| geneid | 79603 |
|---|---|
| ensemblid | ENSG00000090661.12 |
| hgncid | 23747 |
| symbol | CERS4 |
| name | ceramide synthase 4 |
| refseq_nuc | NM_024552.3 |
| refseq_prot | NP_078828.2 |
| ensembl_nuc | ENST00000251363.10 |
| ensembl_prot | ENSP00000251363.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 8209370 |
| end | 8262421 |
| strand | + |
| ver | v1.2 |
| region | chr19:8209370-8262421 |
| region5000 | chr19:8204370-8267421 |
| regionname0 | CERS4_chr19_8209370_8262421 |
| regionname5000 | CERS4_chr19_8204370_8267421 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 394 | 274 | 42 | 60 | 125 | 14 | 33 | 97 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002 | 0/0 | 394 | 56 | 24 | 3 | 26 | 0 | 3 | 20 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003 | 1/1 | 394 | 54 | 21 | 4 | 18 | 2 | 7 | 11 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004 | 0/0 | 394 | 26 | 6 | 8 | 7 | 0 | 5 | 4 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0005 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0006 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0007 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0008 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0009 | 0/0 | 394 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0010 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1185 | 168 | 30 | 27 | 77 | 7 | 27 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0002 | 0/0 | 1185 | 72 | 3 | 24 | 32 | 7 | 6 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0003 | 0/0 | 1185 | 54 | 23 | 3 | 26 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0004 | 1/1 | 1185 | 37 | 9 | 2 | 18 | 1 | 5 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0005 | 0/0 | 1185 | 20 | 3 | 8 | 4 | 0 | 5 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0006 | 0/0 | 1185 | 20 | 0 | 7 | 13 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0007 | 0/0 | 1185 | 15 | 11 | 1 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0008 | 0/0 | 1185 | 9 | 5 | 2 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0009 | 0/0 | 1185 | 5 | 3 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0010 | 0/0 | 1185 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0011 | 0/0 | 1185 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0012 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0013 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0014 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0015 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0016 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0017 | 0/0 | 1185 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0018 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0019 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0020 | 0/0 | 1185 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0021 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0022 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0023 | 0/0 | 1185 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0024 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| c0025 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 595 | 86 | 36 | 10 | 28 | 2 | 9 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0002 | 0/0 | 595 | 85 | 10 | 14 | 46 | 2 | 13 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0003 | 0/0 | 595 | 76 | 16 | 11 | 32 | 4 | 13 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0004 | 1/0 | 595 | 51 | 11 | 3 | 31 | 1 | 4 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0005 | 0/0 | 595 | 37 | 0 | 20 | 11 | 4 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0006 | 0/0 | 595 | 32 | 0 | 8 | 20 | 2 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0007 | 0/0 | 595 | 18 | 8 | 5 | 3 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0008 | 0/0 | 595 | 16 | 7 | 4 | 2 | 0 | 3 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0009 | 0/0 | 595 | 5 | 4 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0010 | 0/0 | 595 | 4 | 3 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0011 | 0/0 | 595 | 2 | 0 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0012 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0013 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0014 | 0/0 | 595 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0015 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0016 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| t0017 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| 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 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0412 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0413 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0414 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0415 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0416 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| g0417 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1185 | 168 | 30 | 27 | 77 | 7 | 27 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002 | 0/0 | 1185 | 72 | 3 | 24 | 32 | 7 | 6 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0006 | 0/0 | 1185 | 20 | 0 | 7 | 13 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0008 | 0/0 | 1185 | 9 | 5 | 2 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0012 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0015 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0019 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0021 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0025 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0003 | 0/0 | 1185 | 54 | 23 | 3 | 26 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0013 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0023 | 0/0 | 1185 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0004 | 1/1 | 1185 | 37 | 9 | 2 | 18 | 1 | 5 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0007 | 0/0 | 1185 | 15 | 11 | 1 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0014 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0020 | 0/0 | 1185 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0005 | 0/0 | 1185 | 20 | 3 | 8 | 4 | 0 | 5 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0009 | 0/0 | 1185 | 5 | 3 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0018 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0005c0011 | 0/0 | 1185 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0006c0010 | 0/0 | 1185 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0007c0022 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0008c0024 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0009c0017 | 0/0 | 1185 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0010c0016 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1779 | 7 | 4 | 0 | 0 | 0 | 3 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0002 | 0/0 | 1779 | 73 | 8 | 12 | 39 | 2 | 12 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0003 | 0/0 | 1779 | 67 | 13 | 10 | 30 | 4 | 10 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0004 | 0/0 | 1779 | 7 | 0 | 0 | 7 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0005 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0006 | 0/0 | 1779 | 5 | 0 | 2 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0008 | 0/0 | 1779 | 2 | 1 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0010 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0012 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0016 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0001t0017 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0001 | 0/0 | 1779 | 14 | 2 | 6 | 5 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0002 | 0/0 | 1779 | 5 | 0 | 2 | 2 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0003 | 0/0 | 1779 | 3 | 0 | 0 | 1 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0004 | 0/0 | 1779 | 9 | 1 | 0 | 7 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0005 | 0/0 | 1779 | 23 | 0 | 11 | 6 | 4 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0006 | 0/0 | 1779 | 17 | 0 | 5 | 11 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0002t0014 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0006t0005 | 0/0 | 1779 | 10 | 0 | 6 | 4 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0006t0006 | 0/0 | 1779 | 9 | 0 | 1 | 8 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0006t0013 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0008t0001 | 0/0 | 1779 | 4 | 3 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0008t0003 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0008t0004 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0008t0005 | 0/0 | 1779 | 2 | 0 | 2 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0012t0002 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0015t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0019t0002 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0021t0005 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0001c0025t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0003t0001 | 0/0 | 1779 | 25 | 16 | 1 | 6 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0003t0002 | 0/0 | 1779 | 5 | 0 | 0 | 5 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0003t0004 | 0/0 | 1779 | 21 | 4 | 2 | 15 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0003t0008 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0013t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0002c0023t0003 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0004t0001 | 0/1 | 1779 | 29 | 5 | 2 | 16 | 1 | 4 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0004t0004 | 1/0 | 1779 | 7 | 4 | 0 | 1 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0004t0009 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0007t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0007t0003 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0007t0004 | 0/0 | 1779 | 4 | 0 | 1 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0007t0009 | 0/0 | 1779 | 4 | 4 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0007t0010 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0014t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0003c0020t0001 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0005t0007 | 0/0 | 1779 | 8 | 1 | 5 | 0 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0005t0008 | 0/0 | 1779 | 10 | 2 | 3 | 2 | 0 | 3 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0005t0011 | 0/0 | 1779 | 2 | 0 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0009t0007 | 0/0 | 1779 | 5 | 3 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0004c0018t0007 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0005c0011t0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0006c0010t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0006c0010t0015 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0007c0022t0004 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0008c0024t0008 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0009c0017t0003 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| a0010c0016t0006 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | copy fasta | chr19 | 8204370 | 8267421 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0007g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0008g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0008g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0016g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0412 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0003g0416 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0003g0417 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0413 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0414 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0014g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0013g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0012t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0015t0001g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0019t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0021t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0025t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0008g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0008g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0013t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0023t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0009g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0014t0001g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0020t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0415 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0011g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0018t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0005c0011t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0005c0011t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0006c0010t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0006c0010t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0007c0022t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0008c0024t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0009c0017t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0010c0016t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0006 | g0386 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00099 | hp2 | a0001 | c0002 | t0005 | g0073 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0220 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00140 | hp2 | a0003 | c0004 | t0001 | g0069 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0065 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0163 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0102 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0302 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00408 | hp1 | a0002 | c0003 | t0004 | g0249 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00408 | hp2 | a0002 | c0003 | t0004 | g0304 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00423 | hp1 | a0002 | c0003 | t0004 | g0332 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0363 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00438 | hp2 | a0003 | c0004 | t0001 | g0151 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00544 | hp1 | a0003 | c0004 | t0001 | g0201 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00558 | hp1 | a0004 | c0005 | t0011 | g0320 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00558 | hp2 | a0001 | c0006 | t0013 | g0260 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0175 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00639 | hp1 | a0001 | c0006 | t0005 | g0194 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0082 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00642 | hp2 | a0001 | c0002 | t0006 | g0247 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00673 | hp1 | a0001 | c0008 | t0003 | g0250 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00673 | hp2 | a0001 | c0006 | t0005 | g0186 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00735 | hp2 | a0001 | c0002 | t0005 | g0059 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00738 | hp1 | a0004 | c0005 | t0007 | g0384 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0378 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00741 | hp1 | a0004 | c0005 | t0008 | g0104 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00741 | hp2 | a0004 | c0005 | t0008 | g0095 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0414 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01069 | hp2 | a0001 | c0006 | t0005 | g0190 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0412 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0079 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01074 | hp2 | a0001 | c0002 | t0005 | g0074 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01081 | hp1 | a0002 | c0003 | t0004 | g0354 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01081 | hp2 | a0003 | c0007 | t0004 | g0299 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01099 | hp1 | a0001 | c0002 | t0005 | g0081 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01099 | hp2 | a0001 | c0006 | t0005 | g0207 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01106 | hp1 | a0009 | c0017 | t0003 | g0162 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01109 | hp1 | a0001 | c0008 | t0005 | g0034 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0057 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01175 | hp1 | a0001 | c0002 | t0006 | g0242 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01243 | hp2 | a0001 | c0002 | t0006 | g0298 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01255 | hp1 | a0003 | c0020 | t0001 | g0080 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01258 | hp1 | a0004 | c0005 | t0008 | g0192 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01261 | hp1 | a0001 | c0006 | t0005 | g0198 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0398 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01346 | hp1 | a0001 | c0002 | t0006 | g0238 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0379 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01358 | hp1 | a0001 | c0002 | t0006 | g0280 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01358 | hp2 | a0001 | c0002 | t0005 | g0090 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0355 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01433 | hp2 | a0003 | c0004 | t0001 | g0041 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01496 | hp2 | a0004 | c0005 | t0007 | g0292 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01515 | hp2 | a0001 | c0002 | t0005 | g0055 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0359 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0067 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0392 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0052 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01928 | hp2 | a0001 | c0006 | t0005 | g0155 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0401 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01934 | hp2 | a0001 | c0002 | t0005 | g0045 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0385 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01952 | hp2 | a0001 | c0002 | t0005 | g0393 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01975 | hp2 | a0001 | c0002 | t0005 | g0072 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0039 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01981 | hp1 | a0002 | c0003 | t0004 | g0293 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01981 | hp2 | a0001 | c0006 | t0005 | g0195 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01993 | hp2 | a0001 | c0006 | t0006 | g0305 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02004 | hp2 | a0004 | c0005 | t0007 | g0294 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02015 | hp2 | a0001 | c0006 | t0005 | g0087 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02027 | hp2 | a0003 | c0004 | t0009 | g0334 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02055 | hp1 | a0001 | c0008 | t0001 | g0188 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02055 | hp2 | a0003 | c0007 | t0010 | g0006 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0157 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02071 | hp2 | a0001 | c0006 | t0006 | g0264 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02080 | hp2 | a0001 | c0002 | t0005 | g0038 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02083 | hp1 | a0004 | c0005 | t0008 | g0394 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02129 | hp2 | a0003 | c0004 | t0001 | g0028 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02135 | hp1 | a0003 | c0004 | t0001 | g0021 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0396 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02148 | hp1 | a0001 | c0008 | t0005 | g0076 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02148 | hp2 | a0004 | c0005 | t0007 | g0217 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02155 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | CDX | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CDX | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02257 | hp2 | a0003 | c0007 | t0009 | g0340 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0037 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02258 | hp2 | a0003 | c0014 | t0001 | g0406 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02273 | hp2 | a0004 | c0005 | t0007 | g0290 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02280 | hp1 | a0001 | c0012 | t0002 | g0145 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02280 | hp2 | a0002 | c0013 | t0001 | g0129 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0365 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02300 | hp2 | a0001 | c0001 | t0016 | g0094 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0402 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02451 | hp2 | a0004 | c0005 | t0008 | g0209 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02523 | hp1 | a0004 | c0005 | t0008 | g0160 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0130 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0400 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02602 | hp2 | a0001 | c0002 | t0005 | g0058 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02615 | hp1 | a0001 | c0008 | t0001 | g0051 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02622 | hp1 | a0004 | c0009 | t0007 | g0291 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0114 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0408 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02630 | hp2 | a0003 | c0004 | t0004 | g0277 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02647 | hp1 | a0003 | c0004 | t0001 | g0132 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02647 | hp2 | a0001 | c0025 | t0001 | g0116 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0405 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02735 | hp1 | a0004 | c0005 | t0008 | g0415 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0411 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02818 | hp1 | a0001 | c0008 | t0004 | g0282 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0062 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02886 | hp2 | a0006 | c0010 | t0001 | g0092 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0106 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02895 | hp2 | a0002 | c0003 | t0004 | g0382 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0043 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0383 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02897 | hp1 | a0002 | c0003 | t0004 | g0276 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0061 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02922 | hp1 | a0003 | c0007 | t0003 | g0127 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02922 | hp2 | a0003 | c0004 | t0004 | g0275 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02965 | hp1 | a0005 | c0011 | t0007 | g0286 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02965 | hp2 | a0001 | c0008 | t0004 | g0357 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02970 | hp1 | a0004 | c0009 | t0007 | g0336 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02970 | hp2 | a0005 | c0011 | t0007 | g0284 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02976 | hp1 | a0003 | c0007 | t0009 | g0387 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02976 | hp2 | a0001 | c0019 | t0002 | g0377 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03017 | hp1 | a0003 | c0004 | t0001 | g0077 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0203 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0404 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03041 | hp2 | a0003 | c0007 | t0009 | g0120 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03098 | hp2 | a0006 | c0010 | t0015 | g0093 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03130 | hp1 | a0003 | c0007 | t0003 | g0126 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0390 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03139 | hp1 | a0004 | c0005 | t0007 | g0002 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03139 | hp2 | a0004 | c0009 | t0007 | g0285 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03195 | hp2 | a0003 | c0007 | t0010 | g0032 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0288 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0040 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03225 | hp1 | a0002 | c0003 | t0008 | g0395 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0369 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0351 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03453 | hp1 | a0003 | c0007 | t0009 | g0141 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03486 | hp1 | a0002 | c0003 | t0004 | g0356 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03486 | hp2 | a0002 | c0003 | t0008 | g0403 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0279 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0216 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0210 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0399 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03540 | hp2 | a0001 | c0015 | t0001 | g0409 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03579 | hp1 | a0008 | c0024 | t0008 | g0108 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03579 | hp2 | a0004 | c0005 | t0008 | g0053 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0119 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03669 | hp2 | a0003 | c0007 | t0004 | g0283 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03688 | hp1 | a0004 | c0005 | t0008 | g0251 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03688 | hp2 | a0004 | c0005 | t0008 | g0054 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0417 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03704 | hp2 | a0003 | c0007 | t0004 | g0317 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03710 | hp2 | a0003 | c0004 | t0004 | g0328 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03831 | hp2 | a0003 | c0004 | t0001 | g0091 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0226 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03927 | hp1 | a0003 | c0004 | t0001 | g0078 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03942 | hp1 | a0004 | c0005 | t0007 | g0124 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0416 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0281 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0337 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04228 | hp1 | a0003 | c0004 | t0001 | g0206 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04228 | hp2 | a0004 | c0005 | t0007 | g0287 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0410 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18522 | hp2 | a0002 | c0003 | t0008 | g0107 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0381 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18747 | hp2 | a0001 | c0002 | t0004 | g0239 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18939 | hp1 | a0003 | c0004 | t0001 | g0023 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18943 | hp1 | a0001 | c0006 | t0005 | g0180 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18943 | hp2 | a0002 | c0003 | t0004 | g0331 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18945 | hp1 | a0001 | c0002 | t0005 | g0086 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18946 | hp1 | a0010 | c0016 | t0006 | g0212 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18948 | hp1 | a0001 | c0006 | t0006 | g0274 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0335 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0215 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0374 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18957 | hp1 | a0003 | c0004 | t0001 | g0044 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18957 | hp2 | a0001 | c0002 | t0006 | g0241 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18959 | hp1 | a0001 | c0006 | t0006 | g0349 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18959 | hp2 | a0003 | c0004 | t0001 | g0017 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18960 | hp2 | a0001 | c0002 | t0006 | g0235 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18963 | hp1 | a0004 | c0005 | t0011 | g0307 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18964 | hp1 | a0002 | c0003 | t0002 | g0306 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0165 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0240 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18969 | hp2 | a0001 | c0002 | t0005 | g0063 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18970 | hp2 | a0002 | c0003 | t0004 | g0227 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18973 | hp2 | a0001 | c0006 | t0006 | g0271 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0389 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18974 | hp2 | a0001 | c0002 | t0006 | g0324 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18977 | hp1 | a0001 | c0002 | t0005 | g0199 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0182 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18979 | hp2 | a0002 | c0003 | t0004 | g0308 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18980 | hp1 | a0003 | c0004 | t0004 | g0272 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18983 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18984 | hp1 | a0001 | c0002 | t0005 | g0084 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0259 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18985 | hp2 | a0001 | c0002 | t0005 | g0200 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18988 | hp1 | a0001 | c0002 | t0006 | g0342 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18988 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18993 | hp1 | a0003 | c0004 | t0001 | g0027 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18993 | hp2 | a0001 | c0006 | t0006 | g0380 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0371 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18995 | hp1 | a0001 | c0002 | t0006 | g0234 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18997 | hp1 | a0001 | c0021 | t0005 | g0189 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18997 | hp2 | a0002 | c0003 | t0004 | g0213 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18999 | hp2 | a0002 | c0003 | t0004 | g0309 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0150 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19000 | hp2 | a0001 | c0006 | t0006 | g0266 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19002 | hp2 | a0004 | c0018 | t0007 | g0325 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19004 | hp1 | a0002 | c0003 | t0004 | g0372 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19004 | hp2 | a0003 | c0004 | t0001 | g0020 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19007 | hp1 | a0001 | c0006 | t0005 | g0193 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19007 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19010 | hp1 | a0001 | c0002 | t0006 | g0268 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19010 | hp2 | a0001 | c0002 | t0006 | g0214 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0366 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0060 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19043 | hp1 | a0003 | c0004 | t0004 | g0278 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0187 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19055 | hp1 | a0001 | c0002 | t0006 | g0310 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19056 | hp1 | a0004 | c0009 | t0007 | g0134 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19057 | hp2 | a0001 | c0006 | t0006 | g0232 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19059 | hp1 | a0001 | c0002 | t0006 | g0322 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0388 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19064 | hp2 | a0007 | c0022 | t0004 | g0224 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19065 | hp1 | a0002 | c0003 | t0004 | g0376 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19065 | hp2 | a0002 | c0003 | t0004 | g0319 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0185 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19070 | hp1 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19074 | hp2 | a0002 | c0003 | t0004 | g0229 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19078 | hp1 | a0002 | c0003 | t0004 | g0367 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0167 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19081 | hp2 | a0001 | c0002 | t0006 | g0237 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19085 | hp2 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19087 | hp1 | a0004 | c0009 | t0007 | g0248 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19087 | hp2 | a0002 | c0003 | t0004 | g0273 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19088 | hp1 | a0001 | c0006 | t0006 | g0261 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0323 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19091 | hp1 | a0001 | c0008 | t0001 | g0085 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19240 | hp1 | a0001 | c0008 | t0001 | g0211 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0407 | AFR | ASW | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | ASW | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20752 | hp1 | a0003 | c0007 | t0004 | g0300 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20752 | hp2 | a0001 | c0002 | t0005 | g0413 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0083 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20805 | hp2 | a0001 | c0002 | t0014 | g0056 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | GIH | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20905 | hp2 | a0002 | c0023 | t0003 | g0009 | SAS | GIH | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02109 | hp1 | a0003 | c0007 | t0003 | g0128 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0391 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02486 | hp1 | a0003 | c0004 | t0004 | g0252 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0118 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0397 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02559 | hp2 | a0003 | c0007 | t0010 | g0033 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0109 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG06807 | hp2 | a0002 | c0003 | t0004 | g0143 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18955 | hp1 | a0002 | c0003 | t0004 | g0233 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0360 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0231 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0001 | g0088 | REF | REF | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| homoSapiens_grch38 | hp1 | a0003 | c0004 | t0004 | g0350 | REF | REF | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8254569
|
G | A | 1 | a0006 | 2 | HG02886.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.244G>A | p.Ala82Thr | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/12 | 527/1780 | 244/1185 | 82/394 | chr19 | 8254569 | ||
| chr19:8255671
|
G | A | 3 | a0002a0007a0008 | 58 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
missense_variant | MODERATE | c.356G>A | p.Arg119Gln | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/12 | 639/1780 | 356/1185 | 119/394 | chr19 | 8255671 | ||
| chr19:8256706
|
G | A | 1 | a0007 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.608G>A | p.Arg203His | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/12 | 891/1780 | 608/1185 | 203/394 | chr19 | 8256706 | ||
| chr19:8257001
|
T | C | 1 | a0005 | 2 | HG02965.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.665T>C | p.Phe222Ser | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/12 | 948/1780 | 665/1185 | 222/394 | chr19 | 8257001 | ||
| chr19:8261740
|
G | A | 1 | a0010 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.901G>A | p.Gly301Ser | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/12 | 1184/1780 | 901/1185 | 301/394 | chr19 | 8261740 | ||
| chr19:8261982
|
C | T | 3 | a0004a0005a0008 | 29 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
missense_variant | MODERATE | c.1058C>T | p.Ala353Val | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 1341/1780 | 1058/1185 | 353/394 | chr19 | 8261982 | ||
| chr19:8262020
|
G | A | 5 | a0001a0002a0006others(2): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
missense_variant | MODERATE | c.1096G>A | p.Ala366Thr | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 1379/1780 | 1096/1185 | 366/394 | chr19 | 8262020 | ||
| chr19:8262060
|
G | A | 3 | a0004a0005a0009 | 29 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
missense_variant | MODERATE | c.1136G>A | p.Arg379Gln | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 1419/1780 | 1136/1185 | 379/394 | chr19 | 8262060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8254571
|
C | T | 5 | a0001c0025a0002c0003a0002c0023others(2): Show | 58 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
synonymous_variant | LOW | c.246C>T | p.Ala82Ala | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/12 | 529/1780 | 246/1185 | 82/394 | chr19 | 8254571 | ||
| chr19:8255645
|
G | A | 1 | a0001c0012 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.330G>A | p.Thr110Thr | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/12 | 613/1780 | 330/1185 | 110/394 | chr19 | 8255645 | ||
| chr19:8256286
|
G | A | 1 | a0003c0014 | 1 | HG02258.hp2 | splice_region_variant&synonymous_variant | LOW | c.519G>A | p.Gln173Gln | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/12 | 802/1780 | 519/1185 | 173/394 | chr19 | 8256286 | ||
| chr19:8256678
|
C | T | 2 | a0001c0006a0001c0021 | 21 | HG00558.hp2 HG00639.hp1 HG00673.hp2 others(18): Show |
synonymous_variant | LOW | c.580C>T | p.Leu194Leu | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/12 | 863/1780 | 580/1185 | 194/394 | chr19 | 8256678 | ||
| chr19:8257053
|
C | T | 8 | a0001c0008a0001c0025a0002c0003others(5): Show | 89 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
synonymous_variant | LOW | c.717C>T | p.His239His | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/12 | 1000/1780 | 717/1185 | 239/394 | chr19 | 8257053 | ||
| chr19:8257062
|
T | C | 8 | a0001c0001a0001c0012a0001c0015others(5): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
synonymous_variant | LOW | c.726T>C | p.Ser242Ser | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/12 | 1009/1780 | 726/1185 | 242/394 | chr19 | 8257062 | ||
| chr19:8257923
|
C | T | 1 | a0001c0015 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.786C>T | p.Asp262Asp | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/12 | 1069/1780 | 786/1185 | 262/394 | chr19 | 8257923 | ||
| chr19:8261724
|
C | T | 1 | a0001c0019 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.885C>T | p.Asn295Asn | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/12 | 1168/1780 | 885/1185 | 295/394 | chr19 | 8261724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8209370
|
A | G | 33 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(30): Show | 223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
5_prime_UTR_variant | MODIFIER | c.-283A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/12 | 41707 | chr19 | 8209370 | |||||
| chr19:8210798
|
C | T | 1 | a0001c0006t0013 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/12 | 40279 | chr19 | 8210798 | |||||
| chr19:8262115
|
C | T | 10 | a0001c0001t0007a0001c0001t0008a0002c0003t0008others(7): Show | 36 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 6 | chr19 | 8262115 | |||||
| chr19:8262171
|
A | G | 1 | a0004c0005t0011 | 2 | HG00558.hp1 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*62A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 62 | chr19 | 8262171 | |||||
| chr19:8262271
|
C | T | 2 | a0001c0001t0012a0001c0001t0017 | 2 | HG02572.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*162C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 162 | chr19 | 8262271 | |||||
| chr19:8262277
|
A | G | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(26): Show | 210 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 168 | chr19 | 8262277 | |||||
| chr19:8262312
|
G | C | 11 | a0001c0001t0005a0001c0001t0006a0001c0001t0016others(8): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 203 | chr19 | 8262312 | |||||
| chr19:8262348
|
C | T | 1 | a0001c0006t0013 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 239 | chr19 | 8262348 | |||||
| chr19:8262360
|
G | A | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(23): Show | 202 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*251G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 251 | chr19 | 8262360 | |||||
| chr19:8262369
|
G | T | 1 | a0001c0002t0014 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 260 | chr19 | 8262369 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8209503
|
G | A | 1 | a0004c0005t0007g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-159+9G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209503 | ||||||
| chr19:8209604
|
T | G | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-159+110T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209604 | ||||||
| chr19:8209666
|
T | C | 1 | a0001c0002t0004g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-159+172T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209666 | ||||||
| chr19:8209687
|
C | G | 3 | a0001c0002t0003g0416a0001c0002t0003g0417a0004c0005t0008g0415 | 3 | HG02735.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-159+193C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209687 | ||||||
| chr19:8209776
|
C | T | 3 | a0001c0002t0001g0412a0001c0002t0005g0413a0001c0002t0005g0414 | 3 | HG01069.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-159+282C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209776 | ||||||
| chr19:8209800
|
G | T | 17 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0003g0397others(14): Show | 17 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-159+306G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209800 | ||||||
| chr19:8209850
|
G | T | 1 | a0004c0005t0008g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-159+356G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209850 | ||||||
| chr19:8209929
|
T | A | 1 | a0001c0001t0003g0005 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-159+435T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209929 | ||||||
| chr19:8209945
|
C | T | 1 | a0001c0002t0005g0393 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-159+451C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209945 | ||||||
| chr19:8210022
|
C | CCAGGAAA others(16): Show |
139 | a0001c0001t0001g0117a0001c0001t0001g0407a0001c0001t0001g0408others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-159+532_-159+533i others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 8210022 | |||||
| chr19:8210269
|
G | A | 2 | a0001c0001t0007g0121a0003c0007t0009g0120 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-158-437G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210269 | ||||||
| chr19:8210336
|
G | A | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-158-370G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210336 | ||||||
| chr19:8210359
|
T | C | 17 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0003g0397others(14): Show | 17 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-158-347T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210359 | ||||||
| chr19:8210393
|
T | C | 1 | a0001c0002t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-158-313T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210393 | ||||||
| chr19:8210559
|
G | A | 1 | a0004c0005t0007g0124 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-158-147G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210559 | ||||||
| chr19:8210562
|
A | G | 3 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0001g0392 | 3 | HG01891.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-158-144A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210562 | ||||||
| chr19:8210565
|
G | T | 1 | a0001c0002t0005g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-158-141G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210565 | ||||||
| chr19:8210602
|
ACTGGGGC others(31): Show |
A | 4 | a0001c0001t0001g0125a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-99_-158-62del others(38): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 8210602 | |||||
| chr19:8210616
|
G | C | 5 | a0001c0001t0003g0131a0001c0001t0003g0133a0001c0001t0017g0130others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-90G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210616 | ||||||
| chr19:8210678
|
C | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0137a0001c0001t0002g0139others(3): Show | 6 | HG00621.hp1 HG02015.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-158-28C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210678 | ||||||
| chr19:8210885
|
G | C | 16 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0003g0397others(13): Show | 16 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2+23G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8210885 | ||||||
| chr19:8211009
|
G | A | 7 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0144others(4): Show | 7 | HG02280.hp1 HG02723.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+147G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211009 | ||||||
| chr19:8211018
|
C | T | 9 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0003g0133others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+156C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211018 | ||||||
| chr19:8211070
|
T | C | 47 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0003g0005others(44): Show | 47 | HG00609.hp1 HG01261.hp2 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.-2+208T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211070 | ||||||
| chr19:8211142
|
C | T | 14 | a0001c0001t0001g0117a0001c0001t0003g0105a0001c0001t0003g0110others(11): Show | 14 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+280C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211142 | ||||||
| chr19:8211182
|
G | A | 13 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(10): Show | 13 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+320G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211182 | ||||||
| chr19:8211196
|
G | C | 125 | a0001c0001t0001g0125a0001c0001t0001g0202a0001c0001t0001g0204others(122): Show | 125 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2+334G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211196 | ||||||
| chr19:8211234
|
CCTGT | C | 63 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2+373_-2+376delCT others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211234 | ||||||
| chr19:8211280
|
G | A | 4 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0015t0001g0409others(1): Show | 4 | HG02630.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+418G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211280 | ||||||
| chr19:8211802
|
G | A | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-2+940G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211802 | ||||||
| chr19:8211890
|
C | CA | 116 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-2+1051dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | |||||
| chr19:8211890
|
C | CAA | 14 | a0001c0001t0001g0125a0001c0001t0001g0407a0001c0001t0001g0408others(11): Show | 14 | HG00438.hp2 HG01943.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2+1050_-2+1051dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | |||||
| chr19:8211890
|
CA | C | 16 | a0001c0001t0002g0385a0001c0001t0002g0388a0001c0001t0002g0389others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2+1051delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | |||||
| chr19:8211890
|
CAA | C | 27 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(24): Show | 27 | HG00609.hp1 HG01891.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-2+1050_-2+1051del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | |||||
| chr19:8212057
|
G | T | 1 | a0001c0001t0002g0389 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-2+1195G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212057 | ||||||
| chr19:8212105
|
A | C | 2 | a0001c0001t0002g0378a0001c0001t0006g0379 | 2 | HG00738.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-2+1243A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212105 | ||||||
| chr19:8212161
|
C | T | 1 | a0001c0002t0002g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2+1299C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212161 | ||||||
| chr19:8212307
|
G | A | 24 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258others(21): Show | 25 | HG00558.hp2 HG02071.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2+1445G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212307 | ||||||
| chr19:8212326
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-2+1464G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212326 | ||||||
| chr19:8212448
|
A | T | 1 | a0001c0019t0002g0377 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+1586A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212448 | ||||||
| chr19:8212591
|
C | T | 1 | a0001c0002t0003g0417 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2+1729C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212591 | ||||||
| chr19:8212633
|
A | T | 216 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(213): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-2+1771A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212633 | ||||||
| chr19:8212640
|
A | AT | 77 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(74): Show | 77 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-2+1786dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8212640 | |||||
| chr19:8212640
|
A | T | 114 | a0001c0001t0001g0117a0001c0001t0003g0005a0001c0001t0003g0011others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-2+1778A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212640 | ||||||
| chr19:8212642
|
T | TA | 4 | a0001c0002t0003g0416a0001c0002t0003g0417a0003c0007t0010g0006others(1): Show | 4 | HG02055.hp2 HG02735.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1780_-2+1781ins others(1): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212642 | ||||||
| chr19:8212643
|
T | A | 5 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0015t0001g0409others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+1781T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212643 | ||||||
| chr19:8212648
|
T | A | 1 | a0001c0002t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-2+1786T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212648 | ||||||
| chr19:8212663
|
A | T | 1 | a0002c0003t0004g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-2+1801A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212663 | ||||||
| chr19:8212715
|
T | G | 100 | a0001c0001t0001g0125a0001c0001t0001g0202a0001c0001t0001g0204others(97): Show | 100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-2+1853T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212715 | ||||||
| chr19:8212732
|
G | A | 116 | a0001c0001t0001g0117a0001c0001t0003g0005a0001c0001t0003g0011others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-2+1870G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212732 | ||||||
| chr19:8212829
|
A | G | 214 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(211): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.-2+1967A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212829 | ||||||
| chr19:8212830
|
A | G | 2 | a0001c0001t0003g0153a0002c0003t0001g0043 | 2 | HG02896.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.-2+1968A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212830 | ||||||
| chr19:8212849
|
T | C | 100 | a0001c0001t0001g0125a0001c0001t0001g0202a0001c0001t0001g0204others(97): Show | 100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-2+1987T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212849 | ||||||
| chr19:8212940
|
G | A | 1 | a0001c0002t0005g0393 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-2+2078G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212940 | ||||||
| chr19:8213319
|
T | C | 1 | a0001c0006t0006g0274 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-2+2457T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213319 | ||||||
| chr19:8213440
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-2+2578A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213440 | ||||||
| chr19:8213478
|
A | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(4): Show | 7 | HG02683.hp2 HG03017.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+2616A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213478 | ||||||
| chr19:8213560
|
A | G | 35 | a0001c0001t0003g0005a0001c0001t0003g0011a0001c0001t0003g0012others(32): Show | 35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+2698A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213560 | ||||||
| chr19:8213597
|
T | C | 266 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0407others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-2+2735T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213597 | ||||||
| chr19:8213701
|
C | T | 1 | a0002c0003t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2+2839C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213701 | ||||||
| chr19:8213708
|
G | A | 64 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+2846G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213708 | ||||||
| chr19:8213731
|
C | T | 65 | a0001c0001t0002g0003a0001c0001t0002g0218a0001c0001t0002g0219others(62): Show | 65 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-2+2869C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213731 | ||||||
| chr19:8213737
|
G | A | 1 | a0003c0007t0009g0387 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-2+2875G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213737 | ||||||
| chr19:8213895
|
G | C | 9 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0003g0133others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+3033G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213895 | ||||||
| chr19:8213920
|
C | T | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2+3058C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213920 | ||||||
| chr19:8214061
|
G | GTC | 5 | a0001c0002t0001g0208a0001c0002t0005g0199a0001c0002t0005g0200others(2): Show | 5 | HG00438.hp2 HG00544.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3200_-2+3201dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214061 | |||||
| chr19:8214062
|
T | TCACA | 29 | a0001c0001t0003g0005a0001c0001t0003g0011a0001c0001t0003g0012others(26): Show | 29 | HG00609.hp1 HG00741.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2+3212_-2+3215dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214062 | |||||
| chr19:8214062
|
T | TCACACA | 5 | a0001c0002t0001g0042a0001c0002t0001g0098a0001c0002t0001g0099others(2): Show | 5 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3210_-2+3215dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214062 | |||||
| chr19:8214072
|
A | G | 107 | a0001c0001t0002g0003a0001c0001t0002g0218a0001c0001t0002g0219others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-2+3210A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214072 | ||||||
| chr19:8214084
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-2+3222G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214084 | ||||||
| chr19:8214159
|
T | C | 34 | a0001c0001t0003g0005a0001c0001t0003g0011a0001c0001t0003g0012others(31): Show | 34 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+3297T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214159 | ||||||
| chr19:8214164
|
CTG | C | 89 | a0001c0001t0001g0117a0001c0001t0001g0407a0001c0001t0001g0408others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-2+3306_-2+3307del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214164 | |||||
| chr19:8214236
|
T | C | 1 | a0002c0003t0001g0399 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2+3374T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214236 | ||||||
| chr19:8214412
|
C | T | 34 | a0001c0001t0003g0005a0001c0001t0003g0011a0001c0001t0003g0012others(31): Show | 34 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+3550C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214412 | ||||||
| chr19:8214631
|
G | A | 5 | a0001c0001t0003g0131a0001c0001t0003g0133a0001c0001t0017g0130others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3769G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214631 | ||||||
| chr19:8214708
|
C | A | 62 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(59): Show | 62 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-2+3846C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214708 | ||||||
| chr19:8214715
|
TG | T | 32 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(29): Show | 32 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2+3857delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214715 | |||||
| chr19:8214773
|
C | T | 5 | a0002c0003t0004g0276a0002c0003t0004g0382a0003c0004t0004g0275others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3911C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214773 | ||||||
| chr19:8214818
|
C | T | 3 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396 | 3 | HG01261.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-2+3956C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214818 | ||||||
| chr19:8214938
|
C | CGAGGGGG others(38): Show |
4 | a0001c0008t0001g0211a0002c0003t0001g0210a0003c0007t0010g0006others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+4099_-2+4143dup others(45): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214938 | |||||
| chr19:8214942
|
G | GGGGAGGA others(2): Show |
35 | a0001c0001t0001g0407a0001c0001t0003g0011a0001c0001t0003g0012others(32): Show | 35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+4089_-2+4097dup others(9): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214942 | |||||
| chr19:8214961
|
GGGAGGAG others(35): Show |
G | 85 | a0001c0001t0001g0117a0001c0001t0003g0035a0001c0001t0003g0036others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.-2+4133_-2+4174del others(42): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214961 | |||||
| chr19:8214975
|
A | AAGGAAGA others(8): Show |
64 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+4118_-2+4132dup others(15): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214975 | |||||
| chr19:8214989
|
G | GGAGGAA | 33 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(30): Show | 33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+4132_-2+4133ins others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214989 | |||||
| chr19:8215037
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-2+4175C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215037 | ||||||
| chr19:8215223
|
G | T | 1 | a0003c0007t0010g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2+4361G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215223 | ||||||
| chr19:8215298
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-2+4436G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215298 | ||||||
| chr19:8215346
|
G | A | 1 | a0001c0002t0005g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2+4484G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215346 | ||||||
| chr19:8215377
|
G | A | 90 | a0001c0001t0001g0117a0001c0001t0003g0035a0001c0001t0003g0036others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-2+4515G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215377 | ||||||
| chr19:8215405
|
G | C | 33 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(30): Show | 33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+4543G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215405 | ||||||
| chr19:8215478
|
C | CA | 15 | a0001c0001t0001g0202a0001c0001t0002g0256a0001c0001t0003g0154others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+4629dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8215478 | |||||
| chr19:8215478
|
C | CAA | 26 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(23): Show | 26 | HG00609.hp1 HG02040.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2+4628_-2+4629dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8215478 | |||||
| chr19:8215487
|
AAAAAC | A | 7 | a0002c0003t0001g0400a0002c0003t0001g0401a0002c0003t0001g0411others(4): Show | 7 | HG01934.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+4630_-2+4634del others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8215487 | |||||
| chr19:8215516
|
T | C | 1 | a0001c0006t0005g0155 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-2+4654T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215516 | ||||||
| chr19:8215577
|
C | G | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+4715C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215577 | ||||||
| chr19:8215596
|
C | G | 3 | a0001c0002t0006g0386a0003c0007t0004g0299a0003c0007t0004g0300 | 3 | HG00099.hp1 HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-2+4734C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215596 | ||||||
| chr19:8215737
|
C | G | 106 | a0001c0001t0001g0117a0001c0001t0001g0407a0001c0001t0001g0408others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-2+4875C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215737 | ||||||
| chr19:8215939
|
C | T | 1 | a0001c0002t0006g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-2+5077C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215939 | ||||||
| chr19:8216056
|
C | A | 1 | a0001c0001t0008g0390 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+5194C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216056 | ||||||
| chr19:8216091
|
T | C | 64 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+5229T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216091 | ||||||
| chr19:8216103
|
G | C | 1 | a0004c0005t0008g0415 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2+5241G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216103 | ||||||
| chr19:8216148
|
G | A | 1 | a0001c0019t0002g0377 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+5286G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216148 | ||||||
| chr19:8216239
|
C | T | 1 | a0004c0005t0007g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-2+5377C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216239 | ||||||
| chr19:8216251
|
C | T | 1 | a0002c0003t0001g0405 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-2+5389C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216251 | ||||||
| chr19:8216358
|
G | A | 3 | a0002c0003t0001g0400a0002c0003t0001g0401a0002c0003t0001g0411 | 3 | HG01934.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-2+5496G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216358 | ||||||
| chr19:8216380
|
G | GA | 12 | a0001c0001t0001g0125a0001c0001t0002g0301a0001c0001t0003g0131others(9): Show | 12 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+5533dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8216380 | |||||
| chr19:8216549
|
G | A | 12 | a0001c0001t0001g0117a0001c0001t0003g0105a0001c0001t0003g0110others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+5687G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216549 | ||||||
| chr19:8216611
|
G | GA | 6 | a0001c0001t0003g0035a0001c0001t0003g0046a0001c0001t0003g0047others(3): Show | 6 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+5757dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8216611 | |||||
| chr19:8216622
|
A | T | 1 | a0002c0003t0004g0233 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+5760A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216622 | ||||||
| chr19:8216685
|
G | GAAATTTC others(29): Show |
1 | a0002c0003t0004g0233 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+5825_-2+5860dup others(36): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8216685 | |||||
| chr19:8216751
|
G | A | 325 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-2+5889G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216751 | ||||||
| chr19:8216760
|
G | T | 64 | a0001c0001t0002g0003a0001c0001t0002g0218a0001c0001t0002g0219others(61): Show | 64 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+5898G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216760 | ||||||
| chr19:8216821
|
C | T | 4 | a0001c0001t0002g0373a0001c0001t0002g0375a0001c0002t0004g0374others(1): Show | 4 | NA18956.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+5959C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216821 | ||||||
| chr19:8217115
|
T | C | 33 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(30): Show | 33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+6253T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217115 | ||||||
| chr19:8217280
|
G | A | 1 | a0004c0005t0008g0415 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2+6418G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217280 | ||||||
| chr19:8217394
|
A | T | 33 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(30): Show | 33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+6532A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217394 | ||||||
| chr19:8217433
|
A | G | 1 | a0001c0019t0002g0377 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+6571A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217433 | ||||||
| chr19:8217437
|
C | T | 90 | a0001c0001t0001g0117a0001c0001t0003g0035a0001c0001t0003g0036others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-2+6575C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217437 | ||||||
| chr19:8217537
|
G | GT | 33 | a0001c0001t0001g0205a0001c0001t0001g0407a0001c0001t0001g0408others(30): Show | 33 | HG00438.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+6692dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8217537 | |||||
| chr19:8217537
|
GT | G | 6 | a0001c0001t0002g0301a0001c0001t0003g0046a0001c0008t0001g0051others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+6692delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8217537 | |||||
| chr19:8217606
|
G | A | 3 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0156 | 3 | NA18944.hp2 NA18955.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-2+6744G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217606 | ||||||
| chr19:8217625
|
C | T | 12 | a0002c0003t0001g0399a0002c0003t0001g0400a0002c0003t0001g0401others(9): Show | 12 | HG01934.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+6763C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217625 | ||||||
| chr19:8217739
|
C | G | 11 | a0001c0001t0003g0149a0001c0001t0003g0191a0001c0001t0003g0196others(8): Show | 11 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+6877C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217739 | ||||||
| chr19:8217755
|
T | C | 2 | a0001c0001t0002g0257a0001c0001t0004g0381 | 2 | NA18612.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-2+6893T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217755 | ||||||
| chr19:8217758
|
C | T | 1 | a0003c0004t0001g0410 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-2+6896C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217758 | ||||||
| chr19:8217784
|
G | A | 35 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(32): Show | 35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+6922G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217784 | ||||||
| chr19:8217861
|
C | T | 1 | a0003c0004t0001g0410 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-2+6999C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217861 | ||||||
| chr19:8217912
|
A | G | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+7050A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217912 | ||||||
| chr19:8218029
|
A | G | 45 | a0001c0001t0001g0117a0001c0001t0003g0011a0001c0001t0003g0012others(42): Show | 45 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-2+7167A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218029 | ||||||
| chr19:8218161
|
C | T | 3 | a0001c0001t0002g0246a0001c0001t0002g0370a0002c0003t0004g0372 | 3 | NA19004.hp1 NA19057.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-2+7299C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218161 | ||||||
| chr19:8218246
|
T | A | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+7384T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218246 | ||||||
| chr19:8218264
|
C | A | 1 | a0004c0005t0007g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-2+7402C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218264 | ||||||
| chr19:8218556
|
G | A | 1 | a0002c0003t0001g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-2+7694G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218556 | ||||||
| chr19:8218650
|
CAG | C | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+7791_-2+7792del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8218650 | |||||
| chr19:8218721
|
A | G | 2 | a0001c0001t0016g0094a0003c0004t0004g0252 | 2 | HG02300.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-2+7859A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218721 | ||||||
| chr19:8218732
|
A | G | 8 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0017g0130others(5): Show | 8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+7870A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218732 | ||||||
| chr19:8218750
|
A | G | 3 | a0001c0002t0003g0416a0001c0002t0003g0417a0004c0005t0008g0415 | 3 | HG02735.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-2+7888A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218750 | ||||||
| chr19:8218766
|
T | C | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+7904T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218766 | ||||||
| chr19:8218935
|
C | A | 225 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(222): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-2+8073C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218935 | ||||||
| chr19:8219148
|
C | T | 8 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0017g0130others(5): Show | 8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+8286C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219148 | ||||||
| chr19:8219218
|
G | A | 63 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2+8356G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219218 | ||||||
| chr19:8219462
|
C | T | 258 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0407others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-2+8600C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219462 | ||||||
| chr19:8219529
|
G | A | 12 | a0001c0001t0001g0117a0001c0001t0003g0105a0001c0001t0003g0110others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+8667G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219529 | ||||||
| chr19:8219534
|
G | C | 1 | a0001c0001t0002g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-2+8672G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219534 | ||||||
| chr19:8219550
|
C | T | 2 | a0001c0001t0002g0146a0001c0012t0002g0145 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2+8688C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219550 | ||||||
| chr19:8219587
|
C | T | 2 | a0001c0019t0002g0377a0003c0007t0009g0387 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-2+8725C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219587 | ||||||
| chr19:8219662
|
C | CA | 95 | a0001c0001t0001g0117a0001c0001t0001g0408a0001c0001t0003g0035others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-2+8807dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219662 | |||||
| chr19:8219814
|
T | C | 13 | a0002c0003t0001g0399a0002c0003t0001g0400a0002c0003t0001g0401others(10): Show | 13 | HG01934.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+8952T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219814 | ||||||
| chr19:8219874
|
T | G | 1 | a0001c0002t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-2+9012T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219874 | ||||||
| chr19:8219924
|
A | C | 6 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0001g0392others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+9062A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219924 | ||||||
| chr19:8219987
|
T | TA | 72 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(69): Show | 72 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-2+9137dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219987 | |||||
| chr19:8219987
|
T | TAA | 245 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0407others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-2+9136_-2+9137dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219987 | |||||
| chr19:8219987
|
T | TAAA | 6 | a0001c0001t0003g0036a0001c0002t0003g0416a0001c0002t0003g0417others(3): Show | 6 | HG02735.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+9135_-2+9137dup others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219987 | |||||
| chr19:8220119
|
C | T | 21 | a0001c0001t0001g0125a0001c0001t0001g0407a0001c0001t0003g0131others(18): Show | 21 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+9257C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220119 | ||||||
| chr19:8220129
|
C | T | 2 | a0001c0001t0002g0368a0001c0001t0006g0369 | 2 | HG03239.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-2+9267C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220129 | ||||||
| chr19:8220139
|
C | T | 58 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0046others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2+9277C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220139 | ||||||
| chr19:8220141
|
C | T | 1 | a0001c0006t0006g0271 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-2+9279C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220141 | ||||||
| chr19:8220202
|
T | C | 1 | a0004c0005t0007g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-2+9340T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220202 | ||||||
| chr19:8220244
|
A | C | 1 | a0003c0014t0001g0406 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+9382A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220244 | ||||||
| chr19:8220286
|
A | G | 1 | a0001c0002t0005g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2+9424A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220286 | ||||||
| chr19:8220373
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0205 | 2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-2+9511C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220373 | ||||||
| chr19:8220418
|
C | T | 1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2+9556C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220418 | ||||||
| chr19:8220511
|
G | A | 55 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(52): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+9649G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220511 | ||||||
| chr19:8220557
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-2+9695G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220557 | ||||||
| chr19:8220600
|
C | T | 3 | a0001c0002t0006g0214a0001c0002t0006g0215a0010c0016t0006g0212 | 3 | NA18946.hp1 NA18954.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-2+9738C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220600 | ||||||
| chr19:8220723
|
G | A | 92 | a0001c0001t0001g0117a0001c0001t0003g0035a0001c0001t0003g0036others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-2+9861G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220723 | ||||||
| chr19:8220743
|
C | T | 6 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0001g0392others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+9881C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220743 | ||||||
| chr19:8220815
|
GTGTTTTT others(5): Show |
G | 1 | a0001c0001t0006g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-2+9966_-2+9977del others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8220815 | |||||
| chr19:8220817
|
G | GT | 99 | a0001c0001t0001g0117a0001c0001t0002g0142a0001c0001t0002g0218others(96): Show | 99 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-2+9966dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8220817 | |||||
| chr19:8220818
|
T | G | 19 | a0001c0001t0001g0125a0001c0001t0001g0407a0001c0001t0003g0131others(16): Show | 19 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2+9956T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220818 | ||||||
| chr19:8220826
|
T | G | 21 | a0001c0001t0001g0125a0001c0001t0001g0407a0001c0001t0003g0131others(18): Show | 21 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+9964T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220826 | ||||||
| chr19:8220829
|
G | T | 2 | a0001c0001t0007g0383a0001c0002t0004g0004 | 2 | HG02602.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-2+9967G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220829 | ||||||
| chr19:8220846
|
G | C | 71 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0046others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-2+9984G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220846 | ||||||
| chr19:8220914
|
T | C | 1 | a0001c0002t0006g0280 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-2+10052T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220914 | ||||||
| chr19:8220956
|
G | C | 6 | a0001c0001t0003g0159a0001c0002t0001g0208a0001c0002t0005g0199others(3): Show | 6 | HG00438.hp2 HG00544.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+10094G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220956 | ||||||
| chr19:8220975
|
C | T | 3 | a0002c0003t0001g0043a0002c0003t0001g0061a0002c0003t0001g0062 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-2+10113C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220975 | ||||||
| chr19:8221010
|
A | G | 254 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0407others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-2+10148A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221010 | ||||||
| chr19:8221015
|
C | T | 16 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0001g0392others(13): Show | 16 | HG01891.hp1 HG01934.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-2+10153C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221015 | ||||||
| chr19:8221105
|
G | A | 1 | a0003c0007t0009g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2+10243G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221105 | ||||||
| chr19:8221130
|
A | AT | 17 | a0001c0001t0002g0139a0001c0001t0002g0230a0001c0001t0002g0269others(14): Show | 17 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2+10285dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221130 | |||||
| chr19:8221130
|
AT | A | 61 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0002g0246others(58): Show | 61 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2+10285delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221130 | |||||
| chr19:8221305
|
T | G | 1 | a0001c0006t0006g0305 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-2+10443T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221305 | ||||||
| chr19:8221380
|
G | T | 1 | a0001c0002t0002g0365 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-2+10518G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221380 | ||||||
| chr19:8221436
|
G | T | 1 | a0001c0001t0008g0390 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+10574G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221436 | ||||||
| chr19:8221551
|
AT | A | 36 | a0001c0001t0001g0408a0001c0001t0002g0246a0001c0001t0003g0011others(33): Show | 36 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-2+10701delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221551 | |||||
| chr19:8221709
|
A | G | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+10847A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221709 | ||||||
| chr19:8221713
|
T | G | 6 | a0001c0002t0001g0042a0001c0002t0001g0098a0001c0002t0001g0099others(3): Show | 6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+10851T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221713 | ||||||
| chr19:8221752
|
A | T | 1 | a0004c0005t0007g0292 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-2+10890A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221752 | ||||||
| chr19:8221870
|
ATG | A | 10 | a0001c0001t0003g0131a0001c0001t0017g0130a0002c0003t0001g0400others(7): Show | 10 | HG01934.hp1 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+11010_-2+11011d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221870 | |||||
| chr19:8221872
|
G | GT | 34 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0144others(31): Show | 34 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-2+11037dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
G | GTT | 68 | a0001c0001t0002g0142a0001c0001t0002g0221a0001c0001t0002g0222others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-2+11036_-2+11037d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
G | GTTT | 105 | a0001c0001t0001g0202a0001c0001t0002g0219a0001c0001t0002g0228others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-2+11035_-2+11037d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
G | GTTTT | 60 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0003g0035others(57): Show | 60 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-2+11034_-2+11037d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
G | GTTTTT | 12 | a0001c0001t0001g0117a0001c0001t0003g0050a0001c0001t0003g0183others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+11033_-2+11037d others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
G | T | 4 | a0001c0001t0001g0125a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11010G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221872 | ||||||
| chr19:8221872
|
GT | G | 6 | a0001c0001t0002g0341a0001c0001t0008g0390a0001c0006t0013g0260others(3): Show | 6 | HG00558.hp2 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+11037delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
GTTTTTTT others(4): Show |
G | 2 | a0001c0008t0001g0211a0004c0005t0008g0209 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+11027_-2+11037d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221872
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0002t0001g0018a0002c0003t0001g0210 | 2 | HG00609.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-2+11026_-2+11037d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | |||||
| chr19:8221878
|
T | A | 4 | a0001c0001t0001g0125a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11016T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221878 | ||||||
| chr19:8221879
|
T | A | 1 | a0002c0013t0001g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2+11017T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221879 | ||||||
| chr19:8221880
|
T | A | 10 | a0001c0001t0003g0131a0001c0001t0017g0130a0002c0003t0001g0400others(7): Show | 10 | HG01934.hp1 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+11018T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221880 | ||||||
| chr19:8221881
|
T | A | 3 | a0001c0001t0001g0407a0003c0007t0009g0141a0003c0007t0010g0006 | 3 | HG02055.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+11019T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221881 | ||||||
| chr19:8221882
|
T | A | 4 | a0001c0001t0001g0125a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11020T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221882 | ||||||
| chr19:8221883
|
T | A | 1 | a0002c0013t0001g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2+11021T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221883 | ||||||
| chr19:8221884
|
T | A | 5 | a0001c0001t0003g0131a0001c0001t0017g0130a0003c0004t0001g0132others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+11022T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221884 | ||||||
| chr19:8221884
|
T | G | 4 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(1): Show | 4 | HG02630.hp1 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11022T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221884 | ||||||
| chr19:8221884
|
T | TTG | 6 | a0001c0002t0001g0042a0001c0002t0001g0098a0001c0002t0001g0099others(3): Show | 6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+11023_-2+11024i others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221884 | |||||
| chr19:8221884
|
T | TTTG | 17 | a0001c0001t0002g0246a0001c0001t0003g0011a0001c0001t0003g0012others(14): Show | 17 | HG02040.hp2 HG02132.hp2 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2+11024_-2+11025i others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221884 | |||||
| chr19:8221885
|
T | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2+11023T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221885 | ||||||
| chr19:8221886
|
T | A | 11 | a0001c0001t0001g0125a0002c0003t0001g0400a0002c0003t0001g0401others(8): Show | 11 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+11024T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221886 | ||||||
| chr19:8221889
|
T | G | 1 | a0003c0004t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-2+11027T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221889 | ||||||
| chr19:8221945
|
G | C | 1 | a0003c0004t0001g0402 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2+11083G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221945 | ||||||
| chr19:8222025
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+11163T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222025 | ||||||
| chr19:8222034
|
T | C | 309 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-2+11172T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222034 | ||||||
| chr19:8222037
|
C | T | 8 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0017g0130others(5): Show | 8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+11175C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222037 | ||||||
| chr19:8222186
|
A | T | 1 | a0004c0005t0008g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-2+11324A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222186 | ||||||
| chr19:8222272
|
G | A | 6 | a0002c0003t0004g0276a0002c0003t0004g0382a0002c0003t0008g0395others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+11410G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222272 | ||||||
| chr19:8222351
|
T | A | 2 | a0001c0019t0002g0377a0003c0007t0009g0387 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-2+11489T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222351 | ||||||
| chr19:8222624
|
G | A | 1 | a0004c0005t0011g0320 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-2+11762G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222624 | ||||||
| chr19:8222726
|
G | C | 1 | a0001c0001t0003g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-2+11864G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222726 | ||||||
| chr19:8222769
|
A | G | 3 | a0002c0003t0001g0040a0006c0010t0001g0092a0006c0010t0015g0093 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+11907A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222769 | ||||||
| chr19:8223028
|
A | G | 2 | a0001c0001t0001g0408a0001c0015t0001g0409 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-2+12166A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223028 | ||||||
| chr19:8223053
|
G | C | 1 | a0001c0001t0004g0265 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-2+12191G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223053 | ||||||
| chr19:8223054
|
C | T | 1 | a0001c0001t0004g0265 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-2+12192C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223054 | ||||||
| chr19:8223055
|
T | G | 1 | a0001c0001t0004g0265 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-2+12193T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223055 | ||||||
| chr19:8223190
|
G | A | 6 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0001g0392others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+12328G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223190 | ||||||
| chr19:8223333
|
G | A | 7 | a0001c0002t0004g0236a0001c0002t0006g0234a0001c0002t0006g0235others(4): Show | 7 | NA18957.hp2 NA18960.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+12471G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223333 | ||||||
| chr19:8223414
|
C | T | 315 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-2+12552C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223414 | ||||||
| chr19:8223492
|
G | A | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+12630G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223492 | ||||||
| chr19:8223510
|
T | C | 1 | a0001c0001t0003g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-2+12648T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223510 | ||||||
| chr19:8223651
|
C | T | 55 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(52): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+12789C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223651 | ||||||
| chr19:8223658
|
C | T | 310 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-2+12796C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223658 | ||||||
| chr19:8223659
|
G | A | 2 | a0001c0001t0003g0070a0003c0004t0001g0069 | 2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-2+12797G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223659 | ||||||
| chr19:8223728
|
G | T | 1 | a0002c0003t0004g0233 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+12866G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223728 | ||||||
| chr19:8223873
|
C | T | 310 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-2+13011C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223873 | ||||||
| chr19:8223911
|
C | T | 3 | a0001c0002t0006g0386a0003c0007t0004g0299a0003c0007t0004g0300 | 3 | HG00099.hp1 HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-2+13049C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223911 | ||||||
| chr19:8223972
|
C | G | 55 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(52): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+13110C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223972 | ||||||
| chr19:8224104
|
T | TA | 47 | a0001c0001t0001g0125a0001c0001t0002g0245a0001c0001t0002g0269others(44): Show | 47 | HG00280.hp2 HG00621.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2+13264dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | |||||
| chr19:8224104
|
T | TAA | 24 | a0001c0001t0001g0408a0001c0001t0002g0246a0001c0001t0003g0011others(21): Show | 24 | HG00609.hp1 HG00741.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2+13263_-2+13264d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | |||||
| chr19:8224104
|
TA | T | 7 | a0001c0001t0002g0267a0001c0001t0002g0339a0001c0001t0002g0371others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+13264delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | |||||
| chr19:8224104
|
TAAAAAAA others(3): Show |
T | 1 | a0002c0003t0004g0372 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-2+13255_-2+13264d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | |||||
| chr19:8224124
|
AAAG | A | 21 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(18): Show | 21 | HG00280.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2+13263_-2+13265d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224124 | ||||||
| chr19:8224125
|
AAG | A | 58 | a0001c0001t0001g0205a0001c0001t0003g0035a0001c0001t0003g0036others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2+13264_-2+13265d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224125 | ||||||
| chr19:8224126
|
AG | A | 11 | a0001c0001t0003g0071a0001c0001t0005g0096a0001c0001t0016g0094others(8): Show | 11 | HG01175.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+13266delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224126 | |||||
| chr19:8224179
|
C | T | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+13317C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224179 | ||||||
| chr19:8224184
|
G | A | 1 | a0001c0001t0003g0005 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-2+13322G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224184 | ||||||
| chr19:8224264
|
G | A | 34 | a0001c0001t0001g0408a0001c0001t0002g0246a0001c0001t0003g0011others(31): Show | 34 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+13402G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224264 | ||||||
| chr19:8224276
|
A | G | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13414A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224276 | ||||||
| chr19:8224277
|
C | G | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13415C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224277 | ||||||
| chr19:8224278
|
G | A | 3 | a0002c0003t0001g0400a0003c0007t0009g0141a0003c0007t0010g0006 | 3 | HG02055.hp2 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+13416G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224278 | ||||||
| chr19:8224280
|
G | A | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13418G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224280 | ||||||
| chr19:8224282
|
T | C | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13420T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224282 | ||||||
| chr19:8224323
|
C | T | 35 | a0001c0001t0001g0408a0001c0001t0002g0246a0001c0001t0003g0011others(32): Show | 35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+13461C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224323 | ||||||
| chr19:8224406
|
C | CA | 23 | a0001c0001t0001g0205a0001c0001t0002g0139a0001c0001t0002g0144others(20): Show | 23 | HG00280.hp1 HG01175.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-2+13563dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224406 | |||||
| chr19:8224406
|
CA | C | 183 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0002g0142others(180): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-2+13563delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224406 | |||||
| chr19:8224406
|
CAAAAA | C | 6 | a0001c0002t0001g0042a0001c0002t0001g0098a0001c0002t0001g0099others(3): Show | 6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+13559_-2+13563d others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224406 | |||||
| chr19:8224415
|
A | T | 1 | a0001c0001t0003g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+13553A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224415 | ||||||
| chr19:8224423
|
A | T | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+13561A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224423 | ||||||
| chr19:8224588
|
T | C | 2 | a0001c0006t0005g0190a0001c0006t0005g0207 | 2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-2+13726T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224588 | ||||||
| chr19:8224635
|
C | A | 352 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(349): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-2+13773C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224635 | ||||||
| chr19:8224767
|
G | A | 1 | a0002c0003t0004g0213 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-2+13905G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224767 | ||||||
| chr19:8224786
|
G | T | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2+13924G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224786 | ||||||
| chr19:8224796
|
C | T | 5 | a0004c0005t0007g0217a0004c0005t0007g0287a0004c0005t0007g0384others(2): Show | 5 | HG00738.hp1 HG01106.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+13934C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224796 | ||||||
| chr19:8224976
|
C | T | 1 | a0004c0005t0008g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-2+14114C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224976 | ||||||
| chr19:8225018
|
G | A | 1 | a0004c0005t0008g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+14156G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225018 | ||||||
| chr19:8225070
|
G | C | 1 | a0001c0002t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+14208G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225070 | ||||||
| chr19:8225204
|
G | A | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+14342G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225204 | ||||||
| chr19:8225417
|
CT | C | 228 | a0001c0001t0001g0125a0001c0001t0001g0202a0001c0001t0001g0204others(225): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-2+14575delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8225417 | |||||
| chr19:8225417
|
CTT | C | 11 | a0001c0001t0003g0047a0001c0002t0003g0416a0001c0002t0003g0417others(8): Show | 11 | HG00323.hp1 HG02132.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+14574_-2+14575d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8225417 | |||||
| chr19:8225473
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0205 | 2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-2+14611G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225473 | ||||||
| chr19:8225509
|
C | T | 4 | a0002c0003t0001g0399a0002c0003t0001g0404a0002c0003t0004g0143others(1): Show | 4 | HG03041.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+14647C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225509 | ||||||
| chr19:8225536
|
G | T | 2 | a0001c0001t0003g0105a0008c0024t0008g0108 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+14674G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225536 | ||||||
| chr19:8225654
|
C | A | 1 | a0001c0001t0002g0364 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-2+14792C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225654 | ||||||
| chr19:8225719
|
C | T | 4 | a0001c0008t0001g0211a0002c0003t0001g0210a0003c0004t0001g0088others(1): Show | 4 | HG02451.hp2 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+14857C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225719 | ||||||
| chr19:8225852
|
CT | C | 128 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(125): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-2+14991delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225852 | ||||||
| chr19:8225921
|
C | T | 1 | a0006c0010t0015g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2+15059C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225921 | ||||||
| chr19:8225935
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2+15073C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225935 | ||||||
| chr19:8225938
|
G | A | 2 | a0002c0003t0001g0166a0003c0004t0001g0165 | 2 | NA18966.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-2+15076G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225938 | ||||||
| chr19:8225994
|
A | G | 347 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.-2+15132A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225994 | ||||||
| chr19:8226025
|
G | A | 347 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.-2+15163G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226025 | ||||||
| chr19:8226093
|
A | T | 31 | a0001c0001t0002g0246a0001c0001t0003g0011a0001c0001t0003g0012others(28): Show | 31 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-2+15231A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226093 | ||||||
| chr19:8226248
|
T | C | 3 | a0001c0002t0005g0055a0001c0002t0005g0059a0004c0005t0008g0054 | 3 | HG00735.hp2 HG01515.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-2+15386T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226248 | ||||||
| chr19:8226264
|
G | A | 1 | a0001c0001t0010g0008 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-2+15402G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226264 | ||||||
| chr19:8226312
|
G | T | 1 | a0001c0001t0003g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+15450G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226312 | ||||||
| chr19:8226450
|
G | C | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+15588G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226450 | ||||||
| chr19:8226731
|
G | A | 1 | a0001c0001t0002g0345 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-2+15869G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226731 | ||||||
| chr19:8226768
|
G | A | 1 | a0003c0004t0001g0167 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-2+15906G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226768 | ||||||
| chr19:8226769
|
G | A | 1 | a0002c0003t0004g0304 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-2+15907G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226769 | ||||||
| chr19:8226769
|
GATTGCCT others(24): Show |
G | 1 | a0001c0001t0003g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+15908_-2+15938d others(33): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226769 | ||||||
| chr19:8226788
|
T | G | 346 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-2+15926T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226788 | ||||||
| chr19:8226871
|
G | A | 4 | a0001c0001t0002g0373a0001c0001t0002g0375a0001c0002t0004g0374others(1): Show | 4 | NA18956.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+16009G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226871 | ||||||
| chr19:8226879
|
A | T | 37 | a0001c0001t0001g0408a0001c0001t0002g0246a0001c0001t0003g0011others(34): Show | 37 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-2+16017A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226879 | ||||||
| chr19:8227130
|
A | G | 1 | a0001c0008t0004g0357 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-2+16268A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227130 | ||||||
| chr19:8227142
|
G | A | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+16280G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227142 | ||||||
| chr19:8227162
|
G | T | 1 | a0002c0003t0001g0404 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2+16300G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227162 | ||||||
| chr19:8227211
|
A | G | 4 | a0001c0001t0002g0244a0001c0001t0002g0295a0001c0001t0002g0296others(1): Show | 4 | HG01243.hp2 HG01258.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+16349A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227211 | ||||||
| chr19:8227327
|
G | A | 55 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(52): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+16465G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227327 | ||||||
| chr19:8227581
|
A | T | 3 | a0001c0002t0005g0086a0001c0006t0005g0087a0002c0003t0001g0103 | 3 | HG02015.hp2 HG02040.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-2+16719A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227581 | ||||||
| chr19:8227637
|
C | G | 156 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-2+16775C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227637 | ||||||
| chr19:8227729
|
A | G | 1 | a0002c0003t0004g0233 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+16867A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227729 | ||||||
| chr19:8227771
|
G | A | 3 | a0001c0002t0002g0123a0001c0002t0004g0311a0001c0002t0004g0323 | 3 | NA18962.hp2 NA19088.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-2+16909G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227771 | ||||||
| chr19:8227978
|
C | T | 3 | a0002c0003t0001g0040a0006c0010t0001g0092a0006c0010t0015g0093 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+17116C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227978 | ||||||
| chr19:8227989
|
G | A | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-2+17127G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227989 | ||||||
| chr19:8228060
|
C | T | 1 | a0005c0011t0007g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-2+17198C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228060 | ||||||
| chr19:8228175
|
G | A | 6 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+17313G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228175 | ||||||
| chr19:8228178
|
C | T | 4 | a0002c0003t0001g0399a0002c0003t0001g0404a0002c0003t0004g0143others(1): Show | 4 | HG03041.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+17316C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228178 | ||||||
| chr19:8228216
|
G | C | 346 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-2+17354G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228216 | ||||||
| chr19:8228368
|
A | G | 1 | a0003c0004t0001g0010 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-2+17506A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228368 | ||||||
| chr19:8228397
|
G | A | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+17535G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228397 | ||||||
| chr19:8228401
|
A | G | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+17539A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228401 | ||||||
| chr19:8228565
|
C | T | 127 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(124): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-2+17703C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228565 | ||||||
| chr19:8228567
|
C | T | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+17705C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228567 | ||||||
| chr19:8228685
|
A | T | 3 | a0002c0003t0004g0227a0002c0003t0004g0229a0002c0003t0004g0233 | 3 | NA18955.hp1 NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-2+17823A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228685 | ||||||
| chr19:8228689
|
T | G | 1 | a0004c0009t0007g0336 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2+17827T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228689 | ||||||
| chr19:8228724
|
T | TA | 179 | a0001c0001t0001g0125a0001c0001t0001g0407a0001c0001t0001g0408others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.-2+17871dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8228724 | |||||
| chr19:8228724
|
T | TAA | 165 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-2+17870_-2+17871d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8228724 | |||||
| chr19:8228724
|
T | TAAA | 6 | a0001c0001t0003g0022a0002c0003t0001g0399a0002c0003t0001g0404others(3): Show | 6 | HG03041.hp1 HG03540.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+17869_-2+17871d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8228724 | |||||
| chr19:8228980
|
C | T | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+18118C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228980 | ||||||
| chr19:8229020
|
T | TA | 7 | a0001c0001t0002g0228a0001c0001t0002g0269a0001c0001t0003g0174others(4): Show | 7 | HG01169.hp2 HG01255.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+18173dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229020 | |||||
| chr19:8229020
|
TA | T | 7 | a0001c0001t0001g0408a0001c0001t0002g0137a0001c0002t0003g0417others(4): Show | 7 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+18173delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229020 | |||||
| chr19:8229080
|
C | T | 55 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(52): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+18218C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229080 | ||||||
| chr19:8229142
|
T | C | 4 | a0001c0001t0002g0312a0001c0001t0002g0338a0001c0002t0006g0322others(1): Show | 4 | HG00609.hp2 NA18974.hp2 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+18280T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229142 | ||||||
| chr19:8229320
|
C | T | 4 | a0001c0001t0001g0125a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+18458C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229320 | ||||||
| chr19:8229395
|
TTTCTTCT others(5): Show |
T | 1 | a0001c0001t0003g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+18536_-2+18547d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229395 | |||||
| chr19:8229395
|
TTTCTTCT others(19): Show |
T | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-2+18548_-2+18573d others(28): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229395 | |||||
| chr19:8229404
|
CTTCTTTC others(6): Show |
C | 154 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-2+18545_-2+18557d others(15): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229404 | |||||
| chr19:8229405
|
TTCTTTCT others(9): Show |
T | 134 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-2+18545_-2+18560d others(18): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229405 | |||||
| chr19:8229405
|
TTCTTTCT others(15): Show |
T | 17 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0017g0130others(14): Show | 17 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2+18545_-2+18566d others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229405 | |||||
| chr19:8229417
|
T | C | 1 | a0001c0001t0003g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+18555T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229417 | ||||||
| chr19:8229418
|
TTTC | T | 37 | a0001c0001t0001g0407a0001c0001t0002g0246a0001c0001t0003g0011others(34): Show | 37 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-2+18572_-2+18574d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229418 | |||||
| chr19:8229436
|
C | A | 131 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(128): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-2+18574C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229436 | ||||||
| chr19:8229908
|
T | C | 1 | a0004c0018t0007g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2+19046T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229908 | ||||||
| chr19:8229942
|
C | T | 1 | a0002c0003t0001g0399 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2+19080C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229942 | ||||||
| chr19:8229973
|
G | A | 2 | a0001c0019t0002g0377a0003c0007t0009g0387 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-2+19111G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229973 | ||||||
| chr19:8230057
|
A | C | 5 | a0001c0001t0001g0117a0001c0025t0001g0116a0002c0003t0001g0109others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+19195A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230057 | ||||||
| chr19:8230179
|
CCTTTTTT others(3): Show |
C | 1 | a0003c0007t0009g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2+19337_-2+19346d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8230179 | |||||
| chr19:8230214
|
G | A | 6 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+19352G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230214 | ||||||
| chr19:8230236
|
A | G | 6 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+19374A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230236 | ||||||
| chr19:8230252
|
A | G | 355 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-2+19390A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230252 | ||||||
| chr19:8230281
|
C | G | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-2+19419C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230281 | ||||||
| chr19:8230401
|
G | A | 6 | a0001c0001t0002g0341a0001c0001t0002g0346a0001c0001t0002g0347others(3): Show | 6 | HG01070.hp2 HG01517.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+19539G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230401 | ||||||
| chr19:8230420
|
A | C | 355 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-2+19558A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230420 | ||||||
| chr19:8230490
|
A | G | 6 | a0001c0001t0003g0035a0001c0001t0003g0046a0001c0001t0003g0047others(3): Show | 6 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+19628A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230490 | ||||||
| chr19:8230852
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2+19990G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230852 | ||||||
| chr19:8230990
|
C | G | 1 | a0001c0001t0002g0270 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-1-20086C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230990 | ||||||
| chr19:8230996
|
C | T | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-20080C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230996 | ||||||
| chr19:8231022
|
TAG | T | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-20050_-1-20049d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231022 | |||||
| chr19:8231028
|
C | T | 3 | a0001c0001t0001g0408a0001c0015t0001g0409a0003c0007t0009g0340 | 3 | HG02257.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-20048C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231028 | ||||||
| chr19:8231094
|
G | C | 355 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-1-19982G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231094 | ||||||
| chr19:8231207
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-19869A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231207 | ||||||
| chr19:8231475
|
T | C | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-19601T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231475 | ||||||
| chr19:8231536
|
C | T | 4 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(1): Show | 4 | HG02630.hp1 HG03540.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-19540C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231536 | ||||||
| chr19:8231630
|
G | T | 1 | a0003c0007t0009g0387 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-19446G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231630 | ||||||
| chr19:8231746
|
G | A | 6 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-19330G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231746 | ||||||
| chr19:8231746
|
G | T | 3 | a0002c0003t0001g0399a0002c0003t0001g0404a0002c0003t0004g0143 | 3 | HG03041.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-1-19330G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231746 | ||||||
| chr19:8231788
|
G | A | 2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-1-19288G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231788 | ||||||
| chr19:8231803
|
T | C | 355 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-1-19273T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231803 | ||||||
| chr19:8231851
|
A | AT | 7 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0002g0375others(4): Show | 7 | HG00423.hp2 HG01168.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-19203dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATT | 122 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-1-19204_-1-19203d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTT | 28 | a0001c0001t0002g0289a0001c0001t0002g0321a0001c0001t0002g0333others(25): Show | 28 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-19205_-1-19203d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(3): Show |
1 | a0001c0002t0006g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1-19212_-1-19203d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0002g0003a0001c0019t0002g0377a0003c0007t0009g0387 | 3 | HG02976.hp1 HG02976.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-1-19216_-1-19203d others(16): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(8): Show |
2 | a0003c0004t0001g0106a0003c0014t0001g0406 | 2 | HG02258.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-1-19217_-1-19203d others(17): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(9): Show |
9 | a0001c0001t0003g0131a0001c0001t0017g0130a0002c0003t0001g0400others(6): Show | 9 | HG01934.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-19218_-1-19203d others(18): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0125a0002c0003t0001g0405a0003c0004t0001g0132 | 3 | HG02647.hp1 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-19219_-1-19203d others(19): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(11): Show |
1 | a0004c0009t0007g0336 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1-19220_-1-19203d others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0002g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(18): Show |
1 | a0003c0007t0009g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(23): Show |
2 | a0001c0001t0002g0355a0001c0008t0004g0357 | 2 | HG01361.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(32): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(24): Show |
3 | a0001c0001t0002g0140a0001c0001t0002g0245a0001c0001t0002g0345 | 3 | HG00735.hp1 HG01243.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(33): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(25): Show |
3 | a0001c0001t0002g0146a0001c0001t0002g0243a0001c0012t0002g0145 | 3 | HG01952.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(34): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(26): Show |
2 | a0001c0001t0002g0144a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(35): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(30): Show |
1 | a0002c0003t0004g0356 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(39): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(31): Show |
1 | a0001c0001t0002g0295 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(40): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(32): Show |
1 | a0001c0001t0002g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(41): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(34): Show |
1 | a0001c0001t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(43): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
A | ATTTTTTT others(35): Show |
1 | a0001c0001t0003g0067 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(44): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
AT | A | 14 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0002g0348others(11): Show | 14 | HG02040.hp2 HG02132.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-19203delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
ATT | A | 31 | a0001c0001t0001g0204a0001c0001t0002g0246a0001c0001t0002g0269others(28): Show | 31 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-19204_-1-19203d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231851
|
ATTT | A | 128 | a0001c0001t0001g0117a0001c0001t0002g0256a0001c0001t0002g0257others(125): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-1-19205_-1-19203d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | |||||
| chr19:8231937
|
C | T | 3 | a0001c0001t0002g0318a0001c0001t0002g0364a0002c0003t0004g0332 | 3 | HG00423.hp1 NA18941.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-1-19139C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231937 | ||||||
| chr19:8232031
|
T | C | 4 | a0001c0001t0001g0408a0001c0002t0003g0416a0001c0002t0003g0417others(1): Show | 4 | HG02630.hp1 HG03540.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-19045T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232031 | ||||||
| chr19:8232066
|
G | A | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-19010G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232066 | ||||||
| chr19:8232119
|
G | A | 2 | a0001c0001t0002g0378a0001c0001t0006g0379 | 2 | HG00738.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-1-18957G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232119 | ||||||
| chr19:8232121
|
C | CA | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0230 | 3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-1-18954dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232121 | |||||
| chr19:8232234
|
G | A | 1 | a0003c0007t0009g0387 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-18842G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232234 | ||||||
| chr19:8232288
|
C | G | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-18788C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232288 | ||||||
| chr19:8232471
|
T | C | 3 | a0001c0008t0001g0211a0002c0003t0001g0210a0004c0005t0008g0209 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-18605T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232471 | ||||||
| chr19:8232481
|
G | A | 3 | a0001c0001t0002g0341a0001c0001t0002g0346a0001c0001t0002g0366 | 3 | HG03471.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-1-18595G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232481 | ||||||
| chr19:8232723
|
C | CT | 21 | a0001c0001t0002g0139a0001c0001t0002g0337a0001c0001t0002g0371others(18): Show | 21 | HG01978.hp2 HG02055.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1-18338dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232723 | |||||
| chr19:8232723
|
CT | C | 178 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-1-18338delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232723 | |||||
| chr19:8232745
|
C | T | 137 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(134): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-1-18331C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232745 | ||||||
| chr19:8232866
|
G | A | 148 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-1-18210G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232866 | ||||||
| chr19:8232885
|
G | A | 4 | a0001c0001t0002g0373a0001c0001t0002g0375a0001c0002t0004g0374others(1): Show | 4 | NA18956.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-18191G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232885 | ||||||
| chr19:8232889
|
A | AT | 23 | a0001c0001t0002g0139a0001c0001t0002g0228a0001c0001t0002g0318others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1-18161dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | |||||
| chr19:8232889
|
AT | A | 178 | a0001c0001t0001g0205a0001c0001t0001g0407a0001c0001t0001g0408others(175): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-1-18161delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | |||||
| chr19:8232889
|
ATT | A | 28 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(25): Show | 28 | HG01109.hp1 HG01109.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.-1-18162_-1-18161d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | |||||
| chr19:8232889
|
ATTT | A | 7 | a0001c0001t0007g0121a0002c0003t0001g0061a0002c0003t0004g0276others(4): Show | 7 | HG02630.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-18163_-1-18161d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | |||||
| chr19:8232889
|
ATTTTTTT others(4): Show |
A | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-18171_-1-18161d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | |||||
| chr19:8232889
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0010g0008 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-1-18173_-1-18161d others(15): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | |||||
| chr19:8232938
|
A | G | 2 | a0002c0003t0001g0166a0003c0004t0001g0165 | 2 | NA18966.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-1-18138A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232938 | ||||||
| chr19:8233013
|
C | T | 4 | a0002c0003t0001g0399a0002c0003t0001g0404a0002c0003t0004g0143others(1): Show | 4 | HG03041.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-18063C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233013 | ||||||
| chr19:8233072
|
G | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02683.hp2 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-1-18004G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233072 | ||||||
| chr19:8233166
|
C | G | 1 | a0001c0001t0004g0255 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-1-17910C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233166 | ||||||
| chr19:8233181
|
T | G | 2 | a0005c0011t0007g0284a0005c0011t0007g0286 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-1-17895T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233181 | ||||||
| chr19:8233229
|
G | A | 13 | a0001c0001t0001g0117a0001c0001t0003g0105a0001c0001t0003g0110others(10): Show | 13 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-17847G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233229 | ||||||
| chr19:8233290
|
C | T | 1 | a0001c0006t0005g0155 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-1-17786C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233290 | ||||||
| chr19:8233322
|
C | T | 1 | a0001c0002t0003g0417 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-1-17754C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233322 | ||||||
| chr19:8233323
|
A | G | 416 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(413): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.-1-17753A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233323 | ||||||
| chr19:8233342
|
T | C | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-17734T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233342 | ||||||
| chr19:8233355
|
C | T | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-17721C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233355 | ||||||
| chr19:8233419
|
G | A | 352 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(349): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-1-17657G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233419 | ||||||
| chr19:8233456
|
C | A | 1 | a0001c0001t0004g0265 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-1-17620C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233456 | ||||||
| chr19:8233497
|
T | A | 1 | a0001c0001t0002g0351 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-1-17579T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233497 | ||||||
| chr19:8233506
|
T | C | 2 | a0001c0001t0001g0408a0001c0015t0001g0409 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-17570T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233506 | ||||||
| chr19:8233527
|
G | A | 197 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(194): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-1-17549G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233527 | ||||||
| chr19:8233734
|
C | T | 197 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(194): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-1-17342C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233734 | ||||||
| chr19:8233738
|
C | T | 1 | a0001c0001t0012g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-1-17338C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233738 | ||||||
| chr19:8233739
|
G | A | 1 | a0004c0005t0008g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-1-17337G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233739 | ||||||
| chr19:8233821
|
C | T | 33 | a0001c0001t0002g0246a0001c0001t0003g0011a0001c0001t0003g0012others(30): Show | 33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1-17255C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233821 | ||||||
| chr19:8233882
|
T | G | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-17194T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233882 | ||||||
| chr19:8233883
|
G | T | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-17193G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233883 | ||||||
| chr19:8234077
|
C | T | 18 | a0001c0001t0001g0125a0001c0001t0001g0407a0001c0001t0003g0131others(15): Show | 18 | HG01934.hp1 HG02071.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1-16999C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234077 | ||||||
| chr19:8234133
|
C | T | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-16943C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234133 | ||||||
| chr19:8234263
|
G | A | 2 | a0001c0001t0012g0288a0003c0007t0009g0340 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-1-16813G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234263 | ||||||
| chr19:8234284
|
C | T | 190 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(187): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-1-16792C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234284 | ||||||
| chr19:8234386
|
C | G | 190 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(187): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-1-16690C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234386 | ||||||
| chr19:8234471
|
A | G | 99 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-1-16605A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234471 | ||||||
| chr19:8234496
|
T | A | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-1-16580T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234496 | ||||||
| chr19:8234542
|
A | AT | 50 | a0001c0001t0001g0125a0001c0001t0002g0139a0001c0001t0002g0142others(47): Show | 50 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-1-16506dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
A | ATT | 9 | a0001c0001t0002g0140a0001c0001t0002g0219a0001c0001t0002g0343others(6): Show | 9 | HG00733.hp2 HG01074.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-16507_-1-16506d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
A | ATTT | 9 | a0001c0001t0002g0246a0001c0001t0002g0257a0001c0001t0003g0012others(6): Show | 9 | HG00741.hp1 HG01168.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-16508_-1-16506d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
A | ATTTT | 12 | a0001c0001t0003g0022a0001c0001t0003g0030a0001c0002t0001g0018others(9): Show | 12 | HG00609.hp1 HG02135.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-16509_-1-16506d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
AT | A | 163 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(160): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-1-16506delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
ATT | A | 11 | a0001c0001t0001g0407a0001c0001t0003g0049a0001c0002t0001g0158others(8): Show | 11 | HG01099.hp2 HG01515.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-16507_-1-16506d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0314a0001c0001t0003g0161 | 2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-1-16517_-1-16506d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234542
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0002g0360 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1-16519_-1-16506d others(16): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | |||||
| chr19:8234543
|
T | C | 1 | a0003c0004t0001g0410 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-16533T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234543 | ||||||
| chr19:8234571
|
G | T | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1-16505G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234571 | ||||||
| chr19:8234598
|
GGCAGGAG others(49): Show |
G | 1 | a0002c0003t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-1-16474_-1-16419d others(58): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234598 | |||||
| chr19:8234623
|
A | T | 1 | a0006c0010t0015g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-16453A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234623 | ||||||
| chr19:8234670
|
T | C | 190 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(187): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-1-16406T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234670 | ||||||
| chr19:8234720
|
A | AT | 200 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(197): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-1-16351dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234720 | |||||
| chr19:8234774
|
G | C | 99 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0219others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-1-16302G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234774 | ||||||
| chr19:8234961
|
G | A | 11 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(8): Show | 11 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-16115G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234961 | ||||||
| chr19:8234995
|
TTTTC | T | 4 | a0001c0001t0002g0289a0001c0002t0006g0238a0001c0002t0006g0242others(1): Show | 4 | HG00642.hp2 HG01175.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-16065_-1-16062d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234995 | |||||
| chr19:8235004
|
TTTC | T | 3 | a0002c0003t0001g0040a0006c0010t0001g0092a0006c0010t0015g0093 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-16069_-1-16067d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235004 | |||||
| chr19:8235007
|
C | CT | 13 | a0001c0001t0002g0345a0001c0001t0003g0196a0001c0001t0007g0121others(10): Show | 13 | HG00735.hp1 HG02055.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-16066dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | |||||
| chr19:8235007
|
C | CTT | 39 | a0001c0001t0001g0117a0001c0001t0002g0246a0001c0001t0002g0263others(36): Show | 39 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-16067_-1-16066d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | |||||
| chr19:8235007
|
C | CTTT | 83 | a0001c0001t0002g0142a0001c0001t0002g0218a0001c0001t0002g0221others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-1-16068_-1-16066d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | |||||
| chr19:8235007
|
C | CTTTT | 4 | a0001c0001t0002g0219a0001c0001t0002g0257a0001c0001t0002g0330others(1): Show | 4 | HG00438.hp1 HG00642.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-16066_-1-16065i others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | |||||
| chr19:8235010
|
TC | T | 18 | a0001c0001t0001g0125a0001c0001t0001g0408a0001c0001t0003g0131others(15): Show | 18 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-1-16065delC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235010 | ||||||
| chr19:8235011
|
C | T | 213 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-1-16065C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235011 | ||||||
| chr19:8235011
|
CT | C | 14 | a0001c0001t0002g0137a0001c0001t0003g0066a0001c0001t0003g0070others(11): Show | 14 | HG01261.hp2 HG01515.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-16051delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235011 | |||||
| chr19:8235026
|
C | T | 3 | a0001c0001t0001g0408a0001c0015t0001g0409a0003c0007t0010g0033 | 3 | HG02559.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-16050C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235026 | ||||||
| chr19:8235028
|
G | A | 3 | a0001c0001t0001g0408a0001c0015t0001g0409a0003c0007t0010g0033 | 3 | HG02559.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-16048G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235028 | ||||||
| chr19:8235039
|
A | G | 331 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-1-16037A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235039 | ||||||
| chr19:8235053
|
G | GA | 5 | a0001c0001t0001g0408a0001c0008t0001g0211a0001c0015t0001g0409others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-16022dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235053 | |||||
| chr19:8235054
|
A | G | 2 | a0002c0003t0008g0395a0003c0004t0004g0278 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-1-16022A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235054 | ||||||
| chr19:8235061
|
T | C | 2 | a0001c0008t0001g0211a0004c0005t0008g0209 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-16015T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235061 | ||||||
| chr19:8235133
|
C | T | 1 | a0001c0001t0003g0083 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1-15943C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235133 | ||||||
| chr19:8235156
|
A | G | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-15920A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235156 | ||||||
| chr19:8235158
|
A | G | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-15918A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235158 | ||||||
| chr19:8235195
|
A | G | 1 | a0003c0004t0004g0278 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1-15881A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235195 | ||||||
| chr19:8235198
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-15878G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235198 | ||||||
| chr19:8235209
|
A | G | 2 | a0001c0001t0012g0288a0003c0007t0009g0340 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-1-15867A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235209 | ||||||
| chr19:8235214
|
G | A | 17 | a0001c0001t0002g0223a0001c0001t0003g0148a0001c0001t0003g0168others(14): Show | 17 | HG00140.hp1 HG01168.hp2 HG02976.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1-15862G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235214 | ||||||
| chr19:8235228
|
T | C | 8 | a0001c0001t0001g0125a0001c0001t0003g0131a0001c0001t0017g0130others(5): Show | 8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-15848T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235228 | ||||||
| chr19:8235286
|
C | CG | 3 | a0001c0001t0002g0245a0001c0001t0002g0297a0001c0001t0017g0130 | 3 | HG01106.hp2 HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-1-15789dupG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235286 | |||||
| chr19:8235291
|
A | G | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-15785A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235291 | ||||||
| chr19:8235293
|
G | C | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-15783G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235293 | ||||||
| chr19:8235313
|
G | A | 355 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(352): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-1-15763G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235313 | ||||||
| chr19:8235391
|
G | A | 5 | a0001c0001t0003g0391a0001c0001t0008g0390a0002c0003t0008g0107others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-15685G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235391 | ||||||
| chr19:8235502
|
A | G | 1 | a0002c0003t0004g0382 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-1-15574A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235502 | ||||||
| chr19:8235539
|
G | A | 1 | a0002c0003t0001g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1-15537G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235539 | ||||||
| chr19:8235657
|
G | A | 1 | a0004c0005t0007g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-1-15419G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235657 | ||||||
| chr19:8235657
|
G | T | 2 | a0001c0002t0003g0416a0001c0002t0003g0417 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-1-15419G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235657 | ||||||
| chr19:8235661
|
G | T | 1 | a0004c0005t0011g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-1-15415G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235661 | ||||||
| chr19:8235724
|
A | G | 1 | a0001c0001t0006g0369 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-1-15352A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235724 | ||||||
| chr19:8235730
|
A | G | 1 | a0004c0005t0008g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-1-15346A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235730 | ||||||
| chr19:8235762
|
C | T | 4 | a0001c0001t0003g0131a0001c0001t0017g0130a0002c0013t0001g0129others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-15314C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235762 | ||||||
| chr19:8235895
|
C | T | 1 | a0003c0004t0004g0272 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-1-15181C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235895 | ||||||
| chr19:8235921
|
C | T | 162 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.-1-15155C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235921 | ||||||
| chr19:8235991
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1-15085C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235991 | ||||||
| chr19:8235992
|
A | G | 416 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(413): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.-1-15084A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235992 | ||||||
| chr19:8236151
|
C | T | 5 | a0001c0001t0002g0360a0001c0001t0002g0361a0001c0001t0002g0385others(2): Show | 5 | HG00423.hp2 HG00544.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-14925C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236151 | ||||||
| chr19:8236164
|
C | T | 261 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(258): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.-1-14912C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236164 | ||||||
| chr19:8236321
|
G | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1-14755G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236321 | ||||||
| chr19:8236387
|
G | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0184 | 2 | NA18950.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-1-14689G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236387 | ||||||
| chr19:8236467
|
G | T | 7 | a0001c0001t0002g0142a0001c0001t0003g0105a0001c0001t0003g0110others(4): Show | 7 | HG02145.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-14609G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236467 | ||||||
| chr19:8236471
|
C | T | 3 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0006t0005g0194 | 3 | HG00280.hp1 HG00639.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-14605C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236471 | ||||||
| chr19:8236526
|
A | G | 1 | a0001c0001t0003g0391 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-14550A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236526 | ||||||
| chr19:8236576
|
T | G | 19 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(16): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14500T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236576 | ||||||
| chr19:8236582
|
G | A | 19 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(16): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14494G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236582 | ||||||
| chr19:8236605
|
A | G | 19 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(16): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14471A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236605 | ||||||
| chr19:8236641
|
G | T | 19 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(16): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14435G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236641 | ||||||
| chr19:8236680
|
T | TAA | 6 | a0001c0001t0003g0397a0001c0002t0001g0396a0002c0003t0004g0276others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-14376_-1-14375d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236680 | |||||
| chr19:8236680
|
TAA | T | 57 | a0001c0001t0001g0125a0001c0001t0002g0243a0001c0001t0002g0302others(54): Show | 57 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-1-14376_-1-14375d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236680 | |||||
| chr19:8236680
|
TAAA | T | 14 | a0001c0001t0002g0142a0001c0001t0003g0105a0001c0001t0003g0110others(11): Show | 14 | HG00280.hp2 HG00741.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-14377_-1-14375d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236680 | |||||
| chr19:8236681
|
A | T | 1 | a0001c0001t0003g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-1-14395A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236681 | ||||||
| chr19:8236691
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0005g0063 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-1-14381_-1-14371d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236691 | |||||
| chr19:8236694
|
AAAAAAAA others(1): Show |
A | 11 | a0001c0002t0003g0416a0001c0002t0006g0241a0001c0006t0005g0193others(8): Show | 11 | HG04115.hp1 HG04228.hp2 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-14378_-1-14371d others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236694 | |||||
| chr19:8236695
|
AAAAAAAG | A | 236 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(233): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.-1-14377_-1-14371d others(9): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236695 | |||||
| chr19:8236695
|
AAAAAAAG others(4): Show |
A | 1 | a0003c0004t0009g0334 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-1-14377_-1-14367d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236695 | |||||
| chr19:8236696
|
AAAAAAG | A | 9 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(6): Show | 9 | HG02071.hp1 HG02976.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-14376_-1-14371d others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236696 | |||||
| chr19:8236701
|
AG | A | 7 | a0002c0003t0001g0114a0002c0003t0008g0395a0003c0004t0001g0106others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-14374delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236701 | ||||||
| chr19:8236702
|
G | A | 10 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(7): Show | 10 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-14374G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236702 | ||||||
| chr19:8236732
|
T | C | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-14344T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236732 | ||||||
| chr19:8236819
|
T | C | 65 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0002g0218others(62): Show | 65 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-14257T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236819 | ||||||
| chr19:8237002
|
C | CA | 98 | a0001c0001t0002g0139a0001c0001t0002g0219a0001c0001t0002g0230others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-1-14049dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | |||||
| chr19:8237002
|
C | CAA | 113 | a0001c0001t0001g0205a0001c0001t0002g0246a0001c0001t0002g0256others(110): Show | 113 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-1-14050_-1-14049d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | |||||
| chr19:8237002
|
C | CAAA | 81 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0204others(78): Show | 82 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-1-14051_-1-14049d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | |||||
| chr19:8237002
|
C | CAAAA | 13 | a0001c0001t0002g0366a0001c0001t0005g0096a0001c0002t0005g0059others(10): Show | 13 | HG00735.hp2 HG01175.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-14052_-1-14049d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | |||||
| chr19:8237002
|
CAA | C | 8 | a0001c0001t0008g0398a0002c0003t0001g0114a0002c0003t0008g0395others(5): Show | 8 | HG01261.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-14050_-1-14049d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | |||||
| chr19:8237002
|
CAAA | C | 9 | a0001c0001t0003g0397a0001c0002t0001g0396a0001c0002t0004g0231others(6): Show | 9 | HG02145.hp1 HG02559.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-14051_-1-14049d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | |||||
| chr19:8237281
|
G | A | 2 | a0003c0007t0009g0141a0003c0007t0010g0006 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-13795G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237281 | ||||||
| chr19:8237297
|
C | A | 19 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(16): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-13779C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237297 | ||||||
| chr19:8237310
|
G | A | 6 | a0001c0001t0002g0218a0002c0003t0004g0227a0002c0003t0004g0229others(3): Show | 6 | HG00408.hp1 HG02523.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-13766G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237310 | ||||||
| chr19:8237530
|
G | A | 59 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0002g0219others(56): Show | 59 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-1-13546G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237530 | ||||||
| chr19:8237536
|
A | G | 2 | a0001c0002t0005g0063a0010c0016t0006g0212 | 2 | NA18946.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-1-13540A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237536 | ||||||
| chr19:8237575
|
G | T | 10 | a0001c0001t0003g0397a0001c0001t0008g0398a0001c0002t0001g0396others(7): Show | 10 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-13501G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237575 | ||||||
| chr19:8237646
|
T | C | 4 | a0001c0001t0002g0243a0001c0001t0002g0302a0001c0001t0002g0345others(1): Show | 4 | HG00323.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13430T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237646 | ||||||
| chr19:8237719
|
T | C | 4 | a0001c0001t0003g0011a0001c0002t0005g0079a0001c0002t0005g0413others(1): Show | 4 | HG01069.hp1 HG01071.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-13357T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237719 | ||||||
| chr19:8237744
|
A | G | 3 | a0002c0003t0001g0040a0006c0010t0001g0092a0006c0010t0015g0093 | 3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-13332A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237744 | ||||||
| chr19:8237768
|
G | A | 4 | a0001c0001t0003g0131a0001c0001t0017g0130a0002c0013t0001g0129others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13308G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237768 | ||||||
| chr19:8237778
|
G | A | 4 | a0001c0001t0002g0243a0001c0001t0002g0302a0001c0001t0002g0345others(1): Show | 4 | HG00323.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13298G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237778 | ||||||
| chr19:8237818
|
A | T | 7 | a0001c0002t0014g0056a0001c0006t0005g0186a0002c0003t0001g0043others(4): Show | 7 | HG00673.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-13258A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237818 | ||||||
| chr19:8237821
|
A | T | 159 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-1-13255A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237821 | ||||||
| chr19:8237830
|
G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-13246G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237830 | ||||||
| chr19:8237830
|
G | T | 1 | a0001c0019t0002g0377 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1-13246G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237830 | ||||||
| chr19:8237837
|
C | T | 2 | a0001c0008t0003g0250a0001c0019t0002g0377 | 2 | HG00673.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-1-13239C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237837 | ||||||
| chr19:8237848
|
G | C | 168 | a0001c0001t0001g0125a0001c0001t0002g0218a0001c0001t0002g0219others(165): Show | 168 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1-13228G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237848 | ||||||
| chr19:8237870
|
T | C | 2 | a0001c0002t0002g0281a0001c0002t0006g0280 | 2 | HG01358.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-13206T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237870 | ||||||
| chr19:8237915
|
T | G | 4 | a0001c0002t0001g0042a0001c0002t0001g0099a0001c0002t0001g0100others(1): Show | 4 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13161T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237915 | ||||||
| chr19:8237991
|
G | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1-13085G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237991 | ||||||
| chr19:8237997
|
A | T | 1 | a0001c0006t0006g0264 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-13079A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237997 | ||||||
| chr19:8238043
|
C | G | 3 | a0001c0001t0002g0228a0001c0001t0006g0379a0001c0002t0006g0247 | 3 | HG00642.hp2 HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-1-13033C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238043 | ||||||
| chr19:8238048
|
A | C | 50 | a0001c0001t0002g0267a0001c0001t0002g0316a0001c0001t0002g0329others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-1-13028A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238048 | ||||||
| chr19:8238050
|
T | C | 348 | a0001c0001t0001g0125a0001c0001t0001g0202a0001c0001t0001g0204others(345): Show | 349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.-1-13026T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238050 | ||||||
| chr19:8238228
|
C | G | 14 | a0001c0001t0007g0383a0001c0001t0012g0288a0001c0001t0017g0130others(11): Show | 14 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-12848C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238228 | ||||||
| chr19:8238289
|
A | AGGGAGGG others(10): Show |
7 | a0001c0002t0004g0236a0001c0002t0005g0063a0001c0002t0006g0214others(4): Show | 7 | NA18960.hp2 NA18969.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-12778_-1-12762d others(19): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8238289 | |||||
| chr19:8238315
|
A | G | 192 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0408others(189): Show | 192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-1-12761A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238315 | ||||||
| chr19:8238469
|
G | C | 1 | a0003c0004t0004g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1-12607G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238469 | ||||||
| chr19:8238549
|
T | A | 2 | a0005c0011t0007g0284a0005c0011t0007g0286 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-1-12527T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238549 | ||||||
| chr19:8238612
|
G | C | 4 | a0001c0001t0003g0036a0001c0001t0003g0068a0001c0002t0005g0084others(1): Show | 4 | NA18970.hp1 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-12464G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238612 | ||||||
| chr19:8238708
|
C | T | 2 | a0001c0001t0003g0131a0003c0007t0010g0032 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-1-12368C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238708 | ||||||
| chr19:8238766
|
C | T | 302 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0002g0003others(299): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.-1-12310C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238766 | ||||||
| chr19:8238811
|
C | T | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-12265C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238811 | ||||||
| chr19:8238821
|
G | A | 10 | a0001c0001t0003g0131a0001c0002t0002g0281a0001c0002t0003g0416others(7): Show | 10 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-12255G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238821 | ||||||
| chr19:8238840
|
G | A | 3 | a0003c0007t0004g0283a0003c0007t0004g0299a0003c0007t0004g0300 | 3 | HG01081.hp2 HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-1-12236G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238840 | ||||||
| chr19:8238895
|
G | A | 1 | a0004c0005t0011g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-1-12181G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238895 | ||||||
| chr19:8239120
|
G | T | 1 | a0001c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-11956G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239120 | ||||||
| chr19:8239136
|
T | G | 2 | a0001c0001t0001g0408a0001c0015t0001g0409 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-11940T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239136 | ||||||
| chr19:8239231
|
G | A | 1 | a0001c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-11845G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239231 | ||||||
| chr19:8239255
|
C | T | 2 | a0001c0001t0001g0407a0003c0004t0004g0328 | 2 | HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-11821C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239255 | ||||||
| chr19:8239292
|
A | G | 322 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0407others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-1-11784A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239292 | ||||||
| chr19:8239324
|
G | A | 3 | a0001c0001t0001g0117a0006c0010t0001g0092a0006c0010t0015g0093 | 3 | HG02257.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-11752G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239324 | ||||||
| chr19:8239354
|
G | A | 7 | a0001c0001t0003g0131a0003c0007t0009g0120a0003c0007t0009g0141others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11722G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239354 | ||||||
| chr19:8239355
|
C | T | 3 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417 | 3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-11721C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239355 | ||||||
| chr19:8239372
|
C | T | 5 | a0001c0001t0002g0246a0001c0001t0002g0256a0001c0001t0002g0263others(2): Show | 5 | HG02129.hp1 NA18951.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-11704C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239372 | ||||||
| chr19:8239394
|
C | T | 137 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-1-11682C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239394 | ||||||
| chr19:8239395
|
G | A | 3 | a0003c0004t0001g0106a0003c0004t0001g0402a0003c0004t0004g0278 | 3 | HG02451.hp1 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-1-11681G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239395 | ||||||
| chr19:8239409
|
AAAG | A | 181 | a0001c0001t0001g0117a0001c0001t0001g0407a0001c0001t0001g0408others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.-1-11664_-1-11662d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8239409 | |||||
| chr19:8239411
|
AG | A | 125 | a0001c0001t0002g0137a0001c0001t0002g0219a0001c0001t0002g0221others(122): Show | 125 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-1-11664delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239411 | ||||||
| chr19:8239412
|
G | A | 3 | a0001c0001t0002g0257a0001c0001t0002g0366a0004c0009t0007g0248 | 3 | NA19030.hp1 NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-1-11664G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239412 | ||||||
| chr19:8239418
|
GA | G | 3 | a0001c0001t0002g0257a0001c0001t0004g0136a0001c0002t0004g0231 | 3 | NA18960.hp1 NA19055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-1-11652delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8239418 | |||||
| chr19:8239422
|
A | G | 1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-11654A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239422 | ||||||
| chr19:8239455
|
C | T | 4 | a0001c0001t0007g0383a0001c0001t0012g0288a0001c0001t0017g0130others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-11621C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239455 | ||||||
| chr19:8239537
|
C | T | 7 | a0001c0001t0003g0131a0003c0007t0009g0120a0003c0007t0009g0141others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11539C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239537 | ||||||
| chr19:8239546
|
G | A | 4 | a0001c0001t0003g0133a0001c0002t0002g0281a0001c0002t0003g0416others(1): Show | 4 | HG03098.hp1 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-11530G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239546 | ||||||
| chr19:8239546
|
G | C | 4 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0008g0390others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-11530G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239546 | ||||||
| chr19:8239609
|
C | T | 3 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417 | 3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-11467C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239609 | ||||||
| chr19:8239748
|
GT | G | 94 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-1-11327delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239748 | ||||||
| chr19:8239875
|
C | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0029 | 2 | NA18941.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-1-11201C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239875 | ||||||
| chr19:8239923
|
T | C | 7 | a0001c0001t0003g0131a0003c0007t0009g0120a0003c0007t0009g0141others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11153T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239923 | ||||||
| chr19:8239962
|
C | A | 1 | a0001c0001t0007g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1-11114C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239962 | ||||||
| chr19:8240176
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-10900G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240176 | ||||||
| chr19:8240321
|
G | C | 1 | a0001c0002t0005g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-1-10755G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240321 | ||||||
| chr19:8240350
|
T | C | 3 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417 | 3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-10726T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240350 | ||||||
| chr19:8240379
|
G | C | 1 | a0001c0006t0005g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-1-10697G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240379 | ||||||
| chr19:8240387
|
A | G | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-10689A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240387 | ||||||
| chr19:8240412
|
C | T | 1 | a0003c0007t0009g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-10664C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240412 | ||||||
| chr19:8240442
|
A | C | 7 | a0001c0001t0001g0117a0001c0001t0003g0391a0001c0001t0007g0121others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-10634A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240442 | ||||||
| chr19:8240502
|
G | T | 7 | a0001c0001t0001g0117a0001c0001t0003g0391a0001c0001t0007g0121others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-10574G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240502 | ||||||
| chr19:8240561
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-1-10515C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240561 | ||||||
| chr19:8240562
|
G | C | 1 | a0003c0007t0009g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-10514G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240562 | ||||||
| chr19:8240568
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1-10508G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240568 | ||||||
| chr19:8240585
|
A | AGT | 8 | a0001c0001t0002g0289a0001c0001t0003g0397a0001c0002t0005g0073others(5): Show | 8 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-10462_-1-10461d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGT | 119 | a0001c0001t0002g0137a0001c0001t0002g0244a0001c0001t0002g0257others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-1-10464_-1-10461d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGT | 17 | a0001c0001t0002g0223a0001c0001t0002g0371a0001c0001t0003g0016others(14): Show | 17 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1-10466_-1-10461d others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(1): Show |
8 | a0001c0001t0002g0301a0001c0001t0003g0183a0003c0004t0001g0106others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-10468_-1-10461d others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(3): Show |
36 | a0001c0001t0001g0407a0001c0001t0002g0326a0001c0001t0002g0327others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1-10470_-1-10461d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(5): Show |
56 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0228others(53): Show | 56 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-1-10472_-1-10461d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(7): Show |
14 | a0001c0001t0001g0117a0001c0001t0002g0316a0001c0001t0002g0321others(11): Show | 14 | HG01943.hp1 HG01943.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-10474_-1-10461d others(16): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(9): Show |
22 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0243others(19): Show | 22 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1-10476_-1-10461d others(18): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(11): Show |
14 | a0001c0001t0001g0125a0001c0001t0001g0408a0001c0001t0002g0135others(11): Show | 14 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-10478_-1-10461d others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(13): Show |
16 | a0001c0001t0002g0003a0001c0001t0002g0139a0001c0001t0002g0140others(13): Show | 16 | HG01074.hp1 HG01168.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-10480_-1-10461d others(22): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(15): Show |
16 | a0001c0001t0002g0144a0001c0001t0002g0267a0001c0001t0002g0339others(13): Show | 16 | HG00741.hp1 HG01169.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-10482_-1-10461d others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(17): Show |
7 | a0001c0001t0003g0047a0001c0001t0003g0191a0001c0002t0002g0281others(4): Show | 7 | HG02273.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-10484_-1-10461d others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
A | AGTGTGTG others(19): Show |
2 | a0001c0002t0003g0416a0001c0008t0004g0282 | 2 | HG02818.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-1-10486_-1-10461d others(28): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240585
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0003g0115a0002c0003t0001g0392 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-10472_-1-10461d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | |||||
| chr19:8240614
|
G | GTGTGTGT others(12): Show |
1 | a0002c0013t0001g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1-10461_-1-10460i others(21): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240614 | |||||
| chr19:8240719
|
C | CA | 7 | a0001c0001t0003g0131a0003c0007t0009g0120a0003c0007t0009g0141others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-10354dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240719 | |||||
| chr19:8240758
|
A | G | 237 | a0001c0001t0001g0117a0001c0001t0001g0407a0001c0001t0001g0408others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.-1-10318A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240758 | ||||||
| chr19:8240784
|
G | A | 2 | a0001c0001t0002g0257a0001c0001t0004g0254 | 2 | NA18971.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-1-10292G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240784 | ||||||
| chr19:8241011
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0146 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-1-10065G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241011 | ||||||
| chr19:8241297
|
A | G | 1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-9779A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241297 | ||||||
| chr19:8241490
|
T | A | 1 | a0001c0001t0002g0364 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-1-9586T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241490 | ||||||
| chr19:8241631
|
G | T | 1 | a0001c0001t0003g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-9445G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241631 | ||||||
| chr19:8241640
|
C | T | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-9436C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241640 | ||||||
| chr19:8241796
|
C | T | 6 | a0001c0002t0002g0253a0001c0002t0002g0365a0003c0007t0004g0283others(3): Show | 6 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-9280C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241796 | ||||||
| chr19:8241798
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-1-9278C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241798 | ||||||
| chr19:8241890
|
G | C | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-9186G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241890 | ||||||
| chr19:8241979
|
T | G | 1 | a0001c0001t0003g0203 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1-9097T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241979 | ||||||
| chr19:8242057
|
T | G | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-9019T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242057 | ||||||
| chr19:8242078
|
C | T | 1 | a0002c0003t0004g0213 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1-8998C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242078 | ||||||
| chr19:8242138
|
C | T | 9 | a0001c0001t0001g0125a0001c0001t0002g0301a0001c0001t0003g0149others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-8938C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242138 | ||||||
| chr19:8242272
|
G | A | 1 | a0002c0003t0004g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-1-8804G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242272 | ||||||
| chr19:8242299
|
T | C | 323 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-1-8777T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242299 | ||||||
| chr19:8242421
|
A | G | 2 | a0001c0002t0006g0238a0001c0002t0006g0242 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-1-8655A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242421 | ||||||
| chr19:8242752
|
G | C | 1 | a0001c0001t0003g0035 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-1-8324G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242752 | ||||||
| chr19:8242765
|
T | C | 27 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0375others(24): Show | 27 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1-8311T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242765 | ||||||
| chr19:8242775
|
G | A | 29 | a0001c0001t0003g0133a0001c0002t0001g0042a0001c0002t0001g0098others(26): Show | 29 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-8301G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242775 | ||||||
| chr19:8242810
|
A | T | 325 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-1-8266A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242810 | ||||||
| chr19:8242908
|
C | G | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-1-8168C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242908 | ||||||
| chr19:8242981
|
GGTCT | G | 325 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-1-8093_-1-8090del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8242981 | |||||
| chr19:8243165
|
G | T | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-7911G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243165 | ||||||
| chr19:8243194
|
TA | T | 62 | a0001c0001t0001g0204a0001c0001t0002g0139a0001c0001t0002g0219others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1-7853delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | |||||
| chr19:8243194
|
TAA | T | 149 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0408others(146): Show | 149 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.-1-7854_-1-7853del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | |||||
| chr19:8243194
|
TAAA | T | 152 | a0001c0001t0002g0137a0001c0001t0002g0140a0001c0001t0002g0144others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.-1-7855_-1-7853del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | |||||
| chr19:8243194
|
TAAAA | T | 9 | a0001c0001t0001g0407a0001c0002t0002g0123a0001c0002t0004g0311others(6): Show | 9 | HG00639.hp1 HG02040.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-7856_-1-7853del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | |||||
| chr19:8243194
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0008g0398 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-1-7864_-1-7853del others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | |||||
| chr19:8243194
|
TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0008g0390 | 3 | HG02109.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-7865_-1-7853del others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | |||||
| chr19:8243216
|
AAAAAAAA others(1): Show |
A | 12 | a0001c0001t0001g0125a0001c0012t0002g0145a0003c0007t0003g0126others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-7858_-1-7851del others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243216 | |||||
| chr19:8243327
|
C | T | 7 | a0001c0002t0002g0253a0001c0002t0002g0365a0001c0019t0002g0377others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-7749C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243327 | ||||||
| chr19:8243428
|
T | C | 109 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(106): Show | 109 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-1-7648T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243428 | ||||||
| chr19:8243560
|
C | T | 15 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-7516C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243560 | ||||||
| chr19:8243562
|
A | G | 353 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(350): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-1-7514A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243562 | ||||||
| chr19:8243629
|
T | C | 4 | a0002c0003t0001g0118a0002c0003t0004g0356a0002c0003t0008g0107others(1): Show | 4 | HG02486.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-7447T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243629 | ||||||
| chr19:8243647
|
CT | C | 345 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(342): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-1-7415delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243647 | |||||
| chr19:8243661
|
T | C | 38 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(35): Show | 38 | HG00323.hp2 HG00621.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1-7415T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243661 | ||||||
| chr19:8243729
|
C | T | 3 | a0001c0001t0002g0312a0001c0001t0002g0338a0004c0005t0008g0160 | 3 | HG00609.hp2 HG02523.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-1-7347C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243729 | ||||||
| chr19:8243848
|
C | G | 4 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0008g0390others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-7228C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243848 | ||||||
| chr19:8243904
|
G | C | 1 | a0001c0001t0003g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-7172G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243904 | ||||||
| chr19:8244073
|
C | T | 19 | a0001c0006t0005g0087a0001c0008t0001g0085a0001c0008t0005g0034others(16): Show | 19 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1-7003C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244073 | ||||||
| chr19:8244074
|
G | A | 1 | a0001c0008t0001g0051 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-7002G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244074 | ||||||
| chr19:8244079
|
C | T | 11 | a0001c0001t0003g0183a0001c0002t0001g0018a0003c0004t0001g0014others(8): Show | 11 | HG00609.hp1 HG02129.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-6997C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244079 | ||||||
| chr19:8244091
|
T | C | 2 | a0006c0010t0001g0092a0006c0010t0015g0093 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-6985T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244091 | ||||||
| chr19:8244099
|
T | G | 4 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417others(1): Show | 4 | HG01928.hp2 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-6977T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244099 | ||||||
| chr19:8244166
|
T | C | 340 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-1-6910T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244166 | ||||||
| chr19:8244308
|
A | G | 1 | a0001c0002t0006g0280 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-1-6768A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244308 | ||||||
| chr19:8244321
|
A | C | 5 | a0002c0003t0004g0276a0002c0003t0004g0382a0003c0004t0001g0410others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-6755A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244321 | ||||||
| chr19:8244358
|
T | C | 324 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-1-6718T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244358 | ||||||
| chr19:8244359
|
G | A | 1 | a0001c0012t0002g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-1-6717G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244359 | ||||||
| chr19:8244429
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-1-6647A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244429 | ||||||
| chr19:8244555
|
G | A | 1 | a0003c0004t0001g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-6521G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244555 | ||||||
| chr19:8244571
|
G | A | 1 | a0001c0008t0004g0357 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-1-6505G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244571 | ||||||
| chr19:8244594
|
A | T | 2 | a0001c0002t0006g0215a0001c0002t0006g0268 | 2 | NA18954.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-1-6482A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244594 | ||||||
| chr19:8244663
|
C | T | 2 | a0003c0007t0003g0127a0003c0007t0003g0128 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-1-6413C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244663 | ||||||
| chr19:8244671
|
T | C | 14 | a0001c0001t0002g0244a0001c0001t0002g0289a0001c0001t0002g0295others(11): Show | 14 | HG00280.hp1 HG01106.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-6405T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244671 | ||||||
| chr19:8244774
|
G | A | 1 | a0002c0003t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1-6302G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244774 | ||||||
| chr19:8244908
|
G | A | 1 | a0002c0003t0008g0395 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-6168G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244908 | ||||||
| chr19:8244922
|
A | G | 14 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-6154A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244922 | ||||||
| chr19:8244960
|
T | C | 340 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-1-6116T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244960 | ||||||
| chr19:8245000
|
C | T | 1 | a0003c0004t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-1-6076C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245000 | ||||||
| chr19:8245005
|
G | A | 15 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0364others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-6071G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245005 | ||||||
| chr19:8245039
|
G | A | 1 | a0003c0007t0009g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-6037G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245039 | ||||||
| chr19:8245094
|
C | A | 337 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-1-5982C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245094 | ||||||
| chr19:8245110
|
T | TCAAAAAA others(20): Show |
5 | a0001c0001t0003g0048a0001c0002t0006g0215a0001c0002t0006g0322others(2): Show | 5 | HG03834.hp1 NA18954.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245110 | |||||
| chr19:8245111
|
C | CA | 7 | a0001c0001t0003g0035a0001c0001t0003g0050a0001c0002t0002g0253others(4): Show | 7 | HG00621.hp2 HG00642.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-5941dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | |||||
| chr19:8245111
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-1-5951_-1-5941dup others(11): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | |||||
| chr19:8245111
|
C | CAAAAAAA others(22): Show |
1 | a0001c0002t0006g0268 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(29): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | |||||
| chr19:8245111
|
CA | C | 8 | a0001c0002t0001g0098a0001c0002t0003g0416a0001c0002t0003g0417others(5): Show | 8 | HG01928.hp2 HG01981.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5941delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | |||||
| chr19:8245111
|
CAA | C | 25 | a0001c0001t0003g0133a0001c0002t0001g0042a0001c0002t0001g0099others(22): Show | 25 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1-5942_-1-5941del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | |||||
| chr19:8245112
|
A | AAAAAAAC others(20): Show |
1 | a0001c0002t0006g0214 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245112 | |||||
| chr19:8245112
|
A | AAAAAAAC others(20): Show |
3 | a0001c0001t0007g0383a0001c0006t0006g0266a0001c0008t0001g0188 | 3 | HG02055.hp1 HG02896.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245112 | |||||
| chr19:8245112
|
A | AAAAAAAC others(19): Show |
88 | a0001c0001t0002g0270a0001c0001t0003g0036a0001c0001t0003g0046others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245112 | |||||
| chr19:8245113
|
A | AAAAAACA others(18): Show |
1 | a0001c0002t0006g0241 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245113 | |||||
| chr19:8245113
|
A | AAAAACAA others(18): Show |
1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-1-5959_-1-5958ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245113 | |||||
| chr19:8245114
|
A | AAAACAAA others(17): Show |
42 | a0001c0001t0002g0137a0001c0001t0002g0244a0001c0001t0002g0257others(39): Show | 42 | HG00280.hp1 HG00733.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.-1-5959_-1-5958ins others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245114 | |||||
| chr19:8245116
|
A | AAACAAAA others(15): Show |
1 | a0001c0001t0002g0223 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(22): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245116 | |||||
| chr19:8245116
|
A | AAACAAAA others(14): Show |
1 | a0003c0007t0009g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(21): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245116 | |||||
| chr19:8245117
|
A | AACAAAAA others(19): Show |
4 | a0001c0002t0001g0075a0001c0002t0001g0412a0001c0002t0005g0045others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245117 | |||||
| chr19:8245118
|
A | AAAAACAA others(13): Show |
2 | a0001c0001t0003g0115a0002c0003t0001g0392 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-5954_-1-5953ins others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245118 | |||||
| chr19:8245119
|
A | C | 36 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(33): Show | 36 | HG00323.hp2 HG00621.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1-5957A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245119 | ||||||
| chr19:8245121
|
A | AACAAAAC others(18): Show |
10 | a0001c0001t0002g0362a0001c0001t0002g0375a0001c0001t0003g0148others(7): Show | 10 | HG02559.hp1 HG03942.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-5954_-1-5953ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245121 | |||||
| chr19:8245121
|
A | C | 7 | a0001c0001t0003g0048a0001c0002t0006g0215a0001c0002t0006g0268others(4): Show | 7 | HG03834.hp1 NA18954.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-5955A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245121 | ||||||
| chr19:8245122
|
A | AACAAAAC others(18): Show |
2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-1-5953_-1-5952ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245122 | |||||
| chr19:8245122
|
A | AACAAACA others(13): Show |
2 | a0001c0001t0003g0083a0003c0004t0004g0252 | 2 | HG02486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-1-5953_-1-5952ins others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245122 | |||||
| chr19:8245122
|
A | ACAAAACA others(17): Show |
126 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(123): Show | 126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-1-5954_-1-5953ins others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245122 | ||||||
| chr19:8245122
|
A | C | 138 | a0001c0001t0002g0137a0001c0001t0002g0244a0001c0001t0002g0257others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-1-5954A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245122 | ||||||
| chr19:8245123
|
A | C | 1 | a0001c0002t0006g0241 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-1-5953A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245123 | ||||||
| chr19:8245125
|
A | C | 3 | a0003c0004t0001g0150a0003c0004t0001g0165a0003c0004t0001g0182 | 3 | NA18966.hp1 NA18979.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-1-5951A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245125 | ||||||
| chr19:8245126
|
A | AACAAAAA others(18): Show |
31 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(28): Show | 31 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-5949_-1-5948ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245126 | |||||
| chr19:8245126
|
A | AACAAAAA others(18): Show |
1 | a0001c0001t0002g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-5949_-1-5948ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245126 | |||||
| chr19:8245126
|
A | C | 8 | a0001c0001t0002g0223a0001c0001t0002g0371a0001c0001t0003g0115others(5): Show | 8 | HG01168.hp2 HG01891.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5950A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245126 | ||||||
| chr19:8245127
|
A | AACAAAAA others(17): Show |
1 | a0001c0001t0003g0391 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-5948_-1-5947ins others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245127 | |||||
| chr19:8245127
|
A | ACAAAAAA others(16): Show |
3 | a0001c0001t0007g0121a0001c0001t0008g0390a0001c0001t0008g0398 | 3 | HG01261.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-5949_-1-5948ins others(23): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245127 | ||||||
| chr19:8245129
|
A | AAAAAAAA others(6): Show |
3 | a0001c0001t0001g0125a0006c0010t0001g0092a0006c0010t0015g0093 | 3 | HG02886.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-5941_-1-5940ins others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245129 | |||||
| chr19:8245129
|
A | AAAAAAAA others(5): Show |
4 | a0001c0012t0002g0145a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-5941_-1-5940ins others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245129 | |||||
| chr19:8245129
|
A | C | 3 | a0001c0001t0002g0301a0001c0001t0003g0149a0001c0001t0003g0196 | 3 | NA18942.hp1 NA18956.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-1-5947A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245129 | ||||||
| chr19:8245177
|
C | A | 372 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(369): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.-1-5899C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245177 | ||||||
| chr19:8245217
|
A | AT | 4 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417others(1): Show | 4 | HG01928.hp2 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-5853dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245217 | |||||
| chr19:8245346
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-1-5730G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245346 | ||||||
| chr19:8245365
|
C | T | 14 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5711C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245365 | ||||||
| chr19:8245384
|
A | G | 13 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0002t0002g0281others(10): Show | 13 | HG01928.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-5692A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245384 | ||||||
| chr19:8245424
|
T | C | 3 | a0001c0006t0005g0087a0004c0005t0011g0307a0004c0005t0011g0320 | 3 | HG00558.hp1 HG02015.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-1-5652T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245424 | ||||||
| chr19:8245472
|
C | T | 1 | a0002c0003t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1-5604C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245472 | ||||||
| chr19:8245596
|
G | C | 5 | a0003c0007t0009g0120a0003c0007t0009g0141a0003c0007t0009g0387others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-5480G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245596 | ||||||
| chr19:8245726
|
G | A | 1 | a0001c0001t0005g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-1-5350G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245726 | ||||||
| chr19:8245771
|
C | T | 1 | a0002c0003t0001g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-1-5305C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245771 | ||||||
| chr19:8245827
|
A | G | 1 | a0004c0005t0008g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-1-5249A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245827 | ||||||
| chr19:8245902
|
C | CA | 74 | a0001c0001t0001g0408a0001c0001t0002g0135a0001c0001t0002g0139others(71): Show | 74 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1-5149dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
C | CAA | 49 | a0001c0001t0002g0223a0001c0001t0003g0046a0001c0001t0003g0183others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-5150_-1-5149dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
C | CAAA | 20 | a0001c0001t0001g0117a0001c0002t0005g0038a0001c0002t0005g0059others(17): Show | 20 | HG00323.hp1 HG00735.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1-5151_-1-5149dup others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
C | CAAAA | 7 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417others(4): Show | 7 | HG01891.hp2 HG01981.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-5152_-1-5149dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
CA | C | 6 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0008g0390others(3): Show | 6 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-5149delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
CAAA | C | 8 | a0001c0001t0002g0219a0001c0001t0002g0245a0001c0001t0002g0338others(5): Show | 8 | HG01081.hp2 HG01243.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5151_-1-5149del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
CAAAA | C | 78 | a0001c0001t0002g0218a0001c0001t0002g0221a0001c0001t0002g0222others(75): Show | 78 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-1-5152_-1-5149del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
CAAAAA | C | 14 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(11): Show | 14 | HG01109.hp2 HG02083.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-5153_-1-5149del others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
CAAAAAA | C | 88 | a0001c0001t0002g0137a0001c0001t0002g0244a0001c0001t0002g0257others(85): Show | 88 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-1-5154_-1-5149del others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245902
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0106 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1-5158_-1-5149del others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | |||||
| chr19:8245998
|
T | C | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-1-5078T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245998 | ||||||
| chr19:8246006
|
G | A | 6 | a0001c0002t0002g0253a0001c0002t0002g0365a0003c0007t0004g0283others(3): Show | 6 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-5070G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246006 | ||||||
| chr19:8246084
|
AAAC | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0002t0004g0231others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-4977_-1-4975del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8246084 | |||||
| chr19:8246096
|
C | CA | 33 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(30): Show | 33 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-4978dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8246096 | |||||
| chr19:8246099
|
C | A | 353 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(350): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-1-4977C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246099 | ||||||
| chr19:8246136
|
G | C | 88 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.-1-4940G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246136 | ||||||
| chr19:8246211
|
G | A | 22 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(19): Show | 22 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1-4865G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246211 | ||||||
| chr19:8246395
|
C | CA | 6 | a0003c0007t0009g0120a0003c0007t0009g0141a0003c0007t0009g0387others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4676dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8246395 | |||||
| chr19:8246454
|
G | T | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1-4622G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246454 | ||||||
| chr19:8246476
|
C | T | 6 | a0001c0002t0002g0253a0001c0002t0002g0365a0003c0007t0004g0283others(3): Show | 6 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4600C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246476 | ||||||
| chr19:8246519
|
T | C | 31 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(28): Show | 31 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-4557T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246519 | ||||||
| chr19:8246535
|
A | G | 1 | a0001c0001t0002g0373 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-1-4541A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246535 | ||||||
| chr19:8246537
|
A | G | 1 | a0001c0012t0002g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-1-4539A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246537 | ||||||
| chr19:8246612
|
A | C | 2 | a0001c0001t0001g0408a0001c0015t0001g0409 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-4464A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246612 | ||||||
| chr19:8246628
|
C | T | 39 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0408others(36): Show | 39 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-4448C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246628 | ||||||
| chr19:8246663
|
C | T | 1 | a0002c0003t0004g0309 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-1-4413C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246663 | ||||||
| chr19:8246743
|
T | C | 371 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(368): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-1-4333T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246743 | ||||||
| chr19:8246850
|
G | T | 6 | a0001c0002t0001g0042a0001c0002t0001g0098a0001c0002t0001g0099others(3): Show | 6 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4226G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246850 | ||||||
| chr19:8246856
|
A | C | 34 | a0001c0001t0003g0397a0001c0006t0005g0087a0001c0008t0001g0051others(31): Show | 34 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1-4220A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246856 | ||||||
| chr19:8246910
|
A | G | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-4166A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246910 | ||||||
| chr19:8246920
|
C | T | 1 | a0001c0002t0006g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-1-4156C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246920 | ||||||
| chr19:8247128
|
G | T | 134 | a0001c0001t0001g0117a0001c0001t0001g0408a0001c0001t0002g0003others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-1-3948G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247128 | ||||||
| chr19:8247132
|
C | T | 1 | a0001c0006t0006g0274 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1-3944C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247132 | ||||||
| chr19:8247199
|
T | C | 1 | a0001c0002t0005g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-1-3877T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247199 | ||||||
| chr19:8247204
|
C | T | 1 | a0003c0007t0009g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-3872C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247204 | ||||||
| chr19:8247284
|
C | T | 3 | a0001c0001t0003g0397a0003c0004t0001g0057a0003c0004t0001g0060 | 3 | HG01109.hp2 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-1-3792C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247284 | ||||||
| chr19:8247296
|
G | A | 2 | a0002c0003t0008g0403a0003c0007t0010g0032 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1-3780G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247296 | ||||||
| chr19:8247360
|
G | A | 6 | a0003c0007t0009g0120a0003c0007t0009g0141a0003c0007t0009g0387others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-3716G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247360 | ||||||
| chr19:8247362
|
G | A | 5 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0007g0383others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-3714G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247362 | ||||||
| chr19:8247563
|
A | G | 4 | a0003c0007t0004g0283a0003c0007t0004g0299a0003c0007t0004g0300others(1): Show | 4 | HG01081.hp2 HG03669.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-3513A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247563 | ||||||
| chr19:8247567
|
G | A | 3 | a0001c0006t0005g0087a0004c0005t0011g0307a0004c0005t0011g0320 | 3 | HG00558.hp1 HG02015.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-1-3509G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247567 | ||||||
| chr19:8247680
|
A | G | 1 | a0001c0006t0005g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-1-3396A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247680 | ||||||
| chr19:8247710
|
T | C | 5 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0007g0383others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-3366T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247710 | ||||||
| chr19:8247728
|
G | A | 40 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(37): Show | 40 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1-3348G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247728 | ||||||
| chr19:8247732
|
C | CT | 16 | a0001c0001t0002g0221a0001c0001t0002g0333a0001c0001t0002g0359others(13): Show | 16 | HG00642.hp1 HG01517.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-3325dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | |||||
| chr19:8247732
|
C | CTT | 184 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.-1-3326_-1-3325dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | |||||
| chr19:8247732
|
C | CTTT | 15 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0137others(12): Show | 15 | HG00544.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-3327_-1-3325dup others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | |||||
| chr19:8247732
|
CT | C | 42 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(39): Show | 42 | HG00621.hp1 HG01070.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-1-3325delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | |||||
| chr19:8247734
|
T | C | 92 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-1-3342T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247734 | ||||||
| chr19:8247735
|
T | C | 2 | a0001c0002t0001g0075a0003c0004t0001g0044 | 2 | HG01070.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-1-3341T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247735 | ||||||
| chr19:8247735
|
T | TTTTTTTT others(2782): Show |
1 | a0002c0003t0004g0356 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-3325_-1-3324ins others(2789): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247735 | |||||
| chr19:8247766
|
C | T | 1 | a0001c0001t0002g0371 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-1-3310C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247766 | ||||||
| chr19:8247800
|
T | C | 353 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(350): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-1-3276T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247800 | ||||||
| chr19:8247881
|
A | G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-3195A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247881 | ||||||
| chr19:8247895
|
G | C | 92 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-1-3181G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247895 | ||||||
| chr19:8247970
|
A | G | 1 | a0001c0001t0002g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1-3106A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247970 | ||||||
| chr19:8248032
|
C | T | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-3044C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248032 | ||||||
| chr19:8248128
|
C | T | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2948C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248128 | ||||||
| chr19:8248134
|
G | A | 1 | a0002c0003t0008g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1-2942G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248134 | ||||||
| chr19:8248328
|
C | T | 1 | a0001c0008t0001g0085 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-1-2748C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248328 | ||||||
| chr19:8248371
|
G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-2705G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248371 | ||||||
| chr19:8248398
|
G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-2678G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248398 | ||||||
| chr19:8248434
|
A | C | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2642A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248434 | ||||||
| chr19:8248450
|
C | T | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2626C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248450 | ||||||
| chr19:8248593
|
GTGAA | G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2480_-1-2477del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248593 | |||||
| chr19:8248608
|
G | A | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2468G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248608 | ||||||
| chr19:8248649
|
T | G | 198 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(195): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-1-2427T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248649 | ||||||
| chr19:8248689
|
G | A | 198 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(195): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-1-2387G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248689 | ||||||
| chr19:8248735
|
A | G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2341A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248735 | ||||||
| chr19:8248828
|
TGATGGGT others(17): Show |
T | 27 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(24): Show | 27 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1-2233_-1-2210del others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248828 | |||||
| chr19:8248843
|
C | T | 4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2233C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248843 | ||||||
| chr19:8248844
|
A | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2232A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248844 | ||||||
| chr19:8248848
|
C | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2228C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248848 | ||||||
| chr19:8248849
|
T | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2227T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248849 | ||||||
| chr19:8248851
|
T | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2225T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248851 | ||||||
| chr19:8248852
|
G | GGTGGGCA others(322): Show |
4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2223_-1-2222ins others(329): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248852 | |||||
| chr19:8248862
|
G | A | 1 | a0006c0010t0015g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-2214G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248862 | ||||||
| chr19:8248871
|
T | TGGTGGGT others(74): Show |
10 | a0003c0007t0004g0283a0003c0007t0004g0299a0003c0007t0004g0300others(7): Show | 10 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-2196_-1-2195ins others(81): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248871 | |||||
| chr19:8248871
|
T | TGGTGGGT others(78): Show |
1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-2196_-1-2195ins others(85): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248871 | |||||
| chr19:8248904
|
T | G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2172T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248904 | ||||||
| chr19:8248906
|
T | C | 99 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.-1-2170T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248906 | ||||||
| chr19:8248977
|
A | G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2099A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248977 | ||||||
| chr19:8248991
|
TGATGGGT others(17): Show |
T | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2070_-1-2047del others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248991 | |||||
| chr19:8249013
|
TTGGA | T | 5 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0007g0383others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-2059_-1-2056del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249013 | |||||
| chr19:8249021
|
G | A | 1 | a0001c0001t0006g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-1-2055G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249021 | ||||||
| chr19:8249058
|
GGAT | G | 31 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(28): Show | 31 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-2012_-1-2010del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249058 | |||||
| chr19:8249079
|
TAGACAGA others(13): Show |
T | 1 | a0003c0004t0001g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-1996_-1-1977del others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249079 | ||||||
| chr19:8249119
|
A | G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-1957A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249119 | ||||||
| chr19:8249131
|
AGTGGGTG others(32): Show |
A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1-1911_-1-1873del others(39): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249131 | |||||
| chr19:8249150
|
GGATGGGT others(47): Show |
G | 1 | a0001c0001t0003g0012 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-1-1875_-1-1822del others(54): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249150 | |||||
| chr19:8249168
|
T | C | 2 | a0001c0001t0003g0115a0002c0003t0001g0392 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-1908T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249168 | ||||||
| chr19:8249175
|
GTGGACAG others(17): Show |
G | 11 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-1895_-1-1872del others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249175 | |||||
| chr19:8249206
|
A | ATGGGTGG others(12): Show |
8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1861_-1-1843dup others(19): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249206 | |||||
| chr19:8249226
|
T | G | 3 | a0002c0003t0001g0400a0002c0003t0001g0401a0002c0003t0001g0411 | 3 | HG01934.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-1-1850T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249226 | ||||||
| chr19:8249231
|
G | A | 2 | a0001c0001t0004g0254a0001c0001t0004g0353 | 2 | HG02083.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-1-1845G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249231 | ||||||
| chr19:8249302
|
C | T | 1 | a0002c0003t0001g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1-1774C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249302 | ||||||
| chr19:8249303
|
G | A | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1773G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249303 | ||||||
| chr19:8249421
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-1655G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249421 | ||||||
| chr19:8249455
|
A | C | 14 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(11): Show | 14 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1621A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249455 | ||||||
| chr19:8249456
|
G | C | 115 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(112): Show | 115 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-1-1620G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249456 | ||||||
| chr19:8249582
|
T | C | 5 | a0001c0002t0002g0253a0001c0002t0002g0281a0001c0002t0002g0365others(2): Show | 5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1494T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249582 | ||||||
| chr19:8249587
|
A | AT | 84 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.-1-1467dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
A | ATT | 15 | a0001c0001t0012g0288a0001c0001t0017g0130a0001c0002t0002g0253others(12): Show | 15 | HG00642.hp1 HG01175.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1-1468_-1-1467dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
A | ATTTT | 46 | a0001c0001t0001g0408a0001c0001t0002g0137a0001c0001t0002g0140others(43): Show | 46 | HG00280.hp2 HG00423.hp2 HG02027.hp1 others(43): Show |
intron_variant | MODIFIER | c.-1-1470_-1-1467dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
A | ATTTTT | 73 | a0001c0001t0001g0204a0001c0001t0002g0003a0001c0001t0002g0135others(70): Show | 73 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-1-1471_-1-1467dup others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
A | ATTTTTT | 81 | a0001c0001t0001g0125a0001c0001t0001g0202a0001c0001t0002g0219others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-1-1472_-1-1467dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
A | ATTTTTTT | 29 | a0001c0001t0001g0205a0001c0001t0002g0218a0001c0001t0002g0221others(26): Show | 29 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-1473_-1-1467dup others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
AT | A | 6 | a0001c0001t0003g0391a0001c0001t0007g0121a0001c0001t0007g0383others(3): Show | 6 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-1467delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
ATTT | A | 7 | a0003c0007t0004g0283a0003c0007t0004g0299a0003c0007t0004g0300others(4): Show | 7 | HG01081.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-1469_-1-1467del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249587
|
ATTTT | A | 7 | a0001c0002t0004g0231a0003c0007t0009g0120a0003c0007t0009g0141others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-1470_-1-1467del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | |||||
| chr19:8249668
|
T | C | 241 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-1-1408T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249668 | ||||||
| chr19:8249735
|
C | T | 5 | a0001c0001t0001g0125a0001c0012t0002g0145a0003c0007t0003g0126others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1341C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249735 | ||||||
| chr19:8249778
|
A | T | 3 | a0004c0009t0007g0285a0004c0009t0007g0291a0004c0009t0007g0336 | 3 | HG02622.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1-1298A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249778 | ||||||
| chr19:8249783
|
G | C | 1 | a0001c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-1293G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249783 | ||||||
| chr19:8249864
|
C | T | 14 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(11): Show | 14 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1212C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249864 | ||||||
| chr19:8249885
|
C | T | 194 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(191): Show | 194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.-1-1191C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249885 | ||||||
| chr19:8249969
|
G | A | 14 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(11): Show | 14 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1107G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249969 | ||||||
| chr19:8249986
|
C | T | 5 | a0001c0001t0001g0125a0001c0012t0002g0145a0003c0007t0003g0126others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1090C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249986 | ||||||
| chr19:8250000
|
A | G | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1076A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250000 | ||||||
| chr19:8250026
|
G | A | 29 | a0001c0002t0001g0024a0001c0002t0001g0158a0001c0002t0001g0163others(26): Show | 29 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-1050G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250026 | ||||||
| chr19:8250194
|
C | CA | 15 | a0001c0002t0004g0231a0003c0007t0004g0283a0003c0007t0004g0299others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1-879dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8250194 | |||||
| chr19:8250270
|
C | T | 8 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0012t0002g0145others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-806C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250270 | ||||||
| chr19:8250362
|
A | C | 1 | a0002c0003t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1-714A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250362 | ||||||
| chr19:8250377
|
A | G | 1 | a0002c0013t0001g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1-699A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250377 | ||||||
| chr19:8250442
|
C | T | 5 | a0001c0002t0002g0253a0001c0002t0002g0281a0001c0002t0002g0365others(2): Show | 5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-634C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250442 | ||||||
| chr19:8250623
|
A | G | 93 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1-453A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250623 | ||||||
| chr19:8250690
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-1-386C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250690 | ||||||
| chr19:8250703
|
C | T | 5 | a0001c0002t0002g0253a0001c0002t0002g0281a0001c0002t0002g0365others(2): Show | 5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-373C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250703 | ||||||
| chr19:8250704
|
C | T | 1 | a0002c0003t0004g0354 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-1-372C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250704 | ||||||
| chr19:8250751
|
G | A | 4 | a0001c0001t0001g0125a0003c0007t0003g0126a0003c0007t0003g0127others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-325G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250751 | ||||||
| chr19:8250816
|
A | G | 1 | a0001c0001t0002g0361 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-1-260A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250816 | ||||||
| chr19:8250893
|
G | A | 4 | a0001c0002t0001g0075a0001c0002t0001g0412a0001c0002t0005g0045others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-183G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250893 | ||||||
| chr19:8250963
|
A | G | 309 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-1-113A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250963 | ||||||
| chr19:8251326
|
C | T | 2 | a0001c0001t0012g0288a0001c0001t0017g0130 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.173+77C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251326 | ||||||
| chr19:8251368
|
C | T | 6 | a0001c0002t0001g0042a0001c0002t0001g0098a0001c0002t0001g0099others(3): Show | 6 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+119C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251368 | ||||||
| chr19:8251426
|
T | C | 55 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(52): Show | 55 | HG00280.hp1 HG00733.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.173+177T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251426 | ||||||
| chr19:8251549
|
C | T | 6 | a0003c0007t0009g0120a0003c0007t0009g0141a0003c0007t0009g0387others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+300C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251549 | ||||||
| chr19:8251594
|
TTGAGGTC others(15): Show |
T | 1 | a0001c0001t0002g0256 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.173+346_173+367del others(22): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251594 | ||||||
| chr19:8251624
|
C | G | 1 | a0001c0006t0006g0264 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.173+375C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251624 | ||||||
| chr19:8251654
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.173+405A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251654 | ||||||
| chr19:8251741
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.173+492T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251741 | ||||||
| chr19:8251800
|
T | TA | 200 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(197): Show | 200 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.173+564dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8251800 | |||||
| chr19:8251813
|
ATGTGAGC | A | 39 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(36): Show | 39 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.173+567_173+573del others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8251813 | |||||
| chr19:8251844
|
G | C | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173+595G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251844 | ||||||
| chr19:8251881
|
G | A | 29 | a0001c0002t0001g0024a0001c0002t0001g0158a0001c0002t0001g0163others(26): Show | 29 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.173+632G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251881 | ||||||
| chr19:8251928
|
A | T | 1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.173+679A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251928 | ||||||
| chr19:8251938
|
G | T | 1 | a0001c0002t0004g0335 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.173+689G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251938 | ||||||
| chr19:8252019
|
G | A | 1 | a0001c0001t0006g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.173+770G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252019 | ||||||
| chr19:8252023
|
T | C | 2 | a0001c0001t0012g0288a0001c0001t0017g0130 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.173+774T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252023 | ||||||
| chr19:8252025
|
G | C | 1 | a0001c0001t0003g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.173+776G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252025 | ||||||
| chr19:8252038
|
G | A | 4 | a0001c0001t0007g0383a0001c0001t0008g0390a0001c0001t0008g0398others(1): Show | 4 | HG01261.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+789G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252038 | ||||||
| chr19:8252064
|
T | TA | 108 | a0001c0001t0002g0003a0001c0001t0002g0135a0001c0001t0002g0139others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.173+828dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252064 | |||||
| chr19:8252064
|
T | TAA | 17 | a0001c0001t0001g0408a0001c0001t0002g0140a0001c0001t0002g0142others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.173+827_173+828dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252064 | |||||
| chr19:8252064
|
TAA | T | 206 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(203): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.173+827_173+828del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252064 | |||||
| chr19:8252073
|
A | T | 1 | a0001c0001t0004g0265 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.173+824A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252073 | ||||||
| chr19:8252094
|
G | C | 1 | a0004c0005t0011g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.173+845G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252094 | ||||||
| chr19:8252096
|
T | C | 3 | a0001c0001t0002g0244a0001c0001t0002g0295a0001c0001t0002g0296 | 3 | HG01258.hp2 HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.173+847T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252096 | ||||||
| chr19:8252106
|
C | T | 2 | a0001c0001t0002g0297a0001c0001t0003g0097 | 2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.173+857C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252106 | ||||||
| chr19:8252167
|
A | G | 1 | a0001c0008t0001g0085 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.173+918A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252167 | ||||||
| chr19:8252185
|
G | A | 139 | a0001c0001t0001g0407a0001c0001t0002g0218a0001c0001t0002g0219others(136): Show | 139 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.173+936G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252185 | ||||||
| chr19:8252316
|
G | A | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173+1067G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252316 | ||||||
| chr19:8252352
|
A | G | 254 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.173+1103A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252352 | ||||||
| chr19:8252369
|
T | TA | 382 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(379): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.173+1131dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252369 | |||||
| chr19:8252369
|
T | TAA | 7 | a0001c0001t0002g0388a0001c0001t0003g0068a0001c0001t0003g0149others(4): Show | 7 | HG00323.hp1 HG01952.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+1130_173+1131d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252369 | |||||
| chr19:8252369
|
T | TAAA | 7 | a0003c0004t0001g0106a0003c0004t0001g0132a0003c0004t0001g0402others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.173+1129_173+1131d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252369 | |||||
| chr19:8252433
|
G | C | 369 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(366): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.173+1184G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252433 | ||||||
| chr19:8252442
|
CT | C | 245 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(242): Show | 246 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.173+1207delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | |||||
| chr19:8252442
|
CTT | C | 20 | a0001c0001t0002g0347a0001c0001t0003g0066a0001c0001t0003g0067others(17): Show | 20 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.173+1206_173+1207d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | |||||
| chr19:8252442
|
CTTTT | C | 33 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(30): Show | 33 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.173+1204_173+1207d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | |||||
| chr19:8252442
|
CTTTTTT | C | 77 | a0001c0001t0002g0223a0001c0001t0002g0270a0001c0001t0003g0036others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.173+1202_173+1207d others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | |||||
| chr19:8252557
|
G | C | 1 | a0001c0001t0003g0029 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.173+1308G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252557 | ||||||
| chr19:8253022
|
A | C | 1 | a0001c0001t0002g0370 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.174-1477A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253022 | ||||||
| chr19:8253077
|
C | T | 48 | a0001c0001t0002g0218a0001c0001t0002g0230a0001c0001t0002g0245others(45): Show | 48 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.174-1422C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253077 | ||||||
| chr19:8253182
|
G | A | 4 | a0002c0003t0004g0213a0002c0003t0004g0308a0002c0003t0004g0319others(1): Show | 4 | NA18979.hp2 NA18997.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-1317G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253182 | ||||||
| chr19:8253239
|
G | GAT | 55 | a0001c0025t0001g0116a0002c0003t0001g0040a0002c0003t0001g0043others(52): Show | 56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174-1259_174-1258d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253239 | |||||
| chr19:8253261
|
A | T | 1 | a0001c0001t0003g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.174-1238A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253261 | ||||||
| chr19:8253292
|
G | GA | 5 | a0001c0008t0004g0282a0004c0005t0007g0002a0004c0005t0008g0053others(2): Show | 5 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.174-1206dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253292 | |||||
| chr19:8253298
|
C | T | 5 | a0001c0001t0003g0070a0001c0001t0003g0110a0001c0001t0003g0111others(2): Show | 5 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-1201C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253298 | ||||||
| chr19:8253325
|
C | G | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.174-1174C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253325 | ||||||
| chr19:8253428
|
TACAG | T | 7 | a0001c0001t0002g0246a0001c0001t0002g0256a0001c0001t0002g0263others(4): Show | 7 | HG02129.hp1 NA18951.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-1067_174-1064d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253428 | |||||
| chr19:8253449
|
C | CT | 118 | a0001c0001t0001g0408a0001c0001t0002g0139a0001c0001t0002g0140others(115): Show | 118 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.174-1028dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | |||||
| chr19:8253449
|
C | CTT | 13 | a0001c0001t0002g0144a0001c0001t0002g0301a0001c0001t0002g0333others(10): Show | 13 | HG02135.hp2 HG02300.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.174-1029_174-1028d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | |||||
| chr19:8253449
|
C | CTTT | 6 | a0001c0001t0003g0070a0001c0001t0003g0112a0001c0001t0003g0113others(3): Show | 6 | HG01081.hp2 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.174-1030_174-1028d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | |||||
| chr19:8253449
|
CT | C | 33 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0002g0223others(30): Show | 33 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.174-1028delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | |||||
| chr19:8253472
|
G | T | 78 | a0001c0001t0002g0270a0001c0001t0003g0029a0001c0002t0001g0042others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.174-1027G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253472 | ||||||
| chr19:8253626
|
G | A | 69 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0003g0115others(66): Show | 70 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.174-873G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253626 | ||||||
| chr19:8253702
|
T | A | 1 | a0001c0002t0004g0240 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.174-797T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253702 | ||||||
| chr19:8253716
|
G | A | 12 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0003g0115others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.174-783G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253716 | ||||||
| chr19:8253716
|
G | T | 79 | a0001c0001t0002g0270a0001c0002t0001g0042a0001c0002t0001g0075others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.174-783G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253716 | ||||||
| chr19:8253802
|
C | T | 29 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(26): Show | 29 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.174-697C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253802 | ||||||
| chr19:8253868
|
A | G | 4 | a0004c0005t0007g0287a0004c0005t0007g0384a0004c0005t0008g0251others(1): Show | 4 | HG00738.hp1 HG02735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-631A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253868 | ||||||
| chr19:8253995
|
G | A | 166 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(163): Show | 166 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.174-504G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253995 | ||||||
| chr19:8254049
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.174-450C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254049 | ||||||
| chr19:8254075
|
C | T | 55 | a0001c0025t0001g0116a0002c0003t0001g0040a0002c0003t0001g0043others(52): Show | 56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174-424C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254075 | ||||||
| chr19:8254141
|
T | C | 29 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(26): Show | 29 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.174-358T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254141 | ||||||
| chr19:8254146
|
C | T | 55 | a0001c0025t0001g0116a0002c0003t0001g0040a0002c0003t0001g0043others(52): Show | 56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174-353C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254146 | ||||||
| chr19:8254150
|
G | A | 5 | a0001c0002t0002g0253a0001c0002t0002g0281a0001c0002t0002g0365others(2): Show | 5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-349G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254150 | ||||||
| chr19:8254183
|
C | T | 6 | a0003c0007t0009g0120a0003c0007t0009g0141a0003c0007t0009g0387others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.174-316C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254183 | ||||||
| chr19:8254192
|
G | A | 1 | a0001c0008t0001g0051 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.174-307G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254192 | ||||||
| chr19:8254212
|
A | G | 2 | a0001c0001t0003g0036a0001c0001t0003g0068 | 2 | NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.174-287A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254212 | ||||||
| chr19:8254220
|
G | A | 12 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0003g0115others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.174-279G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254220 | ||||||
| chr19:8254228
|
C | G | 1 | a0002c0003t0004g0356 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174-271C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254228 | ||||||
| chr19:8254279
|
C | A | 1 | a0005c0011t0007g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.174-220C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254279 | ||||||
| chr19:8254310
|
A | C | 46 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(43): Show | 46 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.174-189A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254310 | ||||||
| chr19:8254322
|
C | CA | 36 | a0001c0001t0002g0219a0001c0001t0002g0303a0001c0001t0002g0312others(33): Show | 36 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.174-157dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAA | 9 | a0001c0001t0002g0301a0001c0001t0002g0338a0001c0001t0003g0133others(6): Show | 9 | HG01261.hp2 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.174-158_174-157dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAA | 24 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(21): Show | 24 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.174-160_174-157dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAA | 14 | a0001c0001t0002g0139a0001c0001t0002g0142a0001c0001t0002g0144others(11): Show | 14 | HG00733.hp2 HG02074.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.174-161_174-157dup others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAAA | 6 | a0001c0001t0001g0125a0001c0001t0002g0230a0001c0002t0001g0098others(3): Show | 6 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.174-162_174-157dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAAAA others(1): Show |
77 | a0001c0001t0002g0218a0001c0001t0002g0221a0001c0001t0002g0222others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.174-164_174-157dup others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAAAA others(2): Show |
68 | a0001c0001t0001g0202a0001c0001t0002g0137a0001c0001t0002g0270others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.174-165_174-157dup others(9): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAAAA others(3): Show |
50 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0002g0223others(47): Show | 50 | HG00558.hp1 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.174-166_174-157dup others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAAAA others(4): Show |
14 | a0001c0001t0002g0243a0001c0001t0002g0347a0001c0002t0002g0253others(11): Show | 14 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.174-167_174-157dup others(11): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
C | CAAAAAAA others(5): Show |
3 | a0001c0002t0002g0281a0001c0002t0003g0416a0001c0002t0003g0417 | 3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.174-168_174-157dup others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254322
|
CA | C | 7 | a0001c0001t0001g0117a0003c0007t0009g0120a0003c0007t0009g0141others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-157delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | |||||
| chr19:8254417
|
C | T | 5 | a0001c0001t0003g0070a0001c0001t0003g0110a0001c0001t0003g0111others(2): Show | 5 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-82C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254417 | ||||||
| chr19:8254461
|
T | A | 1 | a0001c0002t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.174-38T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254461 | ||||||
| chr19:8254629
|
C | T | 2 | a0002c0003t0004g0227a0002c0003t0004g0229 | 2 | NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.291+13C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254629 | ||||||
| chr19:8254638
|
C | T | 29 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(26): Show | 29 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.291+22C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254638 | ||||||
| chr19:8254643
|
C | T | 1 | a0001c0006t0006g0305 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.291+27C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254643 | ||||||
| chr19:8254687
|
C | T | 1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291+71C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254687 | ||||||
| chr19:8254763
|
A | G | 1 | a0001c0012t0002g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291+147A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254763 | ||||||
| chr19:8254783
|
A | AC | 11 | a0001c0001t0002g0301a0001c0001t0002g0303a0001c0001t0002g0312others(8): Show | 11 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.291+173dupC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 8254783 | |||||
| chr19:8254808
|
C | T | 4 | a0001c0001t0003g0046a0001c0001t0003g0047a0001c0001t0003g0048others(1): Show | 4 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+192C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254808 | ||||||
| chr19:8254845
|
C | T | 8 | a0001c0001t0001g0117a0001c0001t0003g0115a0003c0007t0009g0120others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+229C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254845 | ||||||
| chr19:8254875
|
A | AC | 53 | a0001c0001t0002g0139a0001c0001t0002g0219a0001c0001t0002g0228others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.291+267dupC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 8254875 | |||||
| chr19:8254881
|
C | G | 1 | a0002c0003t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.291+265C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254881 | ||||||
| chr19:8254883
|
C | G | 8 | a0001c0001t0003g0133a0003c0007t0004g0283a0003c0007t0004g0299others(5): Show | 8 | HG01081.hp2 HG02622.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+267C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254883 | ||||||
| chr19:8255029
|
A | G | 362 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(359): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.291+413A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255029 | ||||||
| chr19:8255132
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292-475G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255132 | ||||||
| chr19:8255204
|
C | T | 4 | a0001c0001t0007g0121a0001c0001t0007g0383a0001c0001t0008g0390others(1): Show | 4 | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-403C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255204 | ||||||
| chr19:8255303
|
G | A | 1 | a0004c0005t0008g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292-304G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255303 | ||||||
| chr19:8255315
|
C | T | 112 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(109): Show | 112 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.292-292C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255315 | ||||||
| chr19:8255332
|
G | A | 1 | a0001c0002t0005g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.292-275G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255332 | ||||||
| chr19:8255378
|
C | T | 1 | a0001c0001t0003g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.292-229C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255378 | ||||||
| chr19:8255384
|
C | T | 13 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0003g0115others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.292-223C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255384 | ||||||
| chr19:8255399
|
A | T | 1 | a0002c0003t0004g0376 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.292-208A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255399 | ||||||
| chr19:8255594
|
A | AC | 5 | a0001c0001t0003g0161a0001c0006t0006g0266a0001c0021t0005g0189others(2): Show | 5 | HG02135.hp1 HG03209.hp2 HG04204.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.292-8dupC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 8255594 | |||||
| chr19:8255763
|
G | A | 5 | a0001c0002t0002g0253a0001c0002t0002g0365a0001c0002t0003g0416others(2): Show | 5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+38G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/11 | chr19 | 8255763 | ||||||
| chr19:8255772
|
TGGGGCGG others(3): Show |
T | 72 | a0001c0002t0001g0042a0001c0002t0001g0075a0001c0002t0001g0098others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.411-46_411-37delGC others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 8255772 | |||||
| chr19:8255785
|
G | T | 33 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(30): Show | 33 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.411-37G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/11 | chr19 | 8255785 | ||||||
| chr19:8255947
|
G | C | 2 | a0001c0006t0006g0261a0001c0006t0006g0274 | 2 | NA18948.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.468+68G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8255947 | ||||||
| chr19:8255979
|
A | C | 1 | a0001c0001t0003g0026 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.468+100A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8255979 | ||||||
| chr19:8255999
|
C | A | 2 | a0001c0001t0002g0297a0001c0001t0003g0097 | 2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.468+120C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8255999 | ||||||
| chr19:8256006
|
T | G | 78 | a0001c0001t0003g0070a0001c0001t0003g0110a0001c0001t0003g0111others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+127T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256006 | ||||||
| chr19:8256015
|
G | T | 1 | a0001c0001t0003g0005 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.468+136G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256015 | ||||||
| chr19:8256017
|
G | A | 1 | a0001c0001t0002g0339 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.468+138G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256017 | ||||||
| chr19:8256081
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.469-155A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256081 | ||||||
| chr19:8256096
|
G | A | 13 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0003g0115others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-140G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256096 | ||||||
| chr19:8256172
|
C | T | 2 | a0006c0010t0001g0092a0006c0010t0015g0093 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.469-64C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256172 | ||||||
| chr19:8256173
|
G | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.469-63G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256173 | ||||||
| chr19:8256298
|
A | T | 134 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0137others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.519+12A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256298 | ||||||
| chr19:8256444
|
A | ACT | 304 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.519+159_519+160ins others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 8256444 | |||||
| chr19:8256539
|
C | T | 2 | a0001c0001t0002g0316a0001c0001t0002g0329 | 2 | NA18973.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.520-79C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256539 | ||||||
| chr19:8256569
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.520-49G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256569 | ||||||
| chr19:8256571
|
T | C | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.520-47T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256571 | ||||||
| chr19:8256721
|
A | T | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.612+11A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256721 | ||||||
| chr19:8256750
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.612+40C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256750 | ||||||
| chr19:8256774
|
A | G | 1 | a0001c0001t0002g0352 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.612+64A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256774 | ||||||
| chr19:8256829
|
T | C | 2 | a0001c0001t0002g0351a0001c0001t0003g0115 | 2 | HG03225.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.612+119T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256829 | ||||||
| chr19:8256921
|
C | T | 1 | a0001c0002t0005g0413 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.613-28C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256921 | ||||||
| chr19:8257085
|
C | T | 120 | a0001c0001t0002g0137a0001c0001t0002g0218a0001c0001t0002g0219others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
splice_region_variant&intron_variant | LOW | c.741+8C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257085 | ||||||
| chr19:8257176
|
T | C | 89 | a0001c0001t0001g0408a0001c0001t0002g0003a0001c0001t0002g0135others(86): Show | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.741+99T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257176 | ||||||
| chr19:8257177
|
G | A | 2 | a0002c0003t0001g0399a0002c0003t0004g0143 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.741+100G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257177 | ||||||
| chr19:8257185
|
A | G | 291 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(288): Show | 292 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.741+108A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257185 | ||||||
| chr19:8257303
|
C | T | 1 | a0004c0005t0008g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.741+226C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257303 | ||||||
| chr19:8257318
|
T | C | 2 | a0006c0010t0001g0092a0006c0010t0015g0093 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.741+241T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257318 | ||||||
| chr19:8257376
|
G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.741+299G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257376 | ||||||
| chr19:8257440
|
AT | A | 285 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(282): Show | 286 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.741+374delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 8257440 | |||||
| chr19:8257457
|
G | A | 13 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0003g0115others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.741+380G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257457 | ||||||
| chr19:8257588
|
G | A | 1 | a0002c0003t0004g0332 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.742-291G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257588 | ||||||
| chr19:8257608
|
G | C | 1 | a0001c0002t0004g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.742-271G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257608 | ||||||
| chr19:8257633
|
T | C | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.742-246T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257633 | ||||||
| chr19:8257677
|
G | A | 10 | a0001c0002t0001g0042a0001c0002t0001g0075a0001c0002t0001g0098others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-202G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257677 | ||||||
| chr19:8257709
|
C | T | 1 | a0001c0002t0005g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.742-170C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257709 | ||||||
| chr19:8257710
|
G | A | 234 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0137others(231): Show | 235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.742-169G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257710 | ||||||
| chr19:8257768
|
G | A | 1 | a0001c0001t0008g0398 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.742-111G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257768 | ||||||
| chr19:8257801
|
T | A | 6 | a0001c0002t0002g0253a0001c0002t0002g0281a0001c0002t0002g0365others(3): Show | 6 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-78T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257801 | ||||||
| chr19:8257838
|
G | A | 2 | a0001c0008t0001g0211a0004c0005t0008g0209 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.742-41G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257838 | ||||||
| chr19:8257849
|
G | T | 3 | a0001c0002t0006g0238a0001c0002t0006g0242a0001c0002t0006g0247 | 3 | HG00642.hp2 HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.742-30G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257849 | ||||||
| chr19:8257850
|
A | T | 3 | a0001c0002t0006g0238a0001c0002t0006g0242a0001c0002t0006g0247 | 3 | HG00642.hp2 HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.742-29A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257850 | ||||||
| chr19:8258013
|
G | A | 2 | a0001c0001t0012g0288a0001c0001t0017g0130 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.848+28G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258013 | ||||||
| chr19:8258156
|
G | A | 1 | a0002c0003t0004g0293 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.848+171G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258156 | ||||||
| chr19:8258173
|
AATT | A | 5 | a0001c0001t0001g0125a0003c0007t0001g0037a0003c0007t0003g0126others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+196_848+198del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8258173 | |||||
| chr19:8258311
|
A | ATCCCGGC others(3): Show |
1 | a0001c0001t0002g0371 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.848+328_848+337dup others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8258311 | |||||
| chr19:8258408
|
C | T | 2 | a0001c0001t0004g0254a0001c0001t0004g0353 | 2 | HG02083.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.848+423C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258408 | ||||||
| chr19:8258425
|
C | G | 285 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(282): Show | 286 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.848+440C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258425 | ||||||
| chr19:8258507
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.848+522C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258507 | ||||||
| chr19:8258546
|
T | C | 3 | a0002c0003t0001g0392a0002c0003t0001g0404a0002c0003t0004g0143 | 3 | HG01891.hp1 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.848+561T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258546 | ||||||
| chr19:8258619
|
A | C | 365 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(362): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.848+634A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258619 | ||||||
| chr19:8258677
|
TATTAAAA | T | 8 | a0001c0002t0001g0042a0001c0002t0001g0075a0001c0002t0001g0098others(5): Show | 8 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+704_848+710del others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8258677 | |||||
| chr19:8258699
|
G | A | 1 | a0003c0004t0001g0402 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.848+714G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258699 | ||||||
| chr19:8258702
|
C | T | 1 | a0003c0004t0004g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.848+717C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258702 | ||||||
| chr19:8258865
|
G | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0125a0003c0007t0003g0126others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.848+880G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258865 | ||||||
| chr19:8258874
|
C | T | 113 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(110): Show | 113 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.848+889C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258874 | ||||||
| chr19:8258965
|
C | G | 1 | a0002c0003t0004g0304 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.848+980C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258965 | ||||||
| chr19:8259006
|
C | T | 16 | a0001c0008t0004g0282a0001c0008t0004g0357a0002c0003t0001g0040others(13): Show | 16 | HG01891.hp1 HG01981.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.848+1021C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259006 | ||||||
| chr19:8259026
|
C | G | 3 | a0003c0004t0001g0150a0003c0004t0001g0165a0003c0004t0001g0182 | 3 | NA18966.hp1 NA18979.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.848+1041C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259026 | ||||||
| chr19:8259113
|
G | A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.848+1128G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259113 | ||||||
| chr19:8259159
|
G | A | 1 | a0001c0002t0006g0241 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.848+1174G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259159 | ||||||
| chr19:8259220
|
G | A | 6 | a0001c0001t0003g0064a0001c0002t0002g0253a0001c0002t0002g0281others(3): Show | 6 | HG00642.hp1 HG02300.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+1235G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259220 | ||||||
| chr19:8259231
|
G | A | 2 | a0001c0001t0006g0226a0008c0024t0008g0108 | 2 | HG03579.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.848+1246G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259231 | ||||||
| chr19:8259463
|
C | T | 112 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.848+1478C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259463 | ||||||
| chr19:8259549
|
A | C | 1 | a0003c0004t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.848+1564A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259549 | ||||||
| chr19:8259634
|
C | G | 1 | a0002c0003t0008g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.848+1649C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259634 | ||||||
| chr19:8259749
|
G | C | 2 | a0001c0001t0003g0105a0001c0001t0003g0391 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.848+1764G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259749 | ||||||
| chr19:8259764
|
G | A | 16 | a0001c0008t0004g0282a0001c0008t0004g0357a0002c0003t0001g0040others(13): Show | 16 | HG01891.hp1 HG01981.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.848+1779G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259764 | ||||||
| chr19:8259813
|
G | A | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.848+1828G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259813 | ||||||
| chr19:8259856
|
G | A | 1 | a0001c0001t0002g0385 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.849-1832G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259856 | ||||||
| chr19:8259939
|
C | G | 1 | a0001c0012t0002g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849-1749C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259939 | ||||||
| chr19:8259940
|
T | C | 95 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0135others(92): Show | 95 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.849-1748T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259940 | ||||||
| chr19:8259941
|
C | T | 95 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0135others(92): Show | 95 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.849-1747C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259941 | ||||||
| chr19:8259952
|
C | A | 65 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0135others(62): Show | 65 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.849-1736C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259952 | ||||||
| chr19:8259957
|
T | C | 1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1731T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259957 | ||||||
| chr19:8259959
|
C | A | 1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1729C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259959 | ||||||
| chr19:8259960
|
A | G | 1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1728A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259960 | ||||||
| chr19:8259971
|
C | A | 1 | a0001c0002t0004g0239 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.849-1717C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259971 | ||||||
| chr19:8259976
|
T | A | 1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1712T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259976 | ||||||
| chr19:8260006
|
A | AGATAAGG others(3): Show |
1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1682_849-1681i others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260006 | ||||||
| chr19:8260009
|
T | G | 133 | a0001c0001t0002g0003a0001c0001t0002g0137a0001c0001t0002g0218others(130): Show | 134 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.849-1679T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260009 | ||||||
| chr19:8260020
|
T | A | 1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1668T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260020 | ||||||
| chr19:8260021
|
G | T | 1 | a0004c0009t0007g0134 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1667G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260021 | ||||||
| chr19:8260111
|
C | G | 183 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0003others(180): Show | 184 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.849-1577C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260111 | ||||||
| chr19:8260301
|
TCTC | T | 65 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0135others(62): Show | 65 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.849-1384_849-1382d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260301 | |||||
| chr19:8260330
|
A | G | 1 | a0001c0012t0002g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849-1358A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260330 | ||||||
| chr19:8260369
|
A | AT | 65 | a0001c0001t0005g0096a0001c0001t0006g0220a0001c0001t0006g0225others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(62): Show |
intron_variant | MODIFIER | c.849-1302dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | |||||
| chr19:8260369
|
A | ATT | 9 | a0001c0002t0005g0038a0001c0002t0005g0082a0001c0002t0006g0234others(6): Show | 9 | HG00639.hp2 HG00642.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-1303_849-1302d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | |||||
| chr19:8260369
|
AT | A | 50 | a0001c0001t0001g0407a0001c0001t0001g0408a0001c0001t0002g0373others(47): Show | 50 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.849-1302delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | |||||
| chr19:8260369
|
ATT | A | 157 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(154): Show | 158 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.849-1303_849-1302d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | |||||
| chr19:8260369
|
ATTT | A | 24 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0137others(21): Show | 24 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-1304_849-1302d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | |||||
| chr19:8260369
|
ATTTT | A | 41 | a0001c0001t0002g0135a0001c0001t0002g0139a0001c0001t0002g0142others(38): Show | 41 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.849-1305_849-1302d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | |||||
| chr19:8260533
|
G | GA | 160 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(157): Show | 160 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.849-1145dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260533 | |||||
| chr19:8260533
|
G | GAA | 123 | a0001c0001t0001g0407a0001c0001t0002g0003a0001c0001t0002g0137others(120): Show | 124 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.849-1146_849-1145d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260533 | |||||
| chr19:8260651
|
TAAAG | T | 3 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0019 | 3 | HG02040.hp2 NA18747.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.849-1034_849-1031d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260651 | |||||
| chr19:8260675
|
T | C | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101 | 3 | HG01074.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.849-1013T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260675 | ||||||
| chr19:8260681
|
G | A | 1 | a0004c0009t0007g0336 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.849-1007G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260681 | ||||||
| chr19:8260699
|
C | T | 1 | a0002c0003t0004g0304 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.849-989C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260699 | ||||||
| chr19:8260732
|
T | A | 186 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0003others(183): Show | 187 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.849-956T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260732 | ||||||
| chr19:8260752
|
C | A | 1 | a0001c0006t0006g0380 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.849-936C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260752 | ||||||
| chr19:8260915
|
C | T | 10 | a0001c0001t0002g0362a0001c0001t0003g0148a0001c0001t0003g0168others(7): Show | 10 | HG00558.hp2 NA18947.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-773C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260915 | ||||||
| chr19:8260945
|
C | T | 6 | a0001c0001t0003g0133a0003c0007t0001g0037a0003c0007t0004g0283others(3): Show | 6 | HG01081.hp2 HG02258.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-743C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260945 | ||||||
| chr19:8260946
|
A | G | 232 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0003others(229): Show | 233 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.849-742A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260946 | ||||||
| chr19:8260950
|
C | CA | 24 | a0001c0001t0004g0255a0001c0002t0001g0176a0001c0002t0004g0335others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-711dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260950
|
C | CAA | 12 | a0001c0002t0001g0042a0001c0002t0001g0075a0001c0002t0001g0098others(9): Show | 12 | HG00408.hp2 HG00621.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.849-712_849-711dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260950
|
C | CAAAA | 15 | a0001c0002t0001g0396a0001c0002t0004g0236a0001c0002t0005g0058others(12): Show | 15 | HG00642.hp2 HG01069.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-714_849-711dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260950
|
C | CAAAAA | 24 | a0001c0001t0006g0220a0001c0001t0006g0226a0001c0001t0006g0369others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-715_849-711dup others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260950
|
C | CAAAAAA | 19 | a0001c0001t0005g0096a0001c0001t0006g0225a0001c0002t0005g0038others(16): Show | 19 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.849-716_849-711dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260950
|
C | CAAAAAAA | 10 | a0001c0001t0006g0379a0001c0002t0005g0084a0001c0002t0006g0342others(7): Show | 10 | HG01346.hp2 HG02071.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-717_849-711dup others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260950
|
CA | C | 19 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(16): Show | 19 | HG00280.hp2 HG00609.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.849-711delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | |||||
| chr19:8260958
|
A | AAAC | 11 | a0001c0001t0002g0269a0001c0001t0002g0289a0001c0001t0003g0035others(8): Show | 11 | HG01891.hp1 HG01978.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.849-728_849-727ins others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260958 | |||||
| chr19:8260958
|
A | AAC | 212 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0003others(209): Show | 213 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.849-729_849-728ins others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260958 | |||||
| chr19:8260962
|
A | C | 1 | a0004c0005t0007g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849-726A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260962 | ||||||
| chr19:8260966
|
A | C | 2 | a0001c0001t0002g0333a0001c0001t0003g0011 | 2 | HG02135.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.849-722A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260966 | ||||||
| chr19:8260967
|
A | C | 228 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0003others(225): Show | 229 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.849-721A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260967 | ||||||
| chr19:8260968
|
AAAAAAAA others(3): Show |
A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849-717_849-708del others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260968 | |||||
| chr19:8260971
|
A | C | 2 | a0004c0005t0007g0294a0004c0005t0008g0209 | 2 | HG02004.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.849-717A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260971 | ||||||
| chr19:8261052
|
A | G | 1 | a0001c0002t0006g0386 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.849-636A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261052 | ||||||
| chr19:8261122
|
A | G | 1 | a0001c0001t0003g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.849-566A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261122 | ||||||
| chr19:8261183
|
C | T | 99 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(96): Show | 99 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.849-505C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261183 | ||||||
| chr19:8261191
|
G | T | 16 | a0001c0008t0004g0282a0001c0008t0004g0357a0002c0003t0001g0040others(13): Show | 16 | HG01891.hp1 HG01981.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.849-497G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261191 | ||||||
| chr19:8261209
|
T | TA | 114 | a0001c0001t0002g0003a0001c0001t0002g0137a0001c0001t0002g0218others(111): Show | 115 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.849-478dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8261209 | |||||
| chr19:8261253
|
A | T | 199 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0003others(196): Show | 200 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.849-435A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261253 | ||||||
| chr19:8261262
|
T | C | 7 | a0001c0001t0007g0121a0001c0001t0007g0383a0001c0001t0008g0390others(4): Show | 7 | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-426T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261262 | ||||||
| chr19:8261296
|
C | A | 1 | a0001c0001t0008g0390 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849-392C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261296 | ||||||
| chr19:8261360
|
A | G | 278 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0202others(275): Show | 279 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.849-328A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261360 | ||||||
| chr19:8261464
|
G | A | 1 | a0003c0004t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.849-224G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261464 | ||||||
| chr19:8261491
|
G | T | 1 | a0001c0001t0002g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.849-197G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261491 | ||||||
| chr19:8261625
|
C | A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849-63C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261625 | ||||||
| chr19:8261646
|
G | A | 1 | a0001c0006t0006g0232 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.849-42G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261646 | ||||||
| chr19:8261665
|
T | G | 3 | a0001c0001t0002g0314a0001c0001t0012g0288a0001c0001t0017g0130 | 3 | HG02572.hp1 HG03209.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.849-23T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261665 | ||||||
| chr19:8261857
|
C | T | 2 | a0001c0002t0004g0231a0008c0024t0008g0108 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1005+13C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261857 | ||||||
| chr19:8261881
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1005+37C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261881 | ||||||
| chr19:8261888
|
T | C | 9 | a0001c0002t0001g0042a0001c0002t0001g0075a0001c0002t0001g0098others(6): Show | 9 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006-42T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261888 | ||||||
| chr19:8261894
|
C | G | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1006-36C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261894 |