): Show |
G | 12 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+1660_259+1672d others(15): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | ||||||
| chr4:100473373
|
G | GT | 31 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(28): Show | 31 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.259+1664dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | ||||||
| chr4:100473373
|
G | GTT | 50 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0122others(47): Show | 51 | HG00597.hp1 HG00673.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.259+1663_259+1664d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | ||||||
| chr4:100473373
|
G | GTTT | 24 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0181others(21): Show | 24 | HG00597.hp2 HG01123.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.259+1662_259+1664d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | ||||||
| chr4:100473373
|
G | T | 86 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(83): Show | 88 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.259+1665C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | ||||||
| chr4:100473374
|
TTTTTTTT others(5): Show |
T | 6 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(3): Show | 7 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+1652_259+1663d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473374 | ||||||
| chr4:100473375
|
TTTTTTTT others(4): Show |
T | 3 | a0001c0004t0004g0248a0001c0004t0004g0249a0002c0006t0004g0048 | 3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.259+1652_259+1662d others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473375 | ||||||
| chr4:100473381
|
T | TG | 3 | a0001c0001t0005g0256a0004c0005t0017g0019a0004c0005t0017g0020 | 3 | HG00735.hp1 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.259+1656_259+1657i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473381 | ||||||
| chr4:100473386
|
G | T | 184 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(181): Show | 187 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.259+1652C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473386 | ||||||
| chr4:100473499
|
C | T | 3 | a0001c0001t0009g0121a0001c0001t0009g0242a0001c0001t0009g0243 | 3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.259+1539G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473499 | ||||||
| chr4:100473559
|
C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+1479G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473559 | ||||||
| chr4:100473599
|
A | G | 31 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(28): Show | 32 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+1439T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473599 | ||||||
| chr4:100473729
|
T | C | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259+1309A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473729 | ||||||
| chr4:100473812
|
CGAAAATT others(18): Show |
C | 2 | a0001c0001t0013g0246a0001c0001t0027g0247 | 2 | HG00741.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.259+1201_259+1225d others(27): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473812 | ||||||
| chr4:100473820
|
A | T | 1 | a0001c0001t0002g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.259+1218T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473820 | ||||||
| chr4:100473837
|
A | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0129 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.259+1201T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473837 | ||||||
| chr4:100474005
|
T | C | 89 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(86): Show | 90 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.259+1033A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474005 | ||||||
| chr4:100474019
|
A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.259+1019T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474019 | ||||||
| chr4:100474058
|
T | C | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+980A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474058 | ||||||
| chr4:100474487
|
C | T | 2 | a0003c0003t0004g0158a0003c0003t0035g0198 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.259+551G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474487 | ||||||
| chr4:100474513
|
A | C | 6 | a0002c0002t0001g0088a0002c0002t0001g0093a0002c0002t0001g0095others(3): Show | 6 | HG00597.hp2 HG01361.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+525T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474513 | ||||||
| chr4:100474556
|
T | C | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+482A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474556 | ||||||
| chr4:100474601
|
G | A | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+437C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474601 | ||||||
| chr4:100474763
|
T | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0037a0001c0001t0002g0038others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+275A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474763 | ||||||
| chr4:100474829
|
A | G | 138 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(135): Show | 141 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.259+209T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474829 | ||||||
| chr4:100474834
|
G | A | 18 | a0001c0001t0003g0207a0001c0001t0003g0255a0001c0001t0005g0173others(15): Show | 18 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.259+204C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474834 | ||||||
| chr4:100474954
|
G | A | 1 | a0002c0002t0009g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+84C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474954 | ||||||
| chr4:100475195
|
G | A | 89 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(86): Show | 90 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.188-86C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475195 | ||||||
| chr4:100475244
|
G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.188-135C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475244 | ||||||
| chr4:100475302
|
T | TAC | 9 | a0001c0001t0003g0220a0001c0001t0003g0235a0001c0001t0005g0200others(6): Show | 9 | HG01934.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-195_188-194dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACAC | 11 | a0001c0001t0002g0122a0001c0001t0006g0006a0001c0001t0006g0128others(8): Show | 11 | HG00673.hp1 HG00735.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-197_188-194dup others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACACAC | 24 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-199_188-194dup others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACACACA others(1): Show |
33 | a0001c0001t0002g0007a0001c0001t0002g0021a0001c0001t0002g0024others(30): Show | 34 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.188-201_188-194dup others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACACACA others(3): Show |
91 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0002g0003others(88): Show | 93 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.188-203_188-194dup others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACACACA others(5): Show |
17 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0182others(14): Show | 18 | HG00408.hp1 HG00673.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.188-205_188-194dup others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACACACA others(7): Show |
11 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0230others(8): Show | 11 | HG00741.hp2 HG01074.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-207_188-194dup others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
T | TACACACA others(9): Show |
6 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-209_188-194dup others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475302
|
TAC | T | 3 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113 | 3 | HG03041.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.188-195_188-194del others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | ||||||
| chr4:100475472
|
C | T | 11 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.188-363G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475472 | ||||||
| chr4:100475512
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.188-403A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475512 | ||||||
| chr4:100475534
|
T | C | 121 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(118): Show | 123 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.188-425A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475534 | ||||||
| chr4:100475658
|
CCTTTTTT others(1): Show |
C | 25 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0011others(22): Show | 26 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.188-557_188-550del others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475658 | ||||||
| chr4:100475658
|
CCTTTTTT others(2): Show |
C | 94 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(91): Show | 95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-558_188-550del others(9): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475658 | ||||||
| chr4:100475658
|
CCTTTTTT others(3): Show |
C | 17 | a0001c0001t0002g0035a0001c0001t0002g0122a0001c0001t0004g0004others(14): Show | 18 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-559_188-550del others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475658 | ||||||
| chr4:100475659
|
C | CT | 6 | a0001c0001t0003g0255a0001c0001t0005g0174a0001c0001t0005g0187others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-551dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
C | CTT | 5 | a0001c0001t0001g0101a0001c0001t0005g0173a0001c0001t0005g0183others(2): Show | 5 | HG02976.hp2 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-552_188-551dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CT | C | 11 | a0001c0001t0002g0214a0001c0001t0002g0216a0001c0001t0003g0102others(8): Show | 11 | HG00642.hp1 HG00642.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-551delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CTT | C | 6 | a0001c0001t0002g0189a0001c0001t0003g0217a0001c0001t0003g0218others(3): Show | 6 | HG01516.hp1 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-552_188-551del others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CTTTT | C | 13 | a0001c0001t0011g0112a0001c0001t0011g0113a0001c0001t0011g0114others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-554_188-551del others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CTTTTT | C | 8 | a0001c0001t0002g0176a0001c0001t0002g0181a0001c0001t0002g0221others(5): Show | 8 | HG00597.hp1 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-555_188-551del others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CTTTTTT | C | 34 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0127others(31): Show | 35 | HG00673.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.188-556_188-551del others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CTTTTTTT | C | 18 | a0001c0001t0002g0194a0001c0001t0006g0128a0001c0001t0006g0132others(15): Show | 18 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-557_188-551del others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475659
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-566_188-551del others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | ||||||
| chr4:100475666
|
T | A | 2 | a0001c0001t0004g0018a0001c0001t0020g0023 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.188-557A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475666 | ||||||
| chr4:100475666
|
T | G | 7 | a0001c0001t0002g0176a0001c0001t0002g0181a0001c0001t0002g0221others(4): Show | 7 | HG00597.hp1 HG00741.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-557A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475666 | ||||||
| chr4:100475667
|
T | A | 25 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0011others(22): Show | 26 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.188-558A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475667 | ||||||
| chr4:100475667
|
T | G | 34 | a0001c0001t0001g0182a0001c0001t0002g0003a0001c0001t0002g0127others(31): Show | 35 | HG00673.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.188-558A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475667 | ||||||
| chr4:100475668
|
T | A | 94 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185others(91): Show | 95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-559A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475668 | ||||||
| chr4:100475668
|
T | G | 16 | a0001c0001t0002g0194a0001c0001t0006g0128a0001c0001t0006g0132others(13): Show | 16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-559A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475668 | ||||||
| chr4:100475669
|
T | A | 17 | a0001c0001t0002g0035a0001c0001t0002g0122a0001c0001t0004g0004others(14): Show | 18 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-560A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475669 | ||||||
| chr4:100475669
|
T | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.188-560A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475669 | ||||||
| chr4:100475676
|
T | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0232 | 2 | HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188-567A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475676 | ||||||
| chr4:100475956
|
GAGCCACT others(6): Show |
G | 6 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(3): Show | 7 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-860_188-848del others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475956 | ||||||
| chr4:100476162
|
TCTCC | T | 21 | a0001c0001t0002g0122a0001c0001t0003g0212a0001c0001t0004g0154others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.188-1057_188-1054d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476162 | ||||||
| chr4:100476241
|
CTTTCCTT others(9): Show |
C | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.188-1148_188-1133d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476241 | ||||||
| chr4:100476687
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-1578T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476687 | ||||||
| chr4:100476721
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-1612G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476721 | ||||||
| chr4:100476824
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-1715T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476824 | ||||||
| chr4:100476869
|
G | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.188-1760C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476869 | ||||||
| chr4:100476878
|
G | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-1769C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476878 | ||||||
| chr4:100476922
|
C | G | 44 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(41): Show | 45 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.188-1813G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476922 | ||||||
| chr4:100476949
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.188-1840A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476949 | ||||||
| chr4:100476986
|
C | G | 1 | a0001c0001t0038g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.188-1877G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476986 | ||||||
| chr4:100477024
|
G | A | 9 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(6): Show | 10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-1915C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477024 | ||||||
| chr4:100477029
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-1920T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477029 | ||||||
| chr4:100477048
|
T | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-1939A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477048 | ||||||
| chr4:100477220
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-2111A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477220 | ||||||
| chr4:100477261
|
TAAAA | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-2156_188-2153d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477261 | ||||||
| chr4:100477365
|
C | CT | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.188-2257dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477365 | ||||||
| chr4:100477793
|
CT | C | 72 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(69): Show | 74 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.187+2123delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477793 | ||||||
| chr4:100477849
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.187+2068C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477849 | ||||||
| chr4:100477882
|
G | C | 152 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(149): Show | 155 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.187+2035C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477882 | ||||||
| chr4:100477944
|
A | C | 1 | a0001c0001t0005g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187+1973T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477944 | ||||||
| chr4:100477969
|
A | G | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+1948T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477969 | ||||||
| chr4:100478078
|
G | T | 9 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(6): Show | 10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+1839C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478078 | ||||||
| chr4:100478124
|
C | T | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.187+1793G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478124 | ||||||
| chr4:100478127
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(62): Show | 67 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.187+1790T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478127 | ||||||
| chr4:100478156
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(61): Show | 66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.187+1761G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478156 | ||||||
| chr4:100478348
|
C | T | 5 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1569G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478348 | ||||||
| chr4:100478502
|
T | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.187+1415A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478502 | ||||||
| chr4:100478546
|
G | C | 1 | a0001c0001t0002g0003 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.187+1371C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478546 | ||||||
| chr4:100478660
|
A | G | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1257T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478660 | ||||||
| chr4:100478663
|
C | T | 1 | a0002c0002t0001g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.187+1254G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478663 | ||||||
| chr4:100479078
|
C | A | 3 | a0001c0004t0004g0248a0001c0004t0004g0249a0002c0006t0004g0048 | 3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.187+839G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479078 | ||||||
| chr4:100479139
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.187+778C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479139 | ||||||
| chr4:100479268
|
T | A | 5 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0006g0142others(2): Show | 5 | HG00639.hp1 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+649A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479268 | ||||||
| chr4:100479271
|
G | GTTTTTC | 87 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0001g0017others(84): Show | 88 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.187+645_187+646ins others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479271 | ||||||
| chr4:100479348
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0041 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.187+569A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479348 | ||||||
| chr4:100479564
|
C | T | 4 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126others(1): Show | 4 | HG01975.hp1 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+353G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479564 | ||||||
| chr4:100479633
|
C | A | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.187+284G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479633 | ||||||
| chr4:100479681
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.187+236T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479681 | ||||||
| chr4:100479762
|
C | A | 1 | a0001c0001t0012g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.187+155G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479762 | ||||||
| chr4:100479845
|
A | G | 76 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0001g0017others(73): Show | 77 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.187+72T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479845 | ||||||
| chr4:100479858
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.187+59A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479858 | ||||||
| chr4:100480338
|
G | T | 145 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(142): Show | 148 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.65-299C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100480338 | ||||||
| chr4:100480585
|
CAT | C | 78 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0001g0017others(75): Show | 79 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.65-548_65-547delAT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100480585 | ||||||
| chr4:100480710
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-671G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100480710 | ||||||
| chr4:100481064
|
T | C | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-1025A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481064 | ||||||
| chr4:100481083
|
G | A | 1 | a0002c0002t0001g0100 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.65-1044C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481083 | ||||||
| chr4:100481145
|
G | A | 2 | a0001c0001t0011g0109a0001c0001t0011g0113 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.65-1106C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481145 | ||||||
| chr4:100481241
|
C | G | 76 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0001g0017others(73): Show | 77 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.65-1202G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481241 | ||||||
| chr4:100481344
|
T | C | 175 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(172): Show | 178 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(175): Show |
intron_variant | MODIFIER | c.65-1305A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481344 | ||||||
| chr4:100481381
|
G | C | 56 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(53): Show | 57 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.65-1342C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481381 | ||||||
| chr4:100481413
|
A | G | 12 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(9): Show | 12 | HG00735.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-1374T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481413 | ||||||
| chr4:100481492
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.65-1453G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481492 | ||||||
| chr4:100481673
|
A | G | 75 | a0002c0002t0001g0002a0002c0002t0001g0016a0002c0002t0001g0017others(72): Show | 76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.65-1634T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481673 | ||||||
| chr4:100481764
|
C | G | 8 | a0001c0001t0004g0004a0001c0001t0004g0131a0001c0001t0004g0250others(5): Show | 9 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-1725G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481764 | ||||||
| chr4:100481828
|
G | A | 14 | a0001c0001t0002g0122a0001c0001t0004g0004a0001c0001t0004g0131others(11): Show | 15 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-1789C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481828 | ||||||
| chr4:100481856
|
T | A | 1 | a0001c0001t0003g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-1817A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481856 | ||||||
| chr4:100482049
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.65-2010A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482049 | ||||||
| chr4:100482120
|
A | G | 2 | a0001c0001t0015g0022a0001c0001t0015g0115 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.65-2081T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482120 | ||||||
| chr4:100482304
|
T | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(65): Show | 70 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.65-2265A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482304 | ||||||
| chr4:100482310
|
T | C | 1 | a0002c0002t0001g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.65-2271A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482310 | ||||||
| chr4:100482319
|
T | C | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2280A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482319 | ||||||
| chr4:100482440
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-2401T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482440 | ||||||
| chr4:100482459
|
T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.65-2420A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482459 | ||||||
| chr4:100482620
|
T | C | 1 | a0001c0001t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.65-2581A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482620 | ||||||
| chr4:100482625
|
C | T | 1 | a0001c0001t0005g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.65-2586G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482625 | ||||||
| chr4:100482744
|
C | T | 2 | a0004c0005t0017g0019a0004c0005t0017g0020 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.65-2705G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482744 | ||||||
| chr4:100482880
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-2841G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482880 | ||||||
| chr4:100482907
|
A | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-2868T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482907 | ||||||
| chr4:100483033
|
A | G | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | NA18973.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.65-2994T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483033 | ||||||
| chr4:100483437
|
C | T | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-3398G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483437 | ||||||
| chr4:100483448
|
C | T | 1 | a0001c0001t0005g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-3409G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483448 | ||||||
| chr4:100483482
|
T | G | 1 | a0001c0001t0011g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-3443A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483482 | ||||||
| chr4:100483593
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-3554G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483593 | ||||||
| chr4:100484243
|
A | G | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.65-4204T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484243 | ||||||
| chr4:100484435
|
A | G | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-4396T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484435 | ||||||
| chr4:100484478
|
C | T | 3 | a0001c0001t0009g0121a0001c0001t0009g0242a0001c0001t0009g0243 | 3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-4439G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484478 | ||||||
| chr4:100484578
|
T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-4539A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484578 | ||||||
| chr4:100484924
|
T | C | 2 | a0002c0002t0001g0065a0002c0002t0001g0081 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.65-4885A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484924 | ||||||
| chr4:100484961
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-4922G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484961 | ||||||
| chr4:100485056
|
A | T | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5017T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485056 | ||||||
| chr4:100485262
|
G | T | 75 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(72): Show | 76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.65-5223C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485262 | ||||||
| chr4:100485308
|
T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-5269A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485308 | ||||||
| chr4:100485310
|
T | A | 1 | a0001c0001t0013g0246 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-5271A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485310 | ||||||
| chr4:100485429
|
C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-5390G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485429 | ||||||
| chr4:100485752
|
C | A | 127 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(124): Show | 129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.65-5713G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485752 | ||||||
| chr4:100485774
|
G | A | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.65-5735C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485774 | ||||||
| chr4:100485889
|
C | G | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-5850G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485889 | ||||||
| chr4:100485922
|
A | C | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-5883T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485922 | ||||||
| chr4:100486058
|
A | G | 1 | a0002c0002t0006g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-6019T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486058 | ||||||
| chr4:100486139
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-6100C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486139 | ||||||
| chr4:100486516
|
G | GTT | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-6479_65-6478dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486516 | ||||||
| chr4:100486624
|
A | T | 11 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(8): Show | 12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-6585T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486624 | ||||||
| chr4:100486801
|
C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.65-6762G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486801 | ||||||
| chr4:100486809
|
G | T | 28 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(25): Show | 29 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.65-6770C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486809 | ||||||
| chr4:100486882
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-6843T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486882 | ||||||
| chr4:100487401
|
G | T | 1 | a0002c0002t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.65-7362C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487401 | ||||||
| chr4:100487493
|
A | C | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-7454T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487493 | ||||||
| chr4:100487619
|
T | G | 1 | a0001c0001t0002g0245 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.65-7580A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487619 | ||||||
| chr4:100487621
|
T | C | 1 | a0001c0001t0006g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.65-7582A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487621 | ||||||
| chr4:100487649
|
G | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(28): Show | 32 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-7610C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487649 | ||||||
| chr4:100487802
|
C | T | 2 | a0002c0002t0016g0111a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.65-7763G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487802 | ||||||
| chr4:100488879
|
T | A | 7 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-8840A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100488879 | ||||||
| chr4:100489013
|
C | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-8974G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489013 | ||||||
| chr4:100489069
|
G | C | 31 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(28): Show | 32 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-9030C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489069 | ||||||
| chr4:100489233
|
G | T | 73 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(70): Show | 74 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.65-9194C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489233 | ||||||
| chr4:100489252
|
T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-9213A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489252 | ||||||
| chr4:100489497
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-9458T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489497 | ||||||
| chr4:100489625
|
A | G | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-9586T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489625 | ||||||
| chr4:100489749
|
C | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-9710G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489749 | ||||||
| chr4:100489797
|
A | G | 3 | a0002c0002t0007g0163a0002c0002t0007g0164a0002c0002t0007g0165 | 3 | HG01070.hp1 HG01071.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.65-9758T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489797 | ||||||
| chr4:100489819
|
C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-9780G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489819 | ||||||
| chr4:100489926
|
G | C | 7 | a0002c0002t0001g0139a0002c0002t0001g0144a0002c0002t0001g0146others(4): Show | 7 | HG01109.hp1 HG01123.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-9887C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489926 | ||||||
| chr4:100490174
|
T | TA | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.65-10136dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490174 | ||||||
| chr4:100490178
|
A | G | 5 | a0001c0001t0002g0122a0001c0001t0004g0154a0001c0001t0004g0156others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-10139T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490178 | ||||||
| chr4:100490249
|
C | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-10210G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490249 | ||||||
| chr4:100490393
|
C | A | 1 | a0001c0001t0012g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.65-10354G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490393 | ||||||
| chr4:100490750
|
G | T | 129 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(126): Show | 131 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.65-10711C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490750 | ||||||
| chr4:100490922
|
T | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-10883A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490922 | ||||||
| chr4:100491048
|
T | G | 1 | a0002c0002t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.65-11009A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491048 | ||||||
| chr4:100491241
|
C | A | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-11202G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491241 | ||||||
| chr4:100491245
|
A | G | 1 | a0002c0002t0031g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.65-11206T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491245 | ||||||
| chr4:100491261
|
T | C | 1 | a0002c0002t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-11222A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491261 | ||||||
| chr4:100491316
|
G | A | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-11277C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491316 | ||||||
| chr4:100491541
|
A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.65-11502T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491541 | ||||||
| chr4:100491765
|
C | G | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-11726G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491765 | ||||||
| chr4:100491857
|
C | A | 28 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(25): Show | 29 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.65-11818G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491857 | ||||||
| chr4:100491884
|
T | G | 70 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(67): Show | 71 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.65-11845A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491884 | ||||||
| chr4:100491983
|
G | A | 22 | a0001c0001t0006g0006a0001c0001t0006g0128a0001c0001t0006g0133others(19): Show | 22 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-11944C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491983 | ||||||
| chr4:100492103
|
G | A | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12064C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492103 | ||||||
| chr4:100492118
|
A | G | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-12079T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492118 | ||||||
| chr4:100492385
|
G | C | 3 | a0001c0001t0015g0022a0001c0001t0015g0115a0001c0001t0020g0023 | 3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.65-12346C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492385 | ||||||
| chr4:100492426
|
C | T | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-12387G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492426 | ||||||
| chr4:100492453
|
A | G | 1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.65-12414T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492453 | ||||||
| chr4:100492510
|
C | G | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-12471G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492510 | ||||||
| chr4:100492672
|
ACAT | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-12636_65-12634d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492672 | ||||||
| chr4:100492845
|
C | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12806G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492845 | ||||||
| chr4:100493123
|
G | A | 1 | a0001c0001t0012g0238 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.65-13084C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493123 | ||||||
| chr4:100493217
|
C | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-13178G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493217 | ||||||
| chr4:100493241
|
G | A | 3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | HG01257.hp1 HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.65-13202C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493241 | ||||||
| chr4:100493410
|
G | A | 2 | a0001c0008t0005g0197a0002c0002t0001g0066 | 2 | HG02056.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.65-13371C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493410 | ||||||
| chr4:100493554
|
A | T | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-13515T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493554 | ||||||
| chr4:100493599
|
CTTCTA | C | 3 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0014g0137 | 3 | NA18980.hp2 NA19060.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.65-13565_65-13561d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493599 | ||||||
| chr4:100493684
|
C | G | 1 | a0001c0008t0005g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.65-13645G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493684 | ||||||
| chr4:100493763
|
C | G | 1 | a0001c0001t0003g0206 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.65-13724G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493763 | ||||||
| chr4:100493868
|
C | T | 1 | a0002c0002t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.65-13829G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493868 | ||||||
| chr4:100494120
|
G | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035 | 3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-14081C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494120 | ||||||
| chr4:100494272
|
T | C | 135 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(132): Show | 138 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.65-14233A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494272 | ||||||
| chr4:100494422
|
G | T | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-14383C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494422 | ||||||
| chr4:100494761
|
C | T | 69 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(66): Show | 70 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.65-14722G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494761 | ||||||
| chr4:100494787
|
C | CT | 11 | a0001c0001t0002g0122a0002c0002t0001g0169a0002c0002t0001g0170others(8): Show | 11 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-14749dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494787 | ||||||
| chr4:100494947
|
A | AT | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-14909dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494947 | ||||||
| chr4:100495007
|
T | A | 174 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(171): Show | 177 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(174): Show |
intron_variant | MODIFIER | c.65-14968A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495007 | ||||||
| chr4:100495622
|
G | A | 1 | a0001c0001t0011g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-15583C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495622 | ||||||
| chr4:100495648
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.65-15609G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495648 | ||||||
| chr4:100495764
|
A | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-15725T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495764 | ||||||
| chr4:100495874
|
T | C | 139 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(136): Show | 142 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.65-15835A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495874 | ||||||
| chr4:100496016
|
C | T | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.65-15977G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100496016 | ||||||
| chr4:100496517
|
C | G | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.65-16478G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100496517 | ||||||
| chr4:100496604
|
A | C | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.65-16565T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100496604 | ||||||
| chr4:100497066
|
G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-17027C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497066 | ||||||
| chr4:100497113
|
A | G | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-17074T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497113 | ||||||
| chr4:100497239
|
T | C | 29 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0004g0154others(26): Show | 29 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-17200A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497239 | ||||||
| chr4:100497246
|
T | TAA | 8 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(5): Show | 8 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-17209_65-17208d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497246 | ||||||
| chr4:100497246
|
TAA | T | 5 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-17209_65-17208d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497246 | ||||||
| chr4:100497323
|
A | G | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.65-17284T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497323 | ||||||
| chr4:100497387
|
T | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0245a0001c0001t0005g0244 | 3 | HG02886.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.65-17348A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497387 | ||||||
| chr4:100497416
|
G | T | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.65-17377C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497416 | ||||||
| chr4:100497427
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-17388T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497427 | ||||||
| chr4:100497435
|
A | G | 135 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(132): Show | 138 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.65-17396T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497435 | ||||||
| chr4:100497520
|
G | C | 125 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(122): Show | 127 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.65-17481C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497520 | ||||||
| chr4:100497668
|
T | G | 135 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(132): Show | 138 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.65-17629A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497668 | ||||||
| chr4:100497829
|
G | A | 3 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-17790C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497829 | ||||||
| chr4:100498115
|
G | A | 2 | a0001c0001t0006g0128a0001c0001t0006g0149 | 2 | HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.65-18076C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498115 | ||||||
| chr4:100498274
|
A | G | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.65-18235T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498274 | ||||||
| chr4:100498303
|
G | A | 7 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-18264C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498303 | ||||||
| chr4:100498648
|
G | T | 80 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(77): Show | 81 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.65-18609C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498648 | ||||||
| chr4:100498732
|
G | A | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-18693C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498732 | ||||||
| chr4:100499054
|
G | A | 1 | a0001c0001t0008g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.64+18797C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499054 | ||||||
| chr4:100499059
|
AT | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+18791delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499059 | ||||||
| chr4:100499336
|
T | G | 2 | a0001c0001t0011g0109a0001c0001t0011g0113 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64+18515A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499336 | ||||||
| chr4:100499374
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+18477T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499374 | ||||||
| chr4:100499448
|
C | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+18403G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499448 | ||||||
| chr4:100499811
|
G | A | 1 | a0002c0002t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.64+18040C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499811 | ||||||
| chr4:100499998
|
A | G | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.64+17853T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499998 | ||||||
| chr4:100500101
|
T | TA | 7 | a0001c0001t0004g0004a0001c0001t0004g0250a0001c0001t0004g0251others(4): Show | 8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+17749dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500101 | ||||||
| chr4:100500150
|
A | G | 2 | a0002c0002t0026g0049a0002c0006t0004g0048 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+17701T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500150 | ||||||
| chr4:100500303
|
C | A | 1 | a0001c0001t0004g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+17548G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500303 | ||||||
| chr4:100500478
|
T | C | 1 | a0002c0002t0016g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64+17373A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500478 | ||||||
| chr4:100500734
|
A | G | 2 | a0001c0001t0006g0133a0001c0001t0006g0134 | 2 | HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64+17117T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500734 | ||||||
| chr4:100500794
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+17057T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500794 | ||||||
| chr4:100500892
|
A | T | 134 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(131): Show | 137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.64+16959T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500892 | ||||||
| chr4:100500967
|
T | C | 11 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0046others(8): Show | 12 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+16884A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500967 | ||||||
| chr4:100501010
|
T | G | 1 | a0001c0001t0008g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+16841A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501010 | ||||||
| chr4:100501120
|
G | A | 135 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(132): Show | 138 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.64+16731C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501120 | ||||||
| chr4:100501195
|
G | C | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+16656C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501195 | ||||||
| chr4:100501386
|
A | G | 14 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0183others(11): Show | 14 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+16465T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501386 | ||||||
| chr4:100501572
|
T | C | 23 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(20): Show | 23 | HG00597.hp2 HG01192.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+16279A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501572 | ||||||
| chr4:100501594
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64+16257A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501594 | ||||||
| chr4:100501638
|
T | C | 13 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0046others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+16213A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501638 | ||||||
| chr4:100501855
|
G | GT | 33 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(30): Show | 34 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+15995dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501855 | ||||||
| chr4:100502007
|
T | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+15844A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502007 | ||||||
| chr4:100502013
|
G | A | 1 | a0001c0001t0003g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+15838C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502013 | ||||||
| chr4:100502015
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0002g0193others(2): Show | 5 | HG02027.hp1 NA18943.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+15836G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502015 | ||||||
| chr4:100502023
|
A | G | 1 | a0002c0002t0003g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.64+15828T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502023 | ||||||
| chr4:100502106
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+15745C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502106 | ||||||
| chr4:100502162
|
T | C | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64+15689A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502162 | ||||||
| chr4:100502169
|
A | G | 135 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(132): Show | 138 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.64+15682T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502169 | ||||||
| chr4:100502256
|
T | A | 3 | a0001c0001t0015g0022a0001c0001t0015g0115a0001c0001t0020g0023 | 3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64+15595A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502256 | ||||||
| chr4:100502861
|
T | G | 3 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077 | 3 | HG00408.hp2 NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.64+14990A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502861 | ||||||
| chr4:100503231
|
T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+14620A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503231 | ||||||
| chr4:100503248
|
C | T | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64+14603G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503248 | ||||||
| chr4:100503327
|
G | C | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+14524C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503327 | ||||||
| chr4:100503336
|
TTTGGCAT others(12): Show |
T | 6 | a0001c0001t0005g0183a0001c0001t0005g0191a0001c0001t0005g0192others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+14496_64+14514d others(21): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503336 | ||||||
| chr4:100503420
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+14431T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503420 | ||||||
| chr4:100503549
|
T | C | 1 | a0004c0005t0017g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64+14302A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503549 | ||||||
| chr4:100503712
|
A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+14139T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503712 | ||||||
| chr4:100503827
|
A | G | 4 | a0001c0001t0002g0189a0001c0001t0003g0186a0001c0001t0003g0188others(1): Show | 4 | HG01258.hp2 HG01516.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+14024T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503827 | ||||||
| chr4:100504076
|
A | G | 3 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0012g0026 | 3 | HG00738.hp1 HG01106.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.64+13775T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504076 | ||||||
| chr4:100504192
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.64+13659T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504192 | ||||||
| chr4:100504240
|
G | A | 1 | a0001c0001t0027g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64+13611C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504240 | ||||||
| chr4:100504302
|
A | C | 127 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(124): Show | 129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+13549T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504302 | ||||||
| chr4:100504320
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+13531C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504320 | ||||||
| chr4:100504352
|
T | A | 1 | a0002c0002t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.64+13499A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504352 | ||||||
| chr4:100504422
|
T | G | 29 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0004g0154others(26): Show | 29 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+13429A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504422 | ||||||
| chr4:100504517
|
C | A | 3 | a0002c0002t0001g0078a0002c0002t0001g0079a0002c0002t0001g0080 | 3 | HG02132.hp2 NA18984.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.64+13334G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504517 | ||||||
| chr4:100504579
|
TAGG | T | 125 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(122): Show | 127 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.64+13269_64+13271d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504579 | ||||||
| chr4:100504721
|
C | T | 125 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(122): Show | 127 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.64+13130G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504721 | ||||||
| chr4:100504877
|
G | T | 1 | a0001c0001t0008g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+12974C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504877 | ||||||
| chr4:100504940
|
T | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+12911A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504940 | ||||||
| chr4:100505108
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0185 | 3 | HG00408.hp1 NA19012.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.64+12743T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505108 | ||||||
| chr4:100505197
|
G | A | 4 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | NA18747.hp2 NA18955.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+12654C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505197 | ||||||
| chr4:100505241
|
G | C | 2 | a0001c0001t0013g0246a0001c0001t0027g0247 | 2 | HG00741.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.64+12610C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505241 | ||||||
| chr4:100505310
|
G | A | 33 | a0001c0001t0004g0131a0001c0001t0004g0154a0001c0001t0004g0156others(30): Show | 33 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.64+12541C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505310 | ||||||
| chr4:100505505
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(39): Show | 43 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.64+12346G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505505 | ||||||
| chr4:100505571
|
C | A | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+12280G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505571 | ||||||
| chr4:100505575
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64+12276A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505575 | ||||||
| chr4:100505665
|
T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+12186A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505665 | ||||||
| chr4:100505693
|
C | T | 1 | a0001c0001t0003g0085 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.64+12158G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505693 | ||||||
| chr4:100505701
|
C | T | 2 | a0004c0005t0017g0019a0004c0005t0017g0020 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.64+12150G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505701 | ||||||
| chr4:100505732
|
C | G | 40 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(37): Show | 41 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.64+12119G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505732 | ||||||
| chr4:100505804
|
T | TA | 4 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0001t0011g0113others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+12046dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505804 | ||||||
| chr4:100505836
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64+12015G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505836 | ||||||
| chr4:100506075
|
A | T | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64+11776T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506075 | ||||||
| chr4:100506132
|
A | G | 3 | a0001c0001t0015g0022a0001c0001t0015g0115a0001c0001t0020g0023 | 3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64+11719T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506132 | ||||||
| chr4:100506139
|
A | C | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.64+11712T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506139 | ||||||
| chr4:100506255
|
T | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64+11596A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506255 | ||||||
| chr4:100506384
|
A | G | 2 | a0001c0004t0004g0248a0001c0004t0004g0249 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.64+11467T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506384 | ||||||
| chr4:100506414
|
C | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+11437G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506414 | ||||||
| chr4:100506468
|
T | C | 127 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(124): Show | 129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+11383A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506468 | ||||||
| chr4:100506481
|
G | A | 6 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+11370C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506481 | ||||||
| chr4:100506516
|
G | A | 173 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(170): Show | 176 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(173): Show |
intron_variant | MODIFIER | c.64+11335C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506516 | ||||||
| chr4:100506531
|
C | A | 2 | a0001c0001t0028g0175a0003c0003t0036g0160 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64+11320G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506531 | ||||||
| chr4:100506548
|
T | C | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+11303A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506548 | ||||||
| chr4:100506671
|
T | C | 127 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(124): Show | 129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+11180A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506671 | ||||||
| chr4:100506820
|
G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+11031C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506820 | ||||||
| chr4:100507056
|
T | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0037a0001c0001t0002g0038others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+10795A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507056 | ||||||
| chr4:100507097
|
T | A | 125 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(122): Show | 127 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.64+10754A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507097 | ||||||
| chr4:100507657
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.64+10194G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507657 | ||||||
| chr4:100507829
|
C | T | 2 | a0001c0001t0005g0183a0003c0003t0036g0160 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.64+10022G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507829 | ||||||
| chr4:100507901
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+9950T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507901 | ||||||
| chr4:100507910
|
A | G | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+9941T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507910 | ||||||
| chr4:100508232
|
A | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG00408.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64+9619T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508232 | ||||||
| chr4:100508296
|
T | A | 133 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(130): Show | 136 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.64+9555A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508296 | ||||||
| chr4:100508451
|
T | C | 133 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(130): Show | 136 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.64+9400A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508451 | ||||||
| chr4:100508569
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64+9282T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508569 | ||||||
| chr4:100508797
|
T | G | 1 | a0002c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+9054A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508797 | ||||||
| chr4:100508953
|
G | C | 175 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(172): Show | 178 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(175): Show |
intron_variant | MODIFIER | c.64+8898C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508953 | ||||||
| chr4:100509142
|
A | T | 53 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(50): Show | 54 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.64+8709T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509142 | ||||||
| chr4:100509344
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+8507T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509344 | ||||||
| chr4:100509485
|
A | G | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+8366T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509485 | ||||||
| chr4:100509488
|
G | C | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+8363C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509488 | ||||||
| chr4:100509568
|
T | C | 1 | a0001c0001t0006g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64+8283A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509568 | ||||||
| chr4:100509589
|
C | A | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+8262G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509589 | ||||||
| chr4:100509613
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+8238G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509613 | ||||||
| chr4:100509662
|
A | C | 2 | a0002c0002t0016g0110a0002c0002t0016g0111 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.64+8189T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509662 | ||||||
| chr4:100509697
|
G | A | 1 | a0002c0002t0001g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+8154C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509697 | ||||||
| chr4:100509915
|
T | TTAG | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+7933_64+7935dup others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509915 | ||||||
| chr4:100510014
|
T | G | 2 | a0002c0002t0003g0082a0002c0002t0003g0083 | 2 | NA18984.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.64+7837A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510014 | ||||||
| chr4:100510102
|
T | G | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+7749A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510102 | ||||||
| chr4:100510106
|
G | C | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+7745C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510106 | ||||||
| chr4:100510448
|
G | A | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+7403C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510448 | ||||||
| chr4:100510575
|
C | T | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64+7276G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510575 | ||||||
| chr4:100510787
|
A | G | 3 | a0001c0001t0011g0109a0001c0001t0011g0113a0001c0001t0011g0114 | 3 | HG02486.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64+7064T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510787 | ||||||
| chr4:100510928
|
G | A | 75 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(72): Show | 76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.64+6923C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510928 | ||||||
| chr4:100511032
|
A | G | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+6819T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511032 | ||||||
| chr4:100511057
|
G | C | 1 | a0001c0001t0009g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64+6794C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511057 | ||||||
| chr4:100511103
|
C | T | 3 | a0001c0001t0015g0022a0001c0001t0015g0115a0001c0001t0020g0023 | 3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64+6748G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511103 | ||||||
| chr4:100511298
|
A | G | 1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64+6553T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511298 | ||||||
| chr4:100511384
|
T | A | 5 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0006g0157others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+6467A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511384 | ||||||
| chr4:100511488
|
T | A | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+6363A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511488 | ||||||
| chr4:100511537
|
C | A | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.64+6314G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511537 | ||||||
| chr4:100511672
|
G | A | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+6179C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511672 | ||||||
| chr4:100511692
|
G | T | 128 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(125): Show | 130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+6159C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511692 | ||||||
| chr4:100511836
|
T | TA | 134 | a0001c0001t0001g0101a0001c0001t0002g0001a0001c0001t0002g0007others(131): Show | 137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.64+6014dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511836 | ||||||
| chr4:100511985
|
T | C | 1 | a0001c0001t0032g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.64+5866A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511985 | ||||||
| chr4:100511999
|
A | G | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.64+5852T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511999 | ||||||
| chr4:100512097
|
G | A | 23 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(20): Show | 23 | HG00597.hp2 HG01192.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+5754C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512097 | ||||||
| chr4:100512139
|
C | A | 1 | a0002c0002t0001g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+5712G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512139 | ||||||
| chr4:100512178
|
G | A | 34 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(31): Show | 35 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.64+5673C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512178 | ||||||
| chr4:100512186
|
G | A | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+5665C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512186 | ||||||
| chr4:100512517
|
A | T | 1 | a0001c0001t0006g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64+5334T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512517 | ||||||
| chr4:100512622
|
T | C | 1 | a0001c0001t0008g0120 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64+5229A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512622 | ||||||
| chr4:100512750
|
G | A | 75 | a0001c0001t0001g0101a0001c0001t0003g0085a0001c0001t0003g0102others(72): Show | 76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.64+5101C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512750 | ||||||
| chr4:100512786
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.64+5065T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512786 | ||||||
| chr4:100512806
|
CA | C | 5 | a0001c0001t0002g0021a0001c0001t0002g0181a0001c0001t0012g0180others(2): Show | 5 | HG01070.hp1 HG01192.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+5044delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512806 | ||||||
| chr4:100512906
|
T | C | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+4945A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512906 | ||||||
| chr4:100513207
|
G | A | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(126): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+4644C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513207 | ||||||
| chr4:100513584
|
T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64+4267A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513584 | ||||||
| chr4:100513596
|
A | C | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(126): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+4255T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513596 | ||||||
| chr4:100513613
|
G | T | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+4238C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513613 | ||||||
| chr4:100513755
|
T | C | 1 | a0002c0002t0001g0108 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.64+4096A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513755 | ||||||
| chr4:100513999
|
T | C | 1 | a0001c0001t0011g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64+3852A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513999 | ||||||
| chr4:100514140
|
C | T | 3 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0126 | 3 | HG01975.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.64+3711G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514140 | ||||||
| chr4:100514224
|
A | G | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.64+3627T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514224 | ||||||
| chr4:100514236
|
A | C | 13 | a0001c0001t0002g0122a0001c0001t0028g0175a0002c0002t0001g0169others(10): Show | 13 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+3615T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514236 | ||||||
| chr4:100514694
|
T | C | 2 | a0001c0001t0005g0256a0001c0001t0005g0257 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.64+3157A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514694 | ||||||
| chr4:100514955
|
T | C | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.64+2896A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514955 | ||||||
| chr4:100515044
|
A | G | 71 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(68): Show | 72 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.64+2807T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515044 | ||||||
| chr4:100515161
|
G | T | 40 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(37): Show | 41 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.64+2690C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515161 | ||||||
| chr4:100515309
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+2542A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515309 | ||||||
| chr4:100515406
|
G | A | 1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64+2445C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515406 | ||||||
| chr4:100515509
|
G | A | 128 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(125): Show | 130 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+2342C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515509 | ||||||
| chr4:100515701
|
T | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+2150A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515701 | ||||||
| chr4:100515835
|
A | AAAAC | 13 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0010others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+2012_64+2015dup others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515835 | ||||||
| chr4:100516003
|
T | TG | 117 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(114): Show | 119 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.64+1847dupC | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516003 | ||||||
| chr4:100516097
|
C | T | 4 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | NA18747.hp2 NA18955.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1754G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516097 | ||||||
| chr4:100516185
|
G | T | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(126): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+1666C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516185 | ||||||
| chr4:100516208
|
A | G | 38 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0004g0131others(35): Show | 38 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.64+1643T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516208 | ||||||
| chr4:100516357
|
A | G | 130 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.64+1494T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516357 | ||||||
| chr4:100516366
|
C | T | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(126): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+1485G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516366 | ||||||
| chr4:100516372
|
T | C | 1 | a0001c0001t0003g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.64+1479A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516372 | ||||||
| chr4:100516389
|
G | GGA | 10 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0004g0162others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+1460_64+1461dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516389 | ||||||
| chr4:100516427
|
T | C | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(126): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+1424A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516427 | ||||||
| chr4:100516522
|
A | G | 168 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(165): Show | 170 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.64+1329T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516522 | ||||||
| chr4:100516693
|
T | C | 1 | a0001c0001t0015g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64+1158A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516693 | ||||||
| chr4:100516735
|
A | G | 2 | a0001c0001t0005g0173a0001c0001t0005g0174 | 2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.64+1116T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516735 | ||||||
| chr4:100516829
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+1022T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516829 | ||||||
| chr4:100516863
|
T | C | 5 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+988A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516863 | ||||||
| chr4:100516932
|
C | T | 1 | a0003c0003t0002g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.64+919G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516932 | ||||||
| chr4:100517018
|
G | A | 167 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(164): Show | 169 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.64+833C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517018 | ||||||
| chr4:100517233
|
T | C | 168 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(165): Show | 170 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.64+618A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517233 | ||||||
| chr4:100517350
|
C | T | 169 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(166): Show | 171 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(168): Show |
intron_variant | MODIFIER | c.64+501G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517350 | ||||||
| chr4:100517417
|
A | C | 118 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(115): Show | 120 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.64+434T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517417 |