Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9733 |
|---|---|
| ensemblid | ENSG00000075856.12 |
| hgncid | 16860 |
| symbol | SART3 |
| name | spliceosome associated factor 3, U4/U6 recycling protein |
| refseq_nuc | NM_014706.4 |
| refseq_prot | NP_055521.1 |
| ensembl_nuc | ENST00000546815.6 |
| ensembl_prot | ENSP00000449386.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 108522214 |
| end | 108561173 |
| strand | - |
| ver | v1.2 |
| region | chr12:108522214-108561173 |
| region5000 | chr12:108517214-108566173 |
| regionname0 | SART3_chr12_108522214_108561173 |
| regionname5000 | SART3_chr12_108517214_108566173 |
| 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 | 963 | 262 | 82 | 32 | 110 | 9 | 27 | 93 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002 | 0/0 | 963 | 122 | 11 | 25 | 70 | 3 | 13 | 54 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0003 | 0/0 | 963 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0004 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0005 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0006 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0007 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2892 | 162 | 22 | 22 | 91 | 6 | 20 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0002 | 0/0 | 2892 | 65 | 5 | 15 | 42 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0003 | 1/0 | 2892 | 55 | 30 | 5 | 16 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0004 | 0/0 | 2892 | 53 | 3 | 9 | 28 | 1 | 12 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0005 | 0/0 | 2892 | 18 | 9 | 1 | 2 | 1 | 5 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0006 | 0/0 | 2892 | 12 | 11 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0007 | 0/0 | 2892 | 9 | 8 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0008 | 0/0 | 2892 | 5 | 0 | 0 | 5 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0009 | 0/0 | 2892 | 3 | 2 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0010 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0011 | 0/0 | 2892 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0012 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0013 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0014 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0015 | 0/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0016 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0017 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| c0018 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1263 | 295 | 40 | 51 | 161 | 9 | 33 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0002 | 1/0 | 1263 | 81 | 46 | 6 | 18 | 3 | 7 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0003 | 0/0 | 1263 | 6 | 0 | 0 | 6 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0004 | 0/0 | 1263 | 5 | 5 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0005 | 0/0 | 1263 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0006 | 0/0 | 1263 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0007 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| t0008 | 0/0 | 1263 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| 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 | 0/1 | 15 | 0 | 2 | 8 | 1 | 3 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0002 | 0/0 | 13 | 0 | 4 | 8 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0004 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0011 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2892 | 162 | 22 | 22 | 91 | 6 | 20 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0003 | 1/0 | 2892 | 55 | 30 | 5 | 16 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0005 | 0/0 | 2892 | 18 | 9 | 1 | 2 | 1 | 5 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0006 | 0/0 | 2892 | 12 | 11 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0007 | 0/0 | 2892 | 9 | 8 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0010 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0011 | 0/0 | 2892 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0014 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0015 | 0/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0002 | 0/0 | 2892 | 65 | 5 | 15 | 42 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0004 | 0/0 | 2892 | 53 | 3 | 9 | 28 | 1 | 12 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0009 | 0/0 | 2892 | 3 | 2 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0017 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0003c0008 | 0/0 | 2892 | 5 | 0 | 0 | 5 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0004c0012 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0005c0018 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0006c0013 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0007c0016 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4154 | 150 | 17 | 22 | 84 | 6 | 20 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0001t0003 | 0/0 | 4154 | 6 | 0 | 0 | 6 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0001t0004 | 0/0 | 4154 | 5 | 5 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0001t0008 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0003t0002 | 1/0 | 4154 | 54 | 30 | 4 | 16 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0003t0007 | 0/0 | 4154 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0005t0002 | 0/0 | 4154 | 18 | 9 | 1 | 2 | 1 | 5 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0006t0001 | 0/0 | 4154 | 12 | 11 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0007t0002 | 0/0 | 4154 | 7 | 6 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0007t0006 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0010t0001 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0011t0001 | 0/0 | 4154 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0014t0001 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0001c0015t0002 | 0/0 | 4154 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0002t0001 | 0/0 | 4154 | 65 | 5 | 15 | 42 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0004t0001 | 0/0 | 4154 | 50 | 0 | 9 | 28 | 1 | 12 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0004t0005 | 0/0 | 4154 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0009t0001 | 0/0 | 4154 | 3 | 2 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0002c0017t0002 | 0/0 | 4154 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0003c0008t0001 | 0/0 | 4154 | 5 | 0 | 0 | 5 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0004c0012t0001 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0005c0018t0001 | 0/0 | 4154 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0006c0013t0001 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| a0007c0016t0001 | 0/0 | 4154 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | copy fasta | chr12 | 108517214 | 108566173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 15 | 0 | 2 | 8 | 1 | 3 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0011 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0010t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0010t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0011t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0014t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0015t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0002 | 0/0 | 13 | 0 | 4 | 8 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0004 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0009t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0009t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0009t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0017t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0003c0008t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0003c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0003c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0004c0012t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0005c0018t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0006c0013t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0007c0016t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0188 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0256 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0171 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00741 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0035 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01167 | hp1 | a0001 | c0007 | t0002 | g0158 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0271 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01168 | hp1 | a0002 | c0004 | t0001 | g0021 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01168 | hp2 | a0001 | c0011 | t0001 | g0031 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0241 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01169 | hp2 | a0001 | c0011 | t0001 | g0031 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01175 | hp1 | a0002 | c0009 | t0001 | g0213 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0163 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01258 | hp1 | a0001 | c0003 | t0007 | g0173 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0038 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01496 | hp2 | a0005 | c0018 | t0001 | g0281 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0229 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0172 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0186 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0174 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01891 | hp2 | a0002 | c0004 | t0005 | g0049 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01943 | hp1 | a0002 | c0004 | t0001 | g0270 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0041 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01952 | hp2 | a0002 | c0004 | t0001 | g0280 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0206 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0192 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02074 | hp1 | a0002 | c0004 | t0001 | g0275 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02080 | hp1 | a0002 | c0004 | t0001 | g0260 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02080 | hp2 | a0006 | c0013 | t0001 | g0065 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02129 | hp2 | a0002 | c0004 | t0001 | g0265 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0184 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0185 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02155 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02257 | hp1 | a0001 | c0010 | t0001 | g0052 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0157 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02258 | hp2 | a0007 | c0016 | t0001 | g0279 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0252 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02451 | hp2 | a0002 | c0009 | t0001 | g0236 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02523 | hp2 | a0001 | c0014 | t0001 | g0083 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02572 | hp1 | a0001 | c0005 | t0002 | g0204 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0207 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0148 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0150 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0152 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0037 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02717 | hp2 | a0002 | c0009 | t0001 | g0227 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02723 | hp1 | a0001 | c0005 | t0002 | g0040 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02723 | hp2 | a0001 | c0007 | t0002 | g0010 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0277 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02809 | hp1 | a0001 | c0007 | t0002 | g0010 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02818 | hp1 | a0001 | c0007 | t0002 | g0010 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0189 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02886 | hp2 | a0002 | c0017 | t0002 | g0220 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0203 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02896 | hp1 | a0004 | c0012 | t0001 | g0047 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0195 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02897 | hp1 | a0001 | c0005 | t0002 | g0202 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02897 | hp2 | a0004 | c0012 | t0001 | g0047 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0039 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0149 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02976 | hp2 | a0001 | c0007 | t0006 | g0033 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0170 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0190 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0196 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03139 | hp1 | a0002 | c0004 | t0005 | g0049 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0035 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0194 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0168 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03239 | hp2 | a0002 | c0004 | t0001 | g0004 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0155 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03453 | hp2 | a0002 | c0004 | t0005 | g0263 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03486 | hp1 | a0001 | c0005 | t0002 | g0200 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0164 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03490 | hp2 | a0001 | c0005 | t0002 | g0011 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03491 | hp1 | a0001 | c0005 | t0002 | g0201 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03492 | hp2 | a0001 | c0005 | t0002 | g0011 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0156 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03579 | hp2 | a0001 | c0007 | t0002 | g0154 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03669 | hp2 | a0001 | c0005 | t0002 | g0041 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03688 | hp1 | a0002 | c0004 | t0001 | g0249 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0228 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03831 | hp2 | a0002 | c0004 | t0001 | g0262 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03834 | hp2 | a0001 | c0005 | t0002 | g0011 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03927 | hp2 | a0002 | c0004 | t0001 | g0266 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03942 | hp2 | a0002 | c0004 | t0001 | g0048 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04115 | hp2 | a0002 | c0004 | t0001 | g0048 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0274 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04184 | hp2 | a0001 | c0015 | t0002 | g0169 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04199 | hp2 | a0002 | c0004 | t0001 | g0021 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04204 | hp1 | a0002 | c0004 | t0001 | g0245 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0160 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18522 | hp2 | a0001 | c0007 | t0002 | g0010 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18906 | hp1 | a0001 | c0005 | t0002 | g0199 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18906 | hp2 | a0001 | c0007 | t0006 | g0033 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18940 | hp2 | a0001 | c0003 | t0002 | g0167 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18941 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18945 | hp1 | a0001 | c0005 | t0002 | g0042 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18947 | hp2 | a0002 | c0004 | t0001 | g0244 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18951 | hp2 | a0002 | c0004 | t0001 | g0242 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18953 | hp2 | a0002 | c0004 | t0001 | g0264 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18956 | hp2 | a0001 | c0005 | t0002 | g0042 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18959 | hp1 | a0002 | c0004 | t0001 | g0253 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18964 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18965 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18973 | hp2 | a0002 | c0004 | t0001 | g0255 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18974 | hp1 | a0003 | c0008 | t0001 | g0016 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18977 | hp2 | a0002 | c0004 | t0001 | g0268 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18980 | hp2 | a0002 | c0004 | t0001 | g0258 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18982 | hp2 | a0003 | c0008 | t0001 | g0076 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18984 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18985 | hp2 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18988 | hp2 | a0002 | c0004 | t0001 | g0254 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18989 | hp1 | a0002 | c0004 | t0001 | g0250 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18989 | hp2 | a0002 | c0004 | t0001 | g0259 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18990 | hp1 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0181 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18992 | hp1 | a0002 | c0004 | t0001 | g0257 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18994 | hp2 | a0002 | c0004 | t0001 | g0251 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18998 | hp1 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0177 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19003 | hp1 | a0002 | c0004 | t0001 | g0272 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19011 | hp2 | a0003 | c0008 | t0001 | g0080 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19030 | hp2 | a0001 | c0005 | t0002 | g0198 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19043 | hp1 | a0001 | c0005 | t0002 | g0040 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19054 | hp1 | a0002 | c0004 | t0001 | g0243 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19054 | hp2 | a0003 | c0008 | t0001 | g0016 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19055 | hp1 | a0001 | c0003 | t0002 | g0165 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19070 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19074 | hp2 | a0002 | c0004 | t0001 | g0269 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19078 | hp2 | a0002 | c0004 | t0001 | g0278 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19079 | hp1 | a0003 | c0008 | t0001 | g0016 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19083 | hp1 | a0002 | c0004 | t0001 | g0267 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0162 | AFR | ASW | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20752 | hp1 | a0002 | c0004 | t0001 | g0273 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0011 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20905 | hp2 | a0002 | c0004 | t0001 | g0261 | SAS | GIH | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01123 | hp2 | a0002 | c0004 | t0001 | g0021 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02109 | hp1 | a0001 | c0010 | t0001 | g0051 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02109 | hp2 | a0001 | c0007 | t0002 | g0151 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0183 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0191 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0153 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA21309 | hp2 | a0001 | c0005 | t0002 | g0197 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0205 | REF | REF | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108526470
|
C | T | 1 | a0006 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1999G>A | p.Ala667Thr | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/19 | 2018/4154 | 1999/2892 | 667/963 | chr12 | 108526470 | ||
| chr12:108530194
|
C | A | 1 | a0003 | 5 | NA18974.hp1 NA18982.hp2 NA19011.hp2 others(2): Show |
missense_variant | MODERATE | c.1863G>T | p.Glu621Asp | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/19 | 1882/4154 | 1863/2892 | 621/963 | chr12 | 108530194 | ||
| chr12:108536543
|
C | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1417G>C | p.Val473Leu | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/19 | 1436/4154 | 1417/2892 | 473/963 | chr12 | 108536543 | ||
| chr12:108547926
|
C | T | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.505G>A | p.Val169Met | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/19 | 524/4154 | 505/2892 | 169/963 | chr12 | 108547926 | ||
| chr12:108561086
|
G | C | 4 | a0002a0004a0005others(1): Show | 126 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(123): Show |
missense_variant | MODERATE | c.69C>G | p.Asp23Glu | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/19 | 88/4154 | 69/2892 | 23/963 | chr12 | 108561086 | ||
| chr12:108561132
|
G | A | 1 | a0005 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.23C>T | p.Ser8Leu | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/19 | 42/4154 | 23/2892 | 8/963 | chr12 | 108561132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108523541
|
C | T | 1 | a0001c0006 | 12 | HG01109.hp2 HG02257.hp2 HG02615.hp1 others(9): Show |
synonymous_variant | LOW | c.2808G>A | p.Ala936Ala | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 2827/4154 | 2808/2892 | 936/963 | chr12 | 108523541 | ||
| chr12:108523553
|
G | A | 3 | a0002c0009a0004c0012a0007c0016 | 6 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
synonymous_variant | LOW | c.2796C>T | p.Asn932Asn | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 2815/4154 | 2796/2892 | 932/963 | chr12 | 108523553 | ||
| chr12:108524369
|
C | T | 14 | a0001c0001a0001c0006a0001c0007others(11): Show | 319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
synonymous_variant | LOW | c.2661G>A | p.Pro887Pro | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/19 | 2680/4154 | 2661/2892 | 887/963 | chr12 | 108524369 | ||
| chr12:108526396
|
G | A | 1 | a0001c0015 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2073C>T | p.Asp691Asp | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/19 | 2092/4154 | 2073/2892 | 691/963 | chr12 | 108526396 | ||
| chr12:108530173
|
A | G | 15 | a0001c0001a0001c0006a0001c0007others(12): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
synonymous_variant | LOW | c.1884T>C | p.Asp628Asp | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/19 | 1903/4154 | 1884/2892 | 628/963 | chr12 | 108530173 | ||
| chr12:108532253
|
G | A | 1 | a0001c0014 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1638C>T | p.Cys546Cys | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/19 | 1657/4154 | 1638/2892 | 546/963 | chr12 | 108532253 | ||
| chr12:108538156
|
G | A | 1 | a0001c0010 | 2 | HG02109.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.1110C>T | p.Arg370Arg | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/19 | 1129/4154 | 1110/2892 | 370/963 | chr12 | 108538156 | ||
| chr12:108539045
|
G | A | 1 | a0001c0011 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.951C>T | p.Ile317Ile | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/19 | 970/4154 | 951/2892 | 317/963 | chr12 | 108539045 | ||
| chr12:108547903
|
G | A | 1 | a0002c0004 | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
synonymous_variant | LOW | c.528C>T | p.Ala176Ala | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/19 | 547/4154 | 528/2892 | 176/963 | chr12 | 108547903 | ||
| chr12:108547924
|
C | G | 1 | a0001c0005 | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
synonymous_variant | LOW | c.507G>C | p.Val169Val | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/19 | 526/4154 | 507/2892 | 169/963 | chr12 | 108547924 | ||
| chr12:108561047
|
C | T | 13 | a0001c0001a0001c0010a0001c0011others(10): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
synonymous_variant | LOW | c.108G>A | p.Arg36Arg | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/19 | 127/4154 | 108/2892 | 36/963 | chr12 | 108561047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108522762
|
C | T | 1 | a0001c0007t0006 | 2 | HG02976.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*695G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 695 | chr12 | 108522762 | |||||
| chr12:108522900
|
T | G | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 312 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*557A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 557 | chr12 | 108522900 | |||||
| chr12:108523002
|
C | T | 1 | a0001c0001t0004 | 5 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 455 | chr12 | 108523002 | |||||
| chr12:108523013
|
A | T | 1 | a0001c0001t0003 | 6 | NA18966.hp2 NA18984.hp2 NA19063.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*444T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 444 | chr12 | 108523013 | |||||
| chr12:108523130
|
A | G | 1 | a0001c0001t0008 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*327T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 327 | chr12 | 108523130 | |||||
| chr12:108523174
|
C | T | 1 | a0002c0004t0005 | 3 | HG01891.hp2 HG03139.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 283 | chr12 | 108523174 | |||||
| chr12:108523384
|
G | T | 1 | a0001c0003t0007 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 73 | chr12 | 108523384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108523743
|
G | GA | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(216): Show | 314 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.2715-110dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/18 | chr12 | 108523743 | ||||||
| chr12:108523777
|
T | G | 3 | a0001c0003t0002g0189a0001c0003t0002g0190a0001c0003t0002g0191 | 3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2715-143A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/18 | chr12 | 108523777 | ||||||
| chr12:108523846
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2715-212G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/18 | chr12 | 108523846 | ||||||
| chr12:108524553
|
G | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(40): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2524-47C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524553 | ||||||
| chr12:108524654
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(230): Show | 333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.2524-148G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524654 | ||||||
| chr12:108524659
|
CCT | C | 45 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(42): Show | 71 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2524-155_2524-154d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524659 | ||||||
| chr12:108524818
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2524-312T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524818 | ||||||
| chr12:108524897
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2524-391G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524897 | ||||||
| chr12:108525389
|
T | C | 46 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(43): Show | 72 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2523+68A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108525389 | ||||||
| chr12:108525613
|
T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(40): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.2371-4A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525613 | ||||||
| chr12:108525759
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2371-150C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525759 | ||||||
| chr12:108525763
|
C | T | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2371-154G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525763 | ||||||
| chr12:108525771
|
T | G | 1 | a0001c0007t0002g0151 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2371-162A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525771 | ||||||
| chr12:108525897
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.2370+202C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525897 | ||||||
| chr12:108526755
|
CTCGGGT | C | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1916-208_1916-203d others(8): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526755 | ||||||
| chr12:108526829
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1916-276A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526829 | ||||||
| chr12:108526946
|
T | C | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1916-393A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526946 | ||||||
| chr12:108526948
|
C | G | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1916-395G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526948 | ||||||
| chr12:108527014
|
A | G | 41 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(38): Show | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1916-461T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527014 | ||||||
| chr12:108527172
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1916-619T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527172 | ||||||
| chr12:108527369
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1916-816A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527369 | ||||||
| chr12:108527443
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1916-890T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527443 | ||||||
| chr12:108527823
|
C | T | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1916-1270G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527823 | ||||||
| chr12:108527890
|
C | T | 1 | a0001c0003t0007g0173 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1916-1337G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527890 | ||||||
| chr12:108527891
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1916-1338C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527891 | ||||||
| chr12:108527895
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1916-1342T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527895 | ||||||
| chr12:108527928
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(259): Show | 374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.1916-1375T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527928 | ||||||
| chr12:108527954
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1916-1401G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527954 | ||||||
| chr12:108527970
|
T | C | 1 | a0002c0002t0001g0215 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1916-1417A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527970 | ||||||
| chr12:108528008
|
G | A | 1 | a0001c0001t0001g0025 | 2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1916-1455C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528008 | ||||||
| chr12:108528034
|
G | A | 2 | a0002c0004t0001g0259a0002c0004t0001g0269 | 2 | NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1916-1481C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528034 | ||||||
| chr12:108528070
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1916-1517T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528070 | ||||||
| chr12:108528106
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1916-1553T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528106 | ||||||
| chr12:108528125
|
G | A | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1916-1572C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528125 | ||||||
| chr12:108528415
|
G | A | 14 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(11): Show | 20 | HG01943.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1915+1727C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528415 | ||||||
| chr12:108528444
|
C | T | 11 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(8): Show | 17 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.1915+1698G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528444 | ||||||
| chr12:108528462
|
G | A | 1 | a0002c0017t0002g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1915+1680C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528462 | ||||||
| chr12:108528482
|
C | CA | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(114): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1915+1659dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528482 | ||||||
| chr12:108528482
|
CA | C | 26 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(23): Show | 29 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1915+1659delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528482 | ||||||
| chr12:108528508
|
G | T | 55 | a0001c0001t0001g0126a0001c0003t0002g0206a0001c0005t0002g0011others(52): Show | 73 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1915+1634C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528508 | ||||||
| chr12:108528555
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1915+1587C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528555 | ||||||
| chr12:108528692
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1915+1450C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528692 | ||||||
| chr12:108528891
|
G | A | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1915+1251C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528891 | ||||||
| chr12:108528940
|
G | A | 1 | a0002c0004t0001g0046 | 2 | NA18985.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1915+1202C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528940 | ||||||
| chr12:108528989
|
G | A | 16 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(13): Show | 20 | HG01168.hp2 HG01169.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1915+1153C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528989 | ||||||
| chr12:108529004
|
T | G | 39 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(36): Show | 51 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1915+1138A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529004 | ||||||
| chr12:108529089
|
C | T | 1 | a0004c0012t0001g0047 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1915+1053G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529089 | ||||||
| chr12:108529205
|
A | G | 2 | a0002c0004t0001g0270a0002c0004t0001g0280 | 2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1915+937T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529205 | ||||||
| chr12:108529301
|
A | G | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1915+841T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529301 | ||||||
| chr12:108529320
|
C | T | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1915+822G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529320 | ||||||
| chr12:108529425
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1915+717A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529425 | ||||||
| chr12:108529604
|
G | A | 3 | a0002c0004t0001g0256a0002c0004t0001g0260a0002c0004t0001g0278 | 3 | HG00673.hp1 HG02080.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1915+538C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529604 | ||||||
| chr12:108529609
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1915+533T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529609 | ||||||
| chr12:108529772
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1915+370C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529772 | ||||||
| chr12:108529784
|
A | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1915+358T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529784 | ||||||
| chr12:108529806
|
TA | T | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1915+335delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529806 | ||||||
| chr12:108529838
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1915+304G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529838 | ||||||
| chr12:108529876
|
T | A | 1 | a0001c0001t0001g0068 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1915+266A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529876 | ||||||
| chr12:108530332
|
G | A | 1 | a0002c0004t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1747-22C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530332 | ||||||
| chr12:108530333
|
C | A | 1 | a0002c0004t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1747-23G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530333 | ||||||
| chr12:108530380
|
A | C | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1747-70T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530380 | ||||||
| chr12:108530436
|
G | A | 1 | a0001c0005t0002g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1747-126C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530436 | ||||||
| chr12:108530564
|
T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(85): Show | 126 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1747-254A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530564 | ||||||
| chr12:108530719
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0104a0001c0001t0001g0117others(2): Show | 6 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747-409C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530719 | ||||||
| chr12:108530733
|
C | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(222): Show | 322 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.1747-423G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530733 | ||||||
| chr12:108530766
|
A | T | 1 | a0001c0005t0002g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1746+438T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530766 | ||||||
| chr12:108530852
|
C | T | 1 | a0001c0003t0002g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1746+352G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530852 | ||||||
| chr12:108530857
|
CA | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0024others(65): Show | 101 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1746+346delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530857 | ||||||
| chr12:108530972
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1746+232A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530972 | ||||||
| chr12:108530977
|
C | T | 9 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(6): Show | 11 | HG01109.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1746+227G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530977 | ||||||
| chr12:108531127
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(44): Show | 62 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1746+77G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108531127 | ||||||
| chr12:108531154
|
G | C | 1 | a0002c0004t0005g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1746+50C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108531154 | ||||||
| chr12:108531477
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1670-197C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531477 | ||||||
| chr12:108531492
|
C | T | 1 | a0002c0017t0002g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1670-212G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531492 | ||||||
| chr12:108531638
|
C | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.1670-358G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531638 | ||||||
| chr12:108531639
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1670-359T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531639 | ||||||
| chr12:108531639
|
A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(242): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.1670-359T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531639 | ||||||
| chr12:108531640
|
A | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.1670-360T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531640 | ||||||
| chr12:108531847
|
C | T | 2 | a0002c0004t0001g0243a0002c0004t0001g0250 | 2 | NA18989.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1669+375G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531847 | ||||||
| chr12:108531875
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1669+347T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531875 | ||||||
| chr12:108531976
|
C | A | 1 | a0001c0005t0002g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1669+246G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531976 | ||||||
| chr12:108531979
|
C | G | 1 | a0001c0005t0002g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1669+243G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531979 | ||||||
| chr12:108531986
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1669+236C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531986 | ||||||
| chr12:108532108
|
C | T | 1 | a0001c0003t0002g0171 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1669+114G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108532108 | ||||||
| chr12:108532669
|
G | A | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1557-335C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108532669 | ||||||
| chr12:108532678
|
G | A | 1 | a0001c0003t0002g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1557-344C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108532678 | ||||||
| chr12:108532747
|
G | A | 1 | a0001c0010t0001g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1557-413C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108532747 | ||||||
| chr12:108533048
|
G | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(40): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1557-714C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533048 | ||||||
| chr12:108533109
|
C | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0104a0001c0001t0001g0114others(6): Show | 10 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1557-775G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533109 | ||||||
| chr12:108533297
|
C | T | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1557-963G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533297 | ||||||
| chr12:108533317
|
T | C | 5 | a0002c0002t0001g0210a0002c0002t0001g0223a0002c0002t0001g0246others(2): Show | 5 | NA18955.hp1 NA19011.hp1 NA19076.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557-983A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533317 | ||||||
| chr12:108533367
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1557-1033G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533367 | ||||||
| chr12:108533388
|
C | CA | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(157): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1557-1055dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533388 | ||||||
| chr12:108533388
|
C | CAA | 19 | a0001c0001t0001g0060a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 25 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1557-1056_1557-105 others(6): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533388 | ||||||
| chr12:108533407
|
A | G | 41 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(38): Show | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1557-1073T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533407 | ||||||
| chr12:108533545
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1557-1211T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533545 | ||||||
| chr12:108533689
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1557-1355G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533689 | ||||||
| chr12:108533707
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1557-1373A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533707 | ||||||
| chr12:108533764
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0093 | 6 | NA18965.hp2 NA18968.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557-1430C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533764 | ||||||
| chr12:108533833
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1557-1499A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533833 | ||||||
| chr12:108534022
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 111 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1556+1337C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534022 | ||||||
| chr12:108534111
|
CTA | C | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+1246_1556+124 others(6): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534111 | ||||||
| chr12:108534115
|
A | T | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+1244T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534115 | ||||||
| chr12:108534302
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1556+1057G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534302 | ||||||
| chr12:108534304
|
G | A | 4 | a0001c0003t0002g0039a0001c0003t0002g0192a0001c0003t0002g0194others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1556+1055C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534304 | ||||||
| chr12:108534321
|
G | A | 2 | a0002c0004t0001g0242a0002c0004t0001g0258 | 2 | NA18951.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1556+1038C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534321 | ||||||
| chr12:108534398
|
G | A | 34 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(31): Show | 45 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1556+961C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534398 | ||||||
| chr12:108534507
|
T | TA | 5 | a0001c0001t0001g0079a0001c0001t0001g0116a0001c0003t0002g0019others(2): Show | 7 | HG02055.hp1 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1556+851dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534507 | ||||||
| chr12:108534507
|
TA | T | 15 | a0001c0001t0001g0113a0001c0006t0001g0034a0001c0006t0001g0035others(12): Show | 20 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1556+851delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534507 | ||||||
| chr12:108534553
|
G | C | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+806C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534553 | ||||||
| chr12:108534599
|
G | A | 3 | a0001c0003t0002g0189a0001c0003t0002g0190a0001c0003t0002g0191 | 3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1556+760C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534599 | ||||||
| chr12:108534937
|
A | G | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1556+422T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534937 | ||||||
| chr12:108535048
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1556+311A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535048 | ||||||
| chr12:108535179
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1556+180T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535179 | ||||||
| chr12:108535244
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0069a0001c0001t0001g0087others(2): Show | 7 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1556+115T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535244 | ||||||
| chr12:108535310
|
GTGCA | G | 3 | a0002c0004t0001g0242a0002c0004t0001g0258a0002c0004t0001g0267 | 3 | NA18951.hp2 NA18980.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1556+45_1556+48del others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535310 | ||||||
| chr12:108535340
|
C | T | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+19G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535340 | ||||||
| chr12:108535515
|
C | T | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1447-47G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535515 | ||||||
| chr12:108535587
|
G | C | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1447-119C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535587 | ||||||
| chr12:108535674
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1447-206G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535674 | ||||||
| chr12:108535700
|
G | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-232C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535700 | ||||||
| chr12:108535786
|
T | TA | 85 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(82): Show | 126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1447-319dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535786 | ||||||
| chr12:108535786
|
TA | T | 12 | a0001c0001t0001g0136a0001c0003t0002g0019a0001c0003t0002g0039others(9): Show | 15 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1447-319delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535786 | ||||||
| chr12:108535964
|
C | T | 2 | a0002c0004t0001g0251a0002c0004t0001g0255 | 2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1447-496G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535964 | ||||||
| chr12:108535974
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0098a0001c0001t0001g0106 | 4 | HG01081.hp1 HG01175.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-506C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535974 | ||||||
| chr12:108536064
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1446+450T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536064 | ||||||
| chr12:108536246
|
G | A | 40 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(37): Show | 52 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.1446+268C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536246 | ||||||
| chr12:108536251
|
C | T | 1 | a0002c0002t0001g0020 | 3 | NA18957.hp2 NA18968.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1446+263G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536251 | ||||||
| chr12:108536258
|
A | C | 1 | a0002c0004t0005g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1446+256T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536258 | ||||||
| chr12:108536333
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(217): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1446+181T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536333 | ||||||
| chr12:108536484
|
G | A | 4 | a0001c0003t0002g0039a0001c0003t0002g0192a0001c0003t0002g0194others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1446+30C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536484 | ||||||
| chr12:108536508
|
A | T | 13 | a0001c0003t0007g0173a0001c0005t0002g0011a0001c0005t0002g0040others(10): Show | 19 | HG01258.hp1 HG01943.hp2 HG02572.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.1446+6T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536508 | ||||||
| chr12:108537014
|
G | C | 1 | a0001c0003t0007g0173 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1310-229C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537014 | ||||||
| chr12:108537044
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1310-259G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537044 | ||||||
| chr12:108537055
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1310-270C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537055 | ||||||
| chr12:108537168
|
G | A | 1 | a0002c0004t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1309+320C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537168 | ||||||
| chr12:108537199
|
A | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.1309+289T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537199 | ||||||
| chr12:108537367
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+121G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537367 | ||||||
| chr12:108537428
|
C | T | 1 | a0007c0016t0001g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1309+60G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537428 | ||||||
| chr12:108537670
|
C | A | 1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1202-75G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108537670 | ||||||
| chr12:108537707
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1202-112G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108537707 | ||||||
| chr12:108537930
|
C | G | 1 | a0001c0003t0002g0165 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1201+135G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108537930 | ||||||
| chr12:108538003
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 111 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1201+62G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108538003 | ||||||
| chr12:108538222
|
G | A | 1 | a0004c0012t0001g0047 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1063-19C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538222 | ||||||
| chr12:108538277
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1063-74G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538277 | ||||||
| chr12:108538324
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1063-121C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538324 | ||||||
| chr12:108538358
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0069a0001c0001t0001g0087others(2): Show | 7 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1063-155C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538358 | ||||||
| chr12:108538412
|
G | A | 2 | a0002c0002t0001g0229a0002c0002t0001g0230 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1063-209C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538412 | ||||||
| chr12:108538703
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1062+231C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538703 | ||||||
| chr12:108539140
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.907-51G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539140 | ||||||
| chr12:108539540
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.907-451A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539540 | ||||||
| chr12:108539594
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.907-505G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539594 | ||||||
| chr12:108539603
|
A | T | 1 | a0007c0016t0001g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.907-514T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539603 | ||||||
| chr12:108539636
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.907-547C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539636 | ||||||
| chr12:108539652
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0008g0056 | 2 | HG00609.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.907-563G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539652 | ||||||
| chr12:108539783
|
T | C | 2 | a0002c0004t0001g0241a0002c0004t0001g0271 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.907-694A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539783 | ||||||
| chr12:108540155
|
T | TA | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.907-1067dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540155 | ||||||
| chr12:108540212
|
G | A | 1 | a0002c0004t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.907-1123C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540212 | ||||||
| chr12:108540404
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.907-1315A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540404 | ||||||
| chr12:108540459
|
T | C | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.907-1370A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540459 | ||||||
| chr12:108540573
|
TA | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.907-1485delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540573 | ||||||
| chr12:108540641
|
CA | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 318 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.907-1553delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540641 | ||||||
| chr12:108540643
|
A | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0024others(11): Show | 21 | HG00597.hp1 HG00673.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.907-1554T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540643 | ||||||
| chr12:108540659
|
C | T | 1 | a0001c0015t0002g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.907-1570G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540659 | ||||||
| chr12:108540910
|
C | T | 1 | a0002c0002t0001g0225 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.907-1821G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540910 | ||||||
| chr12:108540946
|
G | A | 4 | a0001c0007t0002g0010a0001c0007t0002g0151a0001c0007t0002g0154others(1): Show | 7 | HG01167.hp1 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.907-1857C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540946 | ||||||
| chr12:108541045
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.907-1956G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541045 | ||||||
| chr12:108541321
|
C | T | 1 | a0001c0003t0002g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.906+1707G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541321 | ||||||
| chr12:108541340
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.906+1688C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541340 | ||||||
| chr12:108541543
|
T | A | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.906+1485A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541543 | ||||||
| chr12:108541670
|
C | A | 3 | a0002c0002t0001g0209a0002c0002t0001g0219a0002c0002t0001g0221 | 3 | HG03130.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.906+1358G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541670 | ||||||
| chr12:108541684
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.906+1344C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541684 | ||||||
| chr12:108541712
|
G | C | 1 | a0002c0004t0005g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.906+1316C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541712 | ||||||
| chr12:108541762
|
A | C | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.906+1266T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541762 | ||||||
| chr12:108541767
|
T | C | 6 | a0001c0003t0002g0006a0001c0003t0002g0036a0001c0003t0002g0162others(3): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.906+1261A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541767 | ||||||
| chr12:108541781
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(204): Show | 298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.906+1247T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541781 | ||||||
| chr12:108541792
|
G | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.906+1236C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541792 | ||||||
| chr12:108541954
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.906+1074G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541954 | ||||||
| chr12:108541998
|
C | CT | 24 | a0001c0003t0002g0036a0001c0003t0002g0163a0001c0003t0002g0164others(21): Show | 25 | HG00544.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.906+1029dupA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108541998
|
C | CTTTTTTT others(2987): Show |
1 | a0001c0005t0002g0042 | 2 | NA18945.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.906+1029_906+1030i others(2996): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108541998
|
CTTTTTT | C | 10 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0001g0143others(7): Show | 12 | HG00673.hp1 HG01123.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.906+1024_906+1029d others(8): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108541998
|
CTTTTTTT | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(84): Show | 111 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.906+1023_906+1029d others(9): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108541998
|
CTTTTTTT others(1): Show |
C | 99 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 161 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.906+1022_906+1029d others(10): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108541998
|
CTTTTTTT others(2): Show |
C | 24 | a0001c0001t0001g0030a0001c0001t0001g0074a0001c0001t0001g0131others(21): Show | 31 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.906+1021_906+1029d others(11): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108541998
|
CTTTTTTT others(9): Show |
C | 2 | a0002c0004t0001g0048a0002c0004t0001g0277 | 3 | HG02738.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.906+1014_906+1029d others(18): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | ||||||
| chr12:108542070
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.906+958G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542070 | ||||||
| chr12:108542282
|
C | A | 1 | a0002c0002t0001g0234 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.906+746G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542282 | ||||||
| chr12:108542394
|
C | A | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.906+634G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542394 | ||||||
| chr12:108542473
|
C | T | 2 | a0001c0006t0001g0150a0001c0006t0001g0155 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.906+555G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542473 | ||||||
| chr12:108542538
|
CACAG | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(40): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.906+486_906+489del others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542538 | ||||||
| chr12:108542573
|
C | T | 1 | a0002c0004t0001g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.906+455G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542573 | ||||||
| chr12:108542574
|
G | A | 6 | a0001c0001t0001g0029a0001c0003t0002g0159a0001c0003t0002g0167others(3): Show | 7 | NA18940.hp2 NA18983.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+454C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542574 | ||||||
| chr12:108542652
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 111 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.906+376A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542652 | ||||||
| chr12:108542708
|
G | A | 88 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(85): Show | 126 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.906+320C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542708 | ||||||
| chr12:108542740
|
T | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.906+288A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542740 | ||||||
| chr12:108542743
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.906+285G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542743 | ||||||
| chr12:108542886
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.906+142A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542886 | ||||||
| chr12:108542904
|
G | A | 3 | a0001c0003t0002g0159a0001c0003t0002g0167a0001c0003t0002g0180 | 3 | NA18940.hp2 NA18993.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.906+124C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542904 | ||||||
| chr12:108543279
|
A | C | 1 | a0001c0001t0004g0099 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.782-127T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543279 | ||||||
| chr12:108543352
|
C | T | 1 | a0001c0003t0002g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-200G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543352 | ||||||
| chr12:108543466
|
C | T | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.782-314G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543466 | ||||||
| chr12:108543617
|
G | A | 6 | a0002c0002t0001g0005a0002c0002t0001g0043a0002c0002t0001g0211others(3): Show | 12 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.782-465C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543617 | ||||||
| chr12:108543622
|
T | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0053 | 3 | HG01071.hp2 HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.782-470A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543622 | ||||||
| chr12:108543641
|
G | A | 16 | a0001c0001t0001g0058a0001c0006t0001g0034a0001c0006t0001g0035others(13): Show | 22 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.782-489C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543641 | ||||||
| chr12:108544153
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.781+274G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108544153 | ||||||
| chr12:108544391
|
T | C | 1 | a0001c0005t0002g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781+36A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108544391 | ||||||
| chr12:108544714
|
C | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0133a0001c0001t0001g0135 | 4 | HG02630.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-236G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544714 | ||||||
| chr12:108544779
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.730-301C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544779 | ||||||
| chr12:108544823
|
C | T | 2 | a0001c0003t0002g0177a0001c0003t0002g0178 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.729+316G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544823 | ||||||
| chr12:108544854
|
C | T | 1 | a0002c0004t0005g0049 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.729+285G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544854 | ||||||
| chr12:108544974
|
T | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.729+165A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544974 | ||||||
| chr12:108545407
|
C | T | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.545-84G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545407 | ||||||
| chr12:108545809
|
T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(40): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.545-486A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545809 | ||||||
| chr12:108545967
|
C | CA | 39 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(36): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.545-645dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | ||||||
| chr12:108545967
|
C | CAA | 9 | a0001c0001t0001g0024a0001c0001t0001g0103a0001c0001t0001g0111others(6): Show | 10 | HG02074.hp1 HG02129.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.545-646_545-645dup others(2): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | ||||||
| chr12:108545967
|
C | CAAA | 106 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 155 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.545-647_545-645dup others(3): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | ||||||
| chr12:108545967
|
C | CAAAA | 49 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0084others(46): Show | 75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.545-648_545-645dup others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | ||||||
| chr12:108545967
|
C | CAAAAA | 6 | a0002c0002t0001g0211a0002c0002t0001g0222a0002c0002t0001g0232others(3): Show | 6 | HG01192.hp1 HG01361.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.545-649_545-645dup others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | ||||||
| chr12:108545967
|
CA | C | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.545-645delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | ||||||
| chr12:108545985
|
C | A | 41 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(38): Show | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.545-662G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545985 | ||||||
| chr12:108546104
|
T | C | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545-781A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546104 | ||||||
| chr12:108546125
|
T | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.545-802A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546125 | ||||||
| chr12:108546137
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.545-814A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546137 | ||||||
| chr12:108546231
|
G | A | 2 | a0002c0002t0001g0217a0002c0002t0001g0235 | 2 | HG00609.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.545-908C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546231 | ||||||
| chr12:108546337
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.545-1014G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546337 | ||||||
| chr12:108546367
|
T | A | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.545-1044A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546367 | ||||||
| chr12:108546369
|
T | C | 4 | a0001c0003t0002g0039a0001c0003t0002g0192a0001c0003t0002g0194others(1): Show | 5 | HG02055.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.545-1046A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546369 | ||||||
| chr12:108546522
|
CT | C | 31 | a0001c0001t0001g0061a0001c0003t0002g0193a0001c0005t0002g0011others(28): Show | 43 | HG01109.hp2 HG01167.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.545-1200delA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546522 | ||||||
| chr12:108546522
|
CTT | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(202): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.545-1201_545-1200d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546522 | ||||||
| chr12:108546679
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.544+1208G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546679 | ||||||
| chr12:108546741
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.544+1146C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546741 | ||||||
| chr12:108546776
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1111G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546776 | ||||||
| chr12:108546778
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1109G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546778 | ||||||
| chr12:108546779
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1108G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546779 | ||||||
| chr12:108546780
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1107G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546780 | ||||||
| chr12:108546907
|
C | T | 1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544+980G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546907 | ||||||
| chr12:108547008
|
C | T | 1 | a0002c0002t0001g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.544+879G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547008 | ||||||
| chr12:108547182
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.544+705C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547182 | ||||||
| chr12:108547205
|
T | C | 1 | a0002c0009t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.544+682A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547205 | ||||||
| chr12:108547278
|
G | A | 4 | a0001c0007t0002g0010a0001c0007t0002g0151a0001c0007t0002g0154others(1): Show | 7 | HG01167.hp1 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+609C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547278 | ||||||
| chr12:108547509
|
C | G | 1 | a0003c0008t0001g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.544+378G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547509 | ||||||
| chr12:108547563
|
T | A | 1 | a0001c0005t0002g0042 | 2 | NA18945.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.544+324A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547563 | ||||||
| chr12:108547573
|
T | C | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.544+314A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547573 | ||||||
| chr12:108547671
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.544+216A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547671 | ||||||
| chr12:108547846
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544+41A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547846 | ||||||
| chr12:108548252
|
C | T | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.440-261G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548252 | ||||||
| chr12:108548274
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.440-283A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548274 | ||||||
| chr12:108548281
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.440-290T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548281 | ||||||
| chr12:108548319
|
C | T | 5 | a0002c0002t0001g0210a0002c0002t0001g0223a0002c0002t0001g0246others(2): Show | 5 | NA18955.hp1 NA19011.hp1 NA19076.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-328G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548319 | ||||||
| chr12:108548340
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.440-349A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548340 | ||||||
| chr12:108548774
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.439+314G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548774 | ||||||
| chr12:108548994
|
GT | G | 34 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(31): Show | 45 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.439+93delA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548994 | ||||||
| chr12:108548999
|
C | G | 34 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(31): Show | 45 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.439+89G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548999 | ||||||
| chr12:108549252
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.313-38C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549252 | ||||||
| chr12:108549322
|
G | C | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-108C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549322 | ||||||
| chr12:108549520
|
T | A | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.313-306A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549520 | ||||||
| chr12:108549595
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.313-381G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549595 | ||||||
| chr12:108549781
|
C | T | 8 | a0001c0005t0002g0202a0001c0005t0002g0203a0002c0002t0001g0209others(5): Show | 8 | HG02647.hp1 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-567G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549781 | ||||||
| chr12:108549927
|
C | T | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-713G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549927 | ||||||
| chr12:108549956
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.313-742G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549956 | ||||||
| chr12:108549972
|
C | T | 41 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(38): Show | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.313-758G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549972 | ||||||
| chr12:108550013
|
CA | C | 19 | a0001c0001t0001g0107a0001c0001t0001g0144a0001c0001t0001g0145others(16): Show | 25 | HG01243.hp2 HG01943.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.313-800delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | ||||||
| chr12:108550013
|
CAA | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(125): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.313-801_313-800del others(2): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | ||||||
| chr12:108550013
|
CAAA | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(66): Show | 105 | HG00323.hp1 HG00609.hp2 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.313-802_313-800del others(3): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | ||||||
| chr12:108550013
|
CAAAA | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0074others(3): Show | 9 | HG00597.hp1 HG02809.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-803_313-800del others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | ||||||
| chr12:108550453
|
T | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.313-1239A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550453 | ||||||
| chr12:108550469
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.313-1255C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550469 | ||||||
| chr12:108550535
|
C | A | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-1321G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550535 | ||||||
| chr12:108550715
|
T | C | 12 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(9): Show | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1501A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550715 | ||||||
| chr12:108550721
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.313-1507C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550721 | ||||||
| chr12:108550740
|
G | A | 2 | a0001c0003t0002g0181a0001c0003t0002g0182 | 2 | NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.313-1526C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550740 | ||||||
| chr12:108550776
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.313-1562A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550776 | ||||||
| chr12:108550966
|
C | T | 1 | a0001c0003t0002g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.313-1752G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550966 | ||||||
| chr12:108550981
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.313-1767A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550981 | ||||||
| chr12:108551183
|
G | A | 1 | a0001c0005t0002g0201 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.313-1969C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551183 | ||||||
| chr12:108551209
|
A | G | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-1995T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551209 | ||||||
| chr12:108551222
|
G | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.313-2008C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551222 | ||||||
| chr12:108551457
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.313-2243C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551457 | ||||||
| chr12:108551465
|
G | A | 1 | a0001c0006t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.313-2251C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551465 | ||||||
| chr12:108551473
|
A | G | 2 | a0001c0003t0002g0175a0001c0003t0002g0176 | 2 | HG02027.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.313-2259T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551473 | ||||||
| chr12:108551625
|
G | A | 1 | a0001c0005t0002g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-2411C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551625 | ||||||
| chr12:108551676
|
G | A | 1 | a0002c0002t0001g0208 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.313-2462C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551676 | ||||||
| chr12:108551816
|
G | A | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-2602C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551816 | ||||||
| chr12:108551834
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.313-2620T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551834 | ||||||
| chr12:108551934
|
G | A | 1 | a0001c0006t0001g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.313-2720C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551934 | ||||||
| chr12:108551950
|
T | TA | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-2737dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551950 | ||||||
| chr12:108552145
|
G | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.313-2931C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552145 | ||||||
| chr12:108552206
|
G | C | 1 | a0002c0004t0005g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.313-2992C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552206 | ||||||
| chr12:108552391
|
T | G | 17 | a0001c0003t0002g0038a0001c0003t0002g0159a0001c0003t0002g0160others(14): Show | 18 | HG00544.hp2 HG01496.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-3177A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552391 | ||||||
| chr12:108552442
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.313-3228A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552442 | ||||||
| chr12:108552450
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.313-3236A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552450 | ||||||
| chr12:108552472
|
TA | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(213): Show | 310 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.313-3259delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552472 | ||||||
| chr12:108552542
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.313-3328G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552542 | ||||||
| chr12:108552542
|
C | CA | 93 | a0001c0001t0001g0026a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 132 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.313-3329dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552542 | ||||||
| chr12:108552542
|
C | CAA | 14 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(11): Show | 20 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.313-3330_313-3329d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552542 | ||||||
| chr12:108552554
|
C | A | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-3340G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552554 | ||||||
| chr12:108552676
|
T | C | 1 | a0001c0015t0002g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.313-3462A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552676 | ||||||
| chr12:108552844
|
A | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0102others(9): Show | 16 | NA18942.hp1 NA18946.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.313-3630T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552844 | ||||||
| chr12:108552942
|
C | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(40): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.313-3728G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552942 | ||||||
| chr12:108553022
|
G | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.313-3808C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553022 | ||||||
| chr12:108553099
|
G | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.313-3885C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553099 | ||||||
| chr12:108553178
|
T | C | 12 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(9): Show | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-3964A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553178 | ||||||
| chr12:108553351
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.313-4137A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553351 | ||||||
| chr12:108553787
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313-4573C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553787 | ||||||
| chr12:108553876
|
G | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 104 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.313-4662C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553876 | ||||||
| chr12:108553953
|
C | A | 1 | a0002c0002t0001g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.313-4739G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553953 | ||||||
| chr12:108553984
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.313-4770G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553984 | ||||||
| chr12:108554127
|
G | C | 1 | a0001c0006t0001g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.313-4913C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554127 | ||||||
| chr12:108554131
|
C | CCCCCGCC others(5): Show |
234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.313-4918_313-4917i others(14): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554131 | ||||||
| chr12:108554264
|
T | TG | 280 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(277): Show | 393 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(390): Show |
intron_variant | MODIFIER | c.313-5051_313-5050i others(3): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554264 | ||||||
| chr12:108554300
|
A | G | 1 | a0002c0004t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.313-5086T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554300 | ||||||
| chr12:108554302
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.313-5088T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554302 | ||||||
| chr12:108554392
|
G | A | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-5178C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554392 | ||||||
| chr12:108554844
|
T | C | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-5630A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554844 | ||||||
| chr12:108554886
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-5672G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554886 | ||||||
| chr12:108554896
|
A | G | 1 | a0001c0006t0001g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.313-5682T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554896 | ||||||
| chr12:108555231
|
T | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0102others(9): Show | 16 | NA18942.hp1 NA18946.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.312+5612A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555231 | ||||||
| chr12:108555431
|
G | A | 1 | a0001c0003t0002g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.312+5412C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555431 | ||||||
| chr12:108555483
|
G | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+5360C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555483 | ||||||
| chr12:108555507
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.312+5336G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555507 | ||||||
| chr12:108555580
|
G | A | 2 | a0001c0005t0002g0202a0001c0005t0002g0203 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.312+5263C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555580 | ||||||
| chr12:108555766
|
T | G | 14 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(11): Show | 19 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.312+5077A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555766 | ||||||
| chr12:108555781
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.312+5062G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555781 | ||||||
| chr12:108555820
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+5023A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555820 | ||||||
| chr12:108555884
|
C | G | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0012others(44): Show | 73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.312+4959G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555884 | ||||||
| chr12:108555929
|
G | A | 41 | a0002c0004t0001g0004a0002c0004t0001g0021a0002c0004t0001g0046others(38): Show | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.312+4914C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555929 | ||||||
| chr12:108555963
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+4880A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555963 | ||||||
| chr12:108555989
|
T | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.312+4854A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555989 | ||||||
| chr12:108556100
|
CT | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.312+4742delA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556100 | ||||||
| chr12:108556190
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.312+4653G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556190 | ||||||
| chr12:108556368
|
G | T | 1 | a0001c0003t0002g0161 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.312+4475C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556368 | ||||||
| chr12:108556441
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312+4402A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556441 | ||||||
| chr12:108556574
|
C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312+4269G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556574 | ||||||
| chr12:108556678
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.312+4165A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556678 | ||||||
| chr12:108556793
|
T | C | 1 | a0002c0004t0001g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.312+4050A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556793 | ||||||
| chr12:108556950
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+3893C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556950 | ||||||
| chr12:108557090
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312+3753A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557090 | ||||||
| chr12:108557171
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+3672C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557171 | ||||||
| chr12:108557206
|
G | GT | 98 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0030others(95): Show | 122 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.312+3636dupA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | ||||||
| chr12:108557206
|
G | GTT | 23 | a0001c0001t0001g0024a0001c0001t0001g0131a0001c0003t0002g0192others(20): Show | 32 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.312+3635_312+3636d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | ||||||
| chr12:108557206
|
G | GTTT | 9 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0149others(6): Show | 15 | HG00423.hp2 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.312+3634_312+3636d others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | ||||||
| chr12:108557206
|
GTTT | G | 10 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(7): Show | 16 | HG01943.hp2 HG02723.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.312+3634_312+3636d others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | ||||||
| chr12:108557206
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.312+3622_312+3636d others(17): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | ||||||
| chr12:108557236
|
T | C | 1 | a0001c0001t0001g0026 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.312+3607A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557236 | ||||||
| chr12:108557309
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312+3534C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557309 | ||||||
| chr12:108557317
|
G | A | 2 | a0001c0001t0001g0092a0001c0003t0002g0183 | 2 | HG02165.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.312+3526C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557317 | ||||||
| chr12:108557531
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.312+3312A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557531 | ||||||
| chr12:108557551
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.312+3292C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557551 | ||||||
| chr12:108557711
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0093 | 5 | NA18965.hp2 NA18968.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+3132C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557711 | ||||||
| chr12:108557739
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+3104G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557739 | ||||||
| chr12:108557765
|
G | A | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.312+3078C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557765 | ||||||
| chr12:108557829
|
T | G | 1 | a0001c0001t0001g0094 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.312+3014A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557829 | ||||||
| chr12:108557864
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+2979T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557864 | ||||||
| chr12:108557912
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.312+2931G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557912 | ||||||
| chr12:108557981
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+2862A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557981 | ||||||
| chr12:108558038
|
G | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+2805C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558038 | ||||||
| chr12:108558111
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+2732C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558111 | ||||||
| chr12:108558133
|
C | G | 1 | a0001c0003t0002g0160 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.312+2710G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558133 | ||||||
| chr12:108558140
|
A | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.312+2703T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558140 | ||||||
| chr12:108558175
|
T | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.312+2668A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558175 | ||||||
| chr12:108558178
|
T | C | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.312+2665A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558178 | ||||||
| chr12:108558295
|
A | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 111 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.312+2548T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558295 | ||||||
| chr12:108558612
|
G | A | 13 | a0001c0003t0002g0191a0001c0005t0002g0011a0001c0005t0002g0040others(10): Show | 19 | HG01943.hp2 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.312+2231C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558612 | ||||||
| chr12:108558663
|
C | T | 3 | a0001c0003t0002g0189a0001c0003t0002g0190a0001c0003t0002g0191 | 3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.312+2180G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558663 | ||||||
| chr12:108558715
|
T | A | 3 | a0001c0006t0001g0035a0001c0006t0001g0148a0001c0006t0001g0156 | 4 | HG01109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+2128A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558715 | ||||||
| chr12:108558737
|
T | C | 12 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(9): Show | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+2106A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558737 | ||||||
| chr12:108558756
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+2087T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558756 | ||||||
| chr12:108558815
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(42): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.312+2028G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558815 | ||||||
| chr12:108558958
|
G | A | 1 | a0004c0012t0001g0047 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.312+1885C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558958 | ||||||
| chr12:108558999
|
C | A | 1 | a0002c0004t0001g0274 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.312+1844G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558999 | ||||||
| chr12:108559039
|
G | GA | 107 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 171 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.312+1803dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | ||||||
| chr12:108559039
|
G | GAA | 22 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101others(19): Show | 26 | HG01070.hp2 HG01169.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.312+1802_312+1803d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | ||||||
| chr12:108559039
|
G | GAAA | 82 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(79): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.312+1801_312+1803d others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | ||||||
| chr12:108559039
|
G | GAAAA | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0144others(4): Show | 7 | HG01167.hp1 HG01243.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1800_312+1803d others(6): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | ||||||
| chr12:108559039
|
GAA | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0002c0004t0001g0046others(2): Show | 6 | HG02602.hp2 HG03017.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+1802_312+1803d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | ||||||
| chr12:108559177
|
C | T | 1 | a0001c0006t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.312+1666G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559177 | ||||||
| chr12:108559205
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.312+1638T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559205 | ||||||
| chr12:108559257
|
T | G | 14 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(11): Show | 19 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.312+1586A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559257 | ||||||
| chr12:108559321
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.312+1522T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559321 | ||||||
| chr12:108559322
|
A | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 100 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.312+1521T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559322 | ||||||
| chr12:108559481
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0054 | 3 | NA18947.hp1 NA18988.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.312+1362G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559481 | ||||||
| chr12:108559495
|
G | A | 12 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(9): Show | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+1348C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559495 | ||||||
| chr12:108559547
|
C | G | 3 | a0001c0003t0002g0189a0001c0003t0002g0190a0001c0003t0002g0191 | 3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.312+1296G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559547 | ||||||
| chr12:108559569
|
G | A | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.312+1274C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559569 | ||||||
| chr12:108559664
|
C | CA | 8 | a0001c0003t0002g0184a0001c0003t0002g0185a0001c0003t0002g0186others(5): Show | 11 | HG00544.hp2 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.312+1178dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | ||||||
| chr12:108559664
|
C | CAA | 5 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0194others(2): Show | 8 | HG02895.hp2 HG02896.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1177_312+1178d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | ||||||
| chr12:108559664
|
CA | C | 62 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(59): Show | 82 | HG00639.hp2 HG00673.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.312+1178delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | ||||||
| chr12:108559664
|
CAA | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(155): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.312+1177_312+1178d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | ||||||
| chr12:108559686
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0053 | 3 | HG01071.hp2 HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.312+1157T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559686 | ||||||
| chr12:108559693
|
A | G | 1 | a0002c0004t0001g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.312+1150T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559693 | ||||||
| chr12:108559780
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+1063G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559780 | ||||||
| chr12:108559953
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+890G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559953 | ||||||
| chr12:108559991
|
G | A | 11 | a0001c0003t0002g0019a0001c0003t0002g0039a0001c0003t0002g0189others(8): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.312+852C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559991 | ||||||
| chr12:108560053
|
G | A | 1 | a0007c0016t0001g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.312+790C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560053 | ||||||
| chr12:108560079
|
G | A | 12 | a0001c0005t0002g0011a0001c0005t0002g0040a0001c0005t0002g0041others(9): Show | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+764C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560079 | ||||||
| chr12:108560140
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312+703A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560140 | ||||||
| chr12:108560179
|
G | A | 1 | a0002c0004t0001g0280 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.312+664C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560179 | ||||||
| chr12:108560254
|
C | T | 15 | a0001c0006t0001g0034a0001c0006t0001g0035a0001c0006t0001g0148others(12): Show | 21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.312+589G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560254 | ||||||
| chr12:108560457
|
T | TC | 3 | a0001c0001t0001g0032a0001c0001t0001g0146a0001c0001t0001g0147 | 4 | HG02602.hp2 HG03017.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+385dupG | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560457 | ||||||
| chr12:108560569
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(277): Show | 393 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(390): Show |
intron_variant | MODIFIER | c.312+274T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560569 | ||||||
| chr12:108560570
|
A | G | 2 | a0001c0010t0001g0051a0001c0010t0001g0052 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.312+273T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560570 | ||||||
| chr12:108560648
|
G | A | 1 | a0001c0003t0002g0206 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.312+195C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560648 | ||||||
| chr12:108560702
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.312+141G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560702 | ||||||
| chr12:108560726
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.312+117C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560726 |