Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57586 |
|---|---|
| ensemblid | ENSG00000019505.8 |
| hgncid | 14962 |
| symbol | SYT13 |
| name | synaptotagmin 13 |
| refseq_nuc | NM_020826.3 |
| refseq_prot | NP_065877.1 |
| ensembl_nuc | ENST00000020926.8 |
| ensembl_prot | ENSP00000020926.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 45240302 |
| end | 45286341 |
| strand | - |
| ver | v1.2 |
| region | chr11:45240302-45286341 |
| region5000 | chr11:45235302-45291341 |
| regionname0 | SYT13_chr11_45240302_45286341 |
| regionname5000 | SYT13_chr11_45235302_45291341 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 426 | 359 | 84 | 61 | 169 | 6 | 37 | 131 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0002 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0003 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0004 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0005 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0006 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0007 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0008 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1281 | 355 | 82 | 61 | 169 | 6 | 35 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0002 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0003 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0004 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0005 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0006 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0007 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0008 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0009 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0010 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0011 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| c0012 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| 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 | 1/0 | 3885 | 122 | 15 | 32 | 69 | 0 | 5 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0002 | 0/0 | 3886 | 100 | 27 | 16 | 42 | 4 | 11 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0003 | 0/1 | 3889 | 32 | 4 | 6 | 11 | 0 | 10 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0004 | 0/0 | 3888 | 17 | 3 | 2 | 4 | 2 | 6 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0005 | 0/0 | 3885 | 16 | 1 | 0 | 13 | 0 | 2 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0006 | 0/0 | 3885 | 16 | 0 | 0 | 16 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0007 | 0/0 | 3885 | 8 | 7 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0008 | 0/0 | 3885 | 6 | 5 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0009 | 0/0 | 3886 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0010 | 0/0 | 3885 | 4 | 2 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0011 | 0/0 | 3885 | 4 | 4 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0012 | 0/0 | 3886 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0013 | 0/0 | 3885 | 3 | 3 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0014 | 0/0 | 3886 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0015 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0016 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0017 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0018 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0019 | 0/0 | 3886 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0020 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0021 | 0/0 | 3886 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0022 | 0/0 | 3886 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0023 | 0/0 | 3886 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0024 | 0/0 | 3888 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0025 | 0/0 | 3889 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0026 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0027 | 0/0 | 3886 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0028 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0029 | 0/0 | 3886 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0030 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0031 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0032 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0033 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0034 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0035 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0036 | 0/0 | 3886 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0037 | 0/0 | 3886 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0038 | 0/0 | 3886 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| t0039 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| 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 | 8 | 0 | 0 | 8 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0005 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1281 | 355 | 82 | 61 | 169 | 6 | 35 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0005 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0007 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0010 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0011 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0002c0002 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0003c0012 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0004c0008 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0005c0009 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0006c0006 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0007c0004 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0008c0003 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5165 | 122 | 15 | 32 | 69 | 0 | 5 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0002 | 0/0 | 5166 | 98 | 26 | 16 | 42 | 4 | 10 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0003 | 0/1 | 5169 | 30 | 4 | 5 | 11 | 0 | 9 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0004 | 0/0 | 5168 | 17 | 3 | 2 | 4 | 2 | 6 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0005 | 0/0 | 5165 | 15 | 1 | 0 | 13 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0006 | 0/0 | 5165 | 16 | 0 | 0 | 16 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0007 | 0/0 | 5165 | 8 | 7 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0008 | 0/0 | 5165 | 5 | 4 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0009 | 0/0 | 5166 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0010 | 0/0 | 5165 | 4 | 2 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0011 | 0/0 | 5165 | 4 | 4 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0012 | 0/0 | 5166 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0013 | 0/0 | 5165 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0014 | 0/0 | 5166 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0016 | 0/0 | 5165 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0017 | 0/0 | 5165 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0018 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0019 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0020 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0021 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0023 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0024 | 0/0 | 5168 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0025 | 0/0 | 5169 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0026 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0027 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0028 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0029 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0030 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0031 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0032 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0033 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0034 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0035 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0036 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0037 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0001t0038 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0005t0002 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0007t0015 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0010t0022 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0001c0011t0003 | 0/0 | 5169 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0002c0002t0039 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0003c0012t0013 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0004c0008t0003 | 0/0 | 5169 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0005c0009t0015 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0006c0006t0005 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0007c0004t0008 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| a0008c0003t0002 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | copy fasta | chr11 | 45235302 | 45291341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0007g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0009g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0010g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0013g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0014g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0016g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0017g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0018g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0019g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0020g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0021g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0023g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0024g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0025g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0026g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0027g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0028g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0029g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0030g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0031g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0032g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0033g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0034g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0035g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0036g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0037g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0001t0038g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0007t0015g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0010t0022g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0001c0011t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0002c0002t0039g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0003c0012t0013g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0004c0008t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0005c0009t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0006c0006t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0007c0004t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| a0008c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0174 | EUR | GBR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0222 | EUR | GBR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | FIN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00544 | hp2 | a0001 | c0001 | t0009 | g0075 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0099 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01069 | hp2 | a0001 | c0001 | t0026 | g0214 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0213 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0060 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0050 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0262 | EUR | IBS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01884 | hp2 | a0001 | c0001 | t0030 | g0129 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01952 | hp1 | a0001 | c0001 | t0018 | g0074 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0189 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02004 | hp1 | a0004 | c0008 | t0003 | g0227 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02056 | hp2 | a0001 | c0001 | t0029 | g0273 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | CDX | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CDX | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0020 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02258 | hp2 | a0001 | c0001 | t0028 | g0066 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02280 | hp2 | a0001 | c0001 | t0035 | g0244 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02451 | hp1 | a0005 | c0009 | t0015 | g0067 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0116 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02615 | hp2 | a0001 | c0007 | t0015 | g0068 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02622 | hp1 | a0001 | c0001 | t0036 | g0132 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02647 | hp2 | a0001 | c0010 | t0022 | g0271 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02698 | hp2 | a0001 | c0001 | t0031 | g0158 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0055 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0270 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02818 | hp2 | a0003 | c0012 | t0013 | g0269 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02896 | hp1 | a0007 | c0004 | t0008 | g0044 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0115 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02965 | hp2 | a0001 | c0001 | t0017 | g0020 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0209 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0051 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0027 | AFR | ESN | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0130 | AFR | GWD | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03669 | hp1 | a0001 | c0001 | t0021 | g0081 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03704 | hp1 | a0001 | c0001 | t0023 | g0108 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03710 | hp1 | a0006 | c0006 | t0005 | g0252 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0233 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | STU | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0216 | SAS | STU | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04184 | hp1 | a0001 | c0001 | t0034 | g0165 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0232 | SAS | STU | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04228 | hp1 | a0001 | c0005 | t0002 | g0098 | SAS | STU | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | STU | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18906 | hp1 | a0001 | c0001 | t0037 | g0101 | AFR | YRI | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18944 | hp2 | a0001 | c0001 | t0032 | g0163 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18950 | hp1 | a0001 | c0001 | t0024 | g0218 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18953 | hp1 | a0001 | c0001 | t0012 | g0126 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18963 | hp2 | a0001 | c0001 | t0033 | g0194 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18987 | hp1 | a0001 | c0001 | t0025 | g0219 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19002 | hp1 | a0001 | c0001 | t0038 | g0083 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | LWK | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | LWK | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | LWK | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0138 | AFR | LWK | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19078 | hp2 | a0002 | c0002 | t0039 | g0275 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19081 | hp2 | a0001 | c0001 | t0012 | g0078 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19082 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19087 | hp2 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19089 | hp2 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | YRI | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | ASW | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ASW | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | GIH | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA20905 | hp2 | a0001 | c0011 | t0003 | g0260 | SAS | GIH | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0027 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | ACB | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| HG03471 | hp2 | a0008 | c0003 | t0002 | g0062 | AFR | MSL | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18955 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | USA | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0112 | AFR | USA | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | LWK | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0220 | REF | REF | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0069 | REF | REF | SYT13_chr11_45235302_45291341 | SYT13 | chr11 | 45235302 | 45291341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45240304
|
C | T | 1 | a0001 | 1 | NA18963.hp2 | splice_region_variant | LOW | c.*3748G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | chr11 | 45240304 | ||||||
| chr11:45244167
|
G | A | 1 | a0005 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1166C>T | p.Ala389Val | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1300/5165 | 1166/1281 | 389/426 | chr11 | 45244167 | ||
| chr11:45244320
|
C | T | 1 | a0004 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1013G>A | p.Arg338Gln | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1147/5165 | 1013/1281 | 338/426 | chr11 | 45244320 | ||
| chr11:45252441
|
C | T | 1 | a0006 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.826G>A | p.Glu276Lys | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/6 | 960/5165 | 826/1281 | 276/426 | chr11 | 45252441 | ||
| chr11:45252558
|
C | T | 1 | a0007 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.709G>A | p.Ala237Thr | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/6 | 843/5165 | 709/1281 | 237/426 | chr11 | 45252558 | ||
| chr11:45255714
|
G | A | 1 | a0003 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.361C>T | p.Arg121Cys | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/6 | 495/5165 | 361/1281 | 121/426 | chr11 | 45255714 | ||
| chr11:45255804
|
C | T | 1 | a0008 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.271G>A | p.Ala91Thr | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/6 | 405/5165 | 271/1281 | 91/426 | chr11 | 45255804 | ||
| chr11:45286077
|
T | G | 1 | a0002 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.131A>C | p.Gln44Pro | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/6 | 265/5165 | 131/1281 | 44/426 | chr11 | 45286077 | ||
| chr11:45286083
|
C | T | 1 | a0002 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.125G>A | p.Arg42Gln | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/6 | 259/5165 | 125/1281 | 42/426 | chr11 | 45286083 | ||
| chr11:45286131
|
A | C | 1 | a0002 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.77T>G | p.Val26Gly | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/6 | 211/5165 | 77/1281 | 26/426 | chr11 | 45286131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45244262
|
G | A | 1 | a0001c0010 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1071C>T | p.Asn357Asn | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1205/5165 | 1071/1281 | 357/426 | chr11 | 45244262 | ||
| chr11:45246390
|
C | T | 1 | a0001c0007 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.969G>A | p.Leu323Leu | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/6 | 1103/5165 | 969/1281 | 323/426 | chr11 | 45246390 | ||
| chr11:45252481
|
C | T | 1 | a0001c0005 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.786G>A | p.Leu262Leu | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/6 | 920/5165 | 786/1281 | 262/426 | chr11 | 45252481 | ||
| chr11:45254343
|
G | A | 1 | a0001c0011 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.471C>T | p.Asn157Asn | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/6 | 605/5165 | 471/1281 | 157/426 | chr11 | 45254343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45240306
|
G | A | 2 | a0001c0001t0024a0001c0001t0025 | 2 | NA18950.hp1 NA18987.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3746C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3746 | chr11 | 45240306 | |||||
| chr11:45240575
|
C | T | 14 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(11): Show | 121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*3477G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3477 | chr11 | 45240575 | |||||
| chr11:45240691
|
G | A | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*3361C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3361 | chr11 | 45240691 | |||||
| chr11:45240705
|
A | G | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*3347T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3347 | chr11 | 45240705 | |||||
| chr11:45240731
|
C | T | 1 | a0001c0001t0032 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3321G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3321 | chr11 | 45240731 | |||||
| chr11:45240732
|
G | A | 2 | a0001c0001t0011a0001c0001t0030 | 5 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3320C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3320 | chr11 | 45240732 | |||||
| chr11:45240840
|
C | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3212G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3212 | chr11 | 45240840 | |||||
| chr11:45240855
|
C | T | 3 | a0001c0001t0013a0001c0001t0020a0003c0012t0013 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3197G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 3197 | chr11 | 45240855 | |||||
| chr11:45241111
|
C | T | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*2941G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2941 | chr11 | 45241111 | |||||
| chr11:45241349
|
T | C | 1 | a0001c0001t0034 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2703A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2703 | chr11 | 45241349 | |||||
| chr11:45241513
|
G | A | 3 | a0001c0001t0013a0001c0001t0020a0003c0012t0013 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2539C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2539 | chr11 | 45241513 | |||||
| chr11:45241513
|
G | C | 1 | a0001c0001t0026 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2539C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2539 | chr11 | 45241513 | |||||
| chr11:45241513
|
G | GC | 15 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(12): Show | 119 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2538dupG | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2538 | chr11 | 45241513 | |||||
| chr11:45241513
|
G | GCCC | 3 | a0001c0001t0004a0001c0001t0024a0001c0001t0028 | 19 | HG00099.hp1 HG00597.hp2 HG01074.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2536_*2538dupGGG | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2538 | chr11 | 45241513 | |||||
| chr11:45241513
|
G | GCCCC | 4 | a0001c0001t0003a0001c0001t0025a0001c0011t0003others(1): Show | 33 | HG01099.hp1 HG01109.hp2 HG01168.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2535_*2538dupGGGG | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2538 | chr11 | 45241513 | |||||
| chr11:45241521
|
A | C | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): Show | 81 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2531T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2531 | chr11 | 45241521 | |||||
| chr11:45241595
|
C | T | 1 | a0001c0001t0031 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2457G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2457 | chr11 | 45241595 | |||||
| chr11:45241607
|
C | T | 1 | a0001c0001t0030 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2445G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2445 | chr11 | 45241607 | |||||
| chr11:45241632
|
G | A | 2 | a0001c0001t0008a0007c0004t0008 | 6 | HG01261.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2420C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2420 | chr11 | 45241632 | |||||
| chr11:45241707
|
A | G | 14 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(11): Show | 121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2345T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2345 | chr11 | 45241707 | |||||
| chr11:45241789
|
C | T | 12 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(9): Show | 71 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2263G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2263 | chr11 | 45241789 | |||||
| chr11:45241847
|
C | G | 2 | a0001c0001t0016a0001c0001t0029 | 3 | HG02056.hp2 HG02723.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2205G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2205 | chr11 | 45241847 | |||||
| chr11:45241865
|
C | T | 1 | a0001c0001t0009 | 4 | HG00544.hp2 NA18950.hp2 NA18955.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2187G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2187 | chr11 | 45241865 | |||||
| chr11:45241887
|
C | A | 3 | a0001c0001t0028a0001c0007t0015a0005c0009t0015 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2165G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2165 | chr11 | 45241887 | |||||
| chr11:45242026
|
A | C | 3 | a0001c0001t0013a0001c0001t0020a0003c0012t0013 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2026T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 2026 | chr11 | 45242026 | |||||
| chr11:45242129
|
A | G | 1 | a0001c0001t0023 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1923T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1923 | chr11 | 45242129 | |||||
| chr11:45242143
|
A | C | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1909T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1909 | chr11 | 45242143 | |||||
| chr11:45242250
|
C | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1802G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1802 | chr11 | 45242250 | |||||
| chr11:45242295
|
G | A | 1 | a0001c0001t0007 | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1757C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1757 | chr11 | 45242295 | |||||
| chr11:45242435
|
G | T | 3 | a0001c0001t0013a0001c0001t0020a0003c0012t0013 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1617C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1617 | chr11 | 45242435 | |||||
| chr11:45242474
|
G | C | 32 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(29): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1578C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1578 | chr11 | 45242474 | |||||
| chr11:45242500
|
C | T | 2 | a0001c0001t0006a0002c0002t0039 | 17 | HG00438.hp1 HG02056.hp1 HG02129.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1552G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1552 | chr11 | 45242500 | |||||
| chr11:45242517
|
C | T | 1 | a0001c0010t0022 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1535 | chr11 | 45242517 | |||||
| chr11:45242726
|
C | T | 39 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(36): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*1326G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1326 | chr11 | 45242726 | |||||
| chr11:45242945
|
G | T | 1 | a0001c0001t0021 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1107C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1107 | chr11 | 45242945 | |||||
| chr11:45242968
|
A | G | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1084T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 1084 | chr11 | 45242968 | |||||
| chr11:45243141
|
C | T | 1 | a0001c0001t0014 | 2 | HG02486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*911G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 911 | chr11 | 45243141 | |||||
| chr11:45243156
|
T | C | 1 | a0001c0001t0012 | 4 | NA18953.hp1 NA19081.hp2 NA19087.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*896A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 896 | chr11 | 45243156 | |||||
| chr11:45243284
|
G | T | 1 | a0001c0001t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 768 | chr11 | 45243284 | |||||
| chr11:45243397
|
G | A | 1 | a0001c0001t0035 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 655 | chr11 | 45243397 | |||||
| chr11:45243534
|
G | A | 1 | a0001c0001t0020 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*518C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 518 | chr11 | 45243534 | |||||
| chr11:45243578
|
C | T | 1 | a0001c0001t0020 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*474G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 474 | chr11 | 45243578 | |||||
| chr11:45243634
|
C | G | 1 | a0001c0001t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 418 | chr11 | 45243634 | |||||
| chr11:45243791
|
G | A | 1 | a0001c0001t0036 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 261 | chr11 | 45243791 | |||||
| chr11:45243795
|
T | C | 1 | a0001c0001t0037 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*257A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 257 | chr11 | 45243795 | |||||
| chr11:45243954
|
A | T | 1 | a0001c0001t0018 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 98 | chr11 | 45243954 | |||||
| chr11:45243963
|
T | C | 1 | a0001c0001t0038 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 6/6 | 89 | chr11 | 45243963 | |||||
| chr11:45286314
|
G | C | 1 | a0002c0002t0039 | 1 | NA19078.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/6 | 107 | chr11 | 45286314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45244492
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.977-136A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244492 | ||||||
| chr11:45244612
|
A | G | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.977-256T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244612 | ||||||
| chr11:45244677
|
C | G | 1 | a0001c0001t0009g0076 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.977-321G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244677 | ||||||
| chr11:45244719
|
C | T | 22 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0049others(19): Show | 30 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-363G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244719 | ||||||
| chr11:45244741
|
A | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(223): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.977-385T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244741 | ||||||
| chr11:45244752
|
A | C | 7 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(4): Show | 10 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.977-396T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244752 | ||||||
| chr11:45244753
|
G | A | 7 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(4): Show | 10 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.977-397C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244753 | ||||||
| chr11:45244798
|
C | T | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.977-442G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244798 | ||||||
| chr11:45244844
|
T | C | 149 | a0001c0001t0001g0102a0001c0001t0002g0001a0001c0001t0002g0004others(146): Show | 190 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.977-488A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244844 | ||||||
| chr11:45244849
|
G | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.977-493C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244849 | ||||||
| chr11:45244895
|
T | C | 151 | a0001c0001t0001g0102a0001c0001t0002g0001a0001c0001t0002g0004others(148): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.977-539A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244895 | ||||||
| chr11:45244919
|
T | C | 59 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0049others(56): Show | 67 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.977-563A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45244919 | ||||||
| chr11:45245152
|
C | T | 1 | a0001c0001t0014g0027 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.977-796G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245152 | ||||||
| chr11:45245388
|
A | G | 84 | a0001c0001t0001g0102a0001c0001t0002g0001a0001c0001t0002g0004others(81): Show | 116 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.976+995T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245388 | ||||||
| chr11:45245408
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.976+975A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245408 | ||||||
| chr11:45245460
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.976+923A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245460 | ||||||
| chr11:45245574
|
C | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0142others(2): Show | 6 | NA18981.hp2 NA19001.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.976+809G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245574 | ||||||
| chr11:45245610
|
C | T | 5 | a0001c0001t0003g0217a0001c0001t0003g0220a0001c0001t0004g0188others(2): Show | 5 | HG01069.hp2 HG01099.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+773G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245610 | ||||||
| chr11:45245611
|
G | A | 1 | a0001c0001t0007g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.976+772C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245611 | ||||||
| chr11:45245691
|
C | T | 7 | a0001c0001t0011g0054a0001c0001t0011g0128a0001c0001t0011g0130others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.976+692G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245691 | ||||||
| chr11:45245741
|
C | T | 2 | a0001c0001t0008g0043a0001c0001t0008g0050 | 2 | HG01261.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.976+642G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245741 | ||||||
| chr11:45245785
|
G | T | 6 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.976+598C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245785 | ||||||
| chr11:45245883
|
G | A | 1 | a0001c0001t0011g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.976+500C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45245883 | ||||||
| chr11:45246164
|
A | G | 163 | a0001c0001t0001g0102a0001c0001t0002g0001a0001c0001t0002g0004others(160): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.976+219T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45246164 | ||||||
| chr11:45246180
|
A | G | 5 | a0001c0001t0002g0063a0001c0001t0002g0111a0001c0001t0010g0116others(2): Show | 6 | HG02486.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.976+203T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45246180 | ||||||
| chr11:45246243
|
C | A | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.976+140G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45246243 | ||||||
| chr11:45246260
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.976+123C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45246260 | ||||||
| chr11:45246334
|
A | G | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.976+49T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 5/5 | chr11 | 45246334 | ||||||
| chr11:45246639
|
G | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-127C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45246639 | ||||||
| chr11:45246716
|
G | C | 1 | a0001c0005t0002g0098 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.847-204C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45246716 | ||||||
| chr11:45247058
|
T | C | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.847-546A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247058 | ||||||
| chr11:45247078
|
C | T | 1 | a0001c0001t0008g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.847-566G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247078 | ||||||
| chr11:45247126
|
G | C | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.847-614C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247126 | ||||||
| chr11:45247184
|
C | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02132.hp2 NA18944.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.847-672G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247184 | ||||||
| chr11:45247246
|
C | T | 1 | a0001c0001t0002g0024 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.847-734G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247246 | ||||||
| chr11:45247405
|
T | C | 6 | a0001c0001t0008g0043a0001c0001t0008g0045a0001c0001t0008g0047others(3): Show | 6 | HG01261.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.847-893A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247405 | ||||||
| chr11:45247438
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.847-926C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247438 | ||||||
| chr11:45247696
|
C | T | 4 | a0001c0001t0002g0063a0001c0001t0002g0111a0001c0001t0014g0027others(1): Show | 5 | HG02486.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-1184G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247696 | ||||||
| chr11:45247860
|
G | A | 1 | a0001c0001t0004g0228 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.847-1348C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247860 | ||||||
| chr11:45247872
|
A | G | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-1360T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45247872 | ||||||
| chr11:45248038
|
C | T | 2 | a0001c0001t0029g0273a0001c0001t0035g0244 | 2 | HG02056.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.847-1526G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248038 | ||||||
| chr11:45248198
|
A | C | 82 | a0001c0001t0001g0102a0001c0001t0001g0175a0001c0001t0002g0001others(79): Show | 113 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.847-1686T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248198 | ||||||
| chr11:45248222
|
CATT | C | 7 | a0001c0001t0013g0041a0001c0001t0020g0270a0001c0001t0028g0066others(4): Show | 8 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.847-1713_847-1711d others(5): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248222 | ||||||
| chr11:45248447
|
T | C | 2 | a0001c0001t0016g0048a0001c0001t0016g0055 | 2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.847-1935A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248447 | ||||||
| chr11:45248532
|
A | G | 4 | a0001c0001t0013g0041a0001c0001t0020g0270a0001c0001t0035g0244others(1): Show | 5 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-2020T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248532 | ||||||
| chr11:45248638
|
C | A | 2 | a0001c0001t0016g0048a0001c0001t0016g0055 | 2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.847-2126G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248638 | ||||||
| chr11:45248693
|
T | C | 182 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0124others(179): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.847-2181A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248693 | ||||||
| chr11:45248722
|
G | A | 78 | a0001c0001t0001g0102a0001c0001t0001g0124a0001c0001t0002g0001others(75): Show | 108 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.847-2210C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248722 | ||||||
| chr11:45248802
|
G | T | 1 | a0001c0001t0006g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.847-2290C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248802 | ||||||
| chr11:45248868
|
A | C | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.847-2356T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45248868 | ||||||
| chr11:45249054
|
GA | G | 71 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(68): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.847-2543delT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249054 | ||||||
| chr11:45249213
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.847-2701G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249213 | ||||||
| chr11:45249214
|
G | A | 6 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.847-2702C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249214 | ||||||
| chr11:45249471
|
T | C | 1 | a0005c0009t0015g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.846+2950A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249471 | ||||||
| chr11:45249566
|
C | T | 3 | a0001c0001t0003g0261a0001c0001t0003g0274a0001c0001t0004g0232 | 3 | HG02055.hp2 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.846+2855G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249566 | ||||||
| chr11:45249683
|
G | C | 1 | a0001c0001t0001g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.846+2738C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249683 | ||||||
| chr11:45249758
|
G | GC | 4 | a0001c0001t0001g0166a0001c0001t0001g0265a0001c0001t0005g0251others(1): Show | 4 | HG00408.hp1 HG01255.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2662dupG | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249758 | ||||||
| chr11:45249814
|
G | A | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.846+2607C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249814 | ||||||
| chr11:45249854
|
A | G | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.846+2567T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45249854 | ||||||
| chr11:45250148
|
C | G | 87 | a0001c0001t0001g0102a0001c0001t0001g0124a0001c0001t0002g0001others(84): Show | 119 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.846+2273G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250148 | ||||||
| chr11:45250350
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.846+2071G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250350 | ||||||
| chr11:45250353
|
C | T | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.846+2068G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250353 | ||||||
| chr11:45250365
|
C | T | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.846+2056G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250365 | ||||||
| chr11:45250469
|
G | A | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.846+1952C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250469 | ||||||
| chr11:45250658
|
A | T | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.846+1763T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250658 | ||||||
| chr11:45250728
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.846+1693C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250728 | ||||||
| chr11:45250783
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.846+1638G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250783 | ||||||
| chr11:45250784
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.846+1637C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250784 | ||||||
| chr11:45250902
|
C | T | 80 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(77): Show | 111 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.846+1519G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250902 | ||||||
| chr11:45250942
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.846+1479C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45250942 | ||||||
| chr11:45251000
|
A | G | 164 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(161): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.846+1421T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251000 | ||||||
| chr11:45251137
|
C | A | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.846+1284G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251137 | ||||||
| chr11:45251163
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.846+1258C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251163 | ||||||
| chr11:45251250
|
G | A | 8 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(5): Show | 11 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1171C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251250 | ||||||
| chr11:45251343
|
C | T | 8 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(5): Show | 11 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.846+1078G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251343 | ||||||
| chr11:45251345
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0009g0021others(3): Show | 8 | HG00544.hp2 HG00735.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+1076G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251345 | ||||||
| chr11:45251386
|
T | TA | 29 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0152others(26): Show | 33 | HG01070.hp2 HG01261.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.846+1034dupT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251386 | ||||||
| chr11:45251386
|
T | TAA | 76 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(73): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.846+1033_846+1034d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251386 | ||||||
| chr11:45251386
|
T | TAAA | 57 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0240others(54): Show | 68 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.846+1032_846+1034d others(5): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251386 | ||||||
| chr11:45251386
|
T | TAAAA | 20 | a0001c0001t0001g0239a0001c0001t0002g0018a0001c0001t0002g0229others(17): Show | 24 | HG00323.hp1 HG00408.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.846+1031_846+1034d others(6): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251386 | ||||||
| chr11:45251432
|
G | T | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.846+989C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251432 | ||||||
| chr11:45251509
|
C | G | 1 | a0001c0001t0011g0130 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.846+912G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251509 | ||||||
| chr11:45251545
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(271): Show | 365 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(362): Show |
intron_variant | MODIFIER | c.846+876T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251545 | ||||||
| chr11:45251628
|
C | A | 2 | a0001c0001t0011g0054a0001c0001t0017g0020 | 3 | HG02258.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.846+793G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251628 | ||||||
| chr11:45251707
|
T | G | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.846+714A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251707 | ||||||
| chr11:45251816
|
T | C | 2 | a0001c0001t0003g0249a0001c0001t0003g0250 | 2 | NA18952.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.846+605A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251816 | ||||||
| chr11:45251819
|
C | A | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.846+602G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251819 | ||||||
| chr11:45251863
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.846+558G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251863 | ||||||
| chr11:45251960
|
G | A | 163 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(160): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.846+461C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45251960 | ||||||
| chr11:45252006
|
G | A | 1 | a0001c0001t0014g0027 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.846+415C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45252006 | ||||||
| chr11:45252092
|
C | T | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+329G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45252092 | ||||||
| chr11:45252173
|
G | A | 1 | a0001c0001t0004g0212 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.846+248C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45252173 | ||||||
| chr11:45252270
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.846+151G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 4/5 | chr11 | 45252270 | ||||||
| chr11:45252739
|
C | A | 2 | a0001c0001t0002g0063a0008c0003t0002g0062 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.545-17G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45252739 | ||||||
| chr11:45253302
|
T | C | 1 | a0001c0001t0007g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.545-580A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45253302 | ||||||
| chr11:45253343
|
C | T | 66 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(63): Show | 78 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.545-621G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45253343 | ||||||
| chr11:45253861
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.544+409C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45253861 | ||||||
| chr11:45253871
|
A | G | 5 | a0001c0001t0002g0063a0001c0001t0010g0116a0001c0001t0014g0027others(2): Show | 6 | HG02056.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.544+399T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45253871 | ||||||
| chr11:45254000
|
G | T | 8 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(5): Show | 11 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.544+270C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45254000 | ||||||
| chr11:45254201
|
C | T | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.544+69G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 3/5 | chr11 | 45254201 | ||||||
| chr11:45254424
|
C | T | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.410-20G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254424 | ||||||
| chr11:45254566
|
T | C | 1 | a0001c0001t0034g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.410-162A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254566 | ||||||
| chr11:45254689
|
A | G | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.410-285T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254689 | ||||||
| chr11:45254727
|
C | T | 1 | a0001c0001t0007g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.410-323G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254727 | ||||||
| chr11:45254757
|
A | G | 159 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(156): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.410-353T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254757 | ||||||
| chr11:45254834
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.410-430G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254834 | ||||||
| chr11:45254852
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.410-448C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254852 | ||||||
| chr11:45254874
|
G | A | 85 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(82): Show | 116 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.410-470C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254874 | ||||||
| chr11:45254906
|
G | A | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-502C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254906 | ||||||
| chr11:45254950
|
CA | C | 149 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(146): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.410-547delT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45254950 | ||||||
| chr11:45255057
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.409+609T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255057 | ||||||
| chr11:45255124
|
T | A | 171 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(168): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.409+542A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255124 | ||||||
| chr11:45255199
|
T | C | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+467A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255199 | ||||||
| chr11:45255301
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.409+365G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255301 | ||||||
| chr11:45255370
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.409+296G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255370 | ||||||
| chr11:45255371
|
T | C | 1 | a0001c0001t0004g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.409+295A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255371 | ||||||
| chr11:45255384
|
T | G | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.409+282A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255384 | ||||||
| chr11:45255431
|
A | T | 159 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(156): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.409+235T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255431 | ||||||
| chr11:45255482
|
G | C | 159 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(156): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.409+184C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 2/5 | chr11 | 45255482 | ||||||
| chr11:45255902
|
A | G | 2 | a0001c0001t0003g0052a0001c0001t0005g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.184-11T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45255902 | ||||||
| chr11:45256145
|
G | A | 1 | a0001c0001t0002g0032 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.184-254C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256145 | ||||||
| chr11:45256271
|
G | A | 1 | a0001c0001t0006g0147 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.184-380C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256271 | ||||||
| chr11:45256352
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-461G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256352 | ||||||
| chr11:45256373
|
CCA | C | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-484_184-483del others(2): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256373 | ||||||
| chr11:45256484
|
C | T | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-593G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256484 | ||||||
| chr11:45256486
|
T | C | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-595A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256486 | ||||||
| chr11:45256563
|
C | T | 1 | a0006c0006t0005g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.184-672G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256563 | ||||||
| chr11:45256652
|
G | A | 73 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(70): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.184-761C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256652 | ||||||
| chr11:45256765
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.184-874G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256765 | ||||||
| chr11:45256766
|
G | A | 69 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(66): Show | 81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.184-875C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256766 | ||||||
| chr11:45256952
|
C | A | 74 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(71): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.184-1061G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256952 | ||||||
| chr11:45256956
|
G | A | 4 | a0001c0001t0002g0063a0001c0001t0010g0116a0001c0001t0014g0027others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-1065C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45256956 | ||||||
| chr11:45257198
|
A | G | 1 | a0001c0001t0007g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184-1307T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257198 | ||||||
| chr11:45257380
|
C | G | 1 | a0001c0001t0002g0018 | 3 | HG00323.hp1 HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.184-1489G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257380 | ||||||
| chr11:45257721
|
C | T | 1 | a0001c0001t0014g0027 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.184-1830G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257721 | ||||||
| chr11:45257722
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0157 | 6 | HG01074.hp1 HG01081.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-1831C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257722 | ||||||
| chr11:45257837
|
CG | C | 73 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(70): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.184-1947delC | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257837 | ||||||
| chr11:45257937
|
A | G | 1 | a0001c0001t0016g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.184-2046T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257937 | ||||||
| chr11:45257948
|
C | T | 6 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-2057G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45257948 | ||||||
| chr11:45258063
|
A | T | 1 | a0001c0001t0037g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.184-2172T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258063 | ||||||
| chr11:45258127
|
G | A | 75 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(72): Show | 106 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.184-2236C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258127 | ||||||
| chr11:45258165
|
A | T | 4 | a0001c0001t0002g0063a0001c0001t0010g0116a0001c0001t0014g0027others(1): Show | 5 | HG02486.hp2 HG02572.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-2274T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258165 | ||||||
| chr11:45258366
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.184-2475C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258366 | ||||||
| chr11:45258367
|
C | A | 75 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(72): Show | 106 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.184-2476G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258367 | ||||||
| chr11:45258407
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.184-2516C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258407 | ||||||
| chr11:45258417
|
T | C | 74 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(71): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.184-2526A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258417 | ||||||
| chr11:45258433
|
G | A | 1 | a0001c0001t0004g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.184-2542C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258433 | ||||||
| chr11:45258736
|
C | A | 157 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(154): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.184-2845G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258736 | ||||||
| chr11:45258821
|
G | T | 1 | a0001c0001t0002g0082 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.184-2930C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258821 | ||||||
| chr11:45258847
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.184-2956C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45258847 | ||||||
| chr11:45259027
|
C | G | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-3136G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259027 | ||||||
| chr11:45259102
|
G | A | 72 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(69): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.184-3211C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259102 | ||||||
| chr11:45259176
|
C | T | 1 | a0001c0001t0010g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.184-3285G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259176 | ||||||
| chr11:45259187
|
C | T | 1 | a0001c0001t0018g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.184-3296G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259187 | ||||||
| chr11:45259188
|
G | A | 1 | a0001c0001t0014g0027 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.184-3297C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259188 | ||||||
| chr11:45259306
|
A | G | 72 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(69): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.184-3415T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259306 | ||||||
| chr11:45259415
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.184-3524G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259415 | ||||||
| chr11:45259479
|
C | G | 8 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(5): Show | 11 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-3588G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259479 | ||||||
| chr11:45259747
|
C | A | 1 | a0001c0001t0009g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.184-3856G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259747 | ||||||
| chr11:45259758
|
G | T | 68 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(65): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.184-3867C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259758 | ||||||
| chr11:45259865
|
G | A | 1 | a0001c0005t0002g0098 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.184-3974C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45259865 | ||||||
| chr11:45260001
|
T | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0142others(2): Show | 6 | NA18981.hp2 NA19001.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-4110A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260001 | ||||||
| chr11:45260161
|
T | C | 79 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(76): Show | 111 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.184-4270A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260161 | ||||||
| chr11:45260500
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.184-4609A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260500 | ||||||
| chr11:45260672
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0032 | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-4781C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260672 | ||||||
| chr11:45260738
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.184-4847T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260738 | ||||||
| chr11:45260790
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.184-4899C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260790 | ||||||
| chr11:45260889
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.184-4998C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260889 | ||||||
| chr11:45260940
|
A | G | 171 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(168): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.184-5049T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260940 | ||||||
| chr11:45260980
|
A | G | 76 | a0001c0001t0001g0019a0001c0001t0001g0124a0001c0001t0001g0238others(73): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.184-5089T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45260980 | ||||||
| chr11:45261027
|
C | T | 2 | a0001c0001t0019g0138a0001c0001t0035g0244 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.184-5136G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261027 | ||||||
| chr11:45261057
|
G | A | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-5166C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261057 | ||||||
| chr11:45261186
|
G | A | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-5295C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261186 | ||||||
| chr11:45261245
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.184-5354C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261245 | ||||||
| chr11:45261362
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-5471G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261362 | ||||||
| chr11:45261414
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0186others(6): Show | 16 | HG01099.hp2 HG01255.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.184-5523T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261414 | ||||||
| chr11:45261443
|
C | A | 79 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(76): Show | 111 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.184-5552G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261443 | ||||||
| chr11:45261457
|
A | T | 1 | a0001c0001t0021g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.184-5566T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261457 | ||||||
| chr11:45261511
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(26): Show | 45 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.184-5620A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261511 | ||||||
| chr11:45261514
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.184-5623G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261514 | ||||||
| chr11:45261519
|
A | C | 79 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0102others(76): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.184-5628T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261519 | ||||||
| chr11:45261554
|
C | A | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-5663G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261554 | ||||||
| chr11:45261592
|
G | A | 9 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(6): Show | 12 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-5701C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261592 | ||||||
| chr11:45261612
|
G | C | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-5721C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261612 | ||||||
| chr11:45261617
|
C | G | 50 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(47): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.184-5726G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261617 | ||||||
| chr11:45261751
|
A | G | 1 | a0001c0001t0007g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-5860T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261751 | ||||||
| chr11:45261773
|
C | T | 5 | a0001c0001t0006g0006a0001c0001t0006g0135a0001c0001t0006g0148others(2): Show | 9 | HG00438.hp1 HG02056.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-5882G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261773 | ||||||
| chr11:45261774
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0019g0138a0001c0001t0035g0244 | 3 | HG02280.hp2 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.184-5883C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261774 | ||||||
| chr11:45261786
|
G | A | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-5895C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261786 | ||||||
| chr11:45261857
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(2): Show | 7 | HG00642.hp1 HG01074.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-5966T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261857 | ||||||
| chr11:45261896
|
A | T | 1 | a0001c0001t0002g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.184-6005T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261896 | ||||||
| chr11:45261915
|
C | CA | 74 | a0001c0001t0001g0019a0001c0001t0001g0124a0001c0001t0001g0238others(71): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.184-6025dupT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261915 | ||||||
| chr11:45261915
|
C | CAA | 10 | a0001c0001t0003g0224a0001c0001t0003g0241a0001c0001t0004g0188others(7): Show | 12 | HG01109.hp2 HG01243.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-6026_184-6025d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45261915 | ||||||
| chr11:45262061
|
C | T | 9 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(6): Show | 12 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-6170G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262061 | ||||||
| chr11:45262113
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.184-6222T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262113 | ||||||
| chr11:45262240
|
T | C | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-6349A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262240 | ||||||
| chr11:45262452
|
G | A | 2 | a0001c0001t0003g0123a0001c0001t0029g0273 | 2 | HG02056.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.184-6561C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262452 | ||||||
| chr11:45262462
|
A | G | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.184-6571T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262462 | ||||||
| chr11:45262468
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.184-6577C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262468 | ||||||
| chr11:45262499
|
A | G | 181 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(178): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.184-6608T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262499 | ||||||
| chr11:45262615
|
A | T | 1 | a0001c0001t0003g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.184-6724T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262615 | ||||||
| chr11:45262721
|
T | TCA | 38 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0036others(35): Show | 48 | HG01069.hp2 HG01175.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.184-6832_184-6831d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
T | TCACA | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(43): Show | 73 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.184-6834_184-6831d others(6): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
T | TCACACA | 13 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0141others(10): Show | 15 | HG00099.hp1 HG00642.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.184-6836_184-6831d others(8): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
T | TCACACAC others(1): Show |
4 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0004g0232others(1): Show | 4 | HG01258.hp2 HG04199.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-6838_184-6831d others(10): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0002g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.184-6840_184-6831d others(12): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
TCA | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0002g0139others(2): Show | 5 | HG00597.hp1 HG02056.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-6832_184-6831d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
TCACA | T | 4 | a0001c0001t0011g0054a0001c0001t0013g0041a0001c0001t0020g0270others(1): Show | 5 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-6834_184-6831d others(6): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
TCACACA | T | 5 | a0001c0001t0001g0157a0001c0001t0007g0057a0001c0001t0007g0060others(2): Show | 5 | HG01243.hp1 HG02273.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-6836_184-6831d others(8): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
TCACACAC others(1): Show |
T | 11 | a0001c0001t0002g0042a0001c0001t0003g0052a0001c0001t0005g0046others(8): Show | 11 | HG01261.hp1 HG02970.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-6838_184-6831d others(10): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
TCACACAC others(3): Show |
T | 9 | a0001c0001t0001g0124a0001c0001t0003g0049a0001c0001t0003g0123others(6): Show | 11 | HG01433.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.184-6840_184-6831d others(12): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262721
|
TCACACAC others(7): Show |
T | 2 | a0001c0001t0019g0138a0001c0001t0035g0244 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.184-6844_184-6831d others(16): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262721 | ||||||
| chr11:45262754
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0011g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.184-6879_184-6864d others(18): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262754 | ||||||
| chr11:45262756
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0004g0228 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.184-6879_184-6866d others(16): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262756 | ||||||
| chr11:45262758
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0010g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-6879_184-6868d others(14): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262758 | ||||||
| chr11:45262760
|
CACACACA others(3): Show |
C | 3 | a0001c0001t0002g0063a0001c0001t0014g0027a0008c0003t0002g0062 | 4 | HG02486.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-6879_184-6870d others(12): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262760 | ||||||
| chr11:45262762
|
CACACACA others(1): Show |
C | 50 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(47): Show | 68 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.184-6879_184-6872d others(10): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262762 | ||||||
| chr11:45262764
|
CACACAA | C | 20 | a0001c0001t0002g0001a0001c0001t0002g0028a0001c0001t0002g0029others(17): Show | 31 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-6879_184-6874d others(8): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262764 | ||||||
| chr11:45262766
|
CACAA | C | 23 | a0001c0001t0002g0016a0001c0001t0002g0087a0001c0001t0002g0104others(20): Show | 33 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.184-6879_184-6876d others(6): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262766 | ||||||
| chr11:45262768
|
CAA | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(13): Show | 20 | HG00323.hp1 HG00408.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.184-6879_184-6878d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262768 | ||||||
| chr11:45262769
|
A | ACAC | 4 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0193others(1): Show | 4 | HG03831.hp1 NA18944.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-6879_184-6878i others(5): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262769 | ||||||
| chr11:45262770
|
A | C | 34 | a0001c0001t0001g0240a0001c0001t0002g0222a0001c0001t0002g0225others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.184-6879T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262770 | ||||||
| chr11:45262840
|
A | C | 1 | a0001c0001t0012g0080 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.184-6949T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262840 | ||||||
| chr11:45262872
|
G | A | 6 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-6981C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262872 | ||||||
| chr11:45262972
|
C | A | 2 | a0001c0001t0001g0124a0001c0001t0003g0123 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.184-7081G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45262972 | ||||||
| chr11:45263106
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.184-7215C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263106 | ||||||
| chr11:45263124
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0003g0123a0001c0001t0013g0041others(5): Show | 9 | HG02056.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-7233T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263124 | ||||||
| chr11:45263223
|
G | A | 148 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(145): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.184-7332C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263223 | ||||||
| chr11:45263277
|
G | T | 1 | a0001c0001t0002g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.184-7386C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263277 | ||||||
| chr11:45263333
|
G | A | 1 | a0001c0001t0019g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184-7442C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263333 | ||||||
| chr11:45263353
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.184-7462G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263353 | ||||||
| chr11:45263536
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.184-7645C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263536 | ||||||
| chr11:45263593
|
T | G | 2 | a0001c0001t0001g0106a0001c0001t0002g0107 | 2 | HG03239.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.184-7702A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263593 | ||||||
| chr11:45263681
|
T | G | 8 | a0001c0001t0001g0124a0001c0001t0003g0123a0001c0001t0013g0041others(5): Show | 9 | HG02056.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-7790A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263681 | ||||||
| chr11:45263786
|
G | A | 1 | a0001c0001t0012g0078 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.184-7895C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263786 | ||||||
| chr11:45263935
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.184-8044G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263935 | ||||||
| chr11:45263965
|
G | A | 1 | a0001c0001t0012g0079 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.184-8074C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263965 | ||||||
| chr11:45263990
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.184-8099A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45263990 | ||||||
| chr11:45264015
|
C | G | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0036g0132 | 3 | HG02622.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-8124G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264015 | ||||||
| chr11:45264045
|
A | G | 1 | a0001c0001t0027g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.184-8154T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264045 | ||||||
| chr11:45264124
|
A | G | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-8233T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264124 | ||||||
| chr11:45264223
|
G | A | 2 | a0001c0001t0003g0234a0001c0001t0004g0233 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.184-8332C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264223 | ||||||
| chr11:45264243
|
A | T | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-8352T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264243 | ||||||
| chr11:45264252
|
T | G | 159 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(156): Show | 204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.184-8361A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264252 | ||||||
| chr11:45264303
|
T | C | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-8412A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264303 | ||||||
| chr11:45264305
|
G | C | 1 | a0001c0001t0023g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.184-8414C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264305 | ||||||
| chr11:45264489
|
G | A | 3 | a0001c0001t0003g0224a0001c0001t0003g0241a0001c0001t0004g0223 | 3 | HG01109.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.184-8598C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264489 | ||||||
| chr11:45264534
|
C | G | 67 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(64): Show | 79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-8643G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264534 | ||||||
| chr11:45264551
|
G | C | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-8660C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264551 | ||||||
| chr11:45264721
|
T | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-8830A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264721 | ||||||
| chr11:45264741
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.184-8850G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264741 | ||||||
| chr11:45264810
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.184-8919G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264810 | ||||||
| chr11:45264840
|
A | G | 6 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-8949T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264840 | ||||||
| chr11:45264844
|
T | C | 168 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(165): Show | 215 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.184-8953A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264844 | ||||||
| chr11:45264858
|
A | T | 1 | a0001c0001t0003g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184-8967T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264858 | ||||||
| chr11:45264896
|
G | A | 2 | a0001c0001t0019g0138a0001c0001t0035g0244 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.184-9005C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264896 | ||||||
| chr11:45264926
|
G | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(74): Show | 109 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.184-9035C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45264926 | ||||||
| chr11:45265041
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.184-9150C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265041 | ||||||
| chr11:45265167
|
G | A | 1 | a0001c0001t0009g0076 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.184-9276C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265167 | ||||||
| chr11:45265241
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184-9350G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265241 | ||||||
| chr11:45265260
|
T | C | 1 | a0006c0006t0005g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.184-9369A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265260 | ||||||
| chr11:45265300
|
C | G | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-9409G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265300 | ||||||
| chr11:45265301
|
G | A | 17 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0249others(14): Show | 25 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.184-9410C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265301 | ||||||
| chr11:45265308
|
C | T | 1 | a0008c0003t0002g0062 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-9417G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265308 | ||||||
| chr11:45265309
|
G | A | 1 | a0001c0001t0004g0228 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.184-9418C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265309 | ||||||
| chr11:45265411
|
C | G | 76 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(73): Show | 108 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.184-9520G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265411 | ||||||
| chr11:45265434
|
A | G | 17 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0249others(14): Show | 25 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.184-9543T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265434 | ||||||
| chr11:45265588
|
G | A | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-9697C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265588 | ||||||
| chr11:45265732
|
A | G | 1 | a0001c0001t0004g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.184-9841T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265732 | ||||||
| chr11:45265773
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0002g0237a0001c0001t0003g0123 | 3 | HG02486.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184-9882C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265773 | ||||||
| chr11:45265812
|
A | C | 1 | a0005c0009t0015g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.184-9921T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45265812 | ||||||
| chr11:45266074
|
T | G | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-10183A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266074 | ||||||
| chr11:45266085
|
A | G | 7 | a0001c0001t0001g0124a0001c0001t0003g0123a0001c0001t0013g0041others(4): Show | 8 | HG02280.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-10194T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266085 | ||||||
| chr11:45266503
|
T | TAC | 61 | a0001c0001t0001g0019a0001c0001t0001g0124a0001c0001t0001g0204others(58): Show | 73 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.184-10614_184-1061 others(6): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266503 | ||||||
| chr11:45266503
|
T | TACAC | 8 | a0001c0001t0002g0222a0001c0001t0002g0231a0001c0001t0002g0254others(5): Show | 8 | HG00099.hp2 HG01109.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-10616_184-1061 others(8): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266503 | ||||||
| chr11:45266503
|
T | TACACACA others(7): Show |
2 | a0001c0007t0015g0068a0005c0009t0015g0067 | 2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-10626_184-1061 others(18): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266503 | ||||||
| chr11:45266503
|
T | TACACACA others(11): Show |
1 | a0001c0001t0028g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.184-10630_184-1061 others(22): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266503 | ||||||
| chr11:45266503
|
TAC | T | 39 | a0001c0001t0002g0042a0001c0001t0002g0070a0001c0001t0002g0088others(36): Show | 42 | HG00408.hp2 HG01070.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-10614_184-1061 others(6): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266503 | ||||||
| chr11:45266503
|
TACAC | T | 62 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(59): Show | 94 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.184-10616_184-1061 others(8): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266503 | ||||||
| chr11:45266513
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.184-10622G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266513 | ||||||
| chr11:45266535
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.184-10644A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266535 | ||||||
| chr11:45266559
|
A | G | 3 | a0001c0001t0019g0138a0001c0001t0029g0273a0001c0001t0035g0244 | 3 | HG02056.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.184-10668T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266559 | ||||||
| chr11:45266574
|
A | G | 159 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(156): Show | 204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.184-10683T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266574 | ||||||
| chr11:45266769
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10878A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266769 | ||||||
| chr11:45266773
|
A | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10882T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266773 | ||||||
| chr11:45266780
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10889C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266780 | ||||||
| chr11:45266781
|
A | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10890T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266781 | ||||||
| chr11:45266784
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10893A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266784 | ||||||
| chr11:45266785
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10894C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266785 | ||||||
| chr11:45266786
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10895A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266786 | ||||||
| chr11:45266790
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10899G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266790 | ||||||
| chr11:45266794
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10903G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266794 | ||||||
| chr11:45266796
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10905A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266796 | ||||||
| chr11:45266801
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.184-10910A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266801 | ||||||
| chr11:45266829
|
T | C | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.184-10938A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266829 | ||||||
| chr11:45266831
|
C | G | 8 | a0001c0001t0001g0124a0001c0001t0003g0123a0001c0001t0013g0041others(5): Show | 9 | HG02056.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-10940G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266831 | ||||||
| chr11:45266971
|
C | T | 1 | a0001c0001t0004g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.184-11080G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45266971 | ||||||
| chr11:45267101
|
T | C | 171 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(168): Show | 219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.184-11210A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267101 | ||||||
| chr11:45267113
|
AC | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-11223delG | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267113 | ||||||
| chr11:45267193
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.184-11302G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267193 | ||||||
| chr11:45267283
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.184-11392C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267283 | ||||||
| chr11:45267321
|
G | A | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-11430C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267321 | ||||||
| chr11:45267439
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0003g0123 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.184-11548A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267439 | ||||||
| chr11:45267542
|
G | A | 91 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(88): Show | 124 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.184-11651C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267542 | ||||||
| chr11:45267577
|
C | A | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.184-11686G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267577 | ||||||
| chr11:45267842
|
A | C | 84 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(81): Show | 116 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.184-11951T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267842 | ||||||
| chr11:45267869
|
C | T | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.184-11978G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267869 | ||||||
| chr11:45267939
|
C | G | 1 | a0001c0001t0002g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.184-12048G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267939 | ||||||
| chr11:45267955
|
A | T | 49 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(46): Show | 53 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.184-12064T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45267955 | ||||||
| chr11:45268184
|
C | T | 1 | a0001c0001t0006g0143 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.184-12293G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268184 | ||||||
| chr11:45268263
|
A | G | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0036g0132 | 3 | HG02622.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-12372T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268263 | ||||||
| chr11:45268292
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.184-12401C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268292 | ||||||
| chr11:45268313
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.184-12422C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268313 | ||||||
| chr11:45268380
|
C | A | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0036g0132 | 3 | HG02622.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-12489G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268380 | ||||||
| chr11:45268409
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184-12518G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268409 | ||||||
| chr11:45268581
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.184-12690C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268581 | ||||||
| chr11:45268607
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.184-12716C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268607 | ||||||
| chr11:45268884
|
T | A | 1 | a0001c0001t0002g0097 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.184-12993A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268884 | ||||||
| chr11:45268920
|
C | T | 1 | a0001c0001t0010g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.184-13029G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268920 | ||||||
| chr11:45268929
|
G | C | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0036g0132 | 3 | HG02622.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-13038C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268929 | ||||||
| chr11:45268962
|
G | C | 81 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(78): Show | 113 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.184-13071C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45268962 | ||||||
| chr11:45269098
|
G | C | 1 | a0001c0001t0010g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-13207C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269098 | ||||||
| chr11:45269204
|
G | T | 80 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(77): Show | 112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.184-13313C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269204 | ||||||
| chr11:45269253
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(32): Show | 51 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.184-13362C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269253 | ||||||
| chr11:45269294
|
C | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0036g0132 | 3 | HG02622.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-13403G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269294 | ||||||
| chr11:45269295
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.184-13404C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269295 | ||||||
| chr11:45269320
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.184-13441_184-1343 others(16): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269320 | ||||||
| chr11:45269463
|
A | G | 5 | a0001c0001t0013g0041a0001c0001t0019g0138a0001c0001t0020g0270others(2): Show | 6 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-13572T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269463 | ||||||
| chr11:45269679
|
C | G | 171 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(168): Show | 219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.184-13788G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269679 | ||||||
| chr11:45269764
|
C | G | 171 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(168): Show | 219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.184-13873G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269764 | ||||||
| chr11:45269834
|
T | C | 171 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(168): Show | 219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.184-13943A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45269834 | ||||||
| chr11:45270186
|
A | AT | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-14296dupA | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270186 | ||||||
| chr11:45270206
|
T | C | 3 | a0001c0001t0011g0054a0001c0001t0016g0055a0001c0001t0017g0020 | 4 | HG02258.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-14315A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270206 | ||||||
| chr11:45270277
|
T | C | 6 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-14386A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270277 | ||||||
| chr11:45270413
|
G | A | 2 | a0001c0001t0003g0234a0001c0001t0004g0233 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.184-14522C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270413 | ||||||
| chr11:45270491
|
T | C | 73 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(70): Show | 103 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.184-14600A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270491 | ||||||
| chr11:45270723
|
G | A | 2 | a0001c0001t0002g0114a0001c0001t0010g0115 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.184-14832C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270723 | ||||||
| chr11:45270741
|
G | A | 1 | a0004c0008t0003g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.184-14850C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270741 | ||||||
| chr11:45270826
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.184-14935G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270826 | ||||||
| chr11:45270874
|
A | G | 1 | a0001c0001t0001g0037 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.184-14983T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270874 | ||||||
| chr11:45270905
|
A | G | 1 | a0001c0001t0002g0023 | 2 | NA19070.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.184-15014T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270905 | ||||||
| chr11:45270982
|
A | C | 1 | a0001c0001t0003g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.183+15043T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45270982 | ||||||
| chr11:45271245
|
T | C | 160 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(157): Show | 205 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.183+14780A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271245 | ||||||
| chr11:45271515
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.183+14510G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271515 | ||||||
| chr11:45271537
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.183+14488C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271537 | ||||||
| chr11:45271595
|
G | T | 1 | a0001c0001t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.183+14430C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271595 | ||||||
| chr11:45271624
|
G | A | 2 | a0001c0001t0002g0114a0001c0001t0010g0115 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.183+14401C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271624 | ||||||
| chr11:45271796
|
G | A | 9 | a0001c0001t0007g0015a0001c0001t0007g0057a0001c0001t0007g0058others(6): Show | 12 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.183+14229C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271796 | ||||||
| chr11:45271839
|
A | G | 77 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(74): Show | 108 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.183+14186T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45271839 | ||||||
| chr11:45272050
|
G | A | 183 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(180): Show | 231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.183+13975C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272050 | ||||||
| chr11:45272343
|
C | CAAGA | 9 | a0001c0001t0002g0111a0001c0001t0004g0228a0001c0001t0007g0015others(6): Show | 11 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+13678_183+1368 others(8): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272343 | ||||||
| chr11:45272420
|
G | A | 3 | a0001c0001t0005g0046a0001c0001t0008g0047a0001c0001t0016g0048 | 3 | HG03209.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.183+13605C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272420 | ||||||
| chr11:45272449
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.183+13576A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272449 | ||||||
| chr11:45272601
|
A | G | 66 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(63): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.183+13424T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272601 | ||||||
| chr11:45272636
|
A | T | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+13389T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272636 | ||||||
| chr11:45272647
|
T | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | NA18987.hp2 NA19063.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.183+13378A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272647 | ||||||
| chr11:45272673
|
A | T | 1 | a0001c0001t0003g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.183+13352T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272673 | ||||||
| chr11:45272698
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0003g0123 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.183+13327C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272698 | ||||||
| chr11:45272746
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183+13279C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272746 | ||||||
| chr11:45272805
|
C | T | 77 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(74): Show | 108 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.183+13220G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272805 | ||||||
| chr11:45272885
|
G | A | 183 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0073others(180): Show | 231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.183+13140C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272885 | ||||||
| chr11:45272944
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.183+13081T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45272944 | ||||||
| chr11:45273013
|
T | A | 1 | a0001c0001t0017g0020 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.183+13012A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273013 | ||||||
| chr11:45273035
|
A | G | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+12990T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273035 | ||||||
| chr11:45273106
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.183+12919T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273106 | ||||||
| chr11:45273112
|
T | C | 4 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0113others(1): Show | 6 | HG02280.hp1 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+12913A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273112 | ||||||
| chr11:45273220
|
C | T | 17 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0249others(14): Show | 25 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.183+12805G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273220 | ||||||
| chr11:45273338
|
G | C | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.183+12687C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273338 | ||||||
| chr11:45273680
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+12345C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273680 | ||||||
| chr11:45273760
|
T | C | 3 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231 | 3 | HG00741.hp1 HG01258.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.183+12265A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273760 | ||||||
| chr11:45273782
|
A | T | 3 | a0001c0001t0002g0004a0001c0001t0012g0078a0001c0001t0012g0079 | 7 | HG00621.hp2 NA18952.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+12243T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273782 | ||||||
| chr11:45273796
|
A | G | 42 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(39): Show | 63 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.183+12229T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273796 | ||||||
| chr11:45273838
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.183+12187G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273838 | ||||||
| chr11:45273940
|
G | A | 7 | a0001c0001t0011g0054a0001c0001t0011g0128a0001c0001t0011g0130others(4): Show | 8 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.183+12085C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45273940 | ||||||
| chr11:45274088
|
C | G | 7 | a0001c0001t0002g0056a0001c0001t0007g0015a0001c0001t0007g0057others(4): Show | 9 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+11937G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45274088 | ||||||
| chr11:45274178
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 5 | HG02622.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+11847C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45274178 | ||||||
| chr11:45274281
|
G | A | 1 | a0001c0001t0035g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.183+11744C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45274281 | ||||||
| chr11:45274395
|
C | T | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+11630G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45274395 | ||||||
| chr11:45274567
|
C | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(74): Show | 92 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.183+11458G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45274567 | ||||||
| chr11:45274913
|
TA | T | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+11111delT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45274913 | ||||||
| chr11:45275035
|
G | A | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+10990C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275035 | ||||||
| chr11:45275158
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0003g0123 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.183+10867G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275158 | ||||||
| chr11:45275233
|
C | T | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+10792G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275233 | ||||||
| chr11:45275318
|
G | A | 2 | a0001c0001t0003g0255a0001c0001t0005g0256 | 2 | HG00621.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.183+10707C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275318 | ||||||
| chr11:45275320
|
G | T | 1 | a0005c0009t0015g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.183+10705C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275320 | ||||||
| chr11:45275381
|
C | T | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+10644G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275381 | ||||||
| chr11:45275451
|
A | G | 5 | a0001c0001t0005g0046a0001c0001t0008g0045a0001c0001t0008g0047others(2): Show | 5 | HG02970.hp1 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+10574T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275451 | ||||||
| chr11:45275509
|
A | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 5 | HG02622.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+10516T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275509 | ||||||
| chr11:45275645
|
G | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0009g0021others(3): Show | 8 | HG00544.hp2 HG00735.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+10380C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275645 | ||||||
| chr11:45275807
|
T | TG | 99 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(96): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.183+10217dupC | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275807 | ||||||
| chr11:45275827
|
C | T | 2 | a0001c0001t0011g0130a0001c0001t0030g0129 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.183+10198G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275827 | ||||||
| chr11:45275995
|
C | T | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+10030G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45275995 | ||||||
| chr11:45276048
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(93): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.183+9977A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276048 | ||||||
| chr11:45276123
|
C | T | 3 | a0001c0001t0011g0054a0001c0001t0016g0055a0001c0001t0017g0020 | 4 | HG02258.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+9902G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276123 | ||||||
| chr11:45276237
|
G | A | 1 | a0001c0001t0014g0027 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.183+9788C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276237 | ||||||
| chr11:45276434
|
G | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+9591C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276434 | ||||||
| chr11:45276589
|
A | T | 1 | a0001c0001t0001g0033 | 2 | HG02148.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.183+9436T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276589 | ||||||
| chr11:45276638
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.183+9387C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276638 | ||||||
| chr11:45276639
|
T | G | 23 | a0001c0001t0001g0037a0001c0001t0001g0178a0001c0001t0001g0179others(20): Show | 27 | HG01243.hp1 HG01516.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+9386A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276639 | ||||||
| chr11:45276640
|
T | G | 3 | a0001c0001t0011g0054a0001c0001t0016g0055a0001c0001t0017g0020 | 4 | HG02258.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+9385A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276640 | ||||||
| chr11:45276647
|
T | TA | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+9377dupT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276647 | ||||||
| chr11:45276672
|
C | T | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+9353G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276672 | ||||||
| chr11:45276712
|
TA | T | 13 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG01496.hp1 HG01928.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+9312delT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276712 | ||||||
| chr11:45276712
|
TAAAAA | T | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+9308_183+9312d others(7): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276712 | ||||||
| chr11:45276713
|
A | T | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+9312T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276713 | ||||||
| chr11:45276718
|
A | T | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+9307T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276718 | ||||||
| chr11:45276720
|
A | T | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.183+9305T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276720 | ||||||
| chr11:45276721
|
A | AT | 72 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(69): Show | 102 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.183+9303_183+9304i others(3): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276721 | ||||||
| chr11:45276721
|
A | T | 1 | a0001c0001t0001g0185 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.183+9304T>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276721 | ||||||
| chr11:45276844
|
G | T | 1 | a0007c0004t0008g0044 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.183+9181C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276844 | ||||||
| chr11:45276881
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.183+9144G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276881 | ||||||
| chr11:45276891
|
T | C | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.183+9134A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276891 | ||||||
| chr11:45276963
|
T | C | 2 | a0001c0001t0003g0234a0001c0001t0004g0233 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.183+9062A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45276963 | ||||||
| chr11:45277081
|
A | G | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+8944T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277081 | ||||||
| chr11:45277095
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0003g0123 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.183+8930A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277095 | ||||||
| chr11:45277238
|
AG | A | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+8786delC | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277238 | ||||||
| chr11:45277274
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(93): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.183+8751C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277274 | ||||||
| chr11:45277819
|
A | C | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+8206T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277819 | ||||||
| chr11:45277825
|
C | A | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+8200G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277825 | ||||||
| chr11:45277920
|
G | C | 1 | a0001c0001t0017g0020 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.183+8105C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277920 | ||||||
| chr11:45277954
|
A | G | 1 | a0001c0001t0011g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+8071T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45277954 | ||||||
| chr11:45278010
|
A | G | 103 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(100): Show | 137 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.183+8015T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278010 | ||||||
| chr11:45278044
|
G | A | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+7981C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278044 | ||||||
| chr11:45278082
|
T | C | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.183+7943A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278082 | ||||||
| chr11:45278138
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+7887C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278138 | ||||||
| chr11:45278320
|
G | A | 8 | a0001c0001t0002g0001a0001c0001t0002g0028a0001c0001t0002g0029others(5): Show | 18 | HG00408.hp2 HG00609.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+7705C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278320 | ||||||
| chr11:45278434
|
G | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0235a0001c0001t0002g0236others(1): Show | 6 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+7591C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278434 | ||||||
| chr11:45278743
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.183+7282T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278743 | ||||||
| chr11:45278774
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(74): Show | 92 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.183+7251C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278774 | ||||||
| chr11:45278951
|
T | C | 25 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(22): Show | 28 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.183+7074A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278951 | ||||||
| chr11:45278983
|
G | A | 1 | a0001c0001t0005g0263 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.183+7042C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45278983 | ||||||
| chr11:45279104
|
A | C | 2 | a0001c0001t0003g0071a0001c0001t0003g0072 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.183+6921T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279104 | ||||||
| chr11:45279414
|
T | C | 10 | a0001c0001t0002g0056a0001c0001t0007g0015a0001c0001t0007g0057others(7): Show | 13 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+6611A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279414 | ||||||
| chr11:45279450
|
G | A | 1 | a0001c0001t0002g0032 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.183+6575C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279450 | ||||||
| chr11:45279450
|
G | T | 2 | a0001c0001t0002g0063a0008c0003t0002g0062 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.183+6575C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279450 | ||||||
| chr11:45279505
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 6 | HG00642.hp1 HG01175.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+6520A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279505 | ||||||
| chr11:45279519
|
C | T | 24 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(21): Show | 27 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+6506G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279519 | ||||||
| chr11:45279520
|
G | A | 3 | a0001c0001t0028g0066a0001c0007t0015g0068a0005c0009t0015g0067 | 3 | HG02258.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.183+6505C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279520 | ||||||
| chr11:45279544
|
G | A | 4 | a0001c0001t0011g0128a0001c0001t0011g0130a0001c0001t0011g0131others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+6481C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279544 | ||||||
| chr11:45279580
|
G | C | 104 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(101): Show | 138 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.183+6445C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279580 | ||||||
| chr11:45279623
|
G | A | 1 | a0001c0001t0002g0030 | 2 | NA18945.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.183+6402C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279623 | ||||||
| chr11:45279644
|
C | A | 1 | a0001c0001t0028g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.183+6381G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279644 | ||||||
| chr11:45279651
|
A | C | 27 | a0001c0001t0001g0124a0001c0001t0002g0042a0001c0001t0002g0056others(24): Show | 31 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+6374T>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279651 | ||||||
| chr11:45279683
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.183+6342G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279683 | ||||||
| chr11:45279802
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.183+6223C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279802 | ||||||
| chr11:45279942
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0181 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.183+6083C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45279942 | ||||||
| chr11:45280200
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.183+5825C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280200 | ||||||
| chr11:45280320
|
G | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+5705C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280320 | ||||||
| chr11:45280322
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.183+5703C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280322 | ||||||
| chr11:45280622
|
G | C | 1 | a0001c0001t0003g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+5403C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280622 | ||||||
| chr11:45280694
|
C | T | 7 | a0001c0001t0002g0056a0001c0001t0007g0015a0001c0001t0007g0057others(4): Show | 9 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+5331G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280694 | ||||||
| chr11:45280761
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.183+5264A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280761 | ||||||
| chr11:45280871
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+5154C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280871 | ||||||
| chr11:45280969
|
C | T | 3 | a0001c0001t0011g0054a0001c0001t0016g0055a0001c0001t0017g0020 | 4 | HG02258.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+5056G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45280969 | ||||||
| chr11:45281096
|
T | C | 3 | a0001c0001t0011g0054a0001c0001t0016g0055a0001c0001t0017g0020 | 4 | HG02258.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4929A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281096 | ||||||
| chr11:45281195
|
C | CA | 81 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(78): Show | 113 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.183+4829dupT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281195 | ||||||
| chr11:45281392
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+4633C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281392 | ||||||
| chr11:45281435
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.183+4590C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281435 | ||||||
| chr11:45281645
|
C | T | 1 | a0001c0001t0008g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4380G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281645 | ||||||
| chr11:45281666
|
C | CAA | 5 | a0001c0001t0013g0041a0001c0001t0020g0270a0001c0001t0028g0066others(2): Show | 6 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+4357_183+4358d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281666 | ||||||
| chr11:45281666
|
CA | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(90): Show | 110 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.183+4358delT | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281666 | ||||||
| chr11:45281679
|
A | AAAG | 75 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(72): Show | 105 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.183+4345_183+4346i others(5): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281679 | ||||||
| chr11:45281701
|
T | C | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+4324A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281701 | ||||||
| chr11:45281826
|
A | G | 108 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(105): Show | 142 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.183+4199T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45281826 | ||||||
| chr11:45282136
|
G | T | 79 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(76): Show | 110 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.183+3889C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45282136 | ||||||
| chr11:45282160
|
C | T | 79 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(76): Show | 110 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.183+3865G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45282160 | ||||||
| chr11:45282617
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.183+3408A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45282617 | ||||||
| chr11:45282636
|
C | T | 1 | a0001c0001t0028g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.183+3389G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45282636 | ||||||
| chr11:45282714
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(93): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.183+3311A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45282714 | ||||||
| chr11:45282973
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.183+3052G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45282973 | ||||||
| chr11:45283008
|
C | T | 1 | a0003c0012t0013g0269 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.183+3017G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283008 | ||||||
| chr11:45283009
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.183+3016C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283009 | ||||||
| chr11:45283018
|
C | T | 1 | a0001c0001t0005g0127 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.183+3007G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283018 | ||||||
| chr11:45283357
|
C | A | 1 | a0001c0001t0004g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.183+2668G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283357 | ||||||
| chr11:45283476
|
G | A | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+2549C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283476 | ||||||
| chr11:45283600
|
C | G | 1 | a0001c0001t0002g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.183+2425G>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283600 | ||||||
| chr11:45283644
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.183+2381G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283644 | ||||||
| chr11:45283813
|
CTT | C | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+2210_183+2211d others(4): Show |
SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283813 | ||||||
| chr11:45283858
|
G | A | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+2167C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45283858 | ||||||
| chr11:45284077
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.183+1948C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284077 | ||||||
| chr11:45284080
|
C | T | 12 | a0001c0001t0001g0124a0001c0001t0002g0056a0001c0001t0003g0123others(9): Show | 15 | HG01243.hp1 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.183+1945G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284080 | ||||||
| chr11:45284131
|
G | T | 76 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(73): Show | 107 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.183+1894C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284131 | ||||||
| chr11:45284177
|
T | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | NA18987.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.183+1848A>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284177 | ||||||
| chr11:45284198
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0003g0123 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.183+1827C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284198 | ||||||
| chr11:45284234
|
G | A | 76 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0085others(73): Show | 107 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.183+1791C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284234 | ||||||
| chr11:45284244
|
A | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0065 | 2 | NA18962.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.183+1781T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284244 | ||||||
| chr11:45284421
|
G | A | 1 | a0002c0002t0039g0275 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.183+1604C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284421 | ||||||
| chr11:45284521
|
C | T | 1 | a0001c0001t0012g0126 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.183+1504G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284521 | ||||||
| chr11:45284588
|
G | C | 12 | a0001c0001t0001g0124a0001c0001t0002g0056a0001c0001t0003g0123others(9): Show | 15 | HG01243.hp1 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.183+1437C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284588 | ||||||
| chr11:45284601
|
C | T | 2 | a0001c0001t0002g0063a0008c0003t0002g0062 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.183+1424G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284601 | ||||||
| chr11:45284720
|
G | T | 10 | a0001c0001t0002g0056a0001c0001t0007g0015a0001c0001t0007g0057others(7): Show | 13 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+1305C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284720 | ||||||
| chr11:45284792
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.183+1233C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284792 | ||||||
| chr11:45284844
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.183+1181C>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284844 | ||||||
| chr11:45284980
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.183+1045C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45284980 | ||||||
| chr11:45285076
|
G | A | 3 | a0001c0001t0013g0041a0001c0001t0020g0270a0003c0012t0013g0269 | 4 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+949C>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285076 | ||||||
| chr11:45285102
|
G | C | 1 | a0001c0010t0022g0271 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+923C>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285102 | ||||||
| chr11:45285137
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.183+888A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285137 | ||||||
| chr11:45285334
|
T | C | 1 | a0001c0001t0029g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+691A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285334 | ||||||
| chr11:45285419
|
T | G | 1 | a0002c0002t0039g0275 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.183+606A>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285419 | ||||||
| chr11:45285460
|
A | G | 1 | a0001c0001t0011g0054 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.183+565T>C | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285460 | ||||||
| chr11:45285590
|
C | T | 12 | a0001c0001t0002g0042a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+435G>A | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285590 | ||||||
| chr11:45285701
|
C | A | 1 | a0002c0002t0039g0275 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.183+324G>T | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285701 | ||||||
| chr11:45285723
|
T | C | 1 | a0001c0001t0003g0274 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.183+302A>G | SYT13 | ENSG00000019505.8 | transcript | ENST00000020926.8 | protein_coding | 1/5 | chr11 | 45285723 |