Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6667 |
|---|---|
| ensemblid | ENSG00000185591.10 |
| hgncid | 11205 |
| symbol | SP1 |
| name | Sp1 transcription factor |
| refseq_nuc | NM_138473.3 |
| refseq_prot | NP_612482.2 |
| ensembl_nuc | ENST00000327443.9 |
| ensembl_prot | ENSP00000329357.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 53380176 |
| end | 53416446 |
| strand | + |
| ver | v1.2 |
| region | chr12:53380176-53416446 |
| region5000 | chr12:53375176-53421446 |
| regionname0 | SP1_chr12_53380176_53416446 |
| regionname5000 | SP1_chr12_53375176_53421446 |
| 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 | 785 | 320 | 78 | 65 | 121 | 16 | 38 | 97 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0002 | 0/0 | 785 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0003 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0004 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0005 | 0/0 | 785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0006 | 0/0 | 790 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2358 | 217 | 52 | 50 | 71 | 14 | 28 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0002 | 0/0 | 2358 | 96 | 21 | 14 | 49 | 2 | 10 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0003 | 0/0 | 2358 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0004 | 0/0 | 2358 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0005 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0006 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0007 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0008 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0009 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0010 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| c0011 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| 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 | 5320 | 56 | 1 | 15 | 28 | 1 | 10 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0002 | 0/0 | 5312 | 55 | 4 | 5 | 37 | 1 | 8 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0003 | 1/0 | 5323 | 29 | 4 | 6 | 8 | 3 | 7 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0004 | 0/0 | 5322 | 26 | 2 | 9 | 12 | 2 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0005 | 0/0 | 5317 | 12 | 11 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0006 | 0/0 | 5314 | 9 | 3 | 4 | 1 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0007 | 0/0 | 5321 | 8 | 1 | 4 | 2 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0008 | 0/0 | 5324 | 6 | 1 | 2 | 3 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0009 | 0/0 | 5313 | 4 | 0 | 2 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0010 | 0/0 | 5315 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0011 | 0/0 | 5320 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0012 | 0/0 | 5324 | 4 | 0 | 1 | 2 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0013 | 0/0 | 5323 | 4 | 2 | 1 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0014 | 0/0 | 5322 | 4 | 0 | 0 | 3 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0015 | 0/0 | 5321 | 3 | 0 | 1 | 1 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0016 | 0/0 | 5322 | 3 | 3 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0017 | 0/0 | 5325 | 3 | 0 | 0 | 1 | 1 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0018 | 0/0 | 5314 | 3 | 0 | 0 | 3 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0019 | 0/0 | 5323 | 2 | 1 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0020 | 0/0 | 5324 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0021 | 0/0 | 5315 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0022 | 0/0 | 5317 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0023 | 0/0 | 5321 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0024 | 0/0 | 5322 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0025 | 0/0 | 5323 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0026 | 0/0 | 5325 | 2 | 0 | 1 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0027 | 0/0 | 5312 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0028 | 0/0 | 5313 | 2 | 0 | 1 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0029 | 0/0 | 5313 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0030 | 0/0 | 5317 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0031 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0032 | 0/0 | 5324 | 2 | 1 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0033 | 0/0 | 5321 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0034 | 0/0 | 5317 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0035 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0036 | 0/0 | 5326 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0037 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0038 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0039 | 0/0 | 5316 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0040 | 0/0 | 5313 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0041 | 0/0 | 5312 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0042 | 0/0 | 5315 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0043 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0044 | 0/0 | 5310 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0045 | 0/0 | 5316 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0046 | 0/0 | 5318 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0047 | 0/0 | 5319 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0048 | 0/0 | 5318 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0049 | 0/0 | 5319 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0050 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0051 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0052 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0053 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0054 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0055 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0056 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0057 | 0/0 | 5319 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0058 | 0/0 | 5319 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0059 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0060 | 0/0 | 5323 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0061 | 0/0 | 5321 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0062 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0063 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0064 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0065 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0066 | 0/0 | 5325 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0067 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0068 | 0/0 | 5326 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0069 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0070 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0071 | 0/0 | 5317 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0072 | 0/0 | 5318 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0073 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0074 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0075 | 0/0 | 5314 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0076 | 0/0 | 5315 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0077 | 0/0 | 5311 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0078 | 0/0 | 5318 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0079 | 0/0 | 5316 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0080 | 0/0 | 5317 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0081 | 0/0 | 5316 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0082 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0083 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0084 | 0/0 | 5323 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0085 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0086 | 0/0 | 5326 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0087 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0088 | 0/0 | 5323 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0089 | 0/0 | 5326 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0090 | 0/0 | 5328 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0091 | 0/0 | 5319 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| t0092 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0002 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0003 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0010 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2358 | 217 | 52 | 50 | 71 | 14 | 28 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002 | 0/0 | 2358 | 96 | 21 | 14 | 49 | 2 | 10 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0003 | 0/0 | 2358 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0006 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0008 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0010 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0002c0004 | 0/0 | 2358 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0003c0007 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0004c0009 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0005c0011 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0006c0005 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7677 | 55 | 1 | 14 | 28 | 1 | 10 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0003 | 1/0 | 7680 | 28 | 4 | 5 | 8 | 3 | 7 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0004 | 0/0 | 7679 | 25 | 2 | 9 | 11 | 2 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0005 | 0/0 | 7674 | 12 | 11 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0007 | 0/0 | 7678 | 8 | 1 | 4 | 2 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0008 | 0/0 | 7681 | 6 | 1 | 2 | 3 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0010 | 0/0 | 7672 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0011 | 0/0 | 7677 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0012 | 0/0 | 7681 | 4 | 0 | 1 | 2 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0013 | 0/0 | 7680 | 4 | 2 | 1 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0014 | 0/0 | 7679 | 4 | 0 | 0 | 3 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0015 | 0/0 | 7678 | 3 | 0 | 1 | 1 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0017 | 0/0 | 7682 | 3 | 0 | 0 | 1 | 1 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0019 | 0/0 | 7680 | 2 | 1 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0020 | 0/0 | 7681 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0024 | 0/0 | 7679 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0025 | 0/0 | 7680 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0026 | 0/0 | 7682 | 2 | 0 | 1 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0030 | 0/0 | 7674 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0032 | 0/0 | 7681 | 2 | 1 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0034 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0035 | 0/0 | 7679 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0036 | 0/0 | 7683 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0037 | 0/0 | 7682 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0038 | 0/0 | 7684 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0042 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0045 | 0/0 | 7673 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0046 | 0/0 | 7675 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0047 | 0/0 | 7676 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0048 | 0/0 | 7675 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0049 | 0/0 | 7676 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0050 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0051 | 0/0 | 7678 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0053 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0054 | 0/0 | 7678 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0055 | 0/0 | 7678 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0056 | 0/0 | 7679 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0057 | 0/0 | 7676 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0058 | 0/0 | 7676 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0059 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0061 | 0/0 | 7678 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0062 | 0/0 | 7679 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0063 | 0/0 | 7679 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0064 | 0/0 | 7678 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0065 | 0/0 | 7679 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0066 | 0/0 | 7682 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0067 | 0/0 | 7684 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0068 | 0/0 | 7683 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0069 | 0/0 | 7678 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0070 | 0/0 | 7677 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0071 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0072 | 0/0 | 7675 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0073 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0078 | 0/0 | 7675 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0079 | 0/0 | 7673 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0080 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0082 | 0/0 | 7677 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0084 | 0/0 | 7680 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0086 | 0/0 | 7683 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0089 | 0/0 | 7683 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0090 | 0/0 | 7685 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0091 | 0/0 | 7676 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0001t0092 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0002 | 0/0 | 7669 | 53 | 4 | 5 | 35 | 1 | 8 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0006 | 0/0 | 7671 | 9 | 3 | 4 | 1 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0009 | 0/0 | 7670 | 4 | 0 | 2 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0018 | 0/0 | 7671 | 3 | 0 | 0 | 3 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0021 | 0/0 | 7672 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0022 | 0/0 | 7674 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0023 | 0/0 | 7678 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0027 | 0/0 | 7669 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0028 | 0/0 | 7670 | 2 | 0 | 1 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0029 | 0/0 | 7670 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0031 | 0/0 | 7670 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0033 | 0/0 | 7678 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0039 | 0/0 | 7673 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0040 | 0/0 | 7670 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0041 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0044 | 0/0 | 7667 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0074 | 0/0 | 7669 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0075 | 0/0 | 7671 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0077 | 0/0 | 7668 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0081 | 0/0 | 7673 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0085 | 0/0 | 7678 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0087 | 0/0 | 7679 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0002t0088 | 0/0 | 7680 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0003t0016 | 0/0 | 7679 | 3 | 3 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0003t0052 | 0/0 | 7678 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0006t0043 | 0/0 | 7666 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0008t0001 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0001c0010t0060 | 0/0 | 7680 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0002c0004t0002 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0002c0004t0076 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0003c0007t0002 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0004c0009t0083 | 0/0 | 7678 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0005c0011t0003 | 0/0 | 7680 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| a0006c0005t0004 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | copy fasta | chr12 | 53375176 | 53421446 |
| 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 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0010 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0012g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0013g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0014g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0014g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0015g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0015g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0017g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0017g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0019g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0019g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0020g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0024g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0024g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0025g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0025g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0026g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0026g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0030g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0030g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0032g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0032g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0034g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0035g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0036g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0037g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0038g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0042g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0045g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0046g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0047g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0048g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0049g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0050g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0051g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0053g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0054g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0055g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0056g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0057g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0058g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0059g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0061g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0062g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0063g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0064g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0065g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0066g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0067g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0068g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0069g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0070g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0071g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0072g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0073g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0078g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0079g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0080g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0082g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0084g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0086g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0089g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0090g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0091g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0001t0092g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0009g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0018g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0018g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0018g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0021g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0022g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0022g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0023g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0023g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0027g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0027g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0028g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0028g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0029g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0029g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0031g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0031g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0033g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0033g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0039g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0040g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0041g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0044g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0074g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0075g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0077g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0081g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0085g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0087g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0002t0088g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0003t0016g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0003t0016g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0003t0016g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0003t0052g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0006t0043g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0008t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0001c0010t0060g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0002c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0002c0004t0076g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0003c0007t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0004c0009t0083g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0005c0011t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| a0006c0005t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0005 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00140 | hp1 | a0001 | c0001 | t0048 | g0191 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0139 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00280 | hp2 | a0001 | c0002 | t0006 | g0246 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0176 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00323 | hp2 | a0001 | c0001 | t0061 | g0037 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00597 | hp1 | a0001 | c0002 | t0022 | g0222 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00597 | hp2 | a0001 | c0001 | t0015 | g0017 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00639 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0296 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0118 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00673 | hp2 | a0001 | c0001 | t0024 | g0093 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0099 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00733 | hp2 | a0001 | c0002 | t0006 | g0247 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00738 | hp1 | a0001 | c0001 | t0054 | g0059 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00741 | hp1 | a0001 | c0001 | t0084 | g0142 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG00741 | hp2 | a0005 | c0011 | t0003 | g0153 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0076 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01070 | hp2 | a0001 | c0001 | t0045 | g0007 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01099 | hp1 | a0001 | c0001 | t0032 | g0269 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01106 | hp2 | a0001 | c0001 | t0058 | g0085 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0273 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0297 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01167 | hp1 | a0001 | c0008 | t0001 | g0070 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01167 | hp2 | a0001 | c0002 | t0023 | g0040 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01168 | hp2 | a0001 | c0002 | t0006 | g0261 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01169 | hp1 | a0001 | c0002 | t0006 | g0245 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01169 | hp2 | a0001 | c0002 | t0023 | g0039 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0152 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01175 | hp2 | a0001 | c0002 | t0028 | g0236 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01192 | hp1 | a0001 | c0001 | t0020 | g0293 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0180 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01243 | hp1 | a0001 | c0001 | t0069 | g0149 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01257 | hp2 | a0001 | c0001 | t0026 | g0033 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01361 | hp2 | a0001 | c0001 | t0068 | g0148 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01433 | hp1 | a0001 | c0001 | t0015 | g0096 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01496 | hp1 | a0001 | c0002 | t0006 | g0248 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01496 | hp2 | a0001 | c0002 | t0009 | g0003 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0178 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01516 | hp1 | a0001 | c0001 | t0026 | g0066 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0103 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01884 | hp2 | a0001 | c0006 | t0043 | g0271 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01891 | hp1 | a0001 | c0002 | t0033 | g0044 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01934 | hp1 | a0001 | c0001 | t0020 | g0004 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01934 | hp2 | a0001 | c0001 | t0012 | g0128 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01978 | hp1 | a0001 | c0001 | t0053 | g0129 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01981 | hp1 | a0001 | c0001 | t0059 | g0164 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01993 | hp1 | a0001 | c0002 | t0009 | g0213 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0080 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02015 | hp1 | a0001 | c0001 | t0050 | g0156 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0074 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0065 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02055 | hp2 | a0001 | c0001 | t0078 | g0263 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0146 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0162 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02135 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02145 | hp1 | a0001 | c0001 | t0042 | g0266 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02145 | hp2 | a0001 | c0002 | t0021 | g0028 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | CDX | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | CDX | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02257 | hp2 | a0001 | c0002 | t0088 | g0042 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0298 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0104 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02451 | hp2 | a0001 | c0002 | t0031 | g0225 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02572 | hp2 | a0001 | c0001 | t0025 | g0188 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02602 | hp2 | a0001 | c0001 | t0036 | g0161 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0112 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02622 | hp1 | a0001 | c0001 | t0079 | g0285 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0026 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02630 | hp1 | a0001 | c0001 | t0090 | g0166 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02630 | hp2 | a0001 | c0001 | t0030 | g0278 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02647 | hp1 | a0001 | c0001 | t0037 | g0270 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0234 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02683 | hp2 | a0001 | c0002 | t0075 | g0003 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02723 | hp1 | a0001 | c0002 | t0087 | g0043 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02723 | hp2 | a0001 | c0002 | t0085 | g0041 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02735 | hp2 | a0001 | c0001 | t0017 | g0179 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02809 | hp1 | a0001 | c0001 | t0034 | g0299 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02809 | hp2 | a0001 | c0002 | t0021 | g0024 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02818 | hp1 | a0001 | c0001 | t0080 | g0186 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02818 | hp2 | a0001 | c0001 | t0072 | g0185 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0030 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02886 | hp2 | a0001 | c0001 | t0071 | g0184 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02896 | hp1 | a0001 | c0001 | t0091 | g0015 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02896 | hp2 | a0001 | c0003 | t0016 | g0288 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02897 | hp2 | a0001 | c0003 | t0016 | g0290 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02922 | hp2 | a0001 | c0002 | t0027 | g0216 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02965 | hp2 | a0001 | c0003 | t0052 | g0289 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0174 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03130 | hp1 | a0001 | c0002 | t0027 | g0215 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03130 | hp2 | a0001 | c0001 | t0038 | g0272 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03195 | hp1 | a0001 | c0001 | t0065 | g0123 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03195 | hp2 | a0001 | c0002 | t0033 | g0045 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03225 | hp1 | a0001 | c0002 | t0031 | g0226 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03225 | hp2 | a0001 | c0001 | t0064 | g0160 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03453 | hp1 | a0001 | c0001 | t0089 | g0069 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03453 | hp2 | a0001 | c0002 | t0077 | g0212 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0243 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0239 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0244 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0029 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03516 | hp2 | a0001 | c0001 | t0025 | g0287 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0265 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0267 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03669 | hp2 | a0001 | c0001 | t0046 | g0105 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03688 | hp1 | a0001 | c0001 | t0070 | g0111 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03688 | hp2 | a0001 | c0001 | t0082 | g0121 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0109 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0242 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0182 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04115 | hp1 | a0001 | c0002 | t0040 | g0195 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04184 | hp1 | a0001 | c0001 | t0035 | g0155 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04199 | hp1 | a0001 | c0001 | t0015 | g0137 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04228 | hp1 | a0001 | c0001 | t0049 | g0108 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG04228 | hp2 | a0001 | c0001 | t0047 | g0107 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18522 | hp1 | a0001 | c0002 | t0074 | g0214 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18612 | hp1 | a0001 | c0002 | t0018 | g0003 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0170 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18747 | hp2 | a0001 | c0001 | t0014 | g0172 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18945 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18947 | hp1 | a0001 | c0002 | t0039 | g0295 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18947 | hp2 | a0001 | c0002 | t0018 | g0210 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18951 | hp1 | a0001 | c0002 | t0018 | g0205 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18954 | hp1 | a0002 | c0004 | t0076 | g0259 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18959 | hp2 | a0001 | c0001 | t0092 | g0035 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18961 | hp1 | a0001 | c0001 | t0062 | g0086 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18961 | hp2 | a0001 | c0002 | t0041 | g0238 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18962 | hp1 | a0001 | c0002 | t0009 | g0230 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18968 | hp1 | a0001 | c0001 | t0019 | g0192 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18968 | hp2 | a0001 | c0002 | t0022 | g0227 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18972 | hp1 | a0001 | c0002 | t0029 | g0206 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18972 | hp2 | a0001 | c0001 | t0057 | g0190 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18975 | hp1 | a0001 | c0001 | t0055 | g0154 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18981 | hp2 | a0001 | c0001 | t0073 | g0018 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18982 | hp1 | a0004 | c0009 | t0083 | g0157 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18982 | hp2 | a0001 | c0002 | t0029 | g0197 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18987 | hp2 | a0002 | c0004 | t0002 | g0249 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18992 | hp1 | a0006 | c0005 | t0004 | g0055 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18994 | hp2 | a0001 | c0002 | t0006 | g0228 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18998 | hp1 | a0001 | c0002 | t0009 | g0012 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19000 | hp2 | a0001 | c0002 | t0028 | g0237 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19005 | hp2 | a0003 | c0007 | t0002 | g0255 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19010 | hp2 | a0001 | c0001 | t0024 | g0062 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19011 | hp1 | a0001 | c0001 | t0063 | g0141 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19043 | hp1 | a0001 | c0001 | t0067 | g0292 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19062 | hp2 | a0001 | c0001 | t0051 | g0135 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19063 | hp1 | a0001 | c0002 | t0044 | g0220 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0050 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19068 | hp2 | a0001 | c0010 | t0060 | g0075 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19082 | hp2 | a0001 | c0001 | t0014 | g0082 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19086 | hp2 | a0001 | c0001 | t0056 | g0092 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0021 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0110 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20129 | hp1 | a0001 | c0001 | t0030 | g0286 | AFR | ASW | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ASW | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20752 | hp1 | a0001 | c0001 | t0066 | g0150 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20752 | hp2 | a0001 | c0001 | t0017 | g0119 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0177 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0073 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02486 | hp1 | a0001 | c0003 | t0016 | g0291 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02486 | hp2 | a0001 | c0002 | t0081 | g0025 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02559 | hp1 | a0001 | c0001 | t0086 | g0264 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0268 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0279 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | USA | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | USA | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0140 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0094 | REF | REF | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0010 | REF | REF | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53382438
|
T | TACCTGGA others(8): Show |
1 | a0006 | 1 | NA18992.hp1 | disruptive_inframe_insertion | MODERATE | c.492_506dupACCTGGAG others(7): Show |
p.Pro169_Asn170insPr others(13): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 623/7680 | 507/2358 | 169/785 | INFO_REALIGN_3_PRIME | chr12 | 53382438 | |
| chr12:53382543
|
A | G | 1 | a0005 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.596A>G | p.Asp199Gly | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 712/7680 | 596/2358 | 199/785 | chr12 | 53382543 | ||
| chr12:53382597
|
A | G | 1 | a0002 | 2 | NA18954.hp1 NA18987.hp2 |
missense_variant | MODERATE | c.650A>G | p.Asn217Ser | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 766/7680 | 650/2358 | 217/785 | chr12 | 53382597 | ||
| chr12:53383036
|
G | C | 1 | a0003 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.1089G>C | p.Gln363His | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 1205/7680 | 1089/2358 | 363/785 | chr12 | 53383036 | ||
| chr12:53409367
|
C | T | 1 | a0004 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1850C>T | p.Ser617Leu | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/6 | 1966/7680 | 1850/2358 | 617/785 | chr12 | 53409367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53382190
|
C | G | 1 | a0001c0003 | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.243C>G | p.Ser81Ser | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 359/7680 | 243/2358 | 81/785 | chr12 | 53382190 | ||
| chr12:53382766
|
T | C | 1 | a0001c0006 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.819T>C | p.Ser273Ser | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 935/7680 | 819/2358 | 273/785 | chr12 | 53382766 | ||
| chr12:53383387
|
A | G | 3 | a0001c0002a0002c0004a0003c0007 | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
synonymous_variant | LOW | c.1440A>G | p.Gln480Gln | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 1556/7680 | 1440/2358 | 480/785 | chr12 | 53383387 | ||
| chr12:53406706
|
C | T | 1 | a0001c0010 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.1797C>T | p.Thr599Thr | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/6 | 1913/7680 | 1797/2358 | 599/785 | chr12 | 53406706 | ||
| chr12:53409443
|
C | T | 1 | a0001c0008 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.1926C>T | p.His642His | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/6 | 2042/7680 | 1926/2358 | 642/785 | chr12 | 53409443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53380176
|
A | AC | 13 | a0001c0001t0008a0001c0001t0015a0001c0001t0019others(10): Show | 27 | HG00597.hp1 HG00597.hp2 HG01175.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-108dupC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/6 | 107 | INFO_REALIGN_3_PRIME | chr12 | 53380176 | ||||
| chr12:53380185
|
T | C | 1 | a0001c0001t0034 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/6 | 107 | chr12 | 53380185 | |||||
| chr12:53380240
|
C | T | 1 | a0001c0002t0040 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/6 | 52 | chr12 | 53380240 | |||||
| chr12:53411253
|
G | A | 1 | a0001c0002t0023 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 13 | chr12 | 53411253 | |||||
| chr12:53411518
|
C | G | 1 | a0001c0001t0092 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 278 | chr12 | 53411518 | |||||
| chr12:53411575
|
C | A | 1 | a0001c0002t0041 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 335 | chr12 | 53411575 | |||||
| chr12:53411654
|
T | TTA | 40 | a0001c0001t0005a0001c0001t0014a0001c0001t0017others(37): Show | 129 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*435_*436dupTA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 437 | INFO_REALIGN_3_PRIME | chr12 | 53411654 | ||||
| chr12:53411654
|
T | TTATA | 3 | a0001c0001t0091a0001c0002t0018a0001c0002t0039 | 5 | HG02896.hp1 NA18612.hp1 NA18947.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*433_*436dupTATA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 437 | INFO_REALIGN_3_PRIME | chr12 | 53411654 | ||||
| chr12:53412076
|
T | C | 1 | a0001c0001t0042 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 836 | chr12 | 53412076 | |||||
| chr12:53412152
|
G | T | 1 | a0001c0001t0073 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*912G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 912 | chr12 | 53412152 | |||||
| chr12:53412344
|
C | T | 2 | a0001c0001t0071a0001c0001t0072 | 2 | HG02818.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1104C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1104 | chr12 | 53412344 | |||||
| chr12:53412350
|
C | G | 1 | a0001c0001t0026 | 2 | HG01257.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1110C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1110 | chr12 | 53412350 | |||||
| chr12:53412453
|
A | G | 1 | a0001c0001t0070 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1213 | chr12 | 53412453 | |||||
| chr12:53412871
|
C | T | 3 | a0001c0001t0013a0001c0001t0020a0001c0001t0069 | 7 | HG00280.hp1 HG00639.hp2 HG01192.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1631C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1631 | chr12 | 53412871 | |||||
| chr12:53412930
|
C | CTG | 8 | a0001c0001t0012a0001c0001t0026a0001c0001t0036others(5): Show | 12 | HG00099.hp2 HG01257.hp2 HG01516.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1727dupGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1728 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53412930
|
C | CTGTG | 3 | a0001c0001t0067a0001c0001t0068a0001c0001t0090 | 3 | HG01361.hp2 HG02630.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1724_*1727dupGTGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1728 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53412930
|
CTG | C | 25 | a0001c0001t0001a0001c0001t0007a0001c0001t0014others(22): Show | 94 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1727delGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1726 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53412930
|
CTGTG | C | 7 | a0001c0001t0046a0001c0001t0047a0001c0001t0048others(4): Show | 8 | HG00140.hp1 HG00597.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1727delGTGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1724 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53412930
|
CTGTGTG | C | 6 | a0001c0001t0045a0001c0001t0071a0001c0001t0072others(3): Show | 16 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1722_*1727delGTGT others(2): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1722 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53412930
|
CTGTGTGT others(1): Show |
C | 25 | a0001c0001t0005a0001c0001t0010a0001c0001t0030others(22): Show | 100 | HG00323.hp1 HG00609.hp1 HG00673.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1720_*1727delGTGT others(4): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1720 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53412930
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0006t0043 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1714_*1727delGTGT others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1714 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | ||||
| chr12:53413133
|
C | T | 1 | a0001c0001t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1893C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1893 | chr12 | 53413133 | |||||
| chr12:53413227
|
C | G | 1 | a0001c0001t0064 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1987C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1987 | chr12 | 53413227 | |||||
| chr12:53413297
|
T | G | 2 | a0001c0002t0023a0001c0002t0085 | 3 | HG01167.hp2 HG01169.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2057T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2057 | chr12 | 53413297 | |||||
| chr12:53413299
|
T | C | 1 | a0001c0002t0027 | 2 | HG02922.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2059T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2059 | chr12 | 53413299 | |||||
| chr12:53413571
|
A | G | 1 | a0001c0001t0063 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2331 | chr12 | 53413571 | |||||
| chr12:53413812
|
G | A | 1 | a0001c0001t0024 | 2 | HG00673.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2572G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2572 | chr12 | 53413812 | |||||
| chr12:53414123
|
CAG | C | 26 | a0001c0002t0002a0001c0002t0006a0001c0002t0009others(23): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886delGA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2885 | INFO_REALIGN_3_PRIME | chr12 | 53414123 | ||||
| chr12:53414197
|
G | C | 1 | a0001c0001t0050 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2957 | chr12 | 53414197 | |||||
| chr12:53414275
|
T | C | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG03669.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3035T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3035 | chr12 | 53414275 | |||||
| chr12:53414362
|
C | G | 1 | a0001c0001t0059 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3122C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3122 | chr12 | 53414362 | |||||
| chr12:53414373
|
G | A | 2 | a0001c0001t0051a0001c0002t0074 | 2 | NA18522.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3133G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3133 | chr12 | 53414373 | |||||
| chr12:53414580
|
T | C | 4 | a0001c0001t0025a0001c0001t0067a0001c0003t0016others(1): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3340T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3340 | chr12 | 53414580 | |||||
| chr12:53414808
|
T | C | 1 | a0001c0001t0053 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3568T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3568 | chr12 | 53414808 | |||||
| chr12:53415177
|
C | T | 5 | a0001c0002t0023a0001c0002t0033a0001c0002t0085others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3937C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3937 | chr12 | 53415177 | |||||
| chr12:53415178
|
G | A | 1 | a0001c0001t0054 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3938G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3938 | chr12 | 53415178 | |||||
| chr12:53415582
|
A | G | 1 | a0001c0001t0064 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4342A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4342 | chr12 | 53415582 | |||||
| chr12:53415639
|
G | GA | 6 | a0001c0001t0051a0001c0001t0055a0001c0001t0056others(3): Show | 7 | HG01175.hp2 NA18947.hp1 NA18975.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4416dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4417 | INFO_REALIGN_3_PRIME | chr12 | 53415639 | ||||
| chr12:53415639
|
GA | G | 5 | a0001c0001t0058a0001c0001t0079a0001c0002t0031others(2): Show | 6 | HG01106.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4416delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4416 | INFO_REALIGN_3_PRIME | chr12 | 53415639 | ||||
| chr12:53415640
|
A | G | 4 | a0001c0002t0023a0001c0002t0033a0001c0002t0085others(1): Show | 6 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4400A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4400 | chr12 | 53415640 | |||||
| chr12:53415961
|
A | G | 1 | a0001c0001t0062 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4721A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4721 | chr12 | 53415961 | |||||
| chr12:53415987
|
G | C | 1 | a0001c0002t0041 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4747G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4747 | chr12 | 53415987 | |||||
| chr12:53416080
|
T | C | 1 | a0001c0001t0030 | 2 | HG02630.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4840T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4840 | chr12 | 53416080 | |||||
| chr12:53416136
|
C | G | 2 | a0001c0001t0025a0001c0001t0067 | 3 | HG02572.hp2 HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4896C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4896 | chr12 | 53416136 | |||||
| chr12:53416235
|
C | G | 5 | a0001c0001t0067a0001c0002t0023a0001c0002t0033others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4995C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4995 | chr12 | 53416235 | |||||
| chr12:53416349
|
C | CT | 7 | a0001c0001t0032a0001c0001t0037a0001c0001t0038others(4): Show | 10 | HG01099.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5127dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5128 | INFO_REALIGN_3_PRIME | chr12 | 53416349 | ||||
| chr12:53416349
|
CT | C | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(26): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*5127delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5127 | INFO_REALIGN_3_PRIME | chr12 | 53416349 | ||||
| chr12:53416349
|
CTT | C | 10 | a0001c0001t0057a0001c0001t0061a0001c0001t0064others(7): Show | 13 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5126_*5127delTT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5126 | INFO_REALIGN_3_PRIME | chr12 | 53416349 | ||||
| chr12:53416349
|
CTTT | C | 20 | a0001c0001t0011a0001c0001t0065a0001c0002t0002others(17): Show | 93 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*5125_*5127delTTT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5125 | INFO_REALIGN_3_PRIME | chr12 | 53416349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53380395
|
G | A | 1 | a0001c0001t0010g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7+97G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380395 | ||||||
| chr12:53380427
|
C | T | 1 | a0001c0001t0034g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7+129C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380427 | ||||||
| chr12:53380457
|
G | C | 2 | a0001c0001t0015g0017a0001c0001t0073g0018 | 2 | HG00597.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.7+159G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380457 | ||||||
| chr12:53380494
|
C | A | 3 | a0001c0001t0003g0020a0001c0001t0007g0019a0001c0001t0011g0021 | 3 | HG02559.hp2 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7+196C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380494 | ||||||
| chr12:53380494
|
CCGCCCGC others(25): Show |
C | 1 | a0001c0001t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.7+207_7+238delGGGG others(28): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53380494 | |||||
| chr12:53380536
|
C | T | 3 | a0001c0001t0007g0296a0001c0001t0007g0297a0001c0001t0007g0298 | 3 | HG00642.hp1 HG01109.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.7+238C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380536 | ||||||
| chr12:53380555
|
G | T | 1 | a0001c0002t0039g0295 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7+257G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380555 | ||||||
| chr12:53380711
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7+413C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380711 | ||||||
| chr12:53380716
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7+418C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380716 | ||||||
| chr12:53380841
|
G | T | 1 | a0001c0001t0020g0293 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.7+543G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380841 | ||||||
| chr12:53380854
|
G | A | 7 | a0001c0002t0002g0027a0001c0002t0006g0026a0001c0002t0006g0029others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+556G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380854 | ||||||
| chr12:53380924
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.7+626T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380924 | ||||||
| chr12:53380946
|
C | CT | 124 | a0001c0001t0001g0189a0001c0001t0005g0015a0001c0001t0005g0273others(121): Show | 127 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.7+669dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53380946 | |||||
| chr12:53380946
|
CT | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0034others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.7+669delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53380946 | |||||
| chr12:53380985
|
C | G | 39 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.8-674C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380985 | ||||||
| chr12:53380992
|
C | T | 7 | a0001c0001t0025g0188a0001c0001t0025g0287a0001c0001t0067g0292others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-667C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380992 | ||||||
| chr12:53380995
|
A | G | 95 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(92): Show | 98 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.8-664A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380995 | ||||||
| chr12:53381042
|
C | G | 5 | a0001c0001t0003g0177a0001c0001t0003g0178a0001c0001t0003g0181others(2): Show | 5 | HG01192.hp2 HG01515.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-617C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53381042 | ||||||
| chr12:53381363
|
GA | G | 42 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0027others(39): Show | 44 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-293delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53381363 | |||||
| chr12:53381490
|
G | C | 1 | a0001c0002t0002g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.8-169G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53381490 | ||||||
| chr12:53381539
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.8-120T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53381539 | ||||||
| chr12:53381837
|
G | C | 2 | a0001c0002t0002g0176a0001c0002t0002g0234 | 2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.162+24G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 2/5 | chr12 | 53381837 | ||||||
| chr12:53381958
|
CAA | C | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.162+147_162+148del others(2): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 53381958 | |||||
| chr12:53382012
|
C | T | 1 | a0001c0002t0002g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163-98C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 2/5 | chr12 | 53382012 | ||||||
| chr12:53383807
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0004g0175 | 3 | HG01943.hp1 NA18612.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1675+185C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53383807 | ||||||
| chr12:53383963
|
ATTTTC | A | 20 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1675+351_1675+355d others(7): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53383963 | |||||
| chr12:53383973
|
C | CT | 94 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0003g0168others(91): Show | 97 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1675+365dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53383973 | |||||
| chr12:53384030
|
C | T | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+408C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384030 | ||||||
| chr12:53384098
|
T | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | NA18949.hp1 NA18987.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+476T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384098 | ||||||
| chr12:53384190
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1675+568C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384190 | ||||||
| chr12:53384220
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675+598C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384220 | ||||||
| chr12:53384258
|
C | T | 1 | a0001c0001t0090g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1675+636C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384258 | ||||||
| chr12:53384468
|
A | G | 2 | a0001c0002t0002g0235a0001c0002t0002g0262 | 2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1675+846A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384468 | ||||||
| chr12:53384725
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1675+1103G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384725 | ||||||
| chr12:53384866
|
G | T | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+1244G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384866 | ||||||
| chr12:53384980
|
GA | G | 136 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0005g0015others(133): Show | 139 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.1675+1372delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53384980 | |||||
| chr12:53384995
|
T | A | 2 | a0001c0001t0004g0053a0001c0001t0004g0054 | 2 | NA18970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1675+1373T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384995 | ||||||
| chr12:53384996
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1675+1374A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384996 | ||||||
| chr12:53385356
|
G | A | 1 | a0006c0005t0004g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1734G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385356 | ||||||
| chr12:53385357
|
A | G | 1 | a0006c0005t0004g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1735A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385357 | ||||||
| chr12:53385358
|
G | A | 1 | a0006c0005t0004g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1736G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385358 | ||||||
| chr12:53385511
|
CTT | C | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+1890_1675+189 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385511 | ||||||
| chr12:53385537
|
A | G | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+1915A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385537 | ||||||
| chr12:53385581
|
C | T | 1 | a0001c0001t0008g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1675+1959C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385581 | ||||||
| chr12:53385594
|
C | CA | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG00738.hp1 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+1986dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53385594 | |||||
| chr12:53385603
|
A | T | 1 | a0006c0005t0004g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1981A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385603 | ||||||
| chr12:53385605
|
A | AT | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+1983_1675+198 others(5): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385605 | ||||||
| chr12:53385605
|
A | T | 2 | a0001c0001t0036g0161a0001c0001t0038g0272 | 2 | HG02602.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1675+1983A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385605 | ||||||
| chr12:53385606
|
A | AT | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+1984_1675+198 others(5): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385606 | ||||||
| chr12:53385612
|
A | G | 1 | a0001c0001t0067g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1675+1990A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385612 | ||||||
| chr12:53385625
|
T | C | 2 | a0001c0001t0025g0188a0001c0001t0025g0287 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1675+2003T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385625 | ||||||
| chr12:53385686
|
G | A | 3 | a0001c0001t0005g0273a0001c0001t0005g0274a0001c0001t0005g0275 | 3 | HG01109.hp1 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1675+2064G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385686 | ||||||
| chr12:53385912
|
C | CA | 97 | a0001c0001t0001g0047a0001c0001t0001g0064a0001c0001t0005g0276others(94): Show | 100 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1675+2306dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53385912 | |||||
| chr12:53385912
|
CA | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0158others(3): Show | 6 | HG03225.hp2 NA18948.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+2306delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53385912 | |||||
| chr12:53385991
|
T | C | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+2369T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385991 | ||||||
| chr12:53386038
|
C | T | 2 | a0001c0002t0033g0044a0001c0002t0033g0045 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1675+2416C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386038 | ||||||
| chr12:53386046
|
G | A | 2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1675+2424G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386046 | ||||||
| chr12:53386082
|
C | CT | 5 | a0001c0002t0002g0235a0001c0002t0002g0256a0001c0002t0002g0257others(2): Show | 5 | NA18945.hp1 NA18999.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675+2461dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386082 | |||||
| chr12:53386175
|
A | T | 1 | a0001c0001t0050g0156 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1675+2553A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386175 | ||||||
| chr12:53386300
|
T | G | 1 | a0006c0005t0004g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+2678T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386300 | ||||||
| chr12:53386358
|
T | C | 7 | a0001c0001t0025g0188a0001c0001t0025g0287a0001c0001t0067g0292others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+2736T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386358 | ||||||
| chr12:53386479
|
C | CT | 13 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0052others(10): Show | 13 | HG00741.hp2 HG01175.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1675+2876dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386479 | |||||
| chr12:53386479
|
C | CTT | 92 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(89): Show | 95 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1675+2875_1675+287 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386479 | |||||
| chr12:53386498
|
T | TC | 4 | a0001c0003t0016g0288a0001c0003t0016g0290a0001c0003t0016g0291others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+2877dupC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386498 | |||||
| chr12:53386522
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1675+2900C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386522 | ||||||
| chr12:53386537
|
TAGTG | T | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+2920_1675+292 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386537 | |||||
| chr12:53386609
|
A | G | 7 | a0001c0001t0025g0188a0001c0001t0025g0287a0001c0001t0067g0292others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+2987A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386609 | ||||||
| chr12:53386891
|
C | T | 1 | a0001c0001t0066g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1675+3269C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386891 | ||||||
| chr12:53386908
|
T | C | 6 | a0001c0001t0003g0005a0001c0001t0003g0067a0001c0001t0008g0152others(3): Show | 6 | HG00099.hp2 HG01175.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+3286T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386908 | ||||||
| chr12:53386936
|
G | GT | 14 | a0001c0002t0002g0183a0001c0002t0002g0193a0001c0002t0002g0229others(11): Show | 14 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1675+3317dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386936 | |||||
| chr12:53386940
|
G | GT | 49 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0147others(46): Show | 49 | HG00741.hp1 HG01099.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.1675+3334dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386940 | |||||
| chr12:53386940
|
G | T | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+3318G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386940 | ||||||
| chr12:53386940
|
GT | G | 13 | a0001c0001t0001g0038a0001c0001t0001g0158a0001c0001t0003g0020others(10): Show | 13 | HG01192.hp2 HG01515.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+3334delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386940 | |||||
| chr12:53387097
|
C | T | 9 | a0001c0001t0003g0004a0001c0001t0003g0138a0001c0001t0013g0004others(6): Show | 9 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675+3475C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387097 | ||||||
| chr12:53387139
|
G | T | 1 | a0001c0001t0064g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1675+3517G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387139 | ||||||
| chr12:53387150
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1675+3528A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387150 | ||||||
| chr12:53387243
|
G | A | 1 | a0001c0002t0002g0194 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1675+3621G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387243 | ||||||
| chr12:53387414
|
T | G | 1 | a0005c0011t0003g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1675+3792T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387414 | ||||||
| chr12:53387544
|
T | G | 1 | a0004c0009t0083g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1675+3922T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387544 | ||||||
| chr12:53387558
|
G | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0008t0001g0070 | 4 | HG00140.hp2 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1675+3936G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387558 | ||||||
| chr12:53387761
|
G | A | 3 | a0001c0001t0032g0265a0001c0001t0038g0272a0001c0001t0086g0264 | 3 | HG02559.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1675+4139G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387761 | ||||||
| chr12:53387919
|
G | T | 1 | a0001c0001t0030g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1675+4297G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387919 | ||||||
| chr12:53388282
|
C | G | 1 | a0001c0001t0004g0054 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1675+4660C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388282 | ||||||
| chr12:53388609
|
C | T | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+4987C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388609 | ||||||
| chr12:53388779
|
A | G | 1 | a0001c0001t0015g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1675+5157A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388779 | ||||||
| chr12:53388844
|
G | T | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5222G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388844 | ||||||
| chr12:53388977
|
C | CAAAAAAA others(1): Show |
83 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(80): Show | 86 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1675+5359_1675+536 others(12): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53388977 | |||||
| chr12:53388977
|
C | CAAAAAAA others(2): Show |
8 | a0001c0002t0002g0196a0001c0002t0028g0237a0001c0002t0029g0197others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675+5358_1675+536 others(13): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53388977 | |||||
| chr12:53388977
|
C | CAAAAAAA others(3): Show |
3 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0085g0041 | 3 | HG01167.hp2 HG01169.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1675+5357_1675+536 others(14): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53388977 | |||||
| chr12:53389151
|
G | T | 1 | a0001c0001t0004g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1675+5529G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389151 | ||||||
| chr12:53389175
|
G | A | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5553G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389175 | ||||||
| chr12:53389216
|
C | CT | 20 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0130others(17): Show | 20 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1675+5614dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | |||||
| chr12:53389216
|
C | CTT | 7 | a0001c0002t0002g0239a0001c0002t0002g0240a0001c0002t0023g0039others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+5613_1675+561 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | |||||
| chr12:53389216
|
C | CTTT | 68 | a0001c0002t0002g0003a0001c0002t0002g0013a0001c0002t0002g0027others(65): Show | 70 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1675+5612_1675+561 others(7): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | |||||
| chr12:53389216
|
C | CTTTT | 18 | a0001c0002t0002g0012a0001c0002t0002g0014a0001c0002t0002g0193others(15): Show | 19 | HG00597.hp1 HG01168.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675+5611_1675+561 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | |||||
| chr12:53389232
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1675+5610T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389232 | ||||||
| chr12:53389302
|
A | G | 1 | a0001c0001t0079g0285 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1675+5680A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389302 | ||||||
| chr12:53389390
|
A | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5768A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389390 | ||||||
| chr12:53389392
|
C | A | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5770C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389392 | ||||||
| chr12:53389398
|
T | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5776T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389398 | ||||||
| chr12:53389409
|
A | G | 19 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(16): Show | 19 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675+5787A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389409 | ||||||
| chr12:53389602
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1675+5980C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389602 | ||||||
| chr12:53389612
|
C | T | 133 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(130): Show | 136 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.1675+5990C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389612 | ||||||
| chr12:53390264
|
T | C | 1 | a0001c0006t0043g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1675+6642T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390264 | ||||||
| chr12:53390409
|
G | A | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+6787G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390409 | ||||||
| chr12:53390463
|
G | T | 39 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1675+6841G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390463 | ||||||
| chr12:53390682
|
C | CA | 7 | a0001c0001t0008g0152a0001c0002t0002g0199a0001c0002t0002g0221others(4): Show | 7 | HG01175.hp1 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+7072dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53390682 | |||||
| chr12:53390684
|
A | G | 5 | a0001c0001t0032g0265a0001c0001t0032g0269a0001c0001t0037g0270others(2): Show | 5 | HG01099.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675+7062A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390684 | ||||||
| chr12:53390767
|
T | C | 5 | a0001c0002t0002g0198a0001c0002t0002g0200a0001c0002t0002g0223others(2): Show | 5 | HG00597.hp1 NA18959.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675+7145T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390767 | ||||||
| chr12:53390885
|
G | C | 1 | a0001c0001t0003g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1675+7263G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390885 | ||||||
| chr12:53391129
|
G | A | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+7507G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391129 | ||||||
| chr12:53391153
|
C | G | 4 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0085g0041others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1675+7531C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391153 | ||||||
| chr12:53391160
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1675+7538A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391160 | ||||||
| chr12:53391171
|
A | G | 2 | a0001c0001t0003g0125a0001c0001t0054g0059 | 2 | HG00738.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1675+7549A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391171 | ||||||
| chr12:53391221
|
A | G | 1 | a0001c0006t0043g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1675+7599A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391221 | ||||||
| chr12:53391244
|
A | G | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+7622A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391244 | ||||||
| chr12:53391346
|
C | CT | 10 | a0001c0001t0003g0020a0001c0001t0003g0124a0001c0001t0003g0181others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1675+7745dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | |||||
| chr12:53391346
|
C | CTTTT | 69 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(66): Show | 72 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1675+7742_1675+774 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | |||||
| chr12:53391346
|
C | CTTTTT | 13 | a0001c0002t0002g0183a0001c0002t0002g0193a0001c0002t0002g0198others(10): Show | 13 | HG01361.hp1 HG01952.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+7741_1675+774 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | |||||
| chr12:53391346
|
C | CTTTTTT | 8 | a0001c0002t0002g0027a0001c0002t0006g0026a0001c0002t0021g0028others(5): Show | 8 | HG01167.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675+7740_1675+774 others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | |||||
| chr12:53391346
|
CT | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 91 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.1675+7745delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | |||||
| chr12:53391372
|
C | T | 1 | a0001c0002t0002g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1675+7750C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391372 | ||||||
| chr12:53391427
|
C | T | 2 | a0001c0001t0026g0033a0001c0001t0026g0066 | 2 | HG01257.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1675+7805C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391427 | ||||||
| chr12:53391645
|
T | G | 1 | a0001c0002t0002g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1675+8023T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391645 | ||||||
| chr12:53391719
|
G | A | 1 | a0001c0001t0015g0017 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1675+8097G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391719 | ||||||
| chr12:53391814
|
A | G | 3 | a0001c0001t0003g0020a0001c0001t0007g0019a0001c0001t0011g0021 | 3 | HG02559.hp2 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1675+8192A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391814 | ||||||
| chr12:53391860
|
C | T | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+8238C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391860 | ||||||
| chr12:53391903
|
A | G | 1 | a0001c0002t0002g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1675+8281A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391903 | ||||||
| chr12:53391953
|
C | G | 2 | a0001c0001t0003g0181a0001c0001t0008g0180 | 2 | HG01192.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1675+8331C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391953 | ||||||
| chr12:53392007
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1675+8385T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392007 | ||||||
| chr12:53392013
|
C | T | 1 | a0001c0002t0087g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1675+8391C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392013 | ||||||
| chr12:53392035
|
T | C | 1 | a0001c0001t0090g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1675+8413T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392035 | ||||||
| chr12:53392077
|
G | A | 9 | a0001c0002t0002g0242a0001c0002t0002g0243a0001c0002t0002g0244others(6): Show | 9 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675+8455G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392077 | ||||||
| chr12:53392249
|
C | T | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+8627C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392249 | ||||||
| chr12:53392347
|
A | AT | 35 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0058others(32): Show | 35 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1675+8752dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | |||||
| chr12:53392347
|
AT | A | 34 | a0001c0001t0005g0275a0001c0001t0005g0284a0001c0001t0071g0184others(31): Show | 36 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1675+8752delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | |||||
| chr12:53392347
|
ATT | A | 97 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(94): Show | 98 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1675+8751_1675+875 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | |||||
| chr12:53392347
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0064g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1675+8741_1675+875 others(16): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | |||||
| chr12:53392376
|
A | G | 1 | a0001c0001t0003g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1675+8754A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392376 | ||||||
| chr12:53392458
|
G | A | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+8836G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392458 | ||||||
| chr12:53392556
|
A | C | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+8934A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392556 | ||||||
| chr12:53392601
|
C | T | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+8979C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392601 | ||||||
| chr12:53392606
|
C | T | 1 | a0001c0001t0008g0063 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1675+8984C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392606 | ||||||
| chr12:53392697
|
G | C | 1 | a0001c0001t0065g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1675+9075G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392697 | ||||||
| chr12:53392836
|
T | G | 1 | a0001c0002t0031g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1675+9214T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392836 | ||||||
| chr12:53392909
|
C | T | 1 | a0001c0002t0002g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1675+9287C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392909 | ||||||
| chr12:53393028
|
G | A | 2 | a0001c0002t0002g0256a0001c0002t0002g0258 | 2 | NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1675+9406G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393028 | ||||||
| chr12:53393247
|
G | A | 1 | a0001c0001t0005g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1675+9625G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393247 | ||||||
| chr12:53393345
|
C | A | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+9723C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393345 | ||||||
| chr12:53393362
|
G | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0097others(1): Show | 4 | HG00738.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+9740G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393362 | ||||||
| chr12:53393449
|
A | G | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+9827A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393449 | ||||||
| chr12:53393511
|
G | C | 1 | a0001c0001t0003g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1675+9889G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393511 | ||||||
| chr12:53393592
|
C | CT | 7 | a0001c0001t0019g0192a0001c0001t0032g0265a0001c0001t0032g0269others(4): Show | 7 | HG01099.hp1 HG02602.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+9985dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53393592 | |||||
| chr12:53393592
|
CT | C | 96 | a0001c0001t0030g0278a0001c0002t0002g0003a0001c0002t0002g0012others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+9985delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53393592 | |||||
| chr12:53393610
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1675+9988A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393610 | ||||||
| chr12:53393685
|
C | T | 3 | a0001c0002t0027g0215a0001c0002t0027g0216a0001c0002t0074g0214 | 3 | HG02922.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1675+10063C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393685 | ||||||
| chr12:53393787
|
G | A | 2 | a0001c0001t0025g0188a0001c0001t0025g0287 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1675+10165G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393787 | ||||||
| chr12:53393993
|
T | TC | 7 | a0001c0001t0025g0188a0001c0001t0025g0287a0001c0001t0067g0292others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+10372dupC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53393993 | |||||
| chr12:53394082
|
A | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10460A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394082 | ||||||
| chr12:53394169
|
T | C | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+10547T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394169 | ||||||
| chr12:53394218
|
G | GA | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10605dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394218 | |||||
| chr12:53394385
|
T | G | 1 | a0001c0002t0002g0256 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1675+10763T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394385 | ||||||
| chr12:53394409
|
C | CT | 21 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0057others(18): Show | 22 | HG00738.hp2 HG01243.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1675+10808dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394409 | |||||
| chr12:53394409
|
CT | C | 39 | a0001c0001t0001g0167a0001c0001t0005g0015a0001c0001t0005g0187others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1675+10808delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394409 | |||||
| chr12:53394409
|
CTTTTTT | C | 94 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(91): Show | 97 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1675+10803_1675+10 others(12): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394409 | |||||
| chr12:53394458
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1675+10836T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394458 | ||||||
| chr12:53394486
|
GC | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10867delC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394486 | |||||
| chr12:53394489
|
C | T | 1 | a0001c0001t0014g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1675+10867C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394489 | ||||||
| chr12:53394502
|
G | A | 38 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0182others(35): Show | 39 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1675+10880G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394502 | ||||||
| chr12:53394551
|
G | A | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10929G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394551 | ||||||
| chr12:53394583
|
C | CT | 63 | a0001c0001t0019g0192a0001c0001t0032g0265a0001c0001t0038g0272others(60): Show | 64 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.1675+10973dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394583 | |||||
| chr12:53394583
|
C | CTT | 35 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0176others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1675+10972_1675+10 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394583 | |||||
| chr12:53394607
|
C | CT | 50 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0064others(47): Show | 50 | HG00609.hp2 HG00741.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.1675+11010dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | |||||
| chr12:53394607
|
C | CTT | 8 | a0001c0001t0003g0087a0001c0001t0005g0273a0001c0001t0005g0274others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675+11009_1675+11 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | |||||
| chr12:53394607
|
CT | C | 7 | a0001c0001t0001g0122a0001c0001t0003g0020a0001c0001t0007g0019others(4): Show | 7 | HG00323.hp2 HG00733.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+11010delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | |||||
| chr12:53394607
|
CTT | C | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+11009_1675+11 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | |||||
| chr12:53394607
|
CTTT | C | 9 | a0001c0002t0002g0198a0001c0002t0002g0231a0001c0002t0006g0228others(6): Show | 9 | HG00597.hp1 HG00733.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675+11008_1675+11 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | |||||
| chr12:53394607
|
CTTTT | C | 78 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(75): Show | 81 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1675+11007_1675+11 others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | |||||
| chr12:53394637
|
C | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0138a0001c0001t0013g0004others(5): Show | 8 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1675+11015C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394637 | ||||||
| chr12:53394796
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1675+11174A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394796 | ||||||
| chr12:53394856
|
C | T | 20 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1675+11234C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394856 | ||||||
| chr12:53394957
|
C | T | 1 | a0001c0001t0062g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1675+11335C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394957 | ||||||
| chr12:53394957
|
CT | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0097 | 3 | HG00738.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1675+11336delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394957 | ||||||
| chr12:53395170
|
G | A | 1 | a0001c0001t0010g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1676-11415G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395170 | ||||||
| chr12:53395273
|
G | T | 1 | a0001c0001t0010g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1676-11312G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395273 | ||||||
| chr12:53395645
|
C | CTAGCTTC others(4): Show |
1 | a0001c0001t0056g0092 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1676-10939_1676-10 others(17): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53395645 | |||||
| chr12:53395689
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1676-10896C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395689 | ||||||
| chr12:53395811
|
CA | C | 10 | a0001c0001t0001g0171a0001c0001t0005g0282a0001c0001t0030g0286others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-10758delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53395811 | |||||
| chr12:53395811
|
CAA | C | 90 | a0001c0001t0004g0090a0001c0001t0019g0192a0001c0002t0002g0003others(87): Show | 93 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1676-10759_1676-10 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53395811 | |||||
| chr12:53395838
|
G | A | 4 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0085g0041others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-10747G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395838 | ||||||
| chr12:53395979
|
G | A | 41 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0182others(38): Show | 42 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1676-10606G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395979 | ||||||
| chr12:53396036
|
C | T | 1 | a0003c0007t0002g0255 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1676-10549C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396036 | ||||||
| chr12:53396205
|
C | T | 2 | a0001c0002t0031g0225a0001c0002t0031g0226 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1676-10380C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396205 | ||||||
| chr12:53396274
|
C | CA | 14 | a0001c0001t0001g0091a0001c0001t0001g0131a0001c0001t0003g0067others(11): Show | 14 | HG00609.hp1 HG00609.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-10297dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53396274 | |||||
| chr12:53396289
|
G | A | 24 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-10296G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396289 | ||||||
| chr12:53396298
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1676-10287G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396298 | ||||||
| chr12:53396378
|
G | C | 4 | a0001c0003t0016g0288a0001c0003t0016g0290a0001c0003t0016g0291others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1676-10207G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396378 | ||||||
| chr12:53396512
|
T | G | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-10073T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396512 | ||||||
| chr12:53396568
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0003g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1676-10002_1676-99 others(15): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53396568 | |||||
| chr12:53396666
|
T | C | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-9919T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396666 | ||||||
| chr12:53396907
|
G | T | 1 | a0001c0001t0065g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1676-9678G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396907 | ||||||
| chr12:53396980
|
A | T | 1 | a0001c0002t0002g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1676-9605A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396980 | ||||||
| chr12:53397201
|
A | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-9384A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397201 | ||||||
| chr12:53397387
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0008t0001g0070 | 4 | HG00140.hp2 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-9198G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397387 | ||||||
| chr12:53397464
|
A | AT | 8 | a0001c0001t0001g0056a0001c0001t0001g0126a0001c0001t0001g0163others(5): Show | 8 | HG01981.hp1 HG02647.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-9103dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397464 | |||||
| chr12:53397464
|
AT | A | 41 | a0001c0001t0003g0125a0001c0001t0003g0177a0001c0001t0005g0015others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1676-9103delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397464 | |||||
| chr12:53397464
|
ATT | A | 90 | a0001c0001t0032g0269a0001c0002t0002g0003a0001c0002t0002g0012others(87): Show | 93 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1676-9104_1676-910 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397464 | |||||
| chr12:53397579
|
CTTTTTTT others(5): Show |
C | 95 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(92): Show | 98 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1676-8996_1676-898 others(16): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397579 | |||||
| chr12:53397579
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0004t0076g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1676-8996_1676-898 others(17): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397579 | |||||
| chr12:53397624
|
C | T | 20 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1676-8961C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397624 | ||||||
| chr12:53397826
|
T | G | 1 | a0001c0002t0041g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1676-8759T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397826 | ||||||
| chr12:53397846
|
G | A | 103 | a0001c0001t0004g0090a0001c0001t0012g0074a0001c0001t0012g0146others(100): Show | 106 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1676-8739G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397846 | ||||||
| chr12:53397923
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1676-8662A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397923 | ||||||
| chr12:53397975
|
T | C | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-8610T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397975 | ||||||
| chr12:53398075
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1676-8510T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398075 | ||||||
| chr12:53398129
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1676-8456C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398129 | ||||||
| chr12:53398183
|
T | C | 2 | a0001c0001t0004g0088a0001c0010t0060g0075 | 2 | NA19068.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1676-8402T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398183 | ||||||
| chr12:53398204
|
T | G | 24 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-8381T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398204 | ||||||
| chr12:53398224
|
T | G | 2 | a0001c0001t0003g0100a0001c0001t0066g0150 | 2 | HG01256.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1676-8361T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398224 | ||||||
| chr12:53398363
|
A | G | 1 | a0001c0001t0082g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1676-8222A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398363 | ||||||
| chr12:53398371
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0097 | 3 | HG00738.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1676-8214C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398371 | ||||||
| chr12:53398376
|
G | A | 12 | a0001c0001t0003g0009a0001c0001t0004g0009a0001c0001t0004g0076others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1676-8209G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398376 | ||||||
| chr12:53398480
|
A | G | 24 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-8105A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398480 | ||||||
| chr12:53398548
|
G | T | 2 | a0001c0002t0027g0215a0001c0002t0027g0216 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1676-8037G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398548 | ||||||
| chr12:53398585
|
T | C | 7 | a0001c0001t0025g0188a0001c0001t0025g0287a0001c0001t0067g0292others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1676-8000T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398585 | ||||||
| chr12:53398851
|
T | C | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-7734T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398851 | ||||||
| chr12:53399103
|
T | G | 1 | a0001c0002t0087g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1676-7482T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399103 | ||||||
| chr12:53399130
|
T | G | 97 | a0001c0001t0001g0077a0001c0002t0002g0003a0001c0002t0002g0012others(94): Show | 100 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1676-7455T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399130 | ||||||
| chr12:53399273
|
C | T | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-7312C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399273 | ||||||
| chr12:53399336
|
G | GT | 93 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(90): Show | 96 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1676-7244dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399336 | |||||
| chr12:53399342
|
GT | G | 41 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(38): Show | 41 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1676-7234delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399342 | |||||
| chr12:53399343
|
T | TTTTTG | 93 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(90): Show | 96 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1676-7238_1676-723 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399343 | |||||
| chr12:53399372
|
C | T | 1 | a0001c0006t0043g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1676-7213C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399372 | ||||||
| chr12:53399425
|
G | A | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-7160G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399425 | ||||||
| chr12:53399480
|
C | T | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-7105C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399480 | ||||||
| chr12:53399530
|
C | A | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-7055C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399530 | ||||||
| chr12:53399642
|
AT | A | 95 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(92): Show | 98 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1676-6932delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399642 | |||||
| chr12:53399697
|
C | T | 1 | a0001c0002t0088g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1676-6888C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399697 | ||||||
| chr12:53399820
|
G | A | 3 | a0001c0001t0010g0016a0001c0001t0010g0267a0001c0001t0010g0268 | 3 | HG03209.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1676-6765G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399820 | ||||||
| chr12:53399821
|
G | A | 2 | a0001c0002t0033g0044a0001c0002t0033g0045 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1676-6764G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399821 | ||||||
| chr12:53399851
|
G | T | 1 | a0001c0001t0058g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1676-6734G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399851 | ||||||
| chr12:53399863
|
T | A | 1 | a0001c0001t0011g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1676-6722T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399863 | ||||||
| chr12:53399869
|
C | G | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-6716C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399869 | ||||||
| chr12:53399877
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1676-6708C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399877 | ||||||
| chr12:53400230
|
C | T | 3 | a0001c0001t0032g0265a0001c0001t0038g0272a0001c0001t0086g0264 | 3 | HG02559.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1676-6355C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400230 | ||||||
| chr12:53400263
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1676-6322C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400263 | ||||||
| chr12:53400333
|
C | A | 1 | a0001c0002t0002g0260 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1676-6252C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400333 | ||||||
| chr12:53400385
|
A | AT | 7 | a0001c0001t0025g0188a0001c0001t0025g0287a0001c0001t0067g0292others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1676-6199dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400385 | |||||
| chr12:53400405
|
A | G | 1 | a0002c0004t0076g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1676-6180A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400405 | ||||||
| chr12:53400431
|
T | G | 1 | a0001c0001t0036g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1676-6154T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400431 | ||||||
| chr12:53400452
|
A | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0007g0050 | 3 | NA18949.hp1 NA19002.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1676-6133A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400452 | ||||||
| chr12:53400456
|
A | G | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-6129A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400456 | ||||||
| chr12:53400499
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1676-6086G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400499 | ||||||
| chr12:53400504
|
T | G | 41 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0182others(38): Show | 42 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1676-6081T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400504 | ||||||
| chr12:53400692
|
G | A | 9 | a0001c0002t0002g0242a0001c0002t0002g0243a0001c0002t0002g0244others(6): Show | 9 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-5893G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400692 | ||||||
| chr12:53400700
|
T | C | 1 | a0001c0001t0065g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1676-5885T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400700 | ||||||
| chr12:53400755
|
AT | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1676-5806delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | |||||
| chr12:53400755
|
ATT | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0167a0001c0001t0003g0115others(4): Show | 7 | HG01070.hp1 HG02896.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1676-5807_1676-580 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | |||||
| chr12:53400755
|
ATTT | A | 11 | a0001c0002t0002g0223a0001c0002t0002g0242a0001c0002t0002g0254others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1676-5808_1676-580 others(7): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | |||||
| chr12:53400755
|
ATTTT | A | 83 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(80): Show | 86 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1676-5809_1676-580 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | |||||
| chr12:53400800
|
C | T | 1 | a0001c0001t0014g0082 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1676-5785C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400800 | ||||||
| chr12:53400874
|
G | A | 1 | a0001c0002t0002g0241 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1676-5711G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400874 | ||||||
| chr12:53401003
|
C | T | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1676-5582C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401003 | ||||||
| chr12:53401221
|
C | T | 1 | a0001c0006t0043g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1676-5364C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401221 | ||||||
| chr12:53401254
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1676-5331C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401254 | ||||||
| chr12:53401307
|
C | T | 7 | a0001c0002t0002g0204a0001c0002t0002g0207a0001c0002t0002g0208others(4): Show | 7 | HG00609.hp1 HG00673.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-5278C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401307 | ||||||
| chr12:53401457
|
G | GA | 15 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0003g0124others(12): Show | 15 | HG00738.hp2 HG01099.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1676-5108dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53401457 | |||||
| chr12:53401457
|
GA | G | 94 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0004g0175others(91): Show | 97 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1676-5108delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53401457 | |||||
| chr12:53401459
|
A | G | 9 | a0001c0001t0003g0004a0001c0001t0003g0138a0001c0001t0013g0004others(6): Show | 9 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-5126A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401459 | ||||||
| chr12:53401518
|
A | G | 2 | a0001c0001t0011g0104a0001c0001t0011g0110 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1676-5067A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401518 | ||||||
| chr12:53401524
|
C | CT | 5 | a0001c0002t0006g0245a0001c0002t0006g0246a0001c0002t0006g0247others(2): Show | 5 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1676-5060dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53401524 | |||||
| chr12:53401581
|
C | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(17): Show | 21 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1676-5004C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401581 | ||||||
| chr12:53401838
|
T | C | 1 | a0001c0001t0073g0018 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1676-4747T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401838 | ||||||
| chr12:53401961
|
A | G | 24 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-4624A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401961 | ||||||
| chr12:53402159
|
A | G | 1 | a0001c0001t0078g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1676-4426A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402159 | ||||||
| chr12:53402168
|
A | G | 9 | a0001c0001t0003g0100a0001c0001t0003g0116a0001c0001t0003g0177others(6): Show | 9 | HG00733.hp1 HG01192.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1676-4417A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402168 | ||||||
| chr12:53402220
|
C | CT | 8 | a0001c0001t0001g0167a0001c0001t0014g0082a0001c0001t0015g0096others(5): Show | 8 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-4345dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53402220 | |||||
| chr12:53402220
|
CT | C | 88 | a0001c0001t0001g0077a0001c0001t0001g0145a0001c0001t0003g0100others(85): Show | 91 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1676-4345delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53402220 | |||||
| chr12:53402262
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1676-4323C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402262 | ||||||
| chr12:53402375
|
C | T | 1 | a0001c0002t0002g0229 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1676-4210C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402375 | ||||||
| chr12:53402778
|
A | C | 39 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1676-3807A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402778 | ||||||
| chr12:53402960
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 242 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1676-3625T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402960 | ||||||
| chr12:53402968
|
C | CA | 6 | a0001c0001t0001g0008a0001c0001t0059g0164a0001c0002t0002g0252others(3): Show | 7 | HG01169.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-3616dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53402968 | |||||
| chr12:53402969
|
AG | A | 3 | a0001c0001t0001g0032a0001c0002t0018g0205a0004c0009t0083g0157 | 3 | NA18951.hp1 NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1676-3615delG | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402969 | ||||||
| chr12:53402970
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1676-3615G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402970 | ||||||
| chr12:53402973
|
A | G | 1 | a0001c0001t0065g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1676-3612A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402973 | ||||||
| chr12:53403214
|
G | A | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-3371G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403214 | ||||||
| chr12:53403452
|
A | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(17): Show | 21 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1676-3133A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403452 | ||||||
| chr12:53403519
|
A | AT | 12 | a0001c0001t0003g0117a0001c0001t0008g0063a0001c0002t0002g0176others(9): Show | 12 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1676-3051dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53403519 | |||||
| chr12:53403519
|
AT | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 149 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1676-3051delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53403519 | |||||
| chr12:53403800
|
G | C | 1 | a0001c0001t0067g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1676-2785G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403800 | ||||||
| chr12:53403932
|
G | A | 1 | a0002c0004t0002g0249 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1676-2653G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403932 | ||||||
| chr12:53403933
|
A | G | 1 | a0002c0004t0002g0249 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1676-2652A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403933 | ||||||
| chr12:53404172
|
AAAAAAAA others(15): Show |
A | 1 | a0002c0004t0002g0249 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1676-2412_1676-239 others(26): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404172 | ||||||
| chr12:53404194
|
C | A | 1 | a0001c0001t0004g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1676-2391C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404194 | ||||||
| chr12:53404328
|
G | A | 1 | a0001c0001t0071g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1676-2257G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404328 | ||||||
| chr12:53404484
|
A | G | 1 | a0001c0001t0014g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1676-2101A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404484 | ||||||
| chr12:53404542
|
C | CA | 90 | a0001c0001t0004g0102a0001c0001t0020g0293a0001c0001t0092g0035others(87): Show | 93 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1676-2027dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53404542 | |||||
| chr12:53404566
|
A | G | 5 | a0001c0001t0032g0265a0001c0001t0032g0269a0001c0001t0037g0270others(2): Show | 5 | HG01099.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1676-2019A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404566 | ||||||
| chr12:53404613
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1676-1972A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404613 | ||||||
| chr12:53404763
|
G | A | 9 | a0001c0001t0003g0004a0001c0001t0003g0138a0001c0001t0013g0004others(6): Show | 9 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-1822G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404763 | ||||||
| chr12:53404848
|
T | C | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-1737T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404848 | ||||||
| chr12:53404973
|
A | G | 1 | a0001c0002t0002g0253 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1676-1612A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404973 | ||||||
| chr12:53404984
|
C | T | 39 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0182others(36): Show | 40 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-1601C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404984 | ||||||
| chr12:53404996
|
G | C | 2 | a0001c0001t0011g0104a0001c0001t0011g0110 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1676-1589G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404996 | ||||||
| chr12:53405024
|
T | C | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-1561T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405024 | ||||||
| chr12:53405265
|
A | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1320A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405265 | ||||||
| chr12:53405267
|
A | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1318A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405267 | ||||||
| chr12:53405274
|
T | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1311T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405274 | ||||||
| chr12:53405275
|
A | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1310A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405275 | ||||||
| chr12:53405277
|
A | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1308A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405277 | ||||||
| chr12:53405278
|
T | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1307T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405278 | ||||||
| chr12:53405280
|
G | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1305G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405280 | ||||||
| chr12:53405281
|
G | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1304G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405281 | ||||||
| chr12:53405283
|
A | T | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1302A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405283 | ||||||
| chr12:53405287
|
C | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1298C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405287 | ||||||
| chr12:53405288
|
T | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1297T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405288 | ||||||
| chr12:53405289
|
G | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1296G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405289 | ||||||
| chr12:53405291
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1294T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405291 | ||||||
| chr12:53405292
|
T | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1293T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405292 | ||||||
| chr12:53405293
|
C | T | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1292C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405293 | ||||||
| chr12:53405294
|
A | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1291A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405294 | ||||||
| chr12:53405296
|
A | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1289A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405296 | ||||||
| chr12:53405297
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1288T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405297 | ||||||
| chr12:53405298
|
T | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1287T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405298 | ||||||
| chr12:53405301
|
A | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1284A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405301 | ||||||
| chr12:53405302
|
T | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1283T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405302 | ||||||
| chr12:53405304
|
T | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1281T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405304 | ||||||
| chr12:53405307
|
A | T | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1278A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405307 | ||||||
| chr12:53405308
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1277T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405308 | ||||||
| chr12:53405309
|
T | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1276T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405309 | ||||||
| chr12:53405311
|
A | T | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1274A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405311 | ||||||
| chr12:53405312
|
A | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1273A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405312 | ||||||
| chr12:53405314
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1271T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405314 | ||||||
| chr12:53405325
|
T | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1260T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405325 | ||||||
| chr12:53405326
|
G | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1259G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405326 | ||||||
| chr12:53405331
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1254T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405331 | ||||||
| chr12:53405335
|
A | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1250A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405335 | ||||||
| chr12:53405344
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1241T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405344 | ||||||
| chr12:53405345
|
T | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1240T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405345 | ||||||
| chr12:53405346
|
A | G | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1239A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405346 | ||||||
| chr12:53405359
|
T | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1226T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405359 | ||||||
| chr12:53405363
|
G | C | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1222G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405363 | ||||||
| chr12:53405367
|
G | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1218G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405367 | ||||||
| chr12:53405371
|
A | T | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1214A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405371 | ||||||
| chr12:53405373
|
G | A | 3 | a0001c0001t0032g0269a0001c0001t0037g0270a0001c0002t0044g0220 | 3 | HG01099.hp1 HG02647.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1676-1212G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405373 | ||||||
| chr12:53405374
|
T | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1211T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405374 | ||||||
| chr12:53405375
|
C | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1210C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405375 | ||||||
| chr12:53405377
|
C | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1208C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405377 | ||||||
| chr12:53405378
|
T | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1207T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405378 | ||||||
| chr12:53405396
|
G | A | 1 | a0001c0002t0044g0220 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1189G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405396 | ||||||
| chr12:53405428
|
G | A | 6 | a0001c0001t0003g0005a0001c0001t0003g0067a0001c0001t0008g0152others(3): Show | 6 | HG00099.hp2 HG01175.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1676-1157G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405428 | ||||||
| chr12:53405567
|
G | C | 2 | a0001c0001t0025g0188a0001c0001t0025g0287 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1676-1018G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405567 | ||||||
| chr12:53405600
|
A | G | 1 | a0001c0001t0007g0296 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1676-985A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405600 | ||||||
| chr12:53405660
|
T | G | 2 | a0001c0001t0025g0188a0001c0001t0025g0287 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1676-925T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405660 | ||||||
| chr12:53405697
|
A | AGGAAGGA others(1): Show |
37 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(34): Show | 37 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1676-876_1676-869d others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53405697 | |||||
| chr12:53405832
|
A | G | 9 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(6): Show | 9 | HG00738.hp1 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-753A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405832 | ||||||
| chr12:53405926
|
A | G | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-659A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405926 | ||||||
| chr12:53405930
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 242 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1676-655G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405930 | ||||||
| chr12:53405963
|
T | A | 1 | a0001c0001t0066g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1676-622T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405963 | ||||||
| chr12:53405999
|
T | TA | 231 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(228): Show | 241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1676-577dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53405999 | |||||
| chr12:53406065
|
C | CT | 48 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0189others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1676-496dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53406065 | |||||
| chr12:53406065
|
CT | C | 8 | a0001c0001t0001g0034a0001c0001t0003g0068a0001c0001t0003g0181others(5): Show | 8 | HG00140.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-496delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53406065 | |||||
| chr12:53406070
|
T | C | 39 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1676-515T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406070 | ||||||
| chr12:53406111
|
A | G | 135 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(132): Show | 138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-474A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406111 | ||||||
| chr12:53406141
|
G | C | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-444G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406141 | ||||||
| chr12:53406258
|
G | A | 1 | a0001c0001t0003g0178 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1676-327G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406258 | ||||||
| chr12:53406348
|
C | T | 24 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-237C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406348 | ||||||
| chr12:53406364
|
C | T | 13 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(10): Show | 13 | HG00140.hp1 HG00738.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1676-221C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406364 | ||||||
| chr12:53406436
|
G | A | 1 | a0001c0001t0025g0287 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1676-149G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406436 | ||||||
| chr12:53406539
|
T | C | 2 | a0001c0001t0071g0184a0001c0001t0072g0185 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-46T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406539 | ||||||
| chr12:53406785
|
T | C | 1 | a0001c0001t0066g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1844+32T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53406785 | ||||||
| chr12:53406828
|
AT | A | 134 | a0001c0001t0001g0052a0001c0001t0003g0100a0001c0001t0005g0015others(131): Show | 137 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.1844+89delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53406828 | |||||
| chr12:53406848
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1844+95C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53406848 | ||||||
| chr12:53407074
|
T | G | 1 | a0001c0001t0036g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1844+321T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407074 | ||||||
| chr12:53407075
|
C | T | 1 | a0001c0001t0058g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1844+322C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407075 | ||||||
| chr12:53407318
|
GA | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0023others(73): Show | 81 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1844+578delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53407318 | |||||
| chr12:53407330
|
A | T | 1 | a0001c0006t0043g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1844+577A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407330 | ||||||
| chr12:53407331
|
A | T | 131 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(128): Show | 134 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1844+578A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407331 | ||||||
| chr12:53407357
|
A | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1844+604A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407357 | ||||||
| chr12:53407358
|
G | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1844+605G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407358 | ||||||
| chr12:53407387
|
G | A | 1 | a0001c0001t0042g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1844+634G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407387 | ||||||
| chr12:53407506
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1844+753A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407506 | ||||||
| chr12:53407620
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+867G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407620 | ||||||
| chr12:53407625
|
A | G | 1 | a0001c0001t0013g0139 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1844+872A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407625 | ||||||
| chr12:53407629
|
AATTT | A | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1844+889_1844+892d others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53407629 | |||||
| chr12:53407677
|
C | A | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1844+924C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407677 | ||||||
| chr12:53407785
|
C | T | 1 | a0001c0001t0064g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1844+1032C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407785 | ||||||
| chr12:53407786
|
G | A | 4 | a0001c0001t0010g0016a0001c0001t0010g0267a0001c0001t0010g0268others(1): Show | 4 | HG02145.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844+1033G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407786 | ||||||
| chr12:53407838
|
G | A | 39 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1844+1085G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407838 | ||||||
| chr12:53407914
|
G | T | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1844+1161G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407914 | ||||||
| chr12:53407938
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1844+1185C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407938 | ||||||
| chr12:53407960
|
T | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1844+1207T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407960 | ||||||
| chr12:53407969
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1844+1216G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407969 | ||||||
| chr12:53408185
|
G | A | 3 | a0001c0001t0004g0078a0001c0001t0012g0128a0001c0001t0056g0092 | 3 | HG01934.hp2 NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1845-1177G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408185 | ||||||
| chr12:53408245
|
C | CA | 7 | a0001c0002t0023g0039a0001c0002t0023g0040a0001c0002t0033g0044others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1845-1103dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53408245 | |||||
| chr12:53408245
|
C | CAAAAA | 78 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(75): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1845-1107_1845-110 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53408245 | |||||
| chr12:53408245
|
C | CAAAAAA | 10 | a0001c0002t0002g0203a0001c0002t0002g0207a0001c0002t0002g0211others(7): Show | 10 | HG02145.hp2 HG02970.hp1 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845-1108_1845-110 others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53408245 | |||||
| chr12:53408266
|
C | T | 1 | a0002c0004t0076g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1845-1096C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408266 | ||||||
| chr12:53408306
|
G | A | 1 | a0001c0006t0043g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1845-1056G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408306 | ||||||
| chr12:53408341
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1845-1021A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408341 | ||||||
| chr12:53408364
|
G | C | 1 | a0001c0001t0079g0285 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1845-998G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408364 | ||||||
| chr12:53408375
|
T | G | 1 | a0001c0001t0004g0133 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1845-987T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408375 | ||||||
| chr12:53408403
|
A | T | 1 | a0001c0002t0002g0196 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1845-959A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408403 | ||||||
| chr12:53408511
|
C | T | 3 | a0001c0001t0010g0016a0001c0001t0010g0267a0001c0001t0010g0268 | 3 | HG03209.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1845-851C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408511 | ||||||
| chr12:53408575
|
C | T | 1 | a0001c0001t0003g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1845-787C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408575 | ||||||
| chr12:53408672
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1845-690C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408672 | ||||||
| chr12:53408872
|
C | T | 1 | a0001c0001t0065g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1845-490C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408872 | ||||||
| chr12:53408916
|
A | G | 1 | a0001c0001t0037g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1845-446A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408916 | ||||||
| chr12:53409006
|
C | A | 1 | a0001c0001t0067g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1845-356C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409006 | ||||||
| chr12:53409035
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1845-327G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409035 | ||||||
| chr12:53409060
|
A | G | 1 | a0001c0001t0008g0063 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1845-302A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409060 | ||||||
| chr12:53409218
|
C | CTG | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1845-143_1845-142i others(4): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53409218 | |||||
| chr12:53409249
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1845-113A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409249 | ||||||
| chr12:53409295
|
G | T | 2 | a0001c0001t0025g0188a0001c0001t0025g0287 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1845-67G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409295 | ||||||
| chr12:53409768
|
T | G | 39 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(36): Show | 39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.2044+207T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53409768 | ||||||
| chr12:53409849
|
T | C | 89 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2044+288T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53409849 | ||||||
| chr12:53410328
|
A | G | 4 | a0001c0001t0010g0016a0001c0001t0010g0267a0001c0001t0010g0268others(1): Show | 4 | HG02145.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2045-599A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410328 | ||||||
| chr12:53410482
|
A | G | 1 | a0001c0001t0015g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2045-445A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410482 | ||||||
| chr12:53410516
|
G | GT | 6 | a0001c0001t0001g0023a0001c0001t0003g0120a0001c0001t0004g0101others(3): Show | 6 | HG00609.hp2 HG01099.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2045-401dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 53410516 | |||||
| chr12:53410523
|
T | G | 96 | a0001c0002t0002g0003a0001c0002t0002g0012a0001c0002t0002g0013others(93): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2045-404T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410523 | ||||||
| chr12:53410580
|
C | T | 38 | a0001c0001t0005g0015a0001c0001t0005g0273a0001c0001t0005g0274others(35): Show | 38 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2045-347C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410580 | ||||||
| chr12:53410602
|
C | A | 2 | a0001c0002t0002g0211a0001c0002t0077g0212 | 2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-325C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410602 | ||||||
| chr12:53410666
|
C | A | 1 | a0001c0001t0007g0296 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2045-261C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410666 | ||||||
| chr12:53410706
|
C | T | 24 | a0001c0001t0005g0015a0001c0001t0005g0187a0001c0001t0005g0273others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2045-221C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410706 | ||||||
| chr12:53410752
|
C | A | 1 | a0001c0001t0014g0082 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2045-175C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410752 | ||||||
| chr12:53410785
|
G | A | 1 | a0001c0001t0004g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2045-142G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410785 |