Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 58472 |
|---|---|
| ensemblid | ENSG00000137767.14 |
| hgncid | 20390 |
| symbol | SQOR |
| name | sulfide quinone oxidoreductase |
| refseq_nuc | NM_021199.4 |
| refseq_prot | NP_067022.1 |
| ensembl_nuc | ENST00000260324.12 |
| ensembl_prot | ENSP00000260324.7 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 45635029 |
| end | 45691281 |
| strand | + |
| ver | v1.2 |
| region | chr15:45635029-45691281 |
| region5000 | chr15:45630029-45696281 |
| regionname0 | SQOR_chr15_45635029_45691281 |
| regionname5000 | SQOR_chr15_45630029_45696281 |
| 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 | 450 | 234 | 66 | 43 | 87 | 8 | 28 | 65 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002 | 0/0 | 450 | 90 | 5 | 16 | 57 | 2 | 10 | 43 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0003 | 0/0 | 450 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0004 | 0/0 | 450 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0005 | 0/0 | 450 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0006 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0007 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0008 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0009 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0010 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0011 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| 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 | 1353 | 213 | 59 | 38 | 86 | 5 | 23 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0002 | 0/0 | 1353 | 85 | 5 | 11 | 57 | 2 | 10 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0003 | 0/0 | 1353 | 16 | 3 | 5 | 1 | 3 | 4 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0004 | 0/0 | 1353 | 5 | 0 | 5 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0005 | 0/0 | 1353 | 4 | 0 | 0 | 4 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0006 | 0/0 | 1353 | 3 | 2 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0007 | 0/0 | 1353 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0008 | 0/0 | 1353 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0009 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0010 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0011 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0012 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0013 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0014 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0015 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| c0016 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 349 | 319 | 64 | 56 | 151 | 9 | 37 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0002 | 0/0 | 349 | 5 | 3 | 2 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0003 | 0/0 | 349 | 5 | 5 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0004 | 0/0 | 349 | 4 | 4 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0005 | 0/0 | 349 | 4 | 0 | 2 | 0 | 1 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0006 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0007 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| t0008 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| 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 | 1353 | 213 | 59 | 38 | 86 | 5 | 23 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0003 | 0/0 | 1353 | 16 | 3 | 5 | 1 | 3 | 4 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0007 | 0/0 | 1353 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0013 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0016 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002c0002 | 0/0 | 1353 | 85 | 5 | 11 | 57 | 2 | 10 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002c0004 | 0/0 | 1353 | 5 | 0 | 5 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0003c0005 | 0/0 | 1353 | 4 | 0 | 0 | 4 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0004c0008 | 0/0 | 1353 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0005c0006 | 0/0 | 1353 | 3 | 2 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0006c0009 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0007c0015 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0008c0014 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0009c0012 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0010c0011 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0011c0010 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1701 | 200 | 48 | 36 | 86 | 5 | 23 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0001t0002 | 0/0 | 1701 | 5 | 3 | 2 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0001t0003 | 0/0 | 1701 | 5 | 5 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0001t0004 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0001t0007 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0001t0008 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0003t0001 | 0/0 | 1701 | 16 | 3 | 5 | 1 | 3 | 4 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0007t0001 | 0/0 | 1701 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0013t0001 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0001c0016t0001 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002c0002t0001 | 0/0 | 1701 | 80 | 5 | 9 | 56 | 1 | 9 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002c0002t0005 | 0/0 | 1701 | 4 | 0 | 2 | 0 | 1 | 1 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002c0002t0006 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0002c0004t0001 | 0/0 | 1701 | 5 | 0 | 5 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0003c0005t0001 | 0/0 | 1701 | 4 | 0 | 0 | 4 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0004c0008t0001 | 0/0 | 1701 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0005c0006t0001 | 0/0 | 1701 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0005c0006t0004 | 0/0 | 1701 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0006c0009t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0007c0015t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0008c0014t0001 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0009c0012t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0010c0011t0004 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| a0011c0010t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | copy fasta | chr15 | 45630029 | 45696281 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0007t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0007t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0013t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0016t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0004c0008t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0004c0008t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0004c0008t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0005c0006t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0005c0006t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0005c0006t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0006c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0007c0015t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0008c0014t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0009c0012t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0010c0011t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0011c0010t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0163 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0268 | EUR | FIN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0155 | EUR | FIN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00423 | hp1 | a0007 | c0015 | t0001 | g0234 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01069 | hp2 | a0002 | c0002 | t0005 | g0102 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01074 | hp1 | a0002 | c0004 | t0001 | g0248 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0269 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0267 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01109 | hp2 | a0005 | c0006 | t0001 | g0311 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0143 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0327 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01255 | hp1 | a0002 | c0004 | t0001 | g0110 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01257 | hp2 | a0002 | c0004 | t0001 | g0247 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0249 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01346 | hp2 | a0002 | c0002 | t0005 | g0103 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0129 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0282 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0150 | EUR | IBS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0226 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01981 | hp1 | a0002 | c0004 | t0001 | g0280 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02055 | hp1 | a0010 | c0011 | t0004 | g0325 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02165 | hp1 | a0009 | c0012 | t0001 | g0253 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02523 | hp2 | a0002 | c0002 | t0006 | g0031 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0257 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02809 | hp2 | a0004 | c0008 | t0001 | g0164 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02896 | hp1 | a0005 | c0006 | t0004 | g0319 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02897 | hp1 | a0005 | c0006 | t0004 | g0323 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0233 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03195 | hp1 | a0008 | c0014 | t0001 | g0185 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03486 | hp2 | a0004 | c0008 | t0001 | g0231 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0258 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0212 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0265 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03834 | hp2 | a0001 | c0016 | t0001 | g0256 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04228 | hp1 | a0002 | c0002 | t0005 | g0101 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18906 | hp2 | a0004 | c0008 | t0001 | g0326 | AFR | YRI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18962 | hp2 | a0006 | c0009 | t0001 | g0120 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18967 | hp1 | a0011 | c0010 | t0001 | g0283 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18982 | hp1 | a0003 | c0005 | t0001 | g0306 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18984 | hp2 | a0003 | c0005 | t0001 | g0307 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19012 | hp2 | a0003 | c0005 | t0001 | g0023 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0290 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | ASW | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ASW | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20805 | hp1 | a0002 | c0002 | t0005 | g0118 | EUR | TSI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02559 | hp2 | a0001 | c0013 | t0001 | g0187 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0156 | REF | REF | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0167 | REF | REF | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45635106
|
C | T | 1 | a0001 | 6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
splice_region_variant | LOW | c.-20C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/10 | chr15 | 45635106 | ||||||
| chr15:45658958
|
G | A | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.35G>A | p.Arg12His | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 132/1701 | 35/1353 | 12/450 | chr15 | 45658958 | ||
| chr15:45659038
|
G | A | 1 | a0011 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.115G>A | p.Ala39Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 212/1701 | 115/1353 | 39/450 | chr15 | 45659038 | ||
| chr15:45659090
|
T | C | 1 | a0005 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.167T>C | p.Ile56Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 264/1701 | 167/1353 | 56/450 | chr15 | 45659090 | ||
| chr15:45673634
|
C | T | 1 | a0004 | 3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.487C>T | p.His163Tyr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/10 | 584/1701 | 487/1353 | 163/450 | chr15 | 45673634 | ||
| chr15:45673697
|
G | A | 2 | a0005a0010 | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.550G>A | p.Asp184Asn | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/10 | 647/1701 | 550/1353 | 184/450 | chr15 | 45673697 | ||
| chr15:45676133
|
C | G | 1 | a0003 | 4 | NA18982.hp1 NA18984.hp2 NA19012.hp2 others(1): Show |
missense_variant | MODERATE | c.687C>G | p.Phe229Leu | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/10 | 784/1701 | 687/1353 | 229/450 | chr15 | 45676133 | ||
| chr15:45676237
|
T | C | 1 | a0002 | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
missense_variant | MODERATE | c.791T>C | p.Ile264Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/10 | 888/1701 | 791/1353 | 264/450 | chr15 | 45676237 | ||
| chr15:45682649
|
G | A | 1 | a0009 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1036G>A | p.Ala346Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/10 | 1133/1701 | 1036/1353 | 346/450 | chr15 | 45682649 | ||
| chr15:45689118
|
C | T | 1 | a0007 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1196C>T | p.Pro399Leu | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/10 | 1293/1701 | 1196/1353 | 399/450 | chr15 | 45689118 | ||
| chr15:45691002
|
G | A | 1 | a0008 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1325G>A | p.Arg442His | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 1422/1701 | 1325/1353 | 442/450 | chr15 | 45691002 | ||
| chr15:45691280
|
G | C | 1 | a0002 | 1 | HG02523.hp2 | splice_region_variant | LOW | c.*250G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | chr15 | 45691280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45673630
|
C | T | 1 | a0001c0016 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.483C>T | p.Phe161Phe | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/10 | 580/1701 | 483/1353 | 161/450 | chr15 | 45673630 | ||
| chr15:45689098
|
G | A | 1 | a0001c0007 | 3 | HG01884.hp1 HG02965.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.1176G>A | p.Glu392Glu | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/10 | 1273/1701 | 1176/1353 | 392/450 | chr15 | 45689098 | ||
| chr15:45689119
|
G | A | 2 | a0001c0003a0002c0004 | 21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1197G>A | p.Pro399Pro | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/10 | 1294/1701 | 1197/1353 | 399/450 | chr15 | 45689119 | ||
| chr15:45690994
|
G | A | 1 | a0001c0013 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1317G>A | p.Ala439Ala | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 1414/1701 | 1317/1353 | 439/450 | chr15 | 45690994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45635034
|
A | G | 1 | a0001c0001t0008 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/10 | 23890 | chr15 | 45635034 | |||||
| chr15:45658910
|
G | C | 3 | a0001c0001t0004a0005c0006t0004a0010c0011t0004 | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 14 | chr15 | 45658910 | |||||
| chr15:45691078
|
G | T | 1 | a0002c0002t0005 | 4 | HG01069.hp2 HG01346.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*48G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 48 | chr15 | 45691078 | |||||
| chr15:45691235
|
T | C | 2 | a0001c0001t0002a0001c0001t0007 | 6 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 205 | chr15 | 45691235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45635126
|
C | T | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+18C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635126 | ||||||
| chr15:45635335
|
A | G | 17 | a0001c0001t0001g0312a0001c0001t0001g0320a0001c0001t0001g0321others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+227A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635335 | ||||||
| chr15:45635354
|
G | C | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+246G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635354 | ||||||
| chr15:45635513
|
T | C | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+405T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635513 | ||||||
| chr15:45635680
|
T | C | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+572T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635680 | ||||||
| chr15:45635705
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+597T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635705 | ||||||
| chr15:45635761
|
T | A | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-18+653T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635761 | ||||||
| chr15:45635809
|
G | A | 1 | a0002c0002t0001g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18+701G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635809 | ||||||
| chr15:45635830
|
A | ACTCT | 68 | a0001c0001t0001g0010a0001c0001t0001g0261a0001c0001t0001g0262others(65): Show | 69 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-18+724_-18+727dup others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45635830 | |||||
| chr15:45635987
|
C | T | 1 | a0002c0002t0001g0260 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-18+879C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635987 | ||||||
| chr15:45635997
|
A | C | 32 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(29): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-18+889A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635997 | ||||||
| chr15:45636197
|
C | T | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+1089C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636197 | ||||||
| chr15:45636406
|
C | CT | 67 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0218others(64): Show | 70 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-18+1314dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636406 | |||||
| chr15:45636406
|
CT | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(77): Show | 86 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.-18+1314delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636406 | |||||
| chr15:45636440
|
T | C | 6 | a0001c0001t0001g0092a0002c0002t0001g0088a0002c0002t0001g0089others(3): Show | 6 | HG00408.hp1 HG00438.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+1332T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636440 | ||||||
| chr15:45636498
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-18+1390G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636498 | ||||||
| chr15:45636504
|
A | G | 49 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0264others(46): Show | 50 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+1396A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636504 | ||||||
| chr15:45636618
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+1510G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636618 | ||||||
| chr15:45636635
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-18+1527C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636635 | ||||||
| chr15:45636853
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(97): Show | 107 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.-18+1745A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636853 | ||||||
| chr15:45636869
|
C | T | 1 | a0002c0002t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-18+1761C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636869 | ||||||
| chr15:45636988
|
C | CT | 6 | a0001c0001t0001g0087a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | HG00140.hp2 HG01243.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+1894dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636988 | |||||
| chr15:45636988
|
CT | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0213a0001c0001t0001g0214others(11): Show | 15 | HG01169.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+1894delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636988 | |||||
| chr15:45637226
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(75): Show | 84 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.-18+2118T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637226 | ||||||
| chr15:45637294
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+2186G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637294 | ||||||
| chr15:45637544
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-18+2436G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637544 | ||||||
| chr15:45637778
|
C | T | 2 | a0001c0003t0001g0257a0001c0003t0001g0258 | 2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-18+2670C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637778 | ||||||
| chr15:45637869
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18+2761C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637869 | ||||||
| chr15:45637873
|
C | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+2765C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637873 | ||||||
| chr15:45637991
|
G | C | 1 | a0002c0002t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+2883G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637991 | ||||||
| chr15:45638155
|
C | CA | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG02895.hp2 HG03710.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3054dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45638155 | |||||
| chr15:45638349
|
T | G | 1 | a0002c0002t0001g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+3241T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638349 | ||||||
| chr15:45638350
|
G | A | 1 | a0002c0002t0001g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+3242G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638350 | ||||||
| chr15:45638353
|
A | T | 1 | a0002c0002t0001g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+3245A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638353 | ||||||
| chr15:45638407
|
C | T | 2 | a0002c0002t0001g0327a0004c0008t0001g0326 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+3299C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638407 | ||||||
| chr15:45638450
|
C | T | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-18+3342C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638450 | ||||||
| chr15:45638451
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0218others(2): Show | 6 | HG02451.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3343G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638451 | ||||||
| chr15:45638524
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(156): Show | 167 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18+3416G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638524 | ||||||
| chr15:45638585
|
G | C | 2 | a0002c0002t0001g0327a0004c0008t0001g0326 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+3477G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638585 | ||||||
| chr15:45638588
|
G | A | 1 | a0002c0002t0001g0018 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-18+3480G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638588 | ||||||
| chr15:45638595
|
G | A | 2 | a0001c0001t0001g0230a0004c0008t0001g0231 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+3487G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638595 | ||||||
| chr15:45638632
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-18+3524G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638632 | ||||||
| chr15:45638647
|
C | A | 4 | a0001c0001t0004g0324a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3539C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638647 | ||||||
| chr15:45638648
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+3540G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638648 | ||||||
| chr15:45638756
|
G | A | 7 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0210others(4): Show | 7 | HG00140.hp2 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+3648G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638756 | ||||||
| chr15:45638779
|
G | A | 1 | a0001c0001t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-18+3671G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638779 | ||||||
| chr15:45638792
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+3684C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638792 | ||||||
| chr15:45639125
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+4017T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639125 | ||||||
| chr15:45639448
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-18+4340C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639448 | ||||||
| chr15:45639476
|
A | G | 3 | a0001c0001t0001g0207a0001c0016t0001g0256a0002c0002t0001g0206 | 3 | HG02074.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+4368A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639476 | ||||||
| chr15:45639494
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+4386C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639494 | ||||||
| chr15:45639586
|
T | C | 3 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322 | 3 | HG02717.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+4478T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639586 | ||||||
| chr15:45639589
|
G | A | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+4481G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639589 | ||||||
| chr15:45639609
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18+4501T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639609 | ||||||
| chr15:45640463
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-18+5355C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640463 | ||||||
| chr15:45640497
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-18+5389C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640497 | ||||||
| chr15:45640520
|
T | G | 2 | a0001c0001t0001g0230a0004c0008t0001g0231 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+5412T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640520 | ||||||
| chr15:45640673
|
C | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+5565C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640673 | ||||||
| chr15:45640739
|
G | C | 1 | a0002c0002t0001g0265 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-18+5631G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640739 | ||||||
| chr15:45640981
|
G | A | 53 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0264others(50): Show | 54 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-18+5873G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640981 | ||||||
| chr15:45641077
|
T | G | 6 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+5969T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641077 | ||||||
| chr15:45641098
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18+5990G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641098 | ||||||
| chr15:45641109
|
T | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(81): Show | 90 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-18+6001T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641109 | ||||||
| chr15:45641329
|
T | G | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+6221T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641329 | ||||||
| chr15:45641675
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-18+6567G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641675 | ||||||
| chr15:45641878
|
C | G | 2 | a0002c0002t0001g0083a0002c0002t0001g0084 | 2 | NA18949.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-18+6770C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641878 | ||||||
| chr15:45641894
|
C | T | 13 | a0001c0001t0001g0097a0001c0001t0001g0193a0001c0001t0001g0196others(10): Show | 13 | HG00673.hp1 HG01517.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+6786C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641894 | ||||||
| chr15:45641954
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-18+6846C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641954 | ||||||
| chr15:45641956
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+6848A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641956 | ||||||
| chr15:45642028
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-18+6920C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642028 | ||||||
| chr15:45642404
|
G | A | 1 | a0002c0002t0001g0019 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-18+7296G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642404 | ||||||
| chr15:45642506
|
G | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0264others(46): Show | 50 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+7398G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642506 | ||||||
| chr15:45642547
|
A | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7439A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642547 | ||||||
| chr15:45642579
|
T | C | 30 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(27): Show | 31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+7471T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642579 | ||||||
| chr15:45642612
|
A | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7504A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642612 | ||||||
| chr15:45642642
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7534G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642642 | ||||||
| chr15:45642671
|
C | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7563C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642671 | ||||||
| chr15:45642689
|
C | T | 6 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+7581C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642689 | ||||||
| chr15:45642723
|
A | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(149): Show | 160 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.-18+7615A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642723 | ||||||
| chr15:45642723
|
A | G | 6 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+7615A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642723 | ||||||
| chr15:45642782
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+7674C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642782 | ||||||
| chr15:45642809
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7701C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642809 | ||||||
| chr15:45642823
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7715T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642823 | ||||||
| chr15:45642826
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7718G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642826 | ||||||
| chr15:45642876
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7768T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642876 | ||||||
| chr15:45642958
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+7850T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642958 | ||||||
| chr15:45642961
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7853C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642961 | ||||||
| chr15:45642974
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+7866G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642974 | ||||||
| chr15:45643027
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-18+7919C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643027 | ||||||
| chr15:45643053
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0002g0004a0002c0002t0001g0080others(1): Show | 5 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+7945C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643053 | ||||||
| chr15:45643088
|
G | T | 1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-18+7980G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643088 | ||||||
| chr15:45643152
|
T | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8044T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643152 | ||||||
| chr15:45643174
|
C | A | 1 | a0001c0001t0002g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18+8066C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643174 | ||||||
| chr15:45643195
|
C | A | 55 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0264others(52): Show | 56 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18+8087C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643195 | ||||||
| chr15:45643262
|
C | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0003t0001g0079 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-18+8154C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643262 | ||||||
| chr15:45643321
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(156): Show | 167 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18+8213A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643321 | ||||||
| chr15:45643557
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8449C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643557 | ||||||
| chr15:45643579
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8471G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643579 | ||||||
| chr15:45643618
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8510C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643618 | ||||||
| chr15:45643895
|
T | C | 1 | a0001c0001t0003g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+8787T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643895 | ||||||
| chr15:45643896
|
A | T | 2 | a0002c0002t0001g0327a0004c0008t0001g0326 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+8788A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643896 | ||||||
| chr15:45643929
|
T | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8821T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643929 | ||||||
| chr15:45644018
|
C | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02895.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-18+8910C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644018 | ||||||
| chr15:45644036
|
G | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8928G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644036 | ||||||
| chr15:45644068
|
G | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8960G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644068 | ||||||
| chr15:45644094
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(154): Show | 165 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18+8986T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644094 | ||||||
| chr15:45644147
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9039A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644147 | ||||||
| chr15:45644148
|
C | T | 1 | a0001c0003t0001g0258 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18+9040C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644148 | ||||||
| chr15:45644173
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(154): Show | 165 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18+9065T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644173 | ||||||
| chr15:45644191
|
G | A | 7 | a0001c0001t0001g0100a0001c0001t0001g0208a0001c0001t0001g0210others(4): Show | 7 | HG00140.hp2 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+9083G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644191 | ||||||
| chr15:45644305
|
T | C | 3 | a0001c0001t0001g0207a0001c0016t0001g0256a0002c0002t0001g0206 | 3 | HG02074.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+9197T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644305 | ||||||
| chr15:45644389
|
A | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9281A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644389 | ||||||
| chr15:45644391
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(156): Show | 167 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18+9283G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644391 | ||||||
| chr15:45644417
|
T | A | 2 | a0005c0006t0004g0319a0005c0006t0004g0323 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+9309T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644417 | ||||||
| chr15:45644434
|
G | T | 30 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(27): Show | 31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+9326G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644434 | ||||||
| chr15:45644547
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9439G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644547 | ||||||
| chr15:45644658
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9550G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644658 | ||||||
| chr15:45644664
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+9556G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644664 | ||||||
| chr15:45644666
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9558A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644666 | ||||||
| chr15:45644734
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+9626T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644734 | ||||||
| chr15:45644751
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18+9643A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644751 | ||||||
| chr15:45644785
|
G | GAGCTGCC others(13): Show |
1 | a0001c0001t0001g0020 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-18+9678_-18+9697d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45644785 | |||||
| chr15:45644938
|
C | G | 30 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(27): Show | 31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+9830C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644938 | ||||||
| chr15:45645174
|
C | T | 1 | a0002c0002t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-18+10066C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645174 | ||||||
| chr15:45645279
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-18+10171A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645279 | ||||||
| chr15:45645324
|
C | T | 2 | a0001c0001t0003g0315a0001c0001t0007g0316 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+10216C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645324 | ||||||
| chr15:45645330
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+10222A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645330 | ||||||
| chr15:45645386
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+10278T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645386 | ||||||
| chr15:45645427
|
C | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 42 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-18+10319C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645427 | ||||||
| chr15:45645434
|
G | A | 30 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(27): Show | 31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+10326G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645434 | ||||||
| chr15:45645452
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+10344G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645452 | ||||||
| chr15:45645498
|
A | G | 30 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(27): Show | 31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+10390A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645498 | ||||||
| chr15:45645653
|
T | A | 2 | a0001c0001t0003g0315a0001c0001t0007g0316 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+10545T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645653 | ||||||
| chr15:45645705
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+10597C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645705 | ||||||
| chr15:45645752
|
T | C | 1 | a0001c0001t0003g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+10644T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645752 | ||||||
| chr15:45645973
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-18+10865C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645973 | ||||||
| chr15:45645993
|
C | G | 1 | a0001c0001t0001g0299 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-18+10885C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645993 | ||||||
| chr15:45646115
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+11007T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646115 | ||||||
| chr15:45646163
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+11055G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646163 | ||||||
| chr15:45646312
|
C | A | 7 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322others(4): Show | 7 | HG02055.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+11204C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646312 | ||||||
| chr15:45646441
|
T | A | 1 | a0001c0001t0001g0010 | 2 | NA18947.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-18+11333T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646441 | ||||||
| chr15:45646463
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(88): Show | 98 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-18+11355A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646463 | ||||||
| chr15:45646470
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+11362C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646470 | ||||||
| chr15:45646654
|
T | A | 4 | a0001c0001t0004g0324a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+11546T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646654 | ||||||
| chr15:45646849
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-18+11741C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646849 | ||||||
| chr15:45646885
|
T | A | 49 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0263others(46): Show | 50 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+11777T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646885 | ||||||
| chr15:45647077
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(198): Show | 211 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.-17-11830A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647077 | ||||||
| chr15:45647091
|
A | G | 25 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0286others(22): Show | 25 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-11816A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647091 | ||||||
| chr15:45647141
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-17-11766C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647141 | ||||||
| chr15:45647164
|
G | A | 3 | a0001c0001t0001g0108a0002c0002t0001g0109a0002c0004t0001g0110 | 3 | HG00639.hp2 HG01255.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-17-11743G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647164 | ||||||
| chr15:45647328
|
C | CT | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(160): Show | 172 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-17-11563dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45647328 | |||||
| chr15:45647328
|
C | CTT | 15 | a0001c0001t0001g0074a0001c0001t0001g0232a0001c0001t0001g0235others(12): Show | 16 | HG00423.hp1 HG02080.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-11564_-17-1156 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45647328 | |||||
| chr15:45647328
|
C | CTTT | 19 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(16): Show | 19 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-11565_-17-1156 others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45647328 | |||||
| chr15:45647494
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(179): Show | 191 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.-17-11413A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647494 | ||||||
| chr15:45647565
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(179): Show | 191 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.-17-11342A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647565 | ||||||
| chr15:45647642
|
C | T | 1 | a0001c0001t0003g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-11265C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647642 | ||||||
| chr15:45647650
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-11257C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647650 | ||||||
| chr15:45647779
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(70): Show | 79 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-17-11128G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647779 | ||||||
| chr15:45647780
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(70): Show | 79 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-17-11127G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647780 | ||||||
| chr15:45648153
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10754A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648153 | ||||||
| chr15:45648167
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10740G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648167 | ||||||
| chr15:45648174
|
T | A | 8 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-10733T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648174 | ||||||
| chr15:45648198
|
C | T | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-17-10709C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648198 | ||||||
| chr15:45648399
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10508A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648399 | ||||||
| chr15:45648409
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10498C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648409 | ||||||
| chr15:45648472
|
A | T | 32 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(29): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-10435A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648472 | ||||||
| chr15:45648502
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-17-10405C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648502 | ||||||
| chr15:45648534
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-17-10373G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648534 | ||||||
| chr15:45648628
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10279G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648628 | ||||||
| chr15:45648707
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10200C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648707 | ||||||
| chr15:45648764
|
G | A | 31 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0240others(28): Show | 32 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-17-10143G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648764 | ||||||
| chr15:45648830
|
T | C | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0083others(1): Show | 4 | NA18949.hp2 NA18986.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-10077T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648830 | ||||||
| chr15:45648854
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-17-10053C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648854 | ||||||
| chr15:45648984
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9923T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648984 | ||||||
| chr15:45649119
|
A | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 18 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-9788A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649119 | ||||||
| chr15:45649170
|
G | A | 2 | a0002c0002t0001g0327a0004c0008t0001g0326 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-17-9737G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649170 | ||||||
| chr15:45649267
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17-9640C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649267 | ||||||
| chr15:45649373
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-9534G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649373 | ||||||
| chr15:45649485
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-17-9422C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649485 | ||||||
| chr15:45649491
|
T | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(24): Show | 28 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-9416T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649491 | ||||||
| chr15:45649497
|
A | G | 1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-17-9410A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649497 | ||||||
| chr15:45649512
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9395G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649512 | ||||||
| chr15:45649616
|
A | G | 1 | a0001c0001t0002g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-9291A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649616 | ||||||
| chr15:45649646
|
A | AT | 16 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(13): Show | 17 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-9253dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45649646 | |||||
| chr15:45649749
|
C | G | 1 | a0001c0001t0001g0181 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-17-9158C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649749 | ||||||
| chr15:45649785
|
A | T | 1 | a0001c0001t0001g0284 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-17-9122A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649785 | ||||||
| chr15:45649785
|
AT | A | 3 | a0001c0001t0001g0301a0002c0002t0001g0300a0002c0002t0001g0302 | 3 | HG00423.hp2 NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-17-9116delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45649785 | |||||
| chr15:45649812
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-17-9095G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649812 | ||||||
| chr15:45649813
|
A | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 31 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-9094A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649813 | ||||||
| chr15:45649829
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9078T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649829 | ||||||
| chr15:45649831
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9076T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649831 | ||||||
| chr15:45649844
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9063T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649844 | ||||||
| chr15:45649851
|
T | C | 2 | a0001c0001t0001g0099a0005c0006t0001g0311 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-9056T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649851 | ||||||
| chr15:45649865
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0186others(8): Show | 12 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-9042G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649865 | ||||||
| chr15:45650001
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG02965.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-8906G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650001 | ||||||
| chr15:45650005
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-17-8902G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650005 | ||||||
| chr15:45650068
|
C | T | 1 | a0002c0002t0001g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-17-8839C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650068 | ||||||
| chr15:45650098
|
C | A | 15 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0221others(12): Show | 16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-8809C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650098 | ||||||
| chr15:45650119
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8788A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650119 | ||||||
| chr15:45650141
|
C | CT | 11 | a0001c0001t0001g0069a0001c0001t0001g0174a0001c0001t0001g0177others(8): Show | 11 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-8758dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45650141 | |||||
| chr15:45650198
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-17-8709G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650198 | ||||||
| chr15:45650224
|
C | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(11): Show | 15 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-8683C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650224 | ||||||
| chr15:45650232
|
T | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-8675T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650232 | ||||||
| chr15:45650315
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8592G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650315 | ||||||
| chr15:45650351
|
G | A | 1 | a0002c0002t0001g0300 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-17-8556G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650351 | ||||||
| chr15:45650369
|
C | T | 1 | a0011c0010t0001g0283 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-17-8538C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650369 | ||||||
| chr15:45650373
|
C | T | 1 | a0002c0002t0001g0265 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17-8534C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650373 | ||||||
| chr15:45650498
|
G | A | 1 | a0001c0001t0002g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-8409G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650498 | ||||||
| chr15:45650571
|
G | C | 3 | a0001c0001t0001g0186a0001c0001t0003g0313a0008c0014t0001g0185 | 3 | HG03195.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-17-8336G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650571 | ||||||
| chr15:45650585
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(72): Show | 79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-17-8322C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650585 | ||||||
| chr15:45650588
|
T | C | 3 | a0005c0006t0004g0319a0005c0006t0004g0323a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-8319T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650588 | ||||||
| chr15:45650754
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8153T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650754 | ||||||
| chr15:45650849
|
G | T | 3 | a0005c0006t0004g0319a0005c0006t0004g0323a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-8058G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650849 | ||||||
| chr15:45650885
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8022C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650885 | ||||||
| chr15:45650901
|
C | G | 1 | a0001c0003t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-8006C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650901 | ||||||
| chr15:45650952
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-7955C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650952 | ||||||
| chr15:45650980
|
G | A | 1 | a0001c0001t0004g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17-7927G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650980 | ||||||
| chr15:45650991
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-7916C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650991 | ||||||
| chr15:45650998
|
C | T | 1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-17-7909C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650998 | ||||||
| chr15:45650999
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-17-7908G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650999 | ||||||
| chr15:45651032
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-17-7875G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651032 | ||||||
| chr15:45651052
|
A | C | 1 | a0002c0002t0001g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-17-7855A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651052 | ||||||
| chr15:45651055
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-17-7852G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651055 | ||||||
| chr15:45651200
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-17-7707G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651200 | ||||||
| chr15:45651213
|
T | G | 2 | a0001c0001t0001g0235a0007c0015t0001g0234 | 2 | HG00423.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-17-7694T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651213 | ||||||
| chr15:45651270
|
G | A | 3 | a0005c0006t0004g0319a0005c0006t0004g0323a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-7637G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651270 | ||||||
| chr15:45651335
|
C | T | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-17-7572C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651335 | ||||||
| chr15:45651402
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-17-7505G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651402 | ||||||
| chr15:45651492
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG02965.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-7415C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651492 | ||||||
| chr15:45651518
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(323): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-17-7389T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651518 | ||||||
| chr15:45651519
|
G | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 16 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-17-7388G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651519 | ||||||
| chr15:45651555
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-7352C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651555 | ||||||
| chr15:45651556
|
G | A | 1 | a0001c0003t0001g0034 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-17-7351G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651556 | ||||||
| chr15:45651812
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-7095A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651812 | ||||||
| chr15:45651845
|
A | ATTCTTCT others(29): Show |
2 | a0001c0003t0001g0257a0001c0003t0001g0258 | 2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-17-7047_-17-7012d others(38): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45651845 | |||||
| chr15:45651874
|
T | C | 3 | a0005c0006t0004g0319a0005c0006t0004g0323a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-7033T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651874 | ||||||
| chr15:45651883
|
T | A | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17-7024T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651883 | ||||||
| chr15:45651896
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-7011T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651896 | ||||||
| chr15:45651925
|
G | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6982G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651925 | ||||||
| chr15:45651975
|
C | T | 1 | a0001c0003t0001g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-17-6932C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651975 | ||||||
| chr15:45652000
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6907G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652000 | ||||||
| chr15:45652019
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-17-6888G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652019 | ||||||
| chr15:45652030
|
C | T | 1 | a0002c0004t0001g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-17-6877C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652030 | ||||||
| chr15:45652165
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-6742C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652165 | ||||||
| chr15:45652169
|
C | T | 2 | a0001c0001t0001g0161a0002c0002t0001g0162 | 2 | HG01496.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-17-6738C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652169 | ||||||
| chr15:45652173
|
C | T | 15 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0221others(12): Show | 16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-6734C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652173 | ||||||
| chr15:45652174
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6733G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652174 | ||||||
| chr15:45652327
|
T | C | 1 | a0005c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17-6580T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652327 | ||||||
| chr15:45652396
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(89): Show | 96 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-17-6511G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652396 | ||||||
| chr15:45652427
|
C | A | 1 | a0004c0008t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-6480C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652427 | ||||||
| chr15:45652485
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-6422G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652485 | ||||||
| chr15:45652488
|
C | G | 15 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0221others(12): Show | 16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-6419C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652488 | ||||||
| chr15:45652494
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-17-6413C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652494 | ||||||
| chr15:45652504
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6403G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652504 | ||||||
| chr15:45652510
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-17-6397T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652510 | ||||||
| chr15:45652619
|
T | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(187): Show | 199 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.-17-6288T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652619 | ||||||
| chr15:45652638
|
C | CT | 34 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0086others(31): Show | 35 | HG00408.hp1 HG01106.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17-6243dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | |||||
| chr15:45652638
|
C | CTT | 92 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(89): Show | 97 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-17-6244_-17-6243d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | |||||
| chr15:45652638
|
C | CTTT | 20 | a0001c0001t0001g0029a0001c0001t0001g0061a0001c0001t0001g0062others(17): Show | 20 | HG00621.hp2 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-6245_-17-6243d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | |||||
| chr15:45652638
|
CT | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 46 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-17-6243delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | |||||
| chr15:45652638
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-6252_-17-6243d others(12): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | |||||
| chr15:45652672
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6235C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652672 | ||||||
| chr15:45652673
|
G | A | 1 | a0001c0013t0001g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-17-6234G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652673 | ||||||
| chr15:45652776
|
A | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6131A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652776 | ||||||
| chr15:45652846
|
C | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(92): Show | 99 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-17-6061C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652846 | ||||||
| chr15:45652921
|
C | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(108): Show | 117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-17-5986C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652921 | ||||||
| chr15:45652937
|
C | T | 3 | a0005c0006t0004g0319a0005c0006t0004g0323a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-5970C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652937 | ||||||
| chr15:45652971
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-5936A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652971 | ||||||
| chr15:45653003
|
C | CAATTTTA others(5): Show |
1 | a0001c0001t0001g0116 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-17-5903_-17-5892d others(14): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45653003 | |||||
| chr15:45653008
|
T | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(108): Show | 117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-17-5899T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653008 | ||||||
| chr15:45653098
|
C | G | 1 | a0002c0002t0001g0019 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-17-5809C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653098 | ||||||
| chr15:45653176
|
A | G | 1 | a0001c0001t0007g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-5731A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653176 | ||||||
| chr15:45653246
|
CG | C | 29 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0026others(26): Show | 29 | HG00621.hp2 HG01109.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-5660delG | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653246 | ||||||
| chr15:45653260
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-17-5647G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653260 | ||||||
| chr15:45653276
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(93): Show | 100 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-5631C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653276 | ||||||
| chr15:45653315
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(141): Show | 152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-17-5592C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653315 | ||||||
| chr15:45653372
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(30): Show | 35 | HG01169.hp2 HG01255.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-17-5535A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653372 | ||||||
| chr15:45653387
|
ACT | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 16 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-17-5517_-17-5516d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45653387 | |||||
| chr15:45653455
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(152): Show | 162 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-17-5452T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653455 | ||||||
| chr15:45653456
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-17-5451G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653456 | ||||||
| chr15:45653513
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | NA18993.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-17-5394C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653513 | ||||||
| chr15:45653558
|
A | G | 13 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0182others(10): Show | 13 | HG00735.hp2 HG01081.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-5349A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653558 | ||||||
| chr15:45653614
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(96): Show | 103 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-17-5293G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653614 | ||||||
| chr15:45653639
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(108): Show | 117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-17-5268G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653639 | ||||||
| chr15:45653659
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0308a0002c0002t0001g0019others(2): Show | 5 | HG00621.hp1 HG02015.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-5248C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653659 | ||||||
| chr15:45653663
|
C | T | 1 | a0002c0002t0001g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-17-5244C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653663 | ||||||
| chr15:45653696
|
G | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(10): Show | 14 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-5211G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653696 | ||||||
| chr15:45653702
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(11): Show | 15 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-5205C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653702 | ||||||
| chr15:45653898
|
C | T | 1 | a0002c0002t0001g0327 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-17-5009C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653898 | ||||||
| chr15:45653933
|
C | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-17-4974C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653933 | ||||||
| chr15:45654039
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4868T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654039 | ||||||
| chr15:45654044
|
C | A | 1 | a0002c0002t0001g0175 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-17-4863C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654044 | ||||||
| chr15:45654071
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4836A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654071 | ||||||
| chr15:45654115
|
C | CA | 7 | a0001c0001t0001g0111a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-4773dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654115 | |||||
| chr15:45654115
|
CA | C | 21 | a0001c0001t0001g0042a0001c0001t0001g0082a0001c0001t0001g0104others(18): Show | 21 | HG00735.hp2 HG01081.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4773delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654115 | |||||
| chr15:45654115
|
CAA | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(77): Show | 84 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-4774_-17-4773d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654115 | |||||
| chr15:45654124
|
A | AAAC | 15 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0221others(12): Show | 16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-4781_-17-4780i others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654124 | |||||
| chr15:45654124
|
A | AAC | 72 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(69): Show | 76 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-17-4782_-17-4781i others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654124 | |||||
| chr15:45654130
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4777A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654130 | ||||||
| chr15:45654135
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4772G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654135 | ||||||
| chr15:45654210
|
C | T | 1 | a0002c0002t0001g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17-4697C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654210 | ||||||
| chr15:45654216
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4691T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654216 | ||||||
| chr15:45654243
|
G | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4664G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654243 | ||||||
| chr15:45654419
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(85): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-17-4488A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654419 | ||||||
| chr15:45654433
|
T | C | 4 | a0001c0003t0001g0267a0001c0003t0001g0268a0001c0003t0001g0269others(1): Show | 4 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-4474T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654433 | ||||||
| chr15:45654529
|
T | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0077others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-4378T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654529 | ||||||
| chr15:45654653
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4254G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654653 | ||||||
| chr15:45654672
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4235T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654672 | ||||||
| chr15:45654692
|
C | T | 1 | a0002c0002t0001g0033 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-17-4215C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654692 | ||||||
| chr15:45654779
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(83): Show | 91 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-17-4128T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654779 | ||||||
| chr15:45654884
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4023T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654884 | ||||||
| chr15:45654885
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0021others(69): Show | 75 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-17-4022G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654885 | ||||||
| chr15:45654930
|
G | T | 43 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(40): Show | 44 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-17-3977G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654930 | ||||||
| chr15:45655008
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-3899C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655008 | ||||||
| chr15:45655027
|
G | T | 27 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0055others(24): Show | 29 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-3880G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655027 | ||||||
| chr15:45655195
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(12): Show | 17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-3712C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655195 | ||||||
| chr15:45655212
|
G | A | 2 | a0002c0002t0001g0091a0002c0002t0001g0260 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.-17-3695G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655212 | ||||||
| chr15:45655421
|
G | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0021others(68): Show | 74 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-17-3486G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655421 | ||||||
| chr15:45655427
|
A | G | 1 | a0001c0001t0007g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-3480A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655427 | ||||||
| chr15:45655517
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-17-3390G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655517 | ||||||
| chr15:45655586
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(87): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-3321G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655586 | ||||||
| chr15:45655631
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-3276A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655631 | ||||||
| chr15:45655646
|
G | A | 3 | a0001c0001t0002g0004a0002c0002t0001g0080a0002c0002t0001g0081 | 4 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-3261G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655646 | ||||||
| chr15:45655681
|
C | CT | 7 | a0001c0001t0001g0159a0001c0001t0001g0261a0001c0001t0004g0324others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3212dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655681 | |||||
| chr15:45655681
|
C | CTT | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(138): Show | 149 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.-17-3213_-17-3212d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655681 | |||||
| chr15:45655681
|
C | CTTT | 45 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 46 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-17-3214_-17-3212d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655681 | |||||
| chr15:45655746
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0021others(77): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-3161C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655746 | ||||||
| chr15:45655769
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-17-3138C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655769 | ||||||
| chr15:45655776
|
C | T | 3 | a0001c0003t0001g0268a0001c0003t0001g0269a0001c0003t0001g0282 | 3 | HG00323.hp1 HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-17-3131C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655776 | ||||||
| chr15:45655841
|
G | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0003g0315 | 3 | HG02109.hp1 HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17-3066G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655841 | ||||||
| chr15:45655879
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0021others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-17-3028A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655879 | ||||||
| chr15:45655892
|
G | A | 3 | a0001c0001t0001g0104a0001c0003t0001g0191a0002c0002t0001g0115 | 3 | HG01361.hp1 HG02886.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-17-3015G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655892 | ||||||
| chr15:45655953
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-17-2954A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655953 | ||||||
| chr15:45655971
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 39 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-17-2936C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655971 | ||||||
| chr15:45655986
|
A | AT | 22 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0074others(19): Show | 22 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-2908dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655986 | |||||
| chr15:45655999
|
T | C | 1 | a0001c0001t0004g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17-2908T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655999 | ||||||
| chr15:45655999
|
TC | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0171others(20): Show | 25 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-2904delC | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655999 | |||||
| chr15:45656000
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(150): Show | 160 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-17-2907C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656000 | ||||||
| chr15:45656104
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(198): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-17-2803C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656104 | ||||||
| chr15:45656110
|
A | G | 13 | a0001c0001t0001g0099a0001c0001t0001g0171a0001c0001t0001g0188others(10): Show | 13 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-2797A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656110 | ||||||
| chr15:45656186
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(213): Show | 225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-17-2721G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656186 | ||||||
| chr15:45656335
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-17-2572C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656335 | ||||||
| chr15:45656336
|
T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(216): Show | 228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-17-2571T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656336 | ||||||
| chr15:45656356
|
G | A | 8 | a0001c0001t0001g0232a0001c0001t0001g0259a0001c0003t0001g0079others(5): Show | 8 | HG02647.hp2 HG02698.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-2551G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656356 | ||||||
| chr15:45656456
|
AT | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(133): Show | 142 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-17-2437delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45656456 | |||||
| chr15:45656525
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0209 | 3 | NA18954.hp2 NA19007.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-17-2382C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656525 | ||||||
| chr15:45656536
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.-17-2371T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656536 | ||||||
| chr15:45656731
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(226): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-2176C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656731 | ||||||
| chr15:45656863
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-17-2044G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656863 | ||||||
| chr15:45656880
|
C | CT | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(220): Show | 232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-17-2026dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45656880 | |||||
| chr15:45656917
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(129): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-17-1990G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656917 | ||||||
| chr15:45656944
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(223): Show | 235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-1963A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656944 | ||||||
| chr15:45656961
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-17-1946C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656961 | ||||||
| chr15:45657056
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(226): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-1851T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657056 | ||||||
| chr15:45657107
|
C | CA | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(223): Show | 235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-1800_-17-1799i others(3): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657107 | ||||||
| chr15:45657192
|
T | G | 1 | a0001c0001t0003g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-1715T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657192 | ||||||
| chr15:45657240
|
C | G | 57 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 59 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-1667C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657240 | ||||||
| chr15:45657252
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-1655G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657252 | ||||||
| chr15:45657265
|
A | AT | 19 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(16): Show | 21 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-1631dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | |||||
| chr15:45657265
|
A | ATT | 107 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(104): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-1632_-17-1631d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | |||||
| chr15:45657265
|
A | ATTT | 25 | a0001c0001t0001g0041a0001c0001t0001g0133a0001c0001t0001g0134others(22): Show | 26 | HG00741.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-17-1633_-17-1631d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | |||||
| chr15:45657265
|
A | ATTTT | 76 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0021others(73): Show | 78 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-1634_-17-1631d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | |||||
| chr15:45657288
|
A | T | 10 | a0001c0001t0001g0099a0001c0001t0001g0171a0001c0001t0001g0188others(7): Show | 10 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-1619A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657288 | ||||||
| chr15:45657470
|
T | C | 11 | a0001c0001t0001g0092a0001c0001t0001g0130a0001c0001t0001g0131others(8): Show | 11 | HG00408.hp1 HG00438.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-1437T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657470 | ||||||
| chr15:45657528
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17-1379C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657528 | ||||||
| chr15:45657646
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17-1261A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657646 | ||||||
| chr15:45657676
|
T | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0001g0104others(23): Show | 27 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-1231T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657676 | ||||||
| chr15:45657688
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(120): Show | 127 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-17-1219C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657688 | ||||||
| chr15:45657745
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-1162C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657745 | ||||||
| chr15:45657785
|
T | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(223): Show | 235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-1122T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657785 | ||||||
| chr15:45657940
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(223): Show | 235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-967A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657940 | ||||||
| chr15:45657944
|
A | C | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-17-963A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657944 | ||||||
| chr15:45657961
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(223): Show | 235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-946A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657961 | ||||||
| chr15:45658061
|
G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(225): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-846G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658061 | ||||||
| chr15:45658075
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-832G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658075 | ||||||
| chr15:45658169
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(226): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-738A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658169 | ||||||
| chr15:45658193
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-17-714C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658193 | ||||||
| chr15:45658193
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(222): Show | 234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-17-714C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658193 | ||||||
| chr15:45658203
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-17-704C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658203 | ||||||
| chr15:45658237
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(222): Show | 234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-17-670G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658237 | ||||||
| chr15:45658283
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0165a0001c0001t0001g0171others(39): Show | 45 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-17-624C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658283 | ||||||
| chr15:45658286
|
T | A | 2 | a0001c0001t0001g0098a0004c0008t0001g0164 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-17-621T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658286 | ||||||
| chr15:45658325
|
C | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0244others(15): Show | 20 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-582C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658325 | ||||||
| chr15:45658330
|
C | T | 54 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0061others(51): Show | 56 | HG00323.hp1 HG00438.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.-17-577C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658330 | ||||||
| chr15:45658371
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(221): Show | 233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-17-536G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658371 | ||||||
| chr15:45658484
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0215 | 2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-17-423G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658484 | ||||||
| chr15:45658521
|
C | CACTG | 3 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322 | 3 | HG02717.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-17-385_-17-382dup others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45658521 | |||||
| chr15:45658521
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17-386C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658521 | ||||||
| chr15:45658653
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(220): Show | 233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-17-254A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658653 | ||||||
| chr15:45658663
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-244A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658663 | ||||||
| chr15:45658687
|
C | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(201): Show | 211 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-17-220C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658687 | ||||||
| chr15:45658717
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(199): Show | 209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-17-190C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658717 | ||||||
| chr15:45658760
|
C | T | 81 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0020others(78): Show | 84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-147C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658760 | ||||||
| chr15:45658860
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-17-47C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658860 | ||||||
| chr15:45658866
|
T | G | 51 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0073others(48): Show | 52 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-17-41T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658866 | ||||||
| chr15:45658873
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-17-34C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658873 | ||||||
| chr15:45659195
|
C | CGTGT | 4 | a0001c0001t0004g0324a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+50_234+53dupTG others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45659195 | |||||
| chr15:45659209
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.234+52T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659209 | ||||||
| chr15:45659211
|
A | AGT | 4 | a0001c0001t0001g0099a0001c0001t0001g0312a0001c0003t0001g0079others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+71_234+72dupGT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45659211 | |||||
| chr15:45659211
|
A | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(116): Show | 124 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.234+54A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659211 | ||||||
| chr15:45659215
|
T | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(115): Show | 123 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.234+58T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659215 | ||||||
| chr15:45659273
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(166): Show | 176 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.234+116T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659273 | ||||||
| chr15:45659293
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0299a0002c0002t0001g0048others(3): Show | 6 | NA18982.hp1 NA18984.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+136G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659293 | ||||||
| chr15:45659353
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.234+196A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659353 | ||||||
| chr15:45659462
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234+305A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659462 | ||||||
| chr15:45659512
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0098a0001c0001t0001g0132others(8): Show | 13 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+355C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659512 | ||||||
| chr15:45659523
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234+366T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659523 | ||||||
| chr15:45659540
|
C | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0043others(39): Show | 46 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.234+383C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659540 | ||||||
| chr15:45659613
|
T | C | 8 | a0001c0001t0001g0171a0001c0001t0001g0230a0001c0001t0001g0261others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+456T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659613 | ||||||
| chr15:45659715
|
A | G | 4 | a0001c0001t0001g0183a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+558A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659715 | ||||||
| chr15:45659781
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.234+624C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659781 | ||||||
| chr15:45659797
|
T | G | 1 | a0010c0011t0004g0325 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234+640T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659797 | ||||||
| chr15:45659837
|
CTTTGAGA others(4): Show |
C | 1 | a0001c0001t0001g0291 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.234+682_234+692del others(11): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45659837 | |||||
| chr15:45659962
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234+805G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659962 | ||||||
| chr15:45660229
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.234+1072G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660229 | ||||||
| chr15:45660264
|
A | G | 49 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0041others(46): Show | 49 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.234+1107A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660264 | ||||||
| chr15:45660279
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.234+1122C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660279 | ||||||
| chr15:45660335
|
A | G | 13 | a0001c0001t0001g0026a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+1178A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660335 | ||||||
| chr15:45660455
|
G | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0161a0001c0001t0001g0213others(2): Show | 5 | HG01496.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+1298G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660455 | ||||||
| chr15:45660474
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.234+1317A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660474 | ||||||
| chr15:45660630
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-1325A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660630 | ||||||
| chr15:45660946
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.235-1009C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660946 | ||||||
| chr15:45660950
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0165others(3): Show | 7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-1005G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660950 | ||||||
| chr15:45660961
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-994C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660961 | ||||||
| chr15:45661278
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0263 | 2 | HG00438.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.235-677G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661278 | ||||||
| chr15:45661289
|
T | TA | 3 | a0002c0002t0001g0153a0004c0008t0001g0164a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02809.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.235-666_235-665ins others(1): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAA | 62 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0073others(59): Show | 65 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAA | 31 | a0001c0001t0001g0078a0001c0001t0001g0092a0001c0001t0001g0104others(28): Show | 32 | HG00621.hp2 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(3): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAA | 6 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0099others(3): Show | 6 | HG01257.hp2 HG01981.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAA | 4 | a0001c0001t0001g0069a0001c0001t0001g0116a0001c0001t0001g0261others(1): Show | 4 | HG03669.hp2 HG06807.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAA | 14 | a0001c0001t0001g0074a0001c0001t0001g0097a0001c0001t0001g0121others(11): Show | 14 | HG00639.hp1 HG01243.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAAA | 6 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0106others(3): Show | 6 | HG00558.hp2 HG01106.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0193a0001c0001t0001g0301 | 3 | HG00423.hp2 NA18993.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.235-666_235-665ins others(10): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0061 | 2 | NA18984.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.235-666_235-665ins others(15): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAAA others(9): Show |
8 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0052others(5): Show | 8 | HG00140.hp2 HG01081.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(16): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAAA others(10): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0062others(5): Show | 8 | HG00438.hp1 HG01070.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(17): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAAAAAAA others(15): Show |
1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-666_235-665ins others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAGAA | 29 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0085others(26): Show | 29 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAGAAA | 9 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0197others(6): Show | 9 | HG01099.hp2 HG01346.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
T | TAGAAAAA others(9): Show |
1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.235-666_235-665ins others(16): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
TTAAAA | T | 16 | a0001c0001t0001g0026a0001c0001t0001g0188a0001c0001t0001g0189others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-665_235-661del others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661289
|
TTAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0165others(3): Show | 7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-665_235-657del others(9): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | ||||||
| chr15:45661290
|
T | A | 194 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0027others(191): Show | 198 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.235-665T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661290 | ||||||
| chr15:45661290
|
T | TA | 13 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0001g0146others(10): Show | 13 | HG00140.hp1 HG00741.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-641dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45661290 | |||||
| chr15:45661290
|
TA | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0043others(23): Show | 28 | HG00609.hp2 HG01496.hp1 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-641delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45661290 | |||||
| chr15:45661343
|
A | G | 6 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-612A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661343 | ||||||
| chr15:45661363
|
T | C | 2 | a0001c0003t0001g0150a0001c0003t0001g0163 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.235-592T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661363 | ||||||
| chr15:45661468
|
T | G | 1 | a0001c0003t0001g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235-487T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661468 | ||||||
| chr15:45661557
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-398A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661557 | ||||||
| chr15:45661594
|
A | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | NA18960.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.235-361A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661594 | ||||||
| chr15:45661799
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170 | 3 | HG02165.hp2 HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.235-156C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661799 | ||||||
| chr15:45661810
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0214others(1): Show | 5 | HG01169.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-145C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661810 | ||||||
| chr15:45662136
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.405+11A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662136 | ||||||
| chr15:45662144
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.405+19A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662144 | ||||||
| chr15:45662157
|
A | G | 1 | a0004c0008t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+32A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662157 | ||||||
| chr15:45662278
|
G | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0165others(3): Show | 7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+153G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662278 | ||||||
| chr15:45662280
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0165others(3): Show | 7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+155A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662280 | ||||||
| chr15:45662288
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0165others(3): Show | 7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+163A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662288 | ||||||
| chr15:45662359
|
C | G | 28 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 28 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.405+234C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662359 | ||||||
| chr15:45662608
|
G | A | 26 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0028others(23): Show | 26 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.405+483G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662608 | ||||||
| chr15:45662812
|
A | C | 1 | a0004c0008t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.405+687A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662812 | ||||||
| chr15:45663156
|
T | C | 1 | a0001c0003t0001g0143 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.405+1031T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663156 | ||||||
| chr15:45663303
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0035others(52): Show | 56 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.405+1178C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663303 | ||||||
| chr15:45663634
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0043others(26): Show | 31 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.405+1509G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663634 | ||||||
| chr15:45663733
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.405+1608C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663733 | ||||||
| chr15:45663775
|
T | TA | 5 | a0001c0001t0001g0200a0001c0001t0001g0207a0001c0001t0001g0291others(2): Show | 5 | HG02074.hp2 NA18967.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.405+1658dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45663775 | |||||
| chr15:45663908
|
T | C | 33 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0227others(30): Show | 33 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.405+1783T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663908 | ||||||
| chr15:45663936
|
A | T | 1 | a0001c0001t0001g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.405+1811A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663936 | ||||||
| chr15:45663937
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.405+1812C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663937 | ||||||
| chr15:45663982
|
C | T | 4 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+1857C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663982 | ||||||
| chr15:45663994
|
A | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0028others(22): Show | 25 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.405+1869A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663994 | ||||||
| chr15:45664138
|
A | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0055a0001c0001t0001g0057others(4): Show | 7 | HG00597.hp1 NA18956.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+2013A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664138 | ||||||
| chr15:45664194
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.405+2069T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664194 | ||||||
| chr15:45664195
|
A | G | 2 | a0001c0001t0001g0215a0004c0008t0001g0326 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.405+2070A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664195 | ||||||
| chr15:45664240
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.405+2115T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664240 | ||||||
| chr15:45664584
|
G | A | 4 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+2459G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664584 | ||||||
| chr15:45664595
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+2470C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664595 | ||||||
| chr15:45664607
|
C | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+2482C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664607 | ||||||
| chr15:45664614
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.405+2489A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664614 | ||||||
| chr15:45664654
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.405+2529G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664654 | ||||||
| chr15:45664690
|
G | T | 24 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0028others(21): Show | 24 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.405+2565G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664690 | ||||||
| chr15:45664704
|
G | C | 1 | a0002c0002t0001g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.405+2579G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664704 | ||||||
| chr15:45664940
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.405+2815G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664940 | ||||||
| chr15:45665040
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+2915G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665040 | ||||||
| chr15:45665085
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.405+2960G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665085 | ||||||
| chr15:45665308
|
C | T | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.405+3183C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665308 | ||||||
| chr15:45665321
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.405+3196A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665321 | ||||||
| chr15:45665343
|
A | G | 2 | a0001c0001t0001g0186a0008c0014t0001g0185 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.405+3218A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665343 | ||||||
| chr15:45665537
|
AT | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(176): Show | 185 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.405+3415delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45665537 | |||||
| chr15:45665584
|
C | CT | 15 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0113others(12): Show | 16 | HG00423.hp1 HG01169.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.405+3475dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45665584 | |||||
| chr15:45665584
|
CT | C | 7 | a0001c0001t0001g0100a0001c0001t0001g0232a0002c0002t0001g0153others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+3475delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45665584 | |||||
| chr15:45665704
|
C | T | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.405+3579C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665704 | ||||||
| chr15:45665740
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.405+3615C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665740 | ||||||
| chr15:45665750
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+3625A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665750 | ||||||
| chr15:45665752
|
T | A | 87 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(84): Show | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.405+3627T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665752 | ||||||
| chr15:45665775
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(46): Show | 51 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.405+3650G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665775 | ||||||
| chr15:45665862
|
G | A | 1 | a0004c0008t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+3737G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665862 | ||||||
| chr15:45665924
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.405+3799A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665924 | ||||||
| chr15:45665999
|
G | A | 2 | a0004c0008t0001g0164a0004c0008t0001g0231 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.405+3874G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665999 | ||||||
| chr15:45666033
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.406-3895G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666033 | ||||||
| chr15:45666204
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.406-3724A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666204 | ||||||
| chr15:45666329
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.406-3599C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666329 | ||||||
| chr15:45666342
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.406-3586G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666342 | ||||||
| chr15:45666511
|
G | A | 87 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(84): Show | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.406-3417G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666511 | ||||||
| chr15:45666555
|
A | G | 1 | a0002c0002t0001g0046 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.406-3373A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666555 | ||||||
| chr15:45666651
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(49): Show | 54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.406-3277A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666651 | ||||||
| chr15:45666774
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.406-3154T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666774 | ||||||
| chr15:45666789
|
T | TCTCTCCC others(13): Show |
39 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0047others(36): Show | 40 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.406-3102_406-3083d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666789 | |||||
| chr15:45666803
|
T | C | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.406-3125T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666803 | ||||||
| chr15:45666819
|
C | CCCCTCCT others(20): Show |
1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3083_406-3082i others(29): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666819 | |||||
| chr15:45666831
|
T | TCTCCCCT others(18): Show |
4 | a0001c0001t0001g0165a0001c0003t0001g0143a0001c0003t0001g0233others(1): Show | 4 | HG01169.hp1 HG02698.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3083_406-3082i others(27): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666831 | |||||
| chr15:45666836
|
C | CCTCCCCT others(13): Show |
6 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-3077_406-3058d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666836 | |||||
| chr15:45666836
|
C | CCTCCCCT others(12): Show |
1 | a0001c0001t0001g0064 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.406-3082_406-3081i others(21): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666836 | |||||
| chr15:45666841
|
CCTCCCCT others(3): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.406-3082_406-3073d others(12): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666841 | |||||
| chr15:45666846
|
C | T | 4 | a0001c0001t0001g0165a0001c0003t0001g0143a0001c0003t0001g0233others(1): Show | 4 | HG01169.hp1 HG02698.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3082C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666846 | ||||||
| chr15:45666851
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.406-3077T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666851 | ||||||
| chr15:45666856
|
T | C | 4 | a0001c0001t0001g0165a0001c0003t0001g0143a0001c0003t0001g0233others(1): Show | 4 | HG01169.hp1 HG02698.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3072T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666856 | ||||||
| chr15:45666856
|
T | TCTCCC | 18 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0113others(15): Show | 19 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-3052_406-3048d others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666856 | |||||
| chr15:45666856
|
TCTCCC | T | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(87): Show | 93 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.406-3052_406-3048d others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666856 | |||||
| chr15:45666861
|
C | CCTCCCCT others(13): Show |
48 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(45): Show | 50 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.406-3053_406-3052i others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666861 | |||||
| chr15:45666861
|
C | CCTCCCCT others(13): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.406-3053_406-3052i others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666861 | |||||
| chr15:45666861
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0261 | 2 | HG03669.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.406-3067C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666861 | ||||||
| chr15:45666866
|
C | T | 1 | a0002c0002t0005g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.406-3062C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666866 | ||||||
| chr15:45666909
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0261a0004c0008t0001g0164others(1): Show | 4 | HG00738.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3019T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666909 | ||||||
| chr15:45666924
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3004C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666924 | ||||||
| chr15:45666927
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3001T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666927 | ||||||
| chr15:45666928
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3000C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666928 | ||||||
| chr15:45666939
|
T | TCCTTTCT others(12): Show |
10 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0137others(7): Show | 10 | HG00741.hp1 HG01496.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.406-2985_406-2967d others(21): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666939 | |||||
| chr15:45666956
|
T | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(49): Show | 54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.406-2972T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666956 | ||||||
| chr15:45666989
|
C | T | 89 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(86): Show | 92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.406-2939C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666989 | ||||||
| chr15:45667011
|
C | CCCCT | 84 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(81): Show | 87 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.406-2900_406-2897d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | |||||
| chr15:45667011
|
C | CCCCTCCC others(5): Show |
1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.406-2908_406-2897d others(14): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | |||||
| chr15:45667011
|
C | CCCCTCCC others(13): Show |
1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406-2916_406-2897d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | |||||
| chr15:45667011
|
CCCCT | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-2900_406-2897d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | |||||
| chr15:45667028
|
C | CCCTCCCT others(9): Show |
50 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(47): Show | 52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.406-2897_406-2896i others(18): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667028 | |||||
| chr15:45667028
|
C | CCCTCCCT others(5): Show |
1 | a0001c0001t0001g0065 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.406-2897_406-2896i others(14): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667028 | |||||
| chr15:45667028
|
C | CCCTCCCT others(1): Show |
3 | a0001c0001t0001g0261a0004c0008t0001g0164a0004c0008t0001g0231 | 3 | HG02809.hp2 HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.406-2897_406-2896i others(10): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667028 | |||||
| chr15:45667032
|
T | C | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.406-2896T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667032 | ||||||
| chr15:45667049
|
T | C | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.406-2879T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667049 | ||||||
| chr15:45667127
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406-2801T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667127 | ||||||
| chr15:45667140
|
C | T | 1 | a0002c0002t0001g0199 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.406-2788C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667140 | ||||||
| chr15:45667141
|
T | C | 1 | a0002c0002t0001g0199 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.406-2787T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667141 | ||||||
| chr15:45667142
|
C | T | 1 | a0002c0002t0001g0199 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.406-2786C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667142 | ||||||
| chr15:45667175
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.406-2753T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667175 | ||||||
| chr15:45667255
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(242): Show | 253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.406-2673A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667255 | ||||||
| chr15:45667316
|
A | T | 87 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(84): Show | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.406-2612A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667316 | ||||||
| chr15:45667647
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.406-2281C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667647 | ||||||
| chr15:45667763
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2165G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667763 | ||||||
| chr15:45667764
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2164T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667764 | ||||||
| chr15:45667765
|
T | A | 1 | a0001c0001t0001g0200 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2163T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667765 | ||||||
| chr15:45667768
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2160C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667768 | ||||||
| chr15:45667769
|
A | C | 1 | a0001c0001t0001g0200 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2159A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667769 | ||||||
| chr15:45667778
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2150A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667778 | ||||||
| chr15:45667837
|
G | T | 1 | a0004c0008t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.406-2091G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667837 | ||||||
| chr15:45667859
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-2069C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667859 | ||||||
| chr15:45667918
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.406-2010T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667918 | ||||||
| chr15:45667925
|
A | C | 5 | a0001c0001t0001g0262a0002c0002t0001g0088a0002c0002t0001g0089others(2): Show | 5 | HG02717.hp1 HG02809.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.406-2003A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667925 | ||||||
| chr15:45667941
|
C | CT | 63 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(60): Show | 64 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.406-1966dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667941 | |||||
| chr15:45667941
|
C | CTT | 10 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG01169.hp2 HG01433.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.406-1967_406-1966d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667941 | |||||
| chr15:45667941
|
CT | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0021others(144): Show | 152 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.406-1966delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667941 | |||||
| chr15:45667945
|
T | C | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.406-1983T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667945 | ||||||
| chr15:45667946
|
T | C | 88 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(85): Show | 91 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.406-1982T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667946 | ||||||
| chr15:45667947
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0261 | 2 | HG02145.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.406-1981T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667947 | ||||||
| chr15:45667948
|
T | C | 1 | a0002c0002t0001g0149 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.406-1980T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667948 | ||||||
| chr15:45668006
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.406-1922G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668006 | ||||||
| chr15:45668018
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.406-1910C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668018 | ||||||
| chr15:45668143
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(205): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.406-1785G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668143 | ||||||
| chr15:45668190
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.406-1738C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668190 | ||||||
| chr15:45668205
|
A | T | 2 | a0005c0006t0004g0319a0005c0006t0004g0323 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.406-1723A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668205 | ||||||
| chr15:45668234
|
G | A | 1 | a0002c0002t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.406-1694G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668234 | ||||||
| chr15:45668279
|
G | A | 1 | a0011c0010t0001g0283 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.406-1649G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668279 | ||||||
| chr15:45668350
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.406-1578A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668350 | ||||||
| chr15:45668591
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-1337C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668591 | ||||||
| chr15:45668608
|
A | G | 1 | a0002c0002t0001g0088 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.406-1320A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668608 | ||||||
| chr15:45668626
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.406-1302G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668626 | ||||||
| chr15:45668699
|
C | T | 12 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0137others(9): Show | 12 | HG00741.hp1 HG01496.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.406-1229C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668699 | ||||||
| chr15:45668703
|
C | T | 2 | a0004c0008t0001g0164a0004c0008t0001g0231 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.406-1225C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668703 | ||||||
| chr15:45668927
|
G | A | 1 | a0002c0004t0001g0248 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.406-1001G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668927 | ||||||
| chr15:45668960
|
A | G | 1 | a0002c0002t0001g0157 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.406-968A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668960 | ||||||
| chr15:45669160
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0003g0317others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-768A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669160 | ||||||
| chr15:45669162
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.406-766T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669162 | ||||||
| chr15:45669175
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.406-753T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669175 | ||||||
| chr15:45669176
|
T | A | 4 | a0001c0001t0001g0261a0002c0002t0001g0019a0004c0008t0001g0164others(1): Show | 4 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-752T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669176 | ||||||
| chr15:45669178
|
A | AT | 93 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(90): Show | 96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.406-741dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45669178 | |||||
| chr15:45669178
|
A | ATT | 55 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(52): Show | 57 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.406-742_406-741dup others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45669178 | |||||
| chr15:45669178
|
A | T | 1 | a0002c0002t0001g0019 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.406-750A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669178 | ||||||
| chr15:45669206
|
A | G | 3 | a0001c0001t0001g0228a0001c0007t0001g0008a0001c0007t0001g0226 | 4 | HG01884.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-722A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669206 | ||||||
| chr15:45669413
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.406-515C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669413 | ||||||
| chr15:45669756
|
C | T | 3 | a0001c0001t0001g0261a0004c0008t0001g0164a0004c0008t0001g0231 | 3 | HG02809.hp2 HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.406-172C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669756 | ||||||
| chr15:45669794
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406-134C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669794 | ||||||
| chr15:45669843
|
A | G | 5 | a0001c0003t0001g0143a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.406-85A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669843 | ||||||
| chr15:45669885
|
C | T | 3 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | NA18942.hp2 NA18978.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.406-43C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669885 | ||||||
| chr15:45669986
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp2 | splice_region_variant&intron_variant | LOW | c.459+5C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45669986 | ||||||
| chr15:45670084
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+103C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670084 | ||||||
| chr15:45670094
|
C | A | 1 | a0001c0001t0002g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.459+113C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670094 | ||||||
| chr15:45670158
|
T | C | 1 | a0002c0002t0005g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.459+177T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670158 | ||||||
| chr15:45670389
|
G | A | 1 | a0004c0008t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.459+408G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670389 | ||||||
| chr15:45670402
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.459+421G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670402 | ||||||
| chr15:45670429
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.459+448A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670429 | ||||||
| chr15:45670507
|
T | G | 1 | a0001c0003t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459+526T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670507 | ||||||
| chr15:45670546
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.459+565T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670546 | ||||||
| chr15:45670679
|
C | T | 1 | a0002c0002t0001g0037 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.459+698C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670679 | ||||||
| chr15:45670854
|
T | A | 12 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0137others(9): Show | 12 | HG00741.hp1 HG01496.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+873T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670854 | ||||||
| chr15:45671064
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.459+1083A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671064 | ||||||
| chr15:45671068
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.459+1087T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671068 | ||||||
| chr15:45671308
|
C | A | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.459+1327C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671308 | ||||||
| chr15:45671413
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459+1432C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671413 | ||||||
| chr15:45671442
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(208): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.459+1461A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671442 | ||||||
| chr15:45671589
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.459+1608C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671589 | ||||||
| chr15:45671595
|
C | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.459+1614C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671595 | ||||||
| chr15:45671840
|
A | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0092others(23): Show | 27 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-1767A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671840 | ||||||
| chr15:45672014
|
C | T | 4 | a0002c0002t0001g0025a0004c0008t0001g0164a0004c0008t0001g0231others(1): Show | 4 | HG02809.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1593C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672014 | ||||||
| chr15:45672063
|
C | T | 5 | a0001c0001t0001g0261a0001c0001t0004g0324a0004c0008t0001g0164others(2): Show | 5 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-1544C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672063 | ||||||
| chr15:45672069
|
C | T | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1538C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672069 | ||||||
| chr15:45672105
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0312 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.460-1502T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672105 | ||||||
| chr15:45672381
|
A | C | 1 | a0002c0002t0001g0032 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.460-1226A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672381 | ||||||
| chr15:45672534
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.460-1073A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672534 | ||||||
| chr15:45672612
|
T | C | 5 | a0001c0001t0001g0261a0001c0001t0004g0324a0004c0008t0001g0164others(2): Show | 5 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-995T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672612 | ||||||
| chr15:45672675
|
A | T | 3 | a0004c0008t0001g0164a0004c0008t0001g0231a0004c0008t0001g0326 | 3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460-932A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672675 | ||||||
| chr15:45672950
|
C | CAG | 167 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(164): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.460-656_460-655dup others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 45672950 | |||||
| chr15:45673243
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(49): Show | 54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.460-364A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673243 | ||||||
| chr15:45673316
|
G | A | 1 | a0002c0002t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.460-291G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673316 | ||||||
| chr15:45673443
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.460-164C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673443 | ||||||
| chr15:45673487
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.460-120G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673487 | ||||||
| chr15:45673903
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(49): Show | 54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.654+102C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45673903 | ||||||
| chr15:45674069
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0050others(5): Show | 10 | HG00609.hp2 HG01496.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+268T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674069 | ||||||
| chr15:45674087
|
C | T | 1 | a0011c0010t0001g0283 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.654+286C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674087 | ||||||
| chr15:45674158
|
T | C | 12 | a0001c0001t0001g0218a0001c0001t0001g0232a0001c0001t0001g0242others(9): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.654+357T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674158 | ||||||
| chr15:45674174
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0165others(3): Show | 7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+373C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674174 | ||||||
| chr15:45674301
|
G | A | 11 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0320others(8): Show | 12 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+500G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674301 | ||||||
| chr15:45674427
|
C | T | 19 | a0001c0001t0001g0026a0001c0001t0001g0092a0001c0001t0001g0137others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.654+626C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674427 | ||||||
| chr15:45674435
|
C | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0137others(5): Show | 8 | HG00741.hp1 HG01496.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+634C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674435 | ||||||
| chr15:45674440
|
T | TA | 6 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0214others(3): Show | 7 | HG01169.hp2 HG01243.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+654dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45674440 | |||||
| chr15:45674440
|
TA | T | 10 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0126others(7): Show | 10 | HG01069.hp2 HG02293.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+654delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45674440 | |||||
| chr15:45674455
|
A | G | 1 | a0001c0001t0003g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.654+654A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674455 | ||||||
| chr15:45674620
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.654+819C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674620 | ||||||
| chr15:45674677
|
GA | G | 19 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0106others(16): Show | 19 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.654+880delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45674677 | |||||
| chr15:45674689
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.654+888T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674689 | ||||||
| chr15:45674726
|
C | A | 1 | a0007c0015t0001g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.654+925C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674726 | ||||||
| chr15:45674740
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654+939G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674740 | ||||||
| chr15:45674816
|
G | T | 4 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1015G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674816 | ||||||
| chr15:45674926
|
C | T | 1 | a0002c0002t0001g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.654+1125C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674926 | ||||||
| chr15:45675197
|
G | A | 1 | a0001c0003t0001g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.655-904G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675197 | ||||||
| chr15:45675345
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.655-756A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675345 | ||||||
| chr15:45675399
|
A | AT | 89 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0171others(86): Show | 92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.655-690dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45675399 | |||||
| chr15:45675402
|
T | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.655-699T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675402 | ||||||
| chr15:45675412
|
G | T | 89 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0171others(86): Show | 92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.655-689G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675412 | ||||||
| chr15:45675434
|
A | T | 1 | a0002c0002t0001g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.655-667A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675434 | ||||||
| chr15:45675509
|
C | T | 16 | a0001c0001t0001g0026a0001c0001t0001g0092a0001c0003t0001g0034others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.655-592C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675509 | ||||||
| chr15:45675540
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655-561G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675540 | ||||||
| chr15:45675592
|
C | T | 1 | a0002c0002t0001g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.655-509C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675592 | ||||||
| chr15:45675651
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.655-450C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675651 | ||||||
| chr15:45676039
|
T | TA | 86 | a0001c0001t0001g0171a0002c0002t0001g0003a0002c0002t0001g0005others(83): Show | 89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.655-50dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45676039 | |||||
| chr15:45676061
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.655-40A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45676061 | ||||||
| chr15:45676069
|
T | G | 1 | a0004c0008t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655-32T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45676069 | ||||||
| chr15:45676337
|
A | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(246): Show | 257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.864+27A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676337 | ||||||
| chr15:45676343
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.864+33C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676343 | ||||||
| chr15:45676587
|
C | T | 4 | a0001c0001t0002g0144a0004c0008t0001g0164a0004c0008t0001g0231others(1): Show | 4 | HG02809.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+277C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676587 | ||||||
| chr15:45676657
|
C | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0073others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.864+347C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676657 | ||||||
| chr15:45676933
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.864+623C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676933 | ||||||
| chr15:45676973
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.864+663G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676973 | ||||||
| chr15:45677006
|
A | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 13 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+696A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677006 | ||||||
| chr15:45677039
|
T | TA | 102 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0026others(99): Show | 106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.864+746dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45677039 | |||||
| chr15:45677039
|
T | TAA | 6 | a0002c0002t0001g0018a0002c0002t0001g0140a0002c0002t0001g0212others(3): Show | 6 | HG00597.hp2 HG02055.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+745_864+746dup others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45677039 | |||||
| chr15:45677040
|
A | T | 4 | a0001c0001t0001g0261a0004c0008t0001g0164a0004c0008t0001g0231others(1): Show | 4 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+730A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677040 | ||||||
| chr15:45677053
|
A | G | 2 | a0004c0008t0001g0164a0004c0008t0001g0326 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.864+743A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677053 | ||||||
| chr15:45677065
|
C | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+755C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677065 | ||||||
| chr15:45677167
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0262 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.864+857T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677167 | ||||||
| chr15:45677177
|
TCTTC | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0062others(40): Show | 46 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.864+888_864+891del others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45677177 | |||||
| chr15:45677423
|
A | G | 2 | a0002c0002t0001g0229a0002c0002t0001g0327 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.864+1113A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677423 | ||||||
| chr15:45677582
|
C | T | 17 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0073others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.864+1272C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677582 | ||||||
| chr15:45677724
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1414G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677724 | ||||||
| chr15:45677829
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.864+1519T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677829 | ||||||
| chr15:45677831
|
G | A | 2 | a0001c0003t0001g0079a0001c0003t0001g0172 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.864+1521G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677831 | ||||||
| chr15:45677867
|
A | C | 22 | a0001c0001t0001g0099a0001c0001t0001g0130a0001c0001t0001g0133others(19): Show | 23 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.864+1557A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677867 | ||||||
| chr15:45677905
|
A | G | 1 | a0001c0003t0001g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.864+1595A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677905 | ||||||
| chr15:45677933
|
G | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(212): Show | 221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.864+1623G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677933 | ||||||
| chr15:45678014
|
CTGTT | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0067others(21): Show | 25 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.864+1709_864+1712d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45678014 | |||||
| chr15:45678115
|
T | A | 1 | a0001c0001t0002g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.864+1805T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678115 | ||||||
| chr15:45678478
|
G | A | 21 | a0001c0001t0001g0092a0001c0003t0001g0034a0001c0003t0001g0079others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.864+2168G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678478 | ||||||
| chr15:45678493
|
T | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.864+2183T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678493 | ||||||
| chr15:45678503
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.864+2193C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678503 | ||||||
| chr15:45678605
|
C | T | 2 | a0002c0002t0001g0024a0002c0002t0001g0236 | 2 | NA18948.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.864+2295C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678605 | ||||||
| chr15:45678654
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0227 | 3 | HG01884.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.864+2344C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678654 | ||||||
| chr15:45678656
|
G | C | 21 | a0001c0001t0001g0099a0001c0001t0001g0130a0001c0001t0001g0133others(18): Show | 22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.864+2346G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678656 | ||||||
| chr15:45678707
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.864+2397T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678707 | ||||||
| chr15:45678769
|
T | C | 1 | a0002c0002t0001g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.864+2459T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678769 | ||||||
| chr15:45678885
|
T | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+2575T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678885 | ||||||
| chr15:45678932
|
C | T | 21 | a0001c0001t0001g0092a0001c0003t0001g0034a0001c0003t0001g0079others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.864+2622C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678932 | ||||||
| chr15:45678983
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.864+2673G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678983 | ||||||
| chr15:45679469
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.865-3009C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679469 | ||||||
| chr15:45679557
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.865-2921C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679557 | ||||||
| chr15:45679593
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(245): Show | 256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.865-2885T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679593 | ||||||
| chr15:45679625
|
G | T | 1 | a0011c0010t0001g0283 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.865-2853G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679625 | ||||||
| chr15:45679730
|
A | G | 1 | a0009c0012t0001g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.865-2748A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679730 | ||||||
| chr15:45679847
|
C | T | 4 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-2631C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679847 | ||||||
| chr15:45679968
|
T | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0028others(97): Show | 104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.865-2510T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679968 | ||||||
| chr15:45679994
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(322): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.865-2484G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679994 | ||||||
| chr15:45680044
|
A | G | 47 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.865-2434A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680044 | ||||||
| chr15:45680083
|
TTTTC | T | 9 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0024others(6): Show | 9 | HG00621.hp1 HG02683.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.865-2383_865-2380d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45680083 | |||||
| chr15:45680124
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-2354G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680124 | ||||||
| chr15:45680130
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(102): Show | 107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.865-2348T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680130 | ||||||
| chr15:45680138
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(55): Show | 60 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.865-2340A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680138 | ||||||
| chr15:45680415
|
T | C | 1 | a0002c0002t0001g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.865-2063T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680415 | ||||||
| chr15:45680416
|
C | T | 1 | a0002c0002t0001g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.865-2062C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680416 | ||||||
| chr15:45680806
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.865-1672A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680806 | ||||||
| chr15:45680918
|
G | A | 4 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-1560G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680918 | ||||||
| chr15:45681067
|
C | G | 3 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.865-1411C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681067 | ||||||
| chr15:45681078
|
G | A | 1 | a0001c0001t0001g0010 | 2 | NA18947.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.865-1400G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681078 | ||||||
| chr15:45681087
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.865-1391G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681087 | ||||||
| chr15:45681089
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0052 | 3 | NA18949.hp1 NA18950.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.865-1389G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681089 | ||||||
| chr15:45681128
|
A | G | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.865-1350A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681128 | ||||||
| chr15:45681216
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-1262T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681216 | ||||||
| chr15:45681254
|
T | A | 1 | a0002c0002t0001g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.865-1224T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681254 | ||||||
| chr15:45681305
|
G | C | 47 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.865-1173G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681305 | ||||||
| chr15:45681312
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0027others(58): Show | 63 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.865-1166C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681312 | ||||||
| chr15:45681321
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-1157A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681321 | ||||||
| chr15:45681372
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(230): Show | 240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.865-1106G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681372 | ||||||
| chr15:45681508
|
C | T | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-970C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681508 | ||||||
| chr15:45681519
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-959G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681519 | ||||||
| chr15:45681728
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0028others(79): Show | 86 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.865-750C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681728 | ||||||
| chr15:45681981
|
G | C | 1 | a0002c0002t0001g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.865-497G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681981 | ||||||
| chr15:45682048
|
T | C | 21 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0095others(18): Show | 21 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.865-430T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682048 | ||||||
| chr15:45682145
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.865-333T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682145 | ||||||
| chr15:45682225
|
G | A | 4 | a0002c0002t0001g0019a0002c0002t0001g0053a0002c0002t0001g0070others(1): Show | 4 | HG00621.hp1 NA18612.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-253G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682225 | ||||||
| chr15:45682287
|
A | G | 1 | a0001c0001t0007g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.865-191A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682287 | ||||||
| chr15:45682317
|
A | G | 1 | a0002c0002t0001g0157 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.865-161A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682317 | ||||||
| chr15:45682338
|
G | A | 50 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(47): Show | 50 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.865-140G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682338 | ||||||
| chr15:45682395
|
A | G | 51 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.865-83A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682395 | ||||||
| chr15:45682430
|
G | A | 74 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0100others(71): Show | 77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.865-48G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682430 | ||||||
| chr15:45682454
|
T | C | 8 | a0001c0001t0001g0171a0004c0008t0001g0164a0004c0008t0001g0231others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-24T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682454 | ||||||
| chr15:45682671
|
C | T | 9 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0137others(6): Show | 9 | HG00741.hp1 HG01496.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+10C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682671 | ||||||
| chr15:45682715
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1048+54A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682715 | ||||||
| chr15:45682733
|
C | A | 3 | a0004c0008t0001g0164a0004c0008t0001g0231a0004c0008t0001g0326 | 3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+72C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682733 | ||||||
| chr15:45682899
|
C | T | 1 | a0001c0003t0001g0258 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1048+238C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682899 | ||||||
| chr15:45682914
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1048+253C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682914 | ||||||
| chr15:45682990
|
C | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+329C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682990 | ||||||
| chr15:45683026
|
C | CA | 47 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0099others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1048+381dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | |||||
| chr15:45683026
|
C | CAAAAAAA others(22): Show |
1 | a0004c0008t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048+381_1048+382i others(31): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | |||||
| chr15:45683026
|
C | CAAAAAAA others(24): Show |
2 | a0004c0008t0001g0164a0004c0008t0001g0326 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+381_1048+382i others(33): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | |||||
| chr15:45683026
|
CA | C | 48 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0073others(45): Show | 49 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1048+381delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | |||||
| chr15:45683057
|
A | C | 1 | a0004c0008t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048+396A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683057 | ||||||
| chr15:45683068
|
G | A | 18 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0073others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1048+407G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683068 | ||||||
| chr15:45683072
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0312 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1048+411A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683072 | ||||||
| chr15:45683153
|
G | T | 3 | a0004c0008t0001g0164a0004c0008t0001g0231a0004c0008t0001g0326 | 3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+492G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683153 | ||||||
| chr15:45683177
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0225 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048+516A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683177 | ||||||
| chr15:45683206
|
GCT | G | 20 | a0001c0003t0001g0034a0001c0003t0001g0079a0001c0003t0001g0129others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1048+550_1048+551d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683206 | |||||
| chr15:45683215
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1048+554A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683215 | ||||||
| chr15:45683222
|
T | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(6): Show | 9 | HG00558.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+561T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683222 | ||||||
| chr15:45683245
|
G | A | 3 | a0004c0008t0001g0164a0004c0008t0001g0231a0004c0008t0001g0326 | 3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+584G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683245 | ||||||
| chr15:45683308
|
C | T | 2 | a0002c0002t0001g0091a0002c0002t0001g0260 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1048+647C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683308 | ||||||
| chr15:45683314
|
A | T | 2 | a0002c0002t0001g0091a0002c0002t0001g0260 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1048+653A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683314 | ||||||
| chr15:45683319
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1048+658G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683319 | ||||||
| chr15:45683327
|
T | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(150): Show | 160 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1048+666T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683327 | ||||||
| chr15:45683350
|
G | C | 73 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(70): Show | 74 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1048+689G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683350 | ||||||
| chr15:45683391
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1048+730A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683391 | ||||||
| chr15:45683629
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1048+968A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683629 | ||||||
| chr15:45683679
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0189others(1): Show | 4 | HG00741.hp1 HG02698.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+1018A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683679 | ||||||
| chr15:45683799
|
G | T | 1 | a0002c0002t0001g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1048+1138G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683799 | ||||||
| chr15:45683854
|
A | ATG | 9 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0261others(6): Show | 9 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1048+1211_1048+121 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683854 | |||||
| chr15:45683877
|
T | C | 1 | a0004c0008t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048+1216T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683877 | ||||||
| chr15:45683890
|
A | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1048+1229A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683890 | ||||||
| chr15:45683892
|
TTTTG | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0067others(68): Show | 72 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1048+1255_1048+125 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683892 | |||||
| chr15:45683892
|
TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1048+1247_1048+125 others(16): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683892 | |||||
| chr15:45683896
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1048+1235G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683896 | ||||||
| chr15:45683958
|
C | G | 19 | a0001c0003t0001g0034a0001c0003t0001g0079a0001c0003t0001g0129others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1048+1297C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683958 | ||||||
| chr15:45684005
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1048+1344A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684005 | ||||||
| chr15:45684078
|
AT | A | 69 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(66): Show | 69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1048+1425delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684078 | |||||
| chr15:45684204
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1048+1543C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684204 | ||||||
| chr15:45684220
|
A | G | 1 | a0002c0002t0005g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1048+1559A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684220 | ||||||
| chr15:45684306
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1048+1645G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684306 | ||||||
| chr15:45684309
|
A | G | 19 | a0001c0001t0001g0099a0001c0001t0001g0130a0001c0001t0001g0133others(16): Show | 19 | HG00741.hp1 HG01496.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1048+1648A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684309 | ||||||
| chr15:45684421
|
A | C | 22 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(19): Show | 22 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1048+1760A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684421 | ||||||
| chr15:45684459
|
T | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(2): Show | 5 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+1798T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684459 | ||||||
| chr15:45684498
|
T | G | 73 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1048+1837T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684498 | ||||||
| chr15:45684592
|
T | TTC | 135 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0026others(132): Show | 140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1048+1951_1048+195 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | |||||
| chr15:45684592
|
TTC | T | 73 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1048+1951_1048+195 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | |||||
| chr15:45684592
|
TTCTC | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0227 | 3 | HG01884.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1048+1949_1048+195 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | |||||
| chr15:45684592
|
TTCTCTC | T | 3 | a0002c0002t0001g0072a0002c0002t0001g0117a0002c0002t0006g0031 | 3 | HG00609.hp1 HG02523.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1048+1947_1048+195 others(10): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | |||||
| chr15:45684614
|
T | C | 1 | a0001c0001t0001g0305 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1048+1953T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684614 | ||||||
| chr15:45684916
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1048+2255C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684916 | ||||||
| chr15:45685106
|
A | G | 1 | a0002c0002t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1048+2445A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685106 | ||||||
| chr15:45685114
|
C | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(2): Show | 5 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+2453C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685114 | ||||||
| chr15:45685150
|
C | T | 1 | a0002c0002t0001g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1048+2489C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685150 | ||||||
| chr15:45685162
|
C | T | 70 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1048+2501C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685162 | ||||||
| chr15:45685294
|
T | TCCCA | 4 | a0005c0006t0001g0311a0005c0006t0004g0319a0005c0006t0004g0323others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+2634_1048+263 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45685294 | |||||
| chr15:45685360
|
T | C | 72 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1048+2699T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685360 | ||||||
| chr15:45685431
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0214others(1): Show | 5 | HG01169.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+2770C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685431 | ||||||
| chr15:45685484
|
C | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(2): Show | 5 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+2823C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685484 | ||||||
| chr15:45685554
|
C | T | 69 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0069others(66): Show | 69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1049-2783C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685554 | ||||||
| chr15:45685680
|
C | A | 21 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(18): Show | 21 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1049-2657C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685680 | ||||||
| chr15:45685767
|
G | A | 1 | a0002c0002t0001g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1049-2570G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685767 | ||||||
| chr15:45685994
|
C | G | 76 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0100others(73): Show | 79 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1049-2343C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685994 | ||||||
| chr15:45686077
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1049-2260C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686077 | ||||||
| chr15:45686100
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0078 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1049-2237C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686100 | ||||||
| chr15:45686152
|
A | AAT | 37 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(34): Show | 39 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1049-2170_1049-216 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45686152 | |||||
| chr15:45686152
|
A | AATAT | 76 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0100others(73): Show | 79 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1049-2172_1049-216 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45686152 | |||||
| chr15:45686194
|
C | T | 61 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1049-2143C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686194 | ||||||
| chr15:45686195
|
G | A | 61 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1049-2142G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686195 | ||||||
| chr15:45686256
|
A | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0232a0001c0001t0001g0242others(4): Show | 7 | HG02559.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2081A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686256 | ||||||
| chr15:45686323
|
C | T | 61 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1049-2014C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686323 | ||||||
| chr15:45686437
|
C | A | 1 | a0001c0001t0007g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049-1900C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686437 | ||||||
| chr15:45686439
|
A | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(5): Show | 8 | HG00558.hp1 HG02055.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1898A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686439 | ||||||
| chr15:45686446
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1049-1891C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686446 | ||||||
| chr15:45686448
|
G | A | 118 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0028others(115): Show | 123 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1049-1889G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686448 | ||||||
| chr15:45686648
|
C | A | 78 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0100others(75): Show | 81 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1049-1689C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686648 | ||||||
| chr15:45686716
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1049-1621C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686716 | ||||||
| chr15:45686765
|
A | G | 1 | a0004c0008t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1049-1572A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686765 | ||||||
| chr15:45686974
|
A | C | 1 | a0001c0001t0007g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049-1363A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686974 | ||||||
| chr15:45687048
|
C | T | 2 | a0001c0001t0001g0180a0004c0008t0001g0231 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1049-1289C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687048 | ||||||
| chr15:45687080
|
G | A | 1 | a0001c0001t0004g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1049-1257G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687080 | ||||||
| chr15:45687127
|
G | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(5): Show | 8 | HG00558.hp1 HG02055.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1210G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687127 | ||||||
| chr15:45687493
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0223 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1049-844G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687493 | ||||||
| chr15:45687590
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1049-747C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687590 | ||||||
| chr15:45687593
|
G | GA | 68 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(65): Show | 69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1049-737dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45687593 | |||||
| chr15:45687742
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0014a0001c0001t0002g0107others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-595G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687742 | ||||||
| chr15:45687743
|
TTCTG | T | 80 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0028others(77): Show | 84 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1049-578_1049-575d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45687743 | |||||
| chr15:45687946
|
TG | T | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-387delG | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45687946 | |||||
| chr15:45687965
|
T | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(5): Show | 8 | HG00558.hp1 HG02055.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-372T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687965 | ||||||
| chr15:45688177
|
C | T | 32 | a0001c0001t0001g0099a0001c0001t0001g0180a0001c0001t0001g0232others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1049-160C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45688177 | ||||||
| chr15:45688178
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1049-159G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45688178 | ||||||
| chr15:45688194
|
A | G | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1049-143A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45688194 | ||||||
| chr15:45688515
|
C | CT | 6 | a0001c0001t0001g0259a0002c0002t0001g0016a0003c0005t0001g0307others(3): Show | 6 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+125dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 45688515 | |||||
| chr15:45688515
|
C | CTT | 9 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0093others(6): Show | 10 | HG00558.hp1 HG01169.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1116+124_1116+125d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 45688515 | |||||
| chr15:45688560
|
G | A | 1 | a0002c0002t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1116+156G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688560 | ||||||
| chr15:45688749
|
A | G | 183 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0028others(180): Show | 189 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1117-290A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688749 | ||||||
| chr15:45688760
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0001g0130others(11): Show | 14 | HG00741.hp1 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1117-279G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688760 | ||||||
| chr15:45688889
|
T | C | 1 | a0004c0008t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1117-150T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688889 | ||||||
| chr15:45688919
|
C | T | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1117-120C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688919 | ||||||
| chr15:45689417
|
C | CT | 14 | a0001c0001t0001g0050a0001c0001t0001g0197a0001c0001t0001g0221others(11): Show | 14 | HG00642.hp2 HG02015.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1295+218dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45689417 | |||||
| chr15:45689417
|
CT | C | 28 | a0001c0001t0001g0027a0001c0001t0001g0114a0001c0001t0002g0004others(25): Show | 29 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1295+218delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45689417 | |||||
| chr15:45689426
|
T | G | 6 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0116others(3): Show | 6 | NA18959.hp1 NA18962.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+209T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689426 | ||||||
| chr15:45689482
|
A | G | 3 | a0005c0006t0004g0319a0005c0006t0004g0323a0010c0011t0004g0325 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1295+265A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689482 | ||||||
| chr15:45689535
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1295+318A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689535 | ||||||
| chr15:45689643
|
C | A | 74 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0100others(71): Show | 77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1295+426C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689643 | ||||||
| chr15:45689661
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1295+444C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689661 | ||||||
| chr15:45689662
|
C | T | 74 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0100others(71): Show | 77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1295+445C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689662 | ||||||
| chr15:45689671
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1295+454C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689671 | ||||||
| chr15:45689710
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1295+493G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689710 | ||||||
| chr15:45689951
|
A | G | 8 | a0001c0001t0001g0099a0001c0001t0001g0232a0001c0001t0001g0242others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1295+734A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689951 | ||||||
| chr15:45690064
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0170others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295+847G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690064 | ||||||
| chr15:45690081
|
C | T | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1295+864C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690081 | ||||||
| chr15:45690082
|
C | CT | 115 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0026others(112): Show | 120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1296-875dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | |||||
| chr15:45690082
|
C | CTT | 7 | a0001c0001t0001g0142a0001c0001t0001g0171a0001c0001t0001g0240others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1296-876_1296-875d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | |||||
| chr15:45690082
|
C | CTTT | 39 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(36): Show | 40 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1296-877_1296-875d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | |||||
| chr15:45690082
|
C | CTTTT | 28 | a0001c0001t0001g0099a0001c0001t0001g0180a0001c0001t0001g0232others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1295+878_1296-875d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | |||||
| chr15:45690082
|
CT | C | 15 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0078others(12): Show | 15 | HG00741.hp1 HG01496.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1296-875delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | |||||
| chr15:45690119
|
C | CCACCCAG others(9): Show |
69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-853_1296-852i others(18): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690119 | |||||
| chr15:45690121
|
C | A | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-852C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690121 | ||||||
| chr15:45690140
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1296-833G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690140 | ||||||
| chr15:45690159
|
G | A | 2 | a0001c0007t0001g0008a0001c0007t0001g0226 | 3 | HG01884.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1296-814G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690159 | ||||||
| chr15:45690348
|
G | A | 1 | a0008c0014t0001g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1296-625G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690348 | ||||||
| chr15:45690390
|
T | C | 68 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(65): Show | 69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296-583T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690390 | ||||||
| chr15:45690397
|
C | A | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-576C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690397 | ||||||
| chr15:45690408
|
C | A | 68 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(65): Show | 69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296-565C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690408 | ||||||
| chr15:45690542
|
G | T | 1 | a0008c0014t0001g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1296-431G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690542 | ||||||
| chr15:45690583
|
A | G | 1 | a0001c0001t0004g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1296-390A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690583 | ||||||
| chr15:45690587
|
G | A | 70 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(67): Show | 71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1296-386G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690587 | ||||||
| chr15:45690609
|
C | T | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-364C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690609 | ||||||
| chr15:45690663
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1296-310A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690663 | ||||||
| chr15:45690664
|
T | TCCTGA | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-306_1296-305i others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690664 | |||||
| chr15:45690683
|
G | C | 69 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0086others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-290G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690683 | ||||||
| chr15:45690767
|
A | T | 21 | a0001c0003t0001g0034a0001c0003t0001g0079a0001c0003t0001g0129others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1296-206A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690767 | ||||||
| chr15:45690806
|
G | T | 23 | a0001c0001t0001g0180a0001c0003t0001g0034a0001c0003t0001g0079others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1296-167G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690806 | ||||||
| chr15:45690909
|
C | G | 1 | a0004c0008t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1296-64C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690909 |