Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26035 |
|---|---|
| ensemblid | ENSG00000138604.10 |
| hgncid | 17855 |
| symbol | GLCE |
| name | glucuronic acid epimerase |
| refseq_nuc | NM_015554.3 |
| refseq_prot | NP_056369.1 |
| ensembl_nuc | ENST00000261858.7 |
| ensembl_prot | ENSP00000261858.2 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 69160635 |
| end | 69272207 |
| strand | + |
| ver | v1.2 |
| region | chr15:69160635-69272207 |
| region5000 | chr15:69155635-69277207 |
| regionname0 | GLCE_chr15_69160635_69272207 |
| regionname5000 | GLCE_chr15_69155635_69277207 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 617 | 212 | 41 | 23 | 119 | 5 | 23 | 89 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002 | 1/0 | 617 | 111 | 44 | 15 | 42 | 3 | 6 | 33 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0003 | 0/0 | 617 | 10 | 0 | 2 | 7 | 0 | 1 | 6 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0004 | 0/0 | 617 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0005 | 0/0 | 617 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0006 | 0/0 | 617 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1854 | 193 | 24 | 22 | 118 | 5 | 23 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0002 | 1/0 | 1854 | 111 | 44 | 15 | 42 | 3 | 6 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0003 | 0/0 | 1854 | 15 | 15 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0004 | 0/0 | 1854 | 10 | 0 | 2 | 7 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0005 | 0/0 | 1854 | 6 | 6 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0006 | 0/0 | 1854 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0007 | 0/0 | 1854 | 2 | 0 | 0 | 0 | 2 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0008 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0009 | 0/0 | 1854 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| c0010 | 0/0 | 1854 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3190 | 120 | 8 | 16 | 75 | 4 | 16 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0002 | 1/0 | 3191 | 101 | 28 | 15 | 48 | 4 | 5 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0003 | 0/0 | 3190 | 68 | 15 | 7 | 38 | 1 | 7 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0004 | 0/0 | 3191 | 11 | 11 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0005 | 0/0 | 3191 | 6 | 6 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0006 | 0/0 | 3191 | 5 | 5 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0007 | 0/0 | 3191 | 4 | 4 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0008 | 0/0 | 3190 | 3 | 0 | 0 | 3 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0009 | 0/0 | 3191 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0010 | 0/0 | 3191 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0011 | 0/0 | 3191 | 2 | 0 | 1 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0012 | 0/0 | 3190 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0013 | 0/0 | 3191 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0014 | 0/0 | 3191 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0015 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0016 | 0/0 | 3191 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0017 | 0/0 | 3191 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0018 | 0/0 | 3191 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0019 | 0/0 | 3191 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0020 | 0/0 | 3191 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0021 | 0/0 | 3191 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0022 | 0/0 | 3190 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0023 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0024 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0025 | 0/0 | 3191 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| t0026 | 0/0 | 3191 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| 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 | 0 | 3 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1854 | 193 | 24 | 22 | 118 | 5 | 23 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0003 | 0/0 | 1854 | 15 | 15 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0006 | 0/0 | 1854 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0009 | 0/0 | 1854 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0010 | 0/0 | 1854 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002 | 1/0 | 1854 | 111 | 44 | 15 | 42 | 3 | 6 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0003c0004 | 0/0 | 1854 | 10 | 0 | 2 | 7 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0004c0005 | 0/0 | 1854 | 6 | 6 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0005c0007 | 0/0 | 1854 | 2 | 0 | 0 | 0 | 2 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0006c0008 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5043 | 118 | 8 | 15 | 74 | 4 | 16 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0001t0003 | 0/0 | 5043 | 68 | 15 | 7 | 38 | 1 | 7 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0001t0008 | 0/0 | 5043 | 3 | 0 | 0 | 3 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0001t0015 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0001t0022 | 0/0 | 5043 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0001t0023 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0001t0024 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0003t0005 | 0/0 | 5044 | 6 | 6 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0003t0006 | 0/0 | 5044 | 5 | 5 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0003t0014 | 0/0 | 5044 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0003t0016 | 0/0 | 5044 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0003t0026 | 0/0 | 5044 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0006t0012 | 0/0 | 5043 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0009t0001 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0001c0010t0001 | 0/0 | 5043 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0002 | 1/0 | 5044 | 89 | 28 | 13 | 41 | 2 | 4 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0004 | 0/0 | 5044 | 10 | 10 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0009 | 0/0 | 5044 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0010 | 0/0 | 5044 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0011 | 0/0 | 5044 | 2 | 0 | 1 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0017 | 0/0 | 5044 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0018 | 0/0 | 5044 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0019 | 0/0 | 5044 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0020 | 0/0 | 5044 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0021 | 0/0 | 5044 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0002c0002t0025 | 0/0 | 5044 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0003c0004t0002 | 0/0 | 5044 | 10 | 0 | 2 | 7 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0004c0005t0007 | 0/0 | 5044 | 4 | 4 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0004c0005t0013 | 0/0 | 5044 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0005c0007t0002 | 0/0 | 5044 | 2 | 0 | 0 | 0 | 2 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| a0006c0008t0004 | 0/0 | 5044 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | copy fasta | chr15 | 69155635 | 69277207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0015g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0022g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0023g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0001t0024g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0016g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0003t0026g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0006t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0006t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0001c0010t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0011g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0011g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0017g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0018g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0019g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0021g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0002c0002t0025g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0003c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0004c0005t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0004c0005t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0004c0005t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0004c0005t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0004c0005t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0004c0005t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0005c0007t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0005c0007t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| a0006c0008t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG00741 | hp2 | a0002 | c0002 | t0011 | g0144 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01109 | hp1 | a0002 | c0002 | t0021 | g0023 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01167 | hp1 | a0003 | c0004 | t0002 | g0072 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01169 | hp1 | a0001 | c0010 | t0001 | g0323 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0073 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0124 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | CLM | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01515 | hp1 | a0005 | c0007 | t0002 | g0095 | EUR | IBS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01517 | hp1 | a0005 | c0007 | t0002 | g0094 | EUR | IBS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0114 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0108 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01934 | hp2 | a0003 | c0004 | t0002 | g0071 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02015 | hp1 | a0001 | c0001 | t0024 | g0288 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02015 | hp2 | a0001 | c0001 | t0008 | g0158 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02135 | hp1 | a0003 | c0004 | t0002 | g0098 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CDX | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | CDX | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02257 | hp2 | a0002 | c0002 | t0009 | g0106 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02258 | hp1 | a0001 | c0003 | t0026 | g0143 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02280 | hp1 | a0002 | c0002 | t0010 | g0011 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02280 | hp2 | a0004 | c0005 | t0013 | g0015 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0056 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0102 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0127 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02630 | hp2 | a0001 | c0003 | t0005 | g0003 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0137 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0068 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0107 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02809 | hp1 | a0004 | c0005 | t0007 | g0054 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02895 | hp1 | a0001 | c0006 | t0012 | g0208 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0118 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0117 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02896 | hp2 | a0001 | c0003 | t0014 | g0136 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02897 | hp1 | a0001 | c0006 | t0012 | g0209 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02897 | hp2 | a0001 | c0003 | t0014 | g0131 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0140 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02965 | hp1 | a0002 | c0002 | t0004 | g0104 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02976 | hp2 | a0002 | c0002 | t0020 | g0053 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0077 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03041 | hp2 | a0001 | c0003 | t0006 | g0138 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03098 | hp2 | a0001 | c0003 | t0006 | g0326 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03139 | hp1 | a0001 | c0003 | t0005 | g0003 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0103 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0135 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03209 | hp1 | a0001 | c0003 | t0016 | g0327 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03209 | hp2 | a0006 | c0008 | t0004 | g0109 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03225 | hp1 | a0004 | c0005 | t0007 | g0012 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03225 | hp2 | a0002 | c0002 | t0004 | g0116 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03239 | hp1 | a0003 | c0004 | t0002 | g0096 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03453 | hp1 | a0002 | c0002 | t0009 | g0105 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0112 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03491 | hp2 | a0002 | c0002 | t0017 | g0085 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03516 | hp1 | a0001 | c0003 | t0005 | g0139 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03516 | hp2 | a0004 | c0005 | t0007 | g0014 | AFR | ESN | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03579 | hp1 | a0002 | c0002 | t0004 | g0110 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04115 | hp2 | a0002 | c0002 | t0011 | g0097 | SAS | STU | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0058 | SAS | BEB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | STU | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0041 | SAS | STU | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | YRI | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18522 | hp2 | a0004 | c0005 | t0007 | g0013 | AFR | YRI | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | CHB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18906 | hp1 | a0001 | c0003 | t0006 | g0134 | AFR | YRI | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | YRI | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0034 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0175 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18940 | hp2 | a0001 | c0009 | t0001 | g0217 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18956 | hp2 | a0002 | c0002 | t0025 | g0066 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18975 | hp1 | a0003 | c0004 | t0002 | g0062 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18981 | hp2 | a0001 | c0001 | t0015 | g0227 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18985 | hp2 | a0003 | c0004 | t0002 | g0083 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18987 | hp1 | a0003 | c0004 | t0002 | g0080 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18993 | hp1 | a0003 | c0004 | t0002 | g0063 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0329 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | LWK | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | LWK | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19064 | hp2 | a0001 | c0001 | t0023 | g0212 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19084 | hp1 | a0003 | c0004 | t0002 | g0008 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0332 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA20129 | hp1 | a0002 | c0002 | t0010 | g0010 | AFR | ASW | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA20129 | hp2 | a0002 | c0002 | t0018 | g0036 | AFR | ASW | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA20805 | hp2 | a0002 | c0002 | t0019 | g0045 | EUR | TSI | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02486 | hp1 | a0004 | c0005 | t0013 | g0016 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0126 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0115 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | MSL | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0113 | AFR | USA | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| HG06807 | hp2 | a0001 | c0003 | t0006 | g0142 | AFR | USA | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | USA | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA20300 | hp2 | a0001 | c0003 | t0005 | g0141 | AFR | USA | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA21309 | hp1 | a0001 | c0001 | t0022 | g0146 | AFR | LWK | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | LWK | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0277 | REF | REF | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0051 | REF | REF | GLCE_chr15_69155635_69277207 | GLCE | chr15 | 69155635 | 69277207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:69255999
|
A | G | 2 | a0003a0005 | 12 | HG01167.hp1 HG01515.hp1 HG01517.hp1 others(9): Show |
missense_variant | MODERATE | c.193A>G | p.Met65Val | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/5 | 420/5044 | 193/1854 | 65/617 | chr15 | 69255999 | ||
| chr15:69256008
|
G | A | 1 | a0005 | 2 | HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.202G>A | p.Val68Met | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/5 | 429/5044 | 202/1854 | 68/617 | chr15 | 69256008 | ||
| chr15:69256054
|
A | G | 1 | a0004 | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
missense_variant | MODERATE | c.248A>G | p.Lys83Arg | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/5 | 475/5044 | 248/1854 | 83/617 | chr15 | 69256054 | ||
| chr15:69268531
|
G | A | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1141G>A | p.Val381Ile | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1368/5044 | 1141/1854 | 381/617 | chr15 | 69268531 | ||
| chr15:69269179
|
G | A | 2 | a0001a0004 | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
missense_variant | MODERATE | c.1789G>A | p.Val597Ile | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2016/5044 | 1789/1854 | 597/617 | chr15 | 69269179 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:69255857
|
C | T | 1 | a0001c0010 | 1 | HG01169.hp1 | synonymous_variant | LOW | c.51C>T | p.Cys17Cys | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/5 | 278/5044 | 51/1854 | 17/617 | chr15 | 69255857 | ||
| chr15:69256193
|
A | G | 1 | a0001c0009 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.387A>G | p.Pro129Pro | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/5 | 614/5044 | 387/1854 | 129/617 | chr15 | 69256193 | ||
| chr15:69268830
|
A | G | 1 | a0001c0006 | 2 | HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.1440A>G | p.Leu480Leu | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1667/5044 | 1440/1854 | 480/617 | chr15 | 69268830 | ||
| chr15:69268842
|
T | C | 2 | a0001c0003a0004c0005 | 21 | HG02258.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
synonymous_variant | LOW | c.1452T>C | p.His484His | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1679/5044 | 1452/1854 | 484/617 | chr15 | 69268842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:69160643
|
G | T | 2 | a0002c0002t0004a0006c0008t0004 | 11 | HG01884.hp2 HG01891.hp2 HG02717.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-219G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/5 | 95164 | chr15 | 69160643 | |||||
| chr15:69160675
|
C | A | 1 | a0001c0001t0015 | 1 | NA18981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/5 | 95132 | chr15 | 69160675 | |||||
| chr15:69269518
|
G | A | 1 | a0001c0003t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 274 | chr15 | 69269518 | |||||
| chr15:69269568
|
A | G | 1 | a0001c0003t0026 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*324A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 324 | chr15 | 69269568 | |||||
| chr15:69269650
|
G | A | 1 | a0002c0002t0017 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 406 | chr15 | 69269650 | |||||
| chr15:69269748
|
A | G | 1 | a0002c0002t0025 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 504 | chr15 | 69269748 | |||||
| chr15:69269749
|
A | T | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(10): Show | 205 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*505A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 505 | chr15 | 69269749 | |||||
| chr15:69269916
|
G | A | 1 | a0001c0001t0022 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 672 | chr15 | 69269916 | |||||
| chr15:69270186
|
AT | A | 3 | a0001c0001t0003a0001c0001t0008a0001c0006t0012 | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*947delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 947 | INFO_REALIGN_3_PRIME | chr15 | 69270186 | ||||
| chr15:69270327
|
T | A | 1 | a0002c0002t0018 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1083 | chr15 | 69270327 | |||||
| chr15:69270504
|
G | C | 1 | a0002c0002t0018 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1260 | chr15 | 69270504 | |||||
| chr15:69270608
|
T | A | 1 | a0001c0003t0005 | 6 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1364T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1364 | chr15 | 69270608 | |||||
| chr15:69270639
|
A | G | 1 | a0001c0001t0024 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1395A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1395 | chr15 | 69270639 | |||||
| chr15:69270647
|
G | A | 1 | a0002c0002t0019 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1403G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1403 | chr15 | 69270647 | |||||
| chr15:69270810
|
T | C | 1 | a0002c0002t0009 | 2 | HG02257.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1566T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1566 | chr15 | 69270810 | |||||
| chr15:69270834
|
CA | C | 7 | a0001c0001t0001a0001c0001t0015a0001c0001t0022others(4): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1591delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1591 | chr15 | 69270834 | |||||
| chr15:69270916
|
A | G | 5 | a0001c0003t0005a0001c0003t0006a0001c0003t0014others(2): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1672A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1672 | chr15 | 69270916 | |||||
| chr15:69271032
|
A | T | 1 | a0004c0005t0013 | 2 | HG02280.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1788A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1788 | chr15 | 69271032 | |||||
| chr15:69271053
|
G | A | 1 | a0002c0002t0010 | 2 | HG02280.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1809G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1809 | chr15 | 69271053 | |||||
| chr15:69271148
|
G | A | 1 | a0001c0003t0026 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1904G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1904 | chr15 | 69271148 | |||||
| chr15:69271225
|
A | T | 1 | a0001c0001t0023 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1981A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 1981 | chr15 | 69271225 | |||||
| chr15:69271593
|
G | A | 1 | a0001c0001t0008 | 3 | HG02015.hp2 NA18940.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2349G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2349 | chr15 | 69271593 | |||||
| chr15:69271597
|
T | C | 1 | a0002c0002t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2353T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2353 | chr15 | 69271597 | |||||
| chr15:69271677
|
A | G | 1 | a0002c0002t0011 | 2 | HG00741.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2433A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2433 | chr15 | 69271677 | |||||
| chr15:69271865
|
C | A | 1 | a0002c0002t0021 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2621C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2621 | chr15 | 69271865 | |||||
| chr15:69271869
|
C | T | 1 | a0001c0006t0012 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2625C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2625 | chr15 | 69271869 | |||||
| chr15:69272004
|
C | T | 8 | a0001c0001t0001a0001c0001t0015a0001c0001t0022others(5): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2760C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 5/5 | 2760 | chr15 | 69272004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:69160843
|
G | C | 1 | a0003c0004t0002g0008 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-105+86G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69160843 | ||||||
| chr15:69160985
|
G | T | 1 | a0001c0001t0003g0334 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-105+228G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69160985 | ||||||
| chr15:69160992
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+235G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69160992 | ||||||
| chr15:69161157
|
C | T | 5 | a0002c0002t0002g0329a0002c0002t0002g0330a0002c0002t0002g0331others(2): Show | 5 | NA18994.hp2 NA19005.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+400C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161157 | ||||||
| chr15:69161217
|
C | T | 1 | a0002c0002t0002g0328 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-105+460C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161217 | ||||||
| chr15:69161378
|
G | T | 2 | a0001c0003t0006g0326a0001c0003t0016g0327 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-105+621G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161378 | ||||||
| chr15:69161393
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+636G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161393 | ||||||
| chr15:69161469
|
A | C | 1 | a0001c0001t0001g0325 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-105+712A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161469 | ||||||
| chr15:69161871
|
A | G | 1 | a0001c0003t0016g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105+1114A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161871 | ||||||
| chr15:69161912
|
C | CTG | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 221 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-105+1156_-105+115 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69161912 | |||||
| chr15:69161922
|
C | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+1165C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161922 | ||||||
| chr15:69161932
|
T | A | 1 | a0001c0001t0003g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+1175T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69161932 | ||||||
| chr15:69162026
|
G | A | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-105+1269G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69162026 | ||||||
| chr15:69162316
|
TA | T | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+1570delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69162316 | |||||
| chr15:69162472
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+1715T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69162472 | ||||||
| chr15:69162473
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+1716A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69162473 | ||||||
| chr15:69162538
|
GT | G | 6 | a0002c0002t0002g0018a0002c0002t0010g0010a0002c0002t0010g0011others(3): Show | 6 | HG02280.hp1 HG03225.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+1793delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69162538 | |||||
| chr15:69162647
|
C | A | 1 | a0002c0002t0002g0019 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-105+1890C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69162647 | ||||||
| chr15:69162905
|
T | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+2148T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69162905 | ||||||
| chr15:69162995
|
G | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+2238G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69162995 | ||||||
| chr15:69163095
|
C | T | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-105+2338C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69163095 | ||||||
| chr15:69163290
|
T | A | 2 | a0001c0001t0001g0211a0001c0001t0023g0212 | 2 | NA18950.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-105+2533T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69163290 | ||||||
| chr15:69163475
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-105+2718A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69163475 | ||||||
| chr15:69163540
|
A | G | 1 | a0001c0010t0001g0323 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-105+2783A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69163540 | ||||||
| chr15:69163611
|
C | T | 2 | a0001c0006t0012g0208a0001c0006t0012g0209 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-105+2854C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69163611 | ||||||
| chr15:69164151
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+3394T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164151 | ||||||
| chr15:69164154
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+3397C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164154 | ||||||
| chr15:69164155
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+3398T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164155 | ||||||
| chr15:69164246
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+3489G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164246 | ||||||
| chr15:69164499
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+3742T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164499 | ||||||
| chr15:69164522
|
C | G | 12 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0118others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-105+3765C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164522 | ||||||
| chr15:69164527
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+3770G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164527 | ||||||
| chr15:69164528
|
C | T | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-105+3771C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164528 | ||||||
| chr15:69164529
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+3772C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164529 | ||||||
| chr15:69164552
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+3795A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164552 | ||||||
| chr15:69164604
|
G | A | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 202 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-105+3847G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164604 | ||||||
| chr15:69164609
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+3852G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164609 | ||||||
| chr15:69164758
|
C | T | 3 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207 | 3 | HG00438.hp1 NA18988.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-105+4001C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164758 | ||||||
| chr15:69164840
|
A | G | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-105+4083A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69164840 | ||||||
| chr15:69165182
|
A | T | 12 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0118others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-105+4425A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165182 | ||||||
| chr15:69165201
|
C | G | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+4444C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165201 | ||||||
| chr15:69165273
|
C | G | 1 | a0002c0002t0002g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-105+4516C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165273 | ||||||
| chr15:69165276
|
C | T | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-105+4519C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165276 | ||||||
| chr15:69165504
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-105+4747G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165504 | ||||||
| chr15:69165505
|
C | CT | 64 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0093others(61): Show | 65 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.-105+4769dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69165505 | |||||
| chr15:69165505
|
C | CTT | 9 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0003t0005g0003others(6): Show | 10 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-105+4768_-105+476 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69165505 | |||||
| chr15:69165505
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-105+4748C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165505 | ||||||
| chr15:69165505
|
CT | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0218a0001c0001t0001g0219others(10): Show | 13 | HG00741.hp2 HG01496.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-105+4769delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69165505 | |||||
| chr15:69165526
|
T | TA | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+4770dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69165526 | |||||
| chr15:69165621
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-105+4864A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165621 | ||||||
| chr15:69165709
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+4952G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69165709 | ||||||
| chr15:69166049
|
A | G | 4 | a0001c0003t0006g0326a0001c0003t0014g0131a0001c0003t0014g0136others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+5292A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166049 | ||||||
| chr15:69166254
|
G | A | 15 | a0002c0002t0002g0111a0002c0002t0002g0130a0002c0002t0004g0104others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-105+5497G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166254 | ||||||
| chr15:69166299
|
C | T | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+5542C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166299 | ||||||
| chr15:69166314
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+5557A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166314 | ||||||
| chr15:69166641
|
C | T | 1 | a0002c0002t0002g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-105+5884C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166641 | ||||||
| chr15:69166658
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-105+5901G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166658 | ||||||
| chr15:69166672
|
C | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+5915C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166672 | ||||||
| chr15:69166685
|
C | T | 5 | a0002c0002t0002g0018a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 5 | NA18747.hp1 NA18961.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+5928C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166685 | ||||||
| chr15:69166690
|
C | T | 1 | a0001c0003t0006g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-105+5933C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166690 | ||||||
| chr15:69166749
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+5992G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166749 | ||||||
| chr15:69166765
|
CA | C | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+6013delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69166765 | |||||
| chr15:69166777
|
G | C | 2 | a0002c0002t0002g0102a0002c0002t0002g0103 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-105+6020G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166777 | ||||||
| chr15:69166869
|
G | A | 2 | a0001c0001t0003g0147a0001c0001t0022g0146 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-105+6112G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166869 | ||||||
| chr15:69166908
|
C | CA | 32 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0091others(29): Show | 32 | HG00597.hp1 HG00741.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.-105+6176dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69166908 | |||||
| chr15:69166908
|
CA | C | 23 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(20): Show | 23 | HG00423.hp1 HG00741.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.-105+6176delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69166908 | |||||
| chr15:69166908
|
CAA | C | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 187 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-105+6175_-105+617 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69166908 | |||||
| chr15:69166984
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-105+6227A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69166984 | ||||||
| chr15:69167045
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+6288G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167045 | ||||||
| chr15:69167143
|
G | A | 1 | a0002c0002t0018g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-105+6386G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167143 | ||||||
| chr15:69167347
|
C | T | 1 | a0003c0004t0002g0083 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-105+6590C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167347 | ||||||
| chr15:69167482
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+6725C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167482 | ||||||
| chr15:69167531
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+6774C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167531 | ||||||
| chr15:69167532
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+6775A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167532 | ||||||
| chr15:69167533
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+6776G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167533 | ||||||
| chr15:69167823
|
G | GT | 75 | a0001c0001t0001g0020a0001c0001t0001g0281a0001c0001t0001g0282others(72): Show | 78 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-105+7084dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69167823 | |||||
| chr15:69167823
|
G | GTT | 6 | a0001c0001t0003g0148a0001c0001t0003g0203a0001c0003t0014g0131others(3): Show | 6 | HG00741.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+7083_-105+708 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69167823 | |||||
| chr15:69167823
|
GT | G | 11 | a0001c0001t0015g0227a0002c0002t0002g0021a0002c0002t0002g0037others(8): Show | 11 | HG01175.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105+7084delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69167823 | |||||
| chr15:69167831
|
T | G | 36 | a0001c0001t0001g0007a0001c0001t0001g0213a0001c0001t0001g0214others(33): Show | 37 | HG00408.hp2 HG01257.hp1 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.-105+7074T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167831 | ||||||
| chr15:69167840
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0222 | 2 | NA18966.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-105+7083T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167840 | ||||||
| chr15:69167929
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-105+7172A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167929 | ||||||
| chr15:69167967
|
C | G | 1 | a0002c0002t0017g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-105+7210C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69167967 | ||||||
| chr15:69168082
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-105+7325G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69168082 | ||||||
| chr15:69168398
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+7641T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69168398 | ||||||
| chr15:69168473
|
C | T | 1 | a0003c0004t0002g0034 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-105+7716C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69168473 | ||||||
| chr15:69168536
|
CT | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(220): Show | 230 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.-105+7793delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69168536 | |||||
| chr15:69168693
|
C | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0210a0001c0001t0001g0213others(33): Show | 37 | HG00408.hp2 HG01257.hp1 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.-105+7936C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69168693 | ||||||
| chr15:69168779
|
A | G | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 217 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-105+8022A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69168779 | ||||||
| chr15:69169116
|
A | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-105+8359A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169116 | ||||||
| chr15:69169210
|
G | A | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-105+8453G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169210 | ||||||
| chr15:69169421
|
C | CT | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-105+8667dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69169421 | |||||
| chr15:69169422
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+8665T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169422 | ||||||
| chr15:69169487
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+8730G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169487 | ||||||
| chr15:69169550
|
C | T | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-105+8793C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169550 | ||||||
| chr15:69169576
|
A | G | 1 | a0001c0001t0015g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-105+8819A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169576 | ||||||
| chr15:69169782
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+9025C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169782 | ||||||
| chr15:69169846
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-105+9089A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69169846 | ||||||
| chr15:69170067
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-105+9310G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170067 | ||||||
| chr15:69170082
|
C | G | 9 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(6): Show | 10 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-105+9325C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170082 | ||||||
| chr15:69170122
|
T | A | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-105+9365T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170122 | ||||||
| chr15:69170164
|
AC | A | 3 | a0001c0001t0003g0132a0001c0001t0003g0133a0002c0002t0002g0022 | 3 | HG02809.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-105+9408delC | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170164 | ||||||
| chr15:69170194
|
A | T | 1 | a0001c0001t0023g0212 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-105+9437A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170194 | ||||||
| chr15:69170334
|
T | A | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 236 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.-105+9577T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170334 | ||||||
| chr15:69170354
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-105+9597T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170354 | ||||||
| chr15:69170380
|
A | T | 1 | a0001c0001t0003g0203 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-105+9623A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170380 | ||||||
| chr15:69170382
|
T | C | 1 | a0001c0001t0003g0203 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-105+9625T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170382 | ||||||
| chr15:69170557
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0015g0227 | 2 | NA18979.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-105+9800T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170557 | ||||||
| chr15:69170776
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+10019G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170776 | ||||||
| chr15:69170805
|
T | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+10048T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69170805 | ||||||
| chr15:69171012
|
G | GACAGCTT others(1): Show |
3 | a0001c0001t0001g0223a0001c0001t0001g0229a0001c0001t0001g0281 | 3 | HG00423.hp1 NA18998.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-105+10259_-105+10 others(14): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69171012 | |||||
| chr15:69171080
|
GCAAATAA others(43): Show |
G | 2 | a0001c0003t0006g0326a0001c0003t0016g0327 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-105+10377_-105+10 others(56): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69171080 | |||||
| chr15:69171330
|
A | T | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-105+10573A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171330 | ||||||
| chr15:69171399
|
CT | C | 81 | a0001c0001t0001g0230a0001c0001t0001g0287a0001c0001t0001g0312others(78): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-105+10657delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69171399 | |||||
| chr15:69171429
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+10672C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171429 | ||||||
| chr15:69171435
|
C | T | 2 | a0002c0002t0002g0033a0002c0002t0002g0081 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-105+10678C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171435 | ||||||
| chr15:69171440
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-105+10683G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171440 | ||||||
| chr15:69171542
|
G | A | 1 | a0001c0009t0001g0217 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-105+10785G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171542 | ||||||
| chr15:69171940
|
G | A | 5 | a0002c0002t0002g0024a0002c0002t0002g0039a0002c0002t0002g0040others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-105+11183G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171940 | ||||||
| chr15:69171974
|
A | G | 1 | a0002c0002t0002g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-105+11217A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69171974 | ||||||
| chr15:69172329
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+11572T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69172329 | ||||||
| chr15:69172602
|
TA | T | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 202 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-105+11847delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69172602 | |||||
| chr15:69172678
|
A | G | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-105+11921A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69172678 | ||||||
| chr15:69172805
|
G | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+12048G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69172805 | ||||||
| chr15:69172883
|
T | C | 1 | a0002c0002t0002g0231 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-105+12126T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69172883 | ||||||
| chr15:69173680
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-105+12923A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69173680 | ||||||
| chr15:69173695
|
A | T | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 222 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-105+12938A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69173695 | ||||||
| chr15:69173762
|
T | C | 73 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0313others(70): Show | 76 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-105+13005T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69173762 | ||||||
| chr15:69173781
|
C | T | 217 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(214): Show | 224 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-105+13024C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69173781 | ||||||
| chr15:69173883
|
G | A | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+13126G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69173883 | ||||||
| chr15:69174003
|
G | A | 4 | a0002c0002t0002g0025a0002c0002t0002g0041a0002c0002t0002g0042others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+13246G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174003 | ||||||
| chr15:69174187
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+13430A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174187 | ||||||
| chr15:69174268
|
G | GT | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+13512dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69174268 | |||||
| chr15:69174391
|
C | T | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-105+13634C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174391 | ||||||
| chr15:69174410
|
GACCA | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+13657_-105+13 others(10): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69174410 | |||||
| chr15:69174565
|
G | A | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-105+13808G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174565 | ||||||
| chr15:69174589
|
G | A | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+13832G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174589 | ||||||
| chr15:69174611
|
A | AAAAAC | 4 | a0001c0003t0006g0134a0001c0003t0006g0135a0001c0003t0006g0142others(1): Show | 4 | HG02451.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+13878_-105+13 others(11): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69174611 | |||||
| chr15:69174611
|
AAAAAC | A | 12 | a0001c0003t0006g0326a0001c0003t0014g0131a0001c0003t0014g0136others(9): Show | 12 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-105+13878_-105+13 others(11): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69174611 | |||||
| chr15:69174935
|
T | C | 9 | a0001c0001t0001g0226a0001c0001t0001g0287a0001c0001t0001g0289others(6): Show | 9 | HG00408.hp2 HG02015.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-105+14178T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174935 | ||||||
| chr15:69174966
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-105+14209A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69174966 | ||||||
| chr15:69175107
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+14350G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175107 | ||||||
| chr15:69175232
|
T | G | 1 | a0002c0002t0002g0087 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-105+14475T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175232 | ||||||
| chr15:69175244
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-105+14487A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175244 | ||||||
| chr15:69175520
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-105+14763T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175520 | ||||||
| chr15:69175621
|
T | C | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-105+14864T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175621 | ||||||
| chr15:69175780
|
C | A | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-105+15023C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175780 | ||||||
| chr15:69175841
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+15084T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175841 | ||||||
| chr15:69175988
|
A | C | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+15231A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69175988 | ||||||
| chr15:69176216
|
G | GT | 40 | a0001c0001t0001g0020a0001c0001t0001g0091a0002c0002t0002g0017others(37): Show | 40 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-105+15483dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69176216 | |||||
| chr15:69176216
|
G | GTT | 35 | a0001c0001t0001g0007a0001c0001t0001g0210a0001c0001t0001g0213others(32): Show | 36 | HG01257.hp1 HG01934.hp1 HG01975.hp1 others(33): Show |
intron_variant | MODIFIER | c.-105+15482_-105+15 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69176216 | |||||
| chr15:69176216
|
G | GTTT | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0215others(121): Show | 130 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-105+15481_-105+15 others(9): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69176216 | |||||
| chr15:69176216
|
G | GTTTT | 34 | a0001c0001t0001g0211a0001c0001t0001g0225a0001c0001t0001g0229others(31): Show | 34 | HG00597.hp2 HG00621.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-105+15480_-105+15 others(10): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69176216 | |||||
| chr15:69176216
|
G | GTTTTT | 12 | a0001c0001t0001g0219a0001c0001t0001g0223a0001c0001t0001g0275others(9): Show | 12 | HG00423.hp1 HG00639.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-105+15479_-105+15 others(11): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69176216 | |||||
| chr15:69176546
|
T | C | 91 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(88): Show | 95 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-105+15789T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69176546 | ||||||
| chr15:69176640
|
A | G | 3 | a0002c0002t0002g0123a0002c0002t0002g0125a0002c0002t0002g0126 | 3 | HG02559.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+15883A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69176640 | ||||||
| chr15:69176745
|
A | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+15988A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69176745 | ||||||
| chr15:69176934
|
G | C | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+16177G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69176934 | ||||||
| chr15:69176943
|
C | G | 1 | a0002c0002t0002g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+16186C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69176943 | ||||||
| chr15:69177026
|
C | CT | 9 | a0001c0001t0001g0274a0001c0001t0001g0312a0002c0002t0002g0018others(6): Show | 9 | HG03239.hp1 HG03239.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.-105+16284dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177026 | |||||
| chr15:69177037
|
T | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+16280T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177037 | ||||||
| chr15:69177127
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-105+16370C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177127 | ||||||
| chr15:69177169
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-105+16412G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177169 | ||||||
| chr15:69177220
|
C | T | 13 | a0002c0002t0002g0038a0002c0002t0002g0070a0002c0002t0002g0073others(10): Show | 13 | HG01167.hp1 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-105+16463C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177220 | ||||||
| chr15:69177229
|
AATTTTTG others(1): Show |
A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+16479_-105+16 others(14): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177229 | |||||
| chr15:69177239
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105+16482T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177239 | ||||||
| chr15:69177252
|
CAG | C | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+16498_-105+16 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177252 | |||||
| chr15:69177311
|
C | G | 2 | a0001c0001t0003g0129a0002c0002t0002g0128 | 2 | HG01255.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-105+16554C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177311 | ||||||
| chr15:69177383
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+16626G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177383 | ||||||
| chr15:69177457
|
AG | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+16701delG | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177457 | ||||||
| chr15:69177489
|
A | G | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-105+16732A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177489 | ||||||
| chr15:69177582
|
A | AT | 6 | a0002c0002t0010g0010a0004c0005t0007g0012a0004c0005t0007g0013others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+16826dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177582 | |||||
| chr15:69177601
|
TCATG | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+16850_-105+16 others(10): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177601 | |||||
| chr15:69177605
|
GCATGCCC others(17): Show |
G | 1 | a0001c0001t0001g0314 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-105+16871_-105+16 others(30): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177605 | |||||
| chr15:69177684
|
C | CCTTTATC others(17): Show |
3 | a0001c0001t0003g0334a0001c0003t0005g0139a0001c0003t0006g0135 | 3 | HG03195.hp2 HG03516.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-105+16975_-105+16 others(30): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177684 | |||||
| chr15:69177684
|
C | CCTTTATC others(41): Show |
2 | a0001c0001t0003g0129a0002c0002t0002g0128 | 2 | HG01255.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-105+16951_-105+16 others(54): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177684 | |||||
| chr15:69177684
|
CCTTTATC others(17): Show |
C | 8 | a0001c0001t0001g0237a0001c0001t0001g0266a0001c0001t0001g0276others(5): Show | 8 | HG00738.hp2 HG02055.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-105+16975_-105+16 others(30): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177684 | |||||
| chr15:69177684
|
CCTTTATC others(41): Show |
C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+16951_-105+16 others(54): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69177684 | |||||
| chr15:69177822
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-105+17065G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177822 | ||||||
| chr15:69177924
|
G | T | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+17167G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69177924 | ||||||
| chr15:69178113
|
G | T | 2 | a0002c0002t0002g0197a0002c0002t0002g0198 | 2 | NA18945.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-105+17356G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178113 | ||||||
| chr15:69178333
|
C | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00621.hp1 HG02071.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-105+17576C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178333 | ||||||
| chr15:69178348
|
G | GTTTTATT others(17): Show |
1 | a0003c0004t0002g0080 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-105+17593_-105+17 others(30): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69178348 | |||||
| chr15:69178351
|
G | T | 1 | a0003c0004t0002g0080 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-105+17594G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178351 | ||||||
| chr15:69178409
|
A | G | 2 | a0002c0002t0009g0105a0002c0002t0009g0106 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-105+17652A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178409 | ||||||
| chr15:69178621
|
A | C | 1 | a0003c0004t0002g0034 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-105+17864A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178621 | ||||||
| chr15:69178685
|
T | G | 2 | a0002c0002t0004g0108a0006c0008t0004g0109 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-105+17928T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178685 | ||||||
| chr15:69178709
|
A | G | 1 | a0001c0001t0022g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-105+17952A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178709 | ||||||
| chr15:69178731
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-105+17974A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178731 | ||||||
| chr15:69178744
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-105+17987A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178744 | ||||||
| chr15:69178780
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-105+18023A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178780 | ||||||
| chr15:69178848
|
C | G | 1 | a0001c0001t0022g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-105+18091C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178848 | ||||||
| chr15:69178899
|
A | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+18142A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69178899 | ||||||
| chr15:69179008
|
T | G | 1 | a0002c0002t0002g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-105+18251T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179008 | ||||||
| chr15:69179049
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-105+18292G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179049 | ||||||
| chr15:69179286
|
G | T | 7 | a0001c0001t0003g0148a0001c0001t0003g0151a0001c0001t0003g0152others(4): Show | 7 | NA18968.hp1 NA18969.hp1 NA18997.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+18529G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179286 | ||||||
| chr15:69179378
|
G | A | 1 | a0002c0002t0002g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-105+18621G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179378 | ||||||
| chr15:69179657
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+18900G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179657 | ||||||
| chr15:69179658
|
A | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+18901A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179658 | ||||||
| chr15:69179672
|
C | T | 1 | a0002c0002t0002g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+18915C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179672 | ||||||
| chr15:69179676
|
C | A | 5 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(2): Show | 6 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+18919C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179676 | ||||||
| chr15:69179832
|
C | T | 2 | a0002c0002t0002g0039a0002c0002t0002g0040 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-105+19075C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179832 | ||||||
| chr15:69179944
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-105+19187G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179944 | ||||||
| chr15:69179996
|
T | A | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 220 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-105+19239T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69179996 | ||||||
| chr15:69180312
|
G | C | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+19555G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180312 | ||||||
| chr15:69180325
|
C | A | 4 | a0002c0002t0002g0025a0002c0002t0002g0041a0002c0002t0002g0042others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+19568C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180325 | ||||||
| chr15:69180351
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-105+19594C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180351 | ||||||
| chr15:69180395
|
T | TA | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+19646dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69180395 | |||||
| chr15:69180520
|
G | T | 1 | a0001c0003t0016g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105+19763G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180520 | ||||||
| chr15:69180687
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-105+19930G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180687 | ||||||
| chr15:69180747
|
C | T | 1 | a0001c0001t0003g0192 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-105+19990C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180747 | ||||||
| chr15:69180772
|
C | T | 3 | a0002c0002t0002g0038a0002c0002t0002g0073a0002c0002t0002g0074 | 3 | HG01346.hp1 HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-105+20015C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180772 | ||||||
| chr15:69180798
|
T | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+20041T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180798 | ||||||
| chr15:69180807
|
C | T | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+20050C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180807 | ||||||
| chr15:69180808
|
G | C | 9 | a0002c0002t0002g0021a0002c0002t0002g0025a0002c0002t0002g0031others(6): Show | 9 | HG00738.hp1 HG01106.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+20051G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69180808 | ||||||
| chr15:69181202
|
T | C | 3 | a0002c0002t0002g0163a0002c0002t0002g0197a0002c0002t0002g0198 | 3 | HG02523.hp1 NA18945.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-105+20445T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69181202 | ||||||
| chr15:69181332
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-105+20575G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69181332 | ||||||
| chr15:69181696
|
G | A | 1 | a0001c0001t0015g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-105+20939G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69181696 | ||||||
| chr15:69181778
|
AAG | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+21027_-105+21 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69181778 | |||||
| chr15:69181872
|
C | T | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-105+21115C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69181872 | ||||||
| chr15:69181990
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-105+21233C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69181990 | ||||||
| chr15:69182163
|
A | T | 15 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(12): Show | 16 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.-105+21406A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182163 | ||||||
| chr15:69182230
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+21473C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182230 | ||||||
| chr15:69182269
|
T | TTG | 23 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0211others(20): Show | 23 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-105+21541_-105+21 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69182269 | |||||
| chr15:69182269
|
T | TTGTG | 3 | a0001c0001t0001g0310a0002c0002t0002g0022a0002c0002t0002g0328 | 3 | HG02523.hp2 HG03098.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-105+21539_-105+21 others(10): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69182269 | |||||
| chr15:69182269
|
T | TTGTTTGT others(1): Show |
7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+21515_-105+21 others(14): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69182269 | |||||
| chr15:69182296
|
T | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0147a0001c0001t0003g0157others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-105+21539T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182296 | ||||||
| chr15:69182298
|
T | A | 77 | a0001c0001t0001g0304a0001c0001t0003g0001a0001c0001t0003g0004others(74): Show | 80 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-105+21541T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182298 | ||||||
| chr15:69182298
|
T | TGA | 3 | a0001c0001t0001g0277a0001c0006t0012g0208a0001c0006t0012g0209 | 3 | HG02895.hp1 HG02897.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-105+21559_-105+21 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69182298 | |||||
| chr15:69182385
|
A | AAG | 7 | a0001c0001t0001g0005a0001c0001t0001g0239a0001c0001t0001g0324others(4): Show | 8 | HG02071.hp2 HG02602.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.-105+21649_-105+21 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69182385 | |||||
| chr15:69182486
|
A | C | 1 | a0002c0002t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-105+21729A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182486 | ||||||
| chr15:69182875
|
T | C | 2 | a0002c0002t0002g0102a0002c0002t0002g0103 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-105+22118T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182875 | ||||||
| chr15:69182898
|
C | G | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-105+22141C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69182898 | ||||||
| chr15:69183112
|
C | G | 1 | a0001c0001t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-105+22355C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69183112 | ||||||
| chr15:69183748
|
G | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+22991G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69183748 | ||||||
| chr15:69183766
|
A | G | 1 | a0002c0002t0002g0092 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-105+23009A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69183766 | ||||||
| chr15:69184033
|
C | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+23276C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69184033 | ||||||
| chr15:69184205
|
G | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-105+23448G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69184205 | ||||||
| chr15:69184205
|
G | T | 1 | a0001c0001t0003g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-105+23448G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69184205 | ||||||
| chr15:69184569
|
T | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+23812T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69184569 | ||||||
| chr15:69184590
|
C | G | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+23833C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69184590 | ||||||
| chr15:69184950
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+24193T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69184950 | ||||||
| chr15:69185041
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-105+24284G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185041 | ||||||
| chr15:69185103
|
T | A | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+24346T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185103 | ||||||
| chr15:69185185
|
A | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+24428A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185185 | ||||||
| chr15:69185280
|
A | G | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-105+24523A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185280 | ||||||
| chr15:69185312
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-105+24555C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185312 | ||||||
| chr15:69185312
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-105+24555C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185312 | ||||||
| chr15:69185461
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+24704G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185461 | ||||||
| chr15:69185568
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-24748C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185568 | ||||||
| chr15:69185571
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-24745G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185571 | ||||||
| chr15:69185676
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-104-24640A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185676 | ||||||
| chr15:69185721
|
T | C | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104-24595T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185721 | ||||||
| chr15:69185744
|
A | G | 2 | a0001c0001t0003g0190a0001c0001t0003g0192 | 2 | NA18998.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-104-24572A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185744 | ||||||
| chr15:69185777
|
C | A | 1 | a0001c0001t0001g0306 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-104-24539C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69185777 | ||||||
| chr15:69186035
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-104-24281A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186035 | ||||||
| chr15:69186075
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-24241G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186075 | ||||||
| chr15:69186120
|
C | T | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-104-24196C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186120 | ||||||
| chr15:69186219
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-104-24097A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186219 | ||||||
| chr15:69186514
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-104-23802A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186514 | ||||||
| chr15:69186628
|
A | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-104-23688A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186628 | ||||||
| chr15:69186735
|
T | G | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-104-23581T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186735 | ||||||
| chr15:69186952
|
A | G | 1 | a0002c0002t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-104-23364A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69186952 | ||||||
| chr15:69187008
|
G | C | 14 | a0002c0002t0002g0111a0002c0002t0002g0130a0002c0002t0004g0104others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-104-23308G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187008 | ||||||
| chr15:69187267
|
A | C | 1 | a0002c0002t0002g0121 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-104-23049A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187267 | ||||||
| chr15:69187284
|
AT | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-23024delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69187284 | |||||
| chr15:69187386
|
A | G | 6 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0002t0002g0067others(3): Show | 6 | HG00423.hp2 NA18956.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-104-22930A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187386 | ||||||
| chr15:69187464
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-104-22852A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187464 | ||||||
| chr15:69187706
|
G | A | 4 | a0002c0002t0002g0130a0002c0002t0004g0108a0002c0002t0004g0117others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-22610G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187706 | ||||||
| chr15:69187861
|
G | A | 2 | a0001c0001t0003g0190a0001c0001t0003g0192 | 2 | NA18998.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-104-22455G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187861 | ||||||
| chr15:69187892
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-104-22424G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187892 | ||||||
| chr15:69187898
|
A | G | 1 | a0001c0001t0022g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-104-22418A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69187898 | ||||||
| chr15:69188051
|
G | A | 1 | a0002c0002t0018g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-104-22265G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188051 | ||||||
| chr15:69188074
|
A | C | 5 | a0002c0002t0002g0082a0003c0004t0002g0034a0003c0004t0002g0062others(2): Show | 5 | HG02080.hp2 NA18939.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104-22242A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188074 | ||||||
| chr15:69188086
|
C | A | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 233 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-104-22230C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188086 | ||||||
| chr15:69188138
|
G | T | 1 | a0002c0002t0002g0332 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-104-22178G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188138 | ||||||
| chr15:69188210
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-104-22106C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188210 | ||||||
| chr15:69188421
|
T | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 203 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-104-21895T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188421 | ||||||
| chr15:69188447
|
C | T | 9 | a0001c0001t0003g0157a0001c0001t0003g0162a0001c0001t0003g0166others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-104-21869C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188447 | ||||||
| chr15:69188530
|
C | T | 332 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(329): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-104-21786C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188530 | ||||||
| chr15:69188732
|
T | C | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-21584T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188732 | ||||||
| chr15:69188742
|
A | G | 2 | a0001c0001t0003g0145a0002c0002t0011g0144 | 2 | HG00741.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-104-21574A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188742 | ||||||
| chr15:69188839
|
A | G | 1 | a0001c0003t0005g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-104-21477A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188839 | ||||||
| chr15:69188952
|
C | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-21364C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188952 | ||||||
| chr15:69188995
|
T | G | 1 | a0002c0002t0002g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-104-21321T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69188995 | ||||||
| chr15:69189056
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-104-21260T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189056 | ||||||
| chr15:69189113
|
G | T | 1 | a0001c0001t0003g0165 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104-21203G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189113 | ||||||
| chr15:69189148
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-104-21168A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189148 | ||||||
| chr15:69189291
|
G | A | 13 | a0002c0002t0002g0038a0002c0002t0002g0070a0002c0002t0002g0073others(10): Show | 13 | HG01167.hp1 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104-21025G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189291 | ||||||
| chr15:69189332
|
C | A | 1 | a0002c0002t0002g0070 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-104-20984C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189332 | ||||||
| chr15:69189376
|
C | T | 5 | a0002c0002t0002g0018a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 5 | NA18747.hp1 NA18961.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-20940C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189376 | ||||||
| chr15:69189389
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0223a0001c0001t0001g0229others(16): Show | 20 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.-104-20927C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189389 | ||||||
| chr15:69189460
|
G | A | 1 | a0002c0002t0017g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-104-20856G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189460 | ||||||
| chr15:69189694
|
G | T | 1 | a0001c0001t0003g0189 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-104-20622G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189694 | ||||||
| chr15:69189723
|
C | T | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104-20593C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69189723 | ||||||
| chr15:69190021
|
C | T | 1 | a0001c0003t0006g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-104-20295C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190021 | ||||||
| chr15:69190024
|
G | A | 2 | a0001c0003t0006g0326a0001c0003t0016g0327 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-104-20292G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190024 | ||||||
| chr15:69190057
|
C | G | 2 | a0002c0002t0002g0061a0002c0002t0002g0078 | 2 | HG00438.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-104-20259C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190057 | ||||||
| chr15:69190092
|
A | AT | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-20215dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69190092 | |||||
| chr15:69190318
|
G | A | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104-19998G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190318 | ||||||
| chr15:69190360
|
C | T | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-104-19956C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190360 | ||||||
| chr15:69190501
|
A | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-19815A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190501 | ||||||
| chr15:69190734
|
C | A | 2 | a0002c0002t0004g0104a0002c0002t0004g0112 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104-19582C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190734 | ||||||
| chr15:69190788
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0093 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-104-19528G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69190788 | ||||||
| chr15:69191044
|
C | T | 27 | a0001c0001t0001g0020a0001c0001t0001g0030a0002c0002t0002g0029others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-104-19272C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69191044 | ||||||
| chr15:69191114
|
T | A | 1 | a0002c0002t0002g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-104-19202T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69191114 | ||||||
| chr15:69191865
|
C | G | 1 | a0001c0001t0003g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-104-18451C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69191865 | ||||||
| chr15:69191868
|
G | T | 2 | a0002c0002t0002g0033a0002c0002t0002g0081 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-18448G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69191868 | ||||||
| chr15:69192076
|
G | A | 5 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0002g0077others(2): Show | 5 | HG02451.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-18240G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69192076 | ||||||
| chr15:69192085
|
G | A | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-18231G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69192085 | ||||||
| chr15:69192219
|
A | G | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-104-18097A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69192219 | ||||||
| chr15:69192241
|
A | ATG | 8 | a0001c0001t0001g0313a0001c0001t0003g0148a0001c0001t0003g0151others(5): Show | 8 | NA18968.hp1 NA18969.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104-18059_-104-18 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69192241 | |||||
| chr15:69192351
|
TATA | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-17958_-104-17 others(9): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69192351 | |||||
| chr15:69192354
|
A | AATAATAT others(285): Show |
3 | a0001c0001t0001g0303a0001c0001t0001g0308a0001c0001t0001g0310 | 3 | HG02523.hp2 NA18991.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-104-17951_-104-17 others(298): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69192354 | |||||
| chr15:69192451
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-17865T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69192451 | ||||||
| chr15:69192668
|
A | G | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 221 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-104-17648A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69192668 | ||||||
| chr15:69192735
|
A | G | 2 | a0002c0002t0002g0119a0002c0002t0002g0120 | 2 | HG01496.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-104-17581A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69192735 | ||||||
| chr15:69193127
|
A | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-17189A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193127 | ||||||
| chr15:69193129
|
A | G | 2 | a0001c0001t0003g0152a0001c0001t0003g0195 | 2 | NA18968.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-104-17187A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193129 | ||||||
| chr15:69193246
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0210 | 3 | NA18974.hp2 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-104-17070T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193246 | ||||||
| chr15:69193368
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-16948T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193368 | ||||||
| chr15:69193544
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-104-16772C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193544 | ||||||
| chr15:69193826
|
T | G | 2 | a0002c0002t0002g0031a0002c0002t0002g0075 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-104-16490T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193826 | ||||||
| chr15:69193869
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-104-16447C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193869 | ||||||
| chr15:69193877
|
G | T | 21 | a0002c0002t0002g0111a0002c0002t0002g0130a0002c0002t0004g0104others(18): Show | 21 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-104-16439G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69193877 | ||||||
| chr15:69194001
|
A | C | 1 | a0002c0002t0002g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-104-16315A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194001 | ||||||
| chr15:69194133
|
T | G | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-104-16183T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194133 | ||||||
| chr15:69194254
|
C | T | 4 | a0002c0002t0002g0025a0002c0002t0002g0041a0002c0002t0002g0042others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-16062C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194254 | ||||||
| chr15:69194398
|
G | A | 10 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(7): Show | 11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104-15918G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194398 | ||||||
| chr15:69194569
|
G | A | 1 | a0002c0002t0002g0026 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-104-15747G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194569 | ||||||
| chr15:69194579
|
A | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-15737A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194579 | ||||||
| chr15:69194614
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-104-15702C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194614 | ||||||
| chr15:69194657
|
G | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0030 | 2 | HG00597.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-104-15659G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194657 | ||||||
| chr15:69194702
|
G | A | 11 | a0001c0001t0003g0147a0001c0001t0003g0157a0001c0001t0003g0162others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-104-15614G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194702 | ||||||
| chr15:69194860
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-104-15456A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194860 | ||||||
| chr15:69194870
|
G | A | 69 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(66): Show | 72 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-104-15446G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69194870 | ||||||
| chr15:69195885
|
G | C | 1 | a0003c0004t0002g0083 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-104-14431G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69195885 | ||||||
| chr15:69195934
|
A | G | 1 | a0002c0002t0002g0328 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-104-14382A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69195934 | ||||||
| chr15:69195968
|
A | G | 1 | a0003c0004t0002g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-104-14348A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69195968 | ||||||
| chr15:69196033
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-104-14283T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196033 | ||||||
| chr15:69196134
|
A | T | 2 | a0001c0001t0001g0211a0001c0001t0023g0212 | 2 | NA18950.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-104-14182A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196134 | ||||||
| chr15:69196261
|
C | T | 1 | a0002c0002t0004g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-104-14055C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196261 | ||||||
| chr15:69196408
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-104-13908T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196408 | ||||||
| chr15:69196409
|
A | AT | 330 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(327): Show | 338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-104-13904dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69196409 | |||||
| chr15:69196409
|
A | T | 1 | a0001c0001t0001g0313 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-104-13907A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196409 | ||||||
| chr15:69196592
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-104-13724C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196592 | ||||||
| chr15:69196652
|
A | G | 15 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(12): Show | 16 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.-104-13664A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196652 | ||||||
| chr15:69196947
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-104-13369G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69196947 | ||||||
| chr15:69197047
|
C | G | 1 | a0002c0002t0002g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104-13269C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197047 | ||||||
| chr15:69197064
|
A | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-13252A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197064 | ||||||
| chr15:69197131
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-13185G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197131 | ||||||
| chr15:69197198
|
G | A | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104-13118G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197198 | ||||||
| chr15:69197573
|
A | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-12743A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197573 | ||||||
| chr15:69197574
|
C | T | 4 | a0001c0001t0003g0151a0001c0001t0003g0156a0001c0001t0003g0193others(1): Show | 4 | NA18969.hp1 NA19000.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-12742C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197574 | ||||||
| chr15:69197869
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-12447C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197869 | ||||||
| chr15:69197903
|
A | G | 1 | a0002c0002t0002g0163 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-104-12413A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69197903 | ||||||
| chr15:69198212
|
C | T | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-12104C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198212 | ||||||
| chr15:69198433
|
A | G | 1 | a0002c0002t0002g0019 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-104-11883A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198433 | ||||||
| chr15:69198460
|
C | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | NA19000.hp2 NA19054.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-104-11856C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198460 | ||||||
| chr15:69198484
|
C | T | 5 | a0002c0002t0002g0038a0002c0002t0002g0070a0002c0002t0002g0073others(2): Show | 5 | HG01346.hp1 HG01928.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104-11832C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198484 | ||||||
| chr15:69198566
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-104-11750G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198566 | ||||||
| chr15:69198677
|
T | G | 1 | a0002c0002t0017g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-104-11639T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198677 | ||||||
| chr15:69198848
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-104-11468C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198848 | ||||||
| chr15:69198937
|
G | A | 10 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(7): Show | 11 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104-11379G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198937 | ||||||
| chr15:69198983
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-104-11333A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69198983 | ||||||
| chr15:69199128
|
T | G | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 220 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-104-11188T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199128 | ||||||
| chr15:69199187
|
T | G | 1 | a0001c0003t0006g0135 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-104-11129T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199187 | ||||||
| chr15:69199210
|
T | A | 2 | a0001c0003t0014g0131a0001c0003t0014g0136 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-104-11106T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199210 | ||||||
| chr15:69199443
|
TTATAAA | T | 4 | a0001c0003t0006g0326a0001c0003t0014g0131a0001c0003t0014g0136others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-10872_-104-10 others(12): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199443 | ||||||
| chr15:69199491
|
T | G | 1 | a0001c0003t0006g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-104-10825T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199491 | ||||||
| chr15:69199530
|
G | T | 1 | a0002c0002t0002g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-104-10786G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199530 | ||||||
| chr15:69199601
|
G | C | 1 | a0002c0002t0002g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-104-10715G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199601 | ||||||
| chr15:69199623
|
T | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-10693T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199623 | ||||||
| chr15:69199938
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-104-10378T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69199938 | ||||||
| chr15:69200029
|
A | C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-104-10287A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200029 | ||||||
| chr15:69200137
|
A | G | 3 | a0002c0002t0002g0038a0002c0002t0002g0073a0002c0002t0002g0074 | 3 | HG01346.hp1 HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-104-10179A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200137 | ||||||
| chr15:69200162
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0263 | 2 | HG02027.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-104-10154G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200162 | ||||||
| chr15:69200286
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-10030C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200286 | ||||||
| chr15:69200353
|
T | G | 1 | a0001c0001t0001g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-104-9963T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200353 | ||||||
| chr15:69200353
|
T | TGA | 4 | a0001c0003t0006g0326a0001c0003t0014g0131a0001c0003t0014g0136others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-9962_-104-996 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69200353 | |||||
| chr15:69200571
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-104-9745G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200571 | ||||||
| chr15:69200832
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-104-9484T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69200832 | ||||||
| chr15:69201065
|
A | G | 1 | a0001c0001t0003g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-104-9251A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201065 | ||||||
| chr15:69201130
|
C | T | 104 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0091others(101): Show | 105 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-104-9186C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201130 | ||||||
| chr15:69201192
|
T | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104-9124T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201192 | ||||||
| chr15:69201201
|
A | G | 1 | a0002c0002t0009g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-104-9115A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201201 | ||||||
| chr15:69201296
|
A | C | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104-9020A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201296 | ||||||
| chr15:69201434
|
A | G | 1 | a0002c0002t0002g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104-8882A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201434 | ||||||
| chr15:69201572
|
G | C | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-104-8744G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201572 | ||||||
| chr15:69201883
|
T | C | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-104-8433T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69201883 | ||||||
| chr15:69202101
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-8215G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202101 | ||||||
| chr15:69202208
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-8108C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202208 | ||||||
| chr15:69202514
|
T | C | 1 | a0001c0001t0015g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-104-7802T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202514 | ||||||
| chr15:69202528
|
G | A | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.-104-7788G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202528 | ||||||
| chr15:69202555
|
T | G | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-7761T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202555 | ||||||
| chr15:69202708
|
T | A | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-7608T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202708 | ||||||
| chr15:69202819
|
T | TCCCAAAT others(2614): Show |
1 | a0002c0002t0002g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-104-7482_-104-748 others(2625): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69202819 | |||||
| chr15:69202959
|
A | G | 2 | a0001c0001t0003g0190a0001c0001t0003g0192 | 2 | NA18998.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-104-7357A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202959 | ||||||
| chr15:69202978
|
G | A | 1 | a0002c0002t0010g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-104-7338G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202978 | ||||||
| chr15:69202998
|
T | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG00639.hp1 HG01257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-104-7318T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69202998 | ||||||
| chr15:69203026
|
G | A | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 220 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-104-7290G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69203026 | ||||||
| chr15:69203333
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-6983G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69203333 | ||||||
| chr15:69203717
|
A | G | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-104-6599A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69203717 | ||||||
| chr15:69203734
|
G | C | 4 | a0003c0004t0002g0034a0003c0004t0002g0062a0003c0004t0002g0063others(1): Show | 4 | NA18939.hp1 NA18975.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-6582G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69203734 | ||||||
| chr15:69204124
|
A | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-6192A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204124 | ||||||
| chr15:69204247
|
T | TAA | 4 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0013g0015others(1): Show | 4 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-6064_-104-606 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69204247 | |||||
| chr15:69204277
|
C | CT | 14 | a0001c0001t0001g0254a0001c0001t0003g0162a0001c0001t0003g0186others(11): Show | 14 | HG00621.hp2 HG02055.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-104-6016dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69204277 | |||||
| chr15:69204277
|
CT | C | 128 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-104-6016delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69204277 | |||||
| chr15:69204360
|
A | G | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-5956A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204360 | ||||||
| chr15:69204427
|
C | T | 51 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0145others(48): Show | 54 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-104-5889C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204427 | ||||||
| chr15:69204481
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0210 | 3 | NA18974.hp2 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-104-5835C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204481 | ||||||
| chr15:69204700
|
A | G | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0280others(2): Show | 5 | HG00408.hp1 HG00544.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-5616A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204700 | ||||||
| chr15:69204723
|
T | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-104-5593T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204723 | ||||||
| chr15:69204938
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-104-5378A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69204938 | ||||||
| chr15:69205091
|
A | G | 1 | a0002c0002t0002g0092 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-104-5225A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205091 | ||||||
| chr15:69205167
|
C | A | 1 | a0002c0002t0002g0021 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-104-5149C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205167 | ||||||
| chr15:69205224
|
T | G | 1 | a0001c0001t0024g0288 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-104-5092T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205224 | ||||||
| chr15:69205419
|
T | C | 2 | a0002c0002t0004g0115a0002c0002t0004g0116 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-104-4897T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205419 | ||||||
| chr15:69205485
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104-4831G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205485 | ||||||
| chr15:69205660
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-104-4656G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205660 | ||||||
| chr15:69205832
|
T | C | 1 | a0002c0002t0019g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-104-4484T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205832 | ||||||
| chr15:69205980
|
G | A | 332 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(329): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-104-4336G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69205980 | ||||||
| chr15:69206123
|
C | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-104-4193C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206123 | ||||||
| chr15:69206172
|
A | C | 1 | a0002c0002t0002g0333 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-104-4144A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206172 | ||||||
| chr15:69206192
|
G | C | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-104-4124G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206192 | ||||||
| chr15:69206204
|
G | A | 2 | a0002c0002t0002g0046a0002c0002t0002g0050 | 2 | HG00621.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-104-4112G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206204 | ||||||
| chr15:69206206
|
G | GTTT | 5 | a0001c0003t0006g0326a0001c0003t0014g0131a0001c0003t0014g0136others(2): Show | 5 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-4109_-104-410 others(7): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69206206 | |||||
| chr15:69206604
|
A | G | 1 | a0002c0002t0002g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-104-3712A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206604 | ||||||
| chr15:69206609
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0187 | 3 | HG00673.hp1 HG02040.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-104-3707T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206609 | ||||||
| chr15:69206844
|
A | G | 57 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0129others(54): Show | 60 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-104-3472A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206844 | ||||||
| chr15:69206886
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0253 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-104-3430A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69206886 | ||||||
| chr15:69207225
|
A | G | 4 | a0001c0003t0006g0326a0001c0003t0014g0131a0001c0003t0014g0136others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-3091A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207225 | ||||||
| chr15:69207252
|
T | G | 1 | a0002c0002t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-104-3064T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207252 | ||||||
| chr15:69207577
|
A | G | 2 | a0002c0002t0002g0027a0002c0002t0002g0049 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-104-2739A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207577 | ||||||
| chr15:69207651
|
C | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-2665C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207651 | ||||||
| chr15:69207741
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-104-2575C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207741 | ||||||
| chr15:69207828
|
G | C | 331 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-104-2488G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207828 | ||||||
| chr15:69207964
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-104-2352A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69207964 | ||||||
| chr15:69208320
|
G | A | 1 | a0002c0002t0019g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-104-1996G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208320 | ||||||
| chr15:69208409
|
A | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0218others(69): Show | 74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-104-1907A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208409 | ||||||
| chr15:69208459
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-104-1857A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208459 | ||||||
| chr15:69208471
|
ACT | A | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104-1842_-104-184 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69208471 | |||||
| chr15:69208542
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-104-1774C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208542 | ||||||
| chr15:69208601
|
C | T | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104-1715C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208601 | ||||||
| chr15:69208635
|
C | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 217 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-104-1681C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208635 | ||||||
| chr15:69208978
|
G | C | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 221 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-104-1338G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69208978 | ||||||
| chr15:69209045
|
G | C | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 206 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-104-1271G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69209045 | ||||||
| chr15:69209180
|
C | A | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-104-1136C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69209180 | ||||||
| chr15:69209208
|
A | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104-1108A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69209208 | ||||||
| chr15:69209434
|
C | CA | 65 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0091others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-104-881dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | 69209434 | |||||
| chr15:69209484
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-104-832A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69209484 | ||||||
| chr15:69209555
|
C | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 206 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-104-761C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69209555 | ||||||
| chr15:69210104
|
G | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-104-212G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69210104 | ||||||
| chr15:69210117
|
T | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-199T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69210117 | ||||||
| chr15:69210132
|
T | C | 4 | a0002c0002t0002g0025a0002c0002t0002g0041a0002c0002t0002g0042others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-184T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69210132 | ||||||
| chr15:69210312
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0222 | 2 | NA18966.hp1 NA18968.hp2 |
splice_region_variant&intron_variant | LOW | c.-104-4C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | chr15 | 69210312 | ||||||
| chr15:69210927
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-14+521G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69210927 | ||||||
| chr15:69210977
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14+571A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69210977 | ||||||
| chr15:69211060
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-14+654A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211060 | ||||||
| chr15:69211361
|
G | T | 1 | a0001c0001t0003g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-14+955G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211361 | ||||||
| chr15:69211387
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14+981A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211387 | ||||||
| chr15:69211392
|
T | C | 1 | a0001c0001t0001g0313 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-14+986T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211392 | ||||||
| chr15:69211628
|
C | T | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-14+1222C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211628 | ||||||
| chr15:69211650
|
T | C | 10 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0039others(7): Show | 11 | HG00140.hp2 HG00280.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14+1244T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211650 | ||||||
| chr15:69211671
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-14+1265A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69211671 | ||||||
| chr15:69212062
|
G | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 217 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-14+1656G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212062 | ||||||
| chr15:69212192
|
G | T | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+1786G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212192 | ||||||
| chr15:69212306
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-14+1900C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212306 | ||||||
| chr15:69212383
|
G | A | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+1977G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212383 | ||||||
| chr15:69212426
|
A | G | 2 | a0001c0001t0003g0145a0002c0002t0011g0144 | 2 | HG00741.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-14+2020A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212426 | ||||||
| chr15:69212839
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-14+2433A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212839 | ||||||
| chr15:69212862
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-14+2456G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212862 | ||||||
| chr15:69212919
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0276 | 2 | HG00738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-14+2513T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212919 | ||||||
| chr15:69212980
|
A | T | 1 | a0001c0001t0001g0300 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-14+2574A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69212980 | ||||||
| chr15:69213262
|
A | G | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+2856A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213262 | ||||||
| chr15:69213285
|
T | A | 4 | a0002c0002t0002g0130a0002c0002t0004g0108a0002c0002t0004g0117others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2879T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213285 | ||||||
| chr15:69213287
|
T | G | 4 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0013g0015others(1): Show | 4 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2881T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213287 | ||||||
| chr15:69213311
|
C | T | 9 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(6): Show | 10 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+2905C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213311 | ||||||
| chr15:69213425
|
T | C | 1 | a0002c0002t0002g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-14+3019T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213425 | ||||||
| chr15:69213675
|
T | G | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-14+3269T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213675 | ||||||
| chr15:69213685
|
A | C | 7 | a0002c0002t0010g0010a0002c0002t0010g0011a0004c0005t0007g0012others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+3279A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213685 | ||||||
| chr15:69213823
|
C | T | 2 | a0001c0003t0014g0131a0001c0003t0014g0136 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-14+3417C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213823 | ||||||
| chr15:69213904
|
T | C | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-14+3498T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213904 | ||||||
| chr15:69213938
|
T | C | 53 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0091others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-14+3532T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213938 | ||||||
| chr15:69213981
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-14+3575C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69213981 | ||||||
| chr15:69214186
|
G | T | 1 | a0001c0009t0001g0217 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-14+3780G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214186 | ||||||
| chr15:69214227
|
A | C | 1 | a0001c0001t0001g0325 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-14+3821A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214227 | ||||||
| chr15:69214238
|
G | A | 1 | a0002c0002t0011g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-14+3832G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214238 | ||||||
| chr15:69214246
|
A | G | 39 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0021others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+3840A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214246 | ||||||
| chr15:69214331
|
A | G | 8 | a0002c0002t0002g0128a0002c0002t0010g0010a0002c0002t0010g0011others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+3925A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214331 | ||||||
| chr15:69214661
|
T | G | 4 | a0001c0001t0003g0132a0001c0001t0003g0133a0002c0002t0002g0017others(1): Show | 4 | HG01255.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+4255T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214661 | ||||||
| chr15:69214696
|
CA | C | 5 | a0001c0003t0006g0134a0001c0003t0006g0135a0001c0003t0006g0142others(2): Show | 5 | HG03098.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+4292delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69214696 | |||||
| chr15:69214726
|
C | G | 1 | a0002c0002t0002g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-14+4320C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69214726 | ||||||
| chr15:69215121
|
T | C | 177 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.-14+4715T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215121 | ||||||
| chr15:69215195
|
C | T | 4 | a0001c0001t0003g0185a0001c0003t0006g0134a0001c0003t0006g0326others(1): Show | 4 | HG01884.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+4789C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215195 | ||||||
| chr15:69215273
|
A | T | 2 | a0002c0002t0004g0108a0006c0008t0004g0109 | 2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-14+4867A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215273 | ||||||
| chr15:69215313
|
T | C | 4 | a0002c0002t0004g0113a0002c0002t0004g0114a0002c0002t0004g0115others(1): Show | 4 | HG01884.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+4907T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215313 | ||||||
| chr15:69215414
|
T | C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+5008T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215414 | ||||||
| chr15:69215440
|
A | G | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-14+5034A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215440 | ||||||
| chr15:69215466
|
T | C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+5060T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215466 | ||||||
| chr15:69215539
|
G | GGTGT | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-14+5154_-14+5157d others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69215539 | |||||
| chr15:69215539
|
G | GGTGTGT | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00544.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.-14+5152_-14+5157d others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69215539 | |||||
| chr15:69215539
|
G | GGTGTGTG others(1): Show |
19 | a0001c0001t0001g0299a0001c0001t0003g0155a0001c0001t0003g0192others(16): Show | 20 | HG00438.hp1 HG02280.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14+5150_-14+5157d others(10): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69215539 | |||||
| chr15:69215612
|
T | C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+5206T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215612 | ||||||
| chr15:69215630
|
CCTTAT | C | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+5229_-14+5233d others(7): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69215630 | |||||
| chr15:69215689
|
A | G | 331 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-14+5283A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215689 | ||||||
| chr15:69215693
|
A | T | 3 | a0001c0003t0006g0134a0001c0003t0006g0326a0001c0003t0016g0327 | 3 | HG03098.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-14+5287A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215693 | ||||||
| chr15:69215769
|
A | G | 1 | a0001c0001t0003g0202 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14+5363A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215769 | ||||||
| chr15:69215828
|
G | T | 62 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(59): Show | 65 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-14+5422G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215828 | ||||||
| chr15:69215986
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0222 | 2 | NA18966.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-14+5580C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69215986 | ||||||
| chr15:69216076
|
T | C | 1 | a0001c0001t0003g0192 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-14+5670T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216076 | ||||||
| chr15:69216115
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-14+5709T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216115 | ||||||
| chr15:69216123
|
G | A | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-14+5717G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216123 | ||||||
| chr15:69216326
|
A | G | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+5920A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216326 | ||||||
| chr15:69216475
|
T | C | 1 | a0001c0003t0005g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14+6069T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216475 | ||||||
| chr15:69216517
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14+6111G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216517 | ||||||
| chr15:69216746
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-14+6340A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216746 | ||||||
| chr15:69216824
|
A | G | 1 | a0004c0005t0013g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14+6418A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69216824 | ||||||
| chr15:69217013
|
G | A | 1 | a0001c0003t0006g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-14+6607G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69217013 | ||||||
| chr15:69217404
|
A | G | 3 | a0001c0003t0014g0131a0001c0003t0014g0136a0001c0003t0026g0143 | 3 | HG02258.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-14+6998A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69217404 | ||||||
| chr15:69217487
|
T | G | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-14+7081T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69217487 | ||||||
| chr15:69217620
|
A | T | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+7214A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69217620 | ||||||
| chr15:69217884
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-14+7478G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69217884 | ||||||
| chr15:69217964
|
G | A | 332 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(329): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-14+7558G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69217964 | ||||||
| chr15:69218070
|
A | G | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+7664A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69218070 | ||||||
| chr15:69218149
|
C | CA | 77 | a0001c0001t0001g0005a0001c0001t0001g0091a0001c0001t0001g0093others(74): Show | 81 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-14+7764dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69218149 | |||||
| chr15:69218149
|
CA | C | 10 | a0001c0001t0001g0254a0001c0001t0001g0287a0001c0001t0001g0300others(7): Show | 10 | HG01515.hp1 HG01975.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14+7764delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69218149 | |||||
| chr15:69218265
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-14+7859T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69218265 | ||||||
| chr15:69218278
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-14+7872G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69218278 | ||||||
| chr15:69218794
|
C | T | 77 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(74): Show | 80 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-14+8388C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69218794 | ||||||
| chr15:69218910
|
A | G | 3 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014 | 3 | HG03225.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-14+8504A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69218910 | ||||||
| chr15:69219002
|
C | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+8596C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69219002 | ||||||
| chr15:69219303
|
G | A | 1 | a0002c0002t0002g0333 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-14+8897G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69219303 | ||||||
| chr15:69219365
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-14+8959T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69219365 | ||||||
| chr15:69219774
|
T | C | 1 | a0003c0004t0002g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-14+9368T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69219774 | ||||||
| chr15:69219841
|
T | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+9435T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69219841 | ||||||
| chr15:69220012
|
G | A | 4 | a0002c0002t0004g0113a0002c0002t0004g0114a0002c0002t0004g0115others(1): Show | 4 | HG01884.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+9606G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220012 | ||||||
| chr15:69220048
|
A | G | 41 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0021others(38): Show | 41 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-14+9642A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220048 | ||||||
| chr15:69220342
|
A | G | 1 | a0002c0002t0002g0328 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-14+9936A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220342 | ||||||
| chr15:69220519
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-14+10113G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220519 | ||||||
| chr15:69220579
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-14+10173T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220579 | ||||||
| chr15:69220585
|
G | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+10179G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220585 | ||||||
| chr15:69220624
|
C | T | 4 | a0002c0002t0002g0130a0002c0002t0004g0108a0002c0002t0004g0117others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+10218C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220624 | ||||||
| chr15:69220803
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-14+10397A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220803 | ||||||
| chr15:69220865
|
G | A | 1 | a0002c0002t0002g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-14+10459G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220865 | ||||||
| chr15:69220914
|
T | C | 2 | a0001c0003t0005g0137a0001c0003t0005g0141 | 2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-14+10508T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220914 | ||||||
| chr15:69220917
|
G | C | 2 | a0001c0003t0014g0131a0001c0003t0014g0136 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-14+10511G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220917 | ||||||
| chr15:69220960
|
T | C | 14 | a0002c0002t0002g0111a0002c0002t0002g0130a0002c0002t0004g0104others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14+10554T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220960 | ||||||
| chr15:69220975
|
A | G | 2 | a0002c0002t0009g0105a0002c0002t0009g0106 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+10569A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220975 | ||||||
| chr15:69220980
|
T | G | 231 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(228): Show | 238 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-14+10574T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69220980 | ||||||
| chr15:69221220
|
A | G | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-14+10814A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69221220 | ||||||
| chr15:69221351
|
A | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+10945A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69221351 | ||||||
| chr15:69221382
|
C | G | 77 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(74): Show | 80 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-14+10976C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69221382 | ||||||
| chr15:69221531
|
T | C | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-14+11125T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69221531 | ||||||
| chr15:69221569
|
T | TA | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 141 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-14+11171dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69221569 | |||||
| chr15:69221569
|
T | TAA | 77 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(74): Show | 80 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-14+11170_-14+1117 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69221569 | |||||
| chr15:69221848
|
G | C | 1 | a0001c0001t0001g0306 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-14+11442G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69221848 | ||||||
| chr15:69221862
|
CA | C | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-14+11479delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69221862 | |||||
| chr15:69221862
|
CAA | C | 6 | a0001c0001t0001g0274a0001c0003t0026g0143a0002c0002t0002g0068others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+11478_-14+1147 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69221862 | |||||
| chr15:69221996
|
G | A | 11 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14+11590G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69221996 | ||||||
| chr15:69222076
|
T | C | 1 | a0002c0002t0010g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-14+11670T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69222076 | ||||||
| chr15:69222464
|
G | C | 2 | a0002c0002t0009g0105a0002c0002t0009g0106 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+12058G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69222464 | ||||||
| chr15:69222656
|
T | G | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-14+12250T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69222656 | ||||||
| chr15:69222737
|
C | T | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+12331C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69222737 | ||||||
| chr15:69222806
|
A | G | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+12400A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69222806 | ||||||
| chr15:69223016
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-14+12610G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69223016 | ||||||
| chr15:69223018
|
G | A | 15 | a0002c0002t0002g0029a0002c0002t0002g0052a0002c0002t0002g0058others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.-14+12612G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69223018 | ||||||
| chr15:69223349
|
T | G | 6 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0108others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+12943T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69223349 | ||||||
| chr15:69223680
|
TC | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0263a0001c0001t0001g0308 | 3 | HG02027.hp2 NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-14+13276delC | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69223680 | |||||
| chr15:69223786
|
G | C | 6 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(3): Show | 7 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+13380G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69223786 | ||||||
| chr15:69223842
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+13436A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69223842 | ||||||
| chr15:69223947
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-14+13541G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69223947 | ||||||
| chr15:69224242
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14+13836G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69224242 | ||||||
| chr15:69224296
|
T | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+13890T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69224296 | ||||||
| chr15:69224411
|
T | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+14005T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69224411 | ||||||
| chr15:69224959
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-14+14553A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69224959 | ||||||
| chr15:69224979
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14+14573A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69224979 | ||||||
| chr15:69225028
|
G | A | 1 | a0002c0002t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-14+14622G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69225028 | ||||||
| chr15:69225092
|
C | A | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-14+14686C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69225092 | ||||||
| chr15:69225172
|
CT | C | 125 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 128 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-14+14777delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69225172 | |||||
| chr15:69225196
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-14+14790G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69225196 | ||||||
| chr15:69225594
|
A | C | 3 | a0001c0003t0005g0137a0001c0003t0005g0140a0001c0003t0005g0141 | 3 | HG02647.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-14+15188A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69225594 | ||||||
| chr15:69225615
|
A | G | 231 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(228): Show | 238 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-14+15209A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69225615 | ||||||
| chr15:69225754
|
T | C | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 222 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-14+15348T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69225754 | ||||||
| chr15:69226029
|
C | T | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+15623C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69226029 | ||||||
| chr15:69226042
|
GCACAGAC others(21): Show |
G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 142 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-14+15654_-14+1568 others(32): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226042 | |||||
| chr15:69226047
|
GACAC | G | 13 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14+15665_-14+1566 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226047 | |||||
| chr15:69226047
|
GACACACA others(1): Show |
G | 74 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(71): Show | 77 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-14+15661_-14+1566 others(12): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226047 | |||||
| chr15:69226077
|
C | G | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-14+15671C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69226077 | ||||||
| chr15:69226237
|
T | C | 1 | a0002c0002t0004g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-14+15831T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69226237 | ||||||
| chr15:69226375
|
A | T | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+15969A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69226375 | ||||||
| chr15:69226733
|
CT | C | 28 | a0002c0002t0002g0024a0002c0002t0002g0027a0002c0002t0002g0048others(25): Show | 28 | HG00741.hp2 HG01358.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14+16355delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226733 | |||||
| chr15:69226733
|
CTT | C | 91 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0018others(88): Show | 92 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-14+16354_-14+1635 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226733 | |||||
| chr15:69226733
|
CTTT | C | 21 | a0001c0001t0001g0210a0001c0001t0001g0235a0001c0001t0001g0237others(18): Show | 21 | HG01106.hp1 HG01358.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14+16353_-14+1635 others(7): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226733 | |||||
| chr15:69226733
|
CTTTT | C | 166 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 172 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-14+16352_-14+1635 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226733 | |||||
| chr15:69226733
|
CTTTTT | C | 24 | a0001c0001t0001g0220a0001c0001t0001g0241a0001c0001t0001g0263others(21): Show | 25 | HG01167.hp2 HG02027.hp2 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14+16351_-14+1635 others(9): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69226733 | |||||
| chr15:69226832
|
C | G | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-14+16426C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69226832 | ||||||
| chr15:69226926
|
G | A | 16 | a0001c0001t0003g0132a0001c0001t0003g0133a0001c0003t0005g0003others(13): Show | 17 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14+16520G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69226926 | ||||||
| chr15:69227079
|
C | T | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14+16673C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69227079 | ||||||
| chr15:69227530
|
GA | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+17132delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69227530 | |||||
| chr15:69227835
|
C | T | 79 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(76): Show | 82 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-14+17429C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69227835 | ||||||
| chr15:69227975
|
C | A | 228 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(225): Show | 235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-14+17569C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69227975 | ||||||
| chr15:69228054
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-14+17648G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228054 | ||||||
| chr15:69228089
|
T | C | 2 | a0001c0001t0001g0243a0001c0010t0001g0323 | 2 | HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-14+17683T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228089 | ||||||
| chr15:69228116
|
T | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+17710T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228116 | ||||||
| chr15:69228221
|
A | G | 1 | a0003c0004t0002g0034 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-14+17815A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228221 | ||||||
| chr15:69228398
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+17992A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228398 | ||||||
| chr15:69228581
|
A | G | 11 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14+18175A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228581 | ||||||
| chr15:69228630
|
A | G | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 213 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-14+18224A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228630 | ||||||
| chr15:69228909
|
A | C | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14+18503A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228909 | ||||||
| chr15:69228922
|
A | C | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14+18516A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69228922 | ||||||
| chr15:69229775
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-14+19369C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69229775 | ||||||
| chr15:69229849
|
TA | T | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02280.hp2 HG02486.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14+19452delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69229849 | |||||
| chr15:69229859
|
T | A | 1 | a0002c0002t0018g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-14+19453T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69229859 | ||||||
| chr15:69230047
|
G | A | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-14+19641G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69230047 | ||||||
| chr15:69230212
|
TA | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 216 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-14+19821delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69230212 | |||||
| chr15:69230259
|
G | T | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-14+19853G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69230259 | ||||||
| chr15:69230490
|
T | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+20084T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69230490 | ||||||
| chr15:69231045
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-14+20639G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231045 | ||||||
| chr15:69231049
|
T | G | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+20643T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231049 | ||||||
| chr15:69231050
|
A | G | 1 | a0002c0002t0011g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-14+20644A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231050 | ||||||
| chr15:69231104
|
C | T | 1 | a0001c0003t0006g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-14+20698C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231104 | ||||||
| chr15:69231166
|
G | A | 2 | a0002c0002t0002g0027a0002c0002t0002g0049 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-14+20760G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231166 | ||||||
| chr15:69231286
|
A | AT | 126 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0030others(123): Show | 130 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-14+20895dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69231286 | |||||
| chr15:69231306
|
T | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+20900T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231306 | ||||||
| chr15:69231315
|
G | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+20909G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231315 | ||||||
| chr15:69231375
|
C | T | 71 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(68): Show | 74 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-14+20969C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231375 | ||||||
| chr15:69231433
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-14+21027G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231433 | ||||||
| chr15:69231567
|
G | A | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-14+21161G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231567 | ||||||
| chr15:69231660
|
C | T | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+21254C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231660 | ||||||
| chr15:69231670
|
A | C | 1 | a0002c0002t0004g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14+21264A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231670 | ||||||
| chr15:69231751
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-14+21345G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231751 | ||||||
| chr15:69231763
|
G | C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-14+21357G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231763 | ||||||
| chr15:69231776
|
A | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0091others(80): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14+21370A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231776 | ||||||
| chr15:69231781
|
T | C | 2 | a0001c0003t0005g0137a0001c0003t0005g0141 | 2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-14+21375T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231781 | ||||||
| chr15:69231911
|
G | T | 33 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0021others(30): Show | 33 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14+21505G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231911 | ||||||
| chr15:69231944
|
C | G | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-14+21538C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69231944 | ||||||
| chr15:69232042
|
C | T | 1 | a0002c0002t0004g0115 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14+21636C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232042 | ||||||
| chr15:69232078
|
A | C | 1 | a0002c0002t0002g0130 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14+21672A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232078 | ||||||
| chr15:69232094
|
A | G | 3 | a0002c0002t0002g0163a0002c0002t0002g0197a0002c0002t0002g0198 | 3 | HG02523.hp1 NA18945.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-14+21688A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232094 | ||||||
| chr15:69232159
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-14+21753A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232159 | ||||||
| chr15:69232313
|
T | A | 1 | a0002c0002t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-14+21907T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232313 | ||||||
| chr15:69232323
|
T | C | 2 | a0002c0002t0002g0031a0002c0002t0002g0075 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-14+21917T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232323 | ||||||
| chr15:69232379
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+21973A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232379 | ||||||
| chr15:69232452
|
C | CGT | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-14+22059_-14+2206 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69232452 | |||||
| chr15:69232531
|
G | C | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 216 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-14+22125G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69232531 | ||||||
| chr15:69233034
|
A | G | 1 | a0003c0004t0002g0008 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-14+22628A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69233034 | ||||||
| chr15:69233231
|
A | G | 11 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-22563A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69233231 | ||||||
| chr15:69233234
|
G | A | 14 | a0001c0001t0003g0001a0001c0001t0003g0153a0001c0001t0003g0154others(11): Show | 16 | HG00544.hp2 HG00673.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-22560G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69233234 | ||||||
| chr15:69233236
|
A | T | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-13-22558A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69233236 | ||||||
| chr15:69233686
|
AG | A | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-22106delG | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69233686 | |||||
| chr15:69233849
|
G | A | 1 | a0004c0005t0013g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-21945G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69233849 | ||||||
| chr15:69233982
|
G | GT | 43 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0030others(40): Show | 44 | HG00408.hp2 HG00597.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.-13-21800dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69233982 | |||||
| chr15:69233983
|
T | G | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-13-21811T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69233983 | ||||||
| chr15:69234109
|
C | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-13-21685C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69234109 | ||||||
| chr15:69234266
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-21528A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69234266 | ||||||
| chr15:69234297
|
A | T | 152 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 156 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-13-21497A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69234297 | ||||||
| chr15:69234363
|
A | G | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-21431A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69234363 | ||||||
| chr15:69234379
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-13-21415T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69234379 | ||||||
| chr15:69234527
|
G | GAT | 4 | a0001c0003t0014g0131a0001c0003t0014g0136a0001c0003t0026g0143others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-21256_-13-2125 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69234527 | |||||
| chr15:69235034
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0282 | 2 | HG01515.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-13-20760C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235034 | ||||||
| chr15:69235091
|
T | A | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-20703T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235091 | ||||||
| chr15:69235093
|
C | CT | 19 | a0002c0002t0002g0017a0002c0002t0002g0024a0002c0002t0002g0027others(16): Show | 19 | HG00621.hp2 HG01106.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-13-20669dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235093
|
CT | C | 38 | a0001c0001t0003g0199a0001c0003t0005g0139a0001c0003t0005g0141others(35): Show | 38 | HG00423.hp2 HG00438.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.-13-20669delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235093
|
CTT | C | 30 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0151others(27): Show | 31 | HG01169.hp2 HG01891.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.-13-20670_-13-2066 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235093
|
CTTT | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0210others(57): Show | 63 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-13-20671_-13-2066 others(7): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235093
|
CTTTT | C | 40 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0211others(37): Show | 41 | HG00408.hp2 HG00639.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-13-20672_-13-2066 others(8): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235093
|
CTTTTT | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0093others(70): Show | 75 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-13-20673_-13-2066 others(9): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235093
|
CTTTTTTT others(3): Show |
C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-13-20678_-13-2066 others(14): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235093 | |||||
| chr15:69235297
|
G | A | 1 | a0002c0002t0002g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-13-20497G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235297 | ||||||
| chr15:69235339
|
CTCATGTG others(94): Show |
C | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-20451_-13-2035 others(4): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69235339 | |||||
| chr15:69235386
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-13-20408G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235386 | ||||||
| chr15:69235594
|
A | G | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13-20200A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235594 | ||||||
| chr15:69235728
|
A | C | 7 | a0001c0001t0003g0157a0001c0001t0003g0166a0001c0001t0003g0167others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-20066A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235728 | ||||||
| chr15:69235856
|
G | T | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-19938G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235856 | ||||||
| chr15:69235882
|
G | A | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-19912G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235882 | ||||||
| chr15:69235909
|
C | T | 2 | a0002c0002t0009g0105a0002c0002t0009g0106 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-13-19885C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69235909 | ||||||
| chr15:69236064
|
G | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-19730G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236064 | ||||||
| chr15:69236166
|
G | A | 10 | a0001c0001t0003g0004a0001c0001t0003g0145a0001c0001t0003g0161others(7): Show | 11 | HG00140.hp1 HG00639.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-19628G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236166 | ||||||
| chr15:69236218
|
A | AAATGTAT others(22): Show |
16 | a0001c0001t0003g0132a0001c0001t0003g0133a0001c0003t0005g0003others(13): Show | 17 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13-19574_-13-1957 others(33): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69236218 | |||||
| chr15:69236221
|
C | A | 16 | a0001c0001t0003g0132a0001c0001t0003g0133a0001c0003t0005g0003others(13): Show | 17 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13-19573C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236221 | ||||||
| chr15:69236222
|
T | A | 16 | a0001c0001t0003g0132a0001c0001t0003g0133a0001c0003t0005g0003others(13): Show | 17 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13-19572T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236222 | ||||||
| chr15:69236555
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-13-19239G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236555 | ||||||
| chr15:69236625
|
T | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-13-19169T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236625 | ||||||
| chr15:69236669
|
T | C | 1 | a0002c0002t0002g0076 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-13-19125T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236669 | ||||||
| chr15:69236936
|
C | T | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-13-18858C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236936 | ||||||
| chr15:69236968
|
C | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-18826C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69236968 | ||||||
| chr15:69237101
|
C | T | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-13-18693C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237101 | ||||||
| chr15:69237129
|
A | G | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 216 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-13-18665A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237129 | ||||||
| chr15:69237158
|
A | C | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 216 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-13-18636A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237158 | ||||||
| chr15:69237246
|
G | A | 1 | a0002c0002t0002g0047 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-13-18548G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237246 | ||||||
| chr15:69237261
|
A | G | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-13-18533A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237261 | ||||||
| chr15:69237369
|
T | G | 5 | a0001c0003t0006g0134a0001c0003t0006g0135a0001c0003t0006g0142others(2): Show | 5 | HG03098.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-18425T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237369 | ||||||
| chr15:69237420
|
C | A | 2 | a0001c0001t0003g0190a0001c0001t0003g0192 | 2 | NA18998.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-13-18374C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237420 | ||||||
| chr15:69237607
|
A | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-18187A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237607 | ||||||
| chr15:69237651
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0253 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-13-18143T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237651 | ||||||
| chr15:69237858
|
C | A | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-17936C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69237858 | ||||||
| chr15:69238119
|
A | G | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 216 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-13-17675A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238119 | ||||||
| chr15:69238208
|
T | TAAGATTG others(2909): Show |
1 | a0002c0002t0002g0074 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-13-17570_-13-1756 others(2920): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69238208 | |||||
| chr15:69238215
|
G | T | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-13-17579G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238215 | ||||||
| chr15:69238318
|
C | T | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-17476C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238318 | ||||||
| chr15:69238464
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-13-17330C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238464 | ||||||
| chr15:69238465
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-17329G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238465 | ||||||
| chr15:69238540
|
C | T | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-17254C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238540 | ||||||
| chr15:69238557
|
A | G | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-17237A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238557 | ||||||
| chr15:69238736
|
A | G | 1 | a0002c0002t0002g0092 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-13-17058A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238736 | ||||||
| chr15:69238771
|
G | A | 5 | a0002c0002t0004g0107a0002c0002t0004g0113a0002c0002t0004g0114others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-17023G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238771 | ||||||
| chr15:69238783
|
C | T | 6 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(3): Show | 7 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-17011C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69238783 | ||||||
| chr15:69239177
|
T | C | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16617T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239177 | ||||||
| chr15:69239178
|
G | T | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16616G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239178 | ||||||
| chr15:69239180
|
C | T | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16614C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239180 | ||||||
| chr15:69239181
|
T | A | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16613T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239181 | ||||||
| chr15:69239182
|
A | C | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16612A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239182 | ||||||
| chr15:69239186
|
A | T | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16608A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239186 | ||||||
| chr15:69239187
|
A | G | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16607A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239187 | ||||||
| chr15:69239194
|
G | A | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16600G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239194 | ||||||
| chr15:69239197
|
A | ATGT | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 221 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-13-16596_-13-1659 others(7): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69239197 | |||||
| chr15:69239197
|
A | T | 1 | a0001c0001t0008g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-13-16597A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239197 | ||||||
| chr15:69239391
|
G | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-16403G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239391 | ||||||
| chr15:69239449
|
C | T | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13-16345C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239449 | ||||||
| chr15:69239655
|
C | T | 1 | a0002c0002t0004g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-13-16139C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239655 | ||||||
| chr15:69239965
|
G | A | 2 | a0005c0007t0002g0094a0005c0007t0002g0095 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-15829G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239965 | ||||||
| chr15:69239969
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0030others(36): Show | 40 | HG00408.hp2 HG00597.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.-13-15825A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69239969 | ||||||
| chr15:69240094
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0282 | 2 | HG01515.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-13-15700G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240094 | ||||||
| chr15:69240155
|
A | G | 2 | a0002c0002t0002g0035a0002c0002t0002g0060 | 2 | NA18955.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-13-15639A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240155 | ||||||
| chr15:69240191
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-13-15603G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240191 | ||||||
| chr15:69240230
|
G | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15564G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240230 | ||||||
| chr15:69240231
|
C | CT | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15563_-13-1556 others(5): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240231 | ||||||
| chr15:69240232
|
C | A | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15562C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240232 | ||||||
| chr15:69240232
|
C | T | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13-15562C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240232 | ||||||
| chr15:69240235
|
G | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15559G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240235 | ||||||
| chr15:69240238
|
CCCGCCAC others(52): Show |
C | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15555_-13-1549 others(63): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240238 | ||||||
| chr15:69240239
|
C | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-13-15555C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240239 | ||||||
| chr15:69240240
|
C | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-13-15554C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240240 | ||||||
| chr15:69240242
|
C | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-13-15552C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240242 | ||||||
| chr15:69240243
|
C | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-13-15551C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240243 | ||||||
| chr15:69240247
|
GCACTCCA others(53): Show |
G | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 218 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-13-15546_-13-1548 others(64): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240247 | ||||||
| chr15:69240283
|
C | CA | 45 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0022others(42): Show | 45 | HG00423.hp2 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-13-15484dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69240283 | |||||
| chr15:69240298
|
A | T | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15496A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240298 | ||||||
| chr15:69240300
|
A | G | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15494A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240300 | ||||||
| chr15:69240301
|
A | T | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15493A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240301 | ||||||
| chr15:69240305
|
A | C | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15489A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240305 | ||||||
| chr15:69240306
|
A | T | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15488A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240306 | ||||||
| chr15:69240307
|
A | G | 1 | a0001c0001t0003g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-13-15487A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240307 | ||||||
| chr15:69240309
|
A | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15485A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240309 | ||||||
| chr15:69240311
|
G | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15483G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240311 | ||||||
| chr15:69240313
|
A | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-15481A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240313 | ||||||
| chr15:69240434
|
A | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-15360A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240434 | ||||||
| chr15:69240446
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-13-15348G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240446 | ||||||
| chr15:69240599
|
C | A | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-15195C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240599 | ||||||
| chr15:69240676
|
A | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-15118A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240676 | ||||||
| chr15:69240743
|
T | C | 1 | a0001c0003t0016g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13-15051T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240743 | ||||||
| chr15:69240751
|
G | T | 2 | a0001c0001t0003g0157a0001c0001t0003g0167 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-13-15043G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240751 | ||||||
| chr15:69240791
|
A | G | 15 | a0001c0001t0003g0009a0002c0002t0002g0111a0002c0002t0002g0130others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-15003A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240791 | ||||||
| chr15:69240854
|
A | G | 5 | a0001c0001t0003g0004a0001c0001t0003g0161a0001c0001t0003g0174others(2): Show | 6 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-14940A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240854 | ||||||
| chr15:69240858
|
T | C | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-14936T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69240858 | ||||||
| chr15:69241010
|
A | G | 5 | a0002c0002t0002g0038a0002c0002t0002g0070a0002c0002t0002g0073others(2): Show | 5 | HG01346.hp1 HG01928.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-14784A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69241010 | ||||||
| chr15:69241076
|
T | G | 1 | a0002c0002t0020g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13-14718T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69241076 | ||||||
| chr15:69241103
|
C | T | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-14691C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69241103 | ||||||
| chr15:69241110
|
G | A | 1 | a0001c0003t0006g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-14684G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69241110 | ||||||
| chr15:69241954
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-13-13840G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69241954 | ||||||
| chr15:69241979
|
C | T | 1 | a0002c0002t0002g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13-13815C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69241979 | ||||||
| chr15:69242010
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0260 | 2 | NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-13-13784A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69242010 | ||||||
| chr15:69242098
|
G | A | 7 | a0001c0001t0001g0285a0001c0001t0001g0294a0001c0001t0001g0297others(4): Show | 7 | HG01934.hp1 HG02155.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-13696G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69242098 | ||||||
| chr15:69242811
|
G | A | 4 | a0002c0002t0002g0130a0002c0002t0004g0108a0002c0002t0004g0117others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-12983G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69242811 | ||||||
| chr15:69243057
|
C | CA | 19 | a0001c0001t0001g0210a0001c0001t0001g0215a0001c0001t0001g0239others(16): Show | 19 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-13-12718dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69243057 | |||||
| chr15:69243074
|
AAAG | A | 11 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-12717_-13-1271 others(7): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69243074 | |||||
| chr15:69243179
|
A | G | 3 | a0002c0002t0002g0163a0002c0002t0002g0197a0002c0002t0002g0198 | 3 | HG02523.hp1 NA18945.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-13-12615A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243179 | ||||||
| chr15:69243570
|
C | CA | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 150 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-13-12211dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69243570 | |||||
| chr15:69243570
|
C | CAA | 68 | a0001c0001t0001g0225a0001c0001t0003g0001a0001c0001t0003g0004others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-12212_-13-1221 others(6): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69243570 | |||||
| chr15:69243601
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-13-12193G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243601 | ||||||
| chr15:69243619
|
T | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0091others(80): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-13-12175T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243619 | ||||||
| chr15:69243740
|
CTTGACTT others(68): Show |
C | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-12051_-13-1197 others(79): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69243740 | |||||
| chr15:69243812
|
A | T | 1 | a0002c0002t0020g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13-11982A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243812 | ||||||
| chr15:69243819
|
T | A | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-11975T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243819 | ||||||
| chr15:69243820
|
A | T | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 221 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-13-11974A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243820 | ||||||
| chr15:69243830
|
A | G | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-11964A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69243830 | ||||||
| chr15:69244048
|
T | G | 3 | a0002c0002t0002g0027a0002c0002t0002g0037a0002c0002t0002g0049 | 3 | HG02257.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-13-11746T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244048 | ||||||
| chr15:69244135
|
A | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-11659A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244135 | ||||||
| chr15:69244289
|
A | G | 1 | a0002c0002t0002g0047 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-13-11505A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244289 | ||||||
| chr15:69244443
|
T | A | 2 | a0001c0003t0006g0135a0001c0003t0006g0142 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-13-11351T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244443 | ||||||
| chr15:69244456
|
A | C | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-11338A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244456 | ||||||
| chr15:69244533
|
G | A | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-11261G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244533 | ||||||
| chr15:69244543
|
C | T | 1 | a0001c0001t0015g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-13-11251C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244543 | ||||||
| chr15:69244750
|
A | T | 1 | a0002c0002t0019g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-13-11044A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244750 | ||||||
| chr15:69244986
|
G | A | 5 | a0002c0002t0002g0118a0002c0002t0002g0119a0002c0002t0002g0120others(2): Show | 5 | HG01496.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-10808G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69244986 | ||||||
| chr15:69245053
|
C | T | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-13-10741C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69245053 | ||||||
| chr15:69245095
|
G | A | 5 | a0001c0001t0003g0004a0001c0001t0003g0161a0001c0001t0003g0174others(2): Show | 6 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-10699G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69245095 | ||||||
| chr15:69245180
|
A | G | 6 | a0001c0001t0003g0157a0001c0001t0003g0166a0001c0001t0003g0167others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-10614A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69245180 | ||||||
| chr15:69245258
|
C | T | 2 | a0005c0007t0002g0094a0005c0007t0002g0095 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-10536C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69245258 | ||||||
| chr15:69245332
|
C | CA | 17 | a0001c0001t0001g0091a0001c0001t0001g0225a0001c0001t0001g0229others(14): Show | 17 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13-10441dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69245332 | |||||
| chr15:69245332
|
CA | C | 182 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0001g0311others(179): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-13-10441delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69245332 | |||||
| chr15:69245461
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-13-10333T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69245461 | ||||||
| chr15:69245981
|
G | A | 1 | a0001c0001t0003g0205 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-13-9813G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69245981 | ||||||
| chr15:69246019
|
G | A | 1 | a0001c0003t0006g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-9775G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246019 | ||||||
| chr15:69246040
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-13-9754C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246040 | ||||||
| chr15:69246062
|
G | A | 4 | a0002c0002t0019g0045a0003c0004t0002g0096a0005c0007t0002g0094others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-9732G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246062 | ||||||
| chr15:69246487
|
G | C | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-13-9307G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246487 | ||||||
| chr15:69246520
|
A | T | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-13-9274A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246520 | ||||||
| chr15:69246636
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-13-9158A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246636 | ||||||
| chr15:69246717
|
G | GA | 82 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(79): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-13-9060dupA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69246717 | |||||
| chr15:69246945
|
C | T | 3 | a0002c0002t0002g0163a0002c0002t0002g0197a0002c0002t0002g0198 | 3 | HG02523.hp1 NA18945.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-13-8849C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69246945 | ||||||
| chr15:69247047
|
A | G | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-8747A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69247047 | ||||||
| chr15:69247240
|
C | T | 1 | a0002c0002t0002g0047 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-13-8554C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69247240 | ||||||
| chr15:69247542
|
G | T | 1 | a0001c0001t0015g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-13-8252G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69247542 | ||||||
| chr15:69247558
|
A | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0030others(32): Show | 36 | HG00408.hp2 HG00597.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.-13-8236A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69247558 | ||||||
| chr15:69247769
|
A | G | 1 | a0002c0002t0002g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-13-8025A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69247769 | ||||||
| chr15:69247771
|
G | A | 5 | a0001c0003t0006g0134a0001c0003t0006g0135a0001c0003t0006g0142others(2): Show | 5 | HG03098.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-8023G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69247771 | ||||||
| chr15:69248000
|
T | C | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0248others(1): Show | 4 | HG00735.hp2 HG01106.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-7794T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248000 | ||||||
| chr15:69248010
|
C | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-7784C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248010 | ||||||
| chr15:69248133
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0239a0001c0001t0001g0324others(1): Show | 5 | HG02602.hp2 HG02683.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-7661C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248133 | ||||||
| chr15:69248213
|
A | T | 5 | a0001c0001t0003g0004a0001c0001t0003g0161a0001c0001t0003g0174others(2): Show | 6 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-7581A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248213 | ||||||
| chr15:69248370
|
G | C | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-7424G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248370 | ||||||
| chr15:69248418
|
G | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-7376G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248418 | ||||||
| chr15:69248532
|
G | C | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 221 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-13-7262G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248532 | ||||||
| chr15:69248621
|
C | G | 6 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(3): Show | 7 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-7173C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248621 | ||||||
| chr15:69248626
|
C | G | 5 | a0002c0002t0002g0118a0002c0002t0002g0119a0002c0002t0002g0120others(2): Show | 5 | HG01496.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-7168C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248626 | ||||||
| chr15:69248670
|
A | G | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-7124A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248670 | ||||||
| chr15:69248855
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-13-6939T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69248855 | ||||||
| chr15:69249160
|
G | A | 70 | a0001c0001t0001g0211a0001c0001t0003g0001a0001c0001t0003g0004others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-13-6634G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69249160 | ||||||
| chr15:69249172
|
G | T | 1 | a0003c0004t0002g0034 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-13-6622G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69249172 | ||||||
| chr15:69249656
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0222 | 2 | NA18966.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-13-6138G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69249656 | ||||||
| chr15:69249677
|
C | G | 5 | a0002c0002t0004g0107a0002c0002t0004g0113a0002c0002t0004g0114others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-6117C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69249677 | ||||||
| chr15:69249708
|
A | G | 29 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0026others(26): Show | 29 | HG00621.hp2 HG00741.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13-6086A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69249708 | ||||||
| chr15:69249757
|
A | G | 1 | a0002c0002t0002g0048 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-13-6037A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69249757 | ||||||
| chr15:69249907
|
TA | T | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-5885delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69249907 | |||||
| chr15:69250052
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-13-5742G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250052 | ||||||
| chr15:69250215
|
G | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-5579G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250215 | ||||||
| chr15:69250390
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-13-5404C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250390 | ||||||
| chr15:69250515
|
T | A | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-5279T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250515 | ||||||
| chr15:69250629
|
G | A | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-13-5165G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250629 | ||||||
| chr15:69250664
|
C | T | 14 | a0001c0001t0003g0009a0001c0001t0003g0147a0001c0001t0003g0157others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13-5130C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250664 | ||||||
| chr15:69250665
|
G | A | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-5129G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250665 | ||||||
| chr15:69250713
|
A | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-5081A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250713 | ||||||
| chr15:69250759
|
C | T | 2 | a0001c0001t0003g0157a0001c0001t0003g0167 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-13-5035C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69250759 | ||||||
| chr15:69250805
|
TA | T | 172 | a0001c0001t0001g0218a0001c0001t0001g0254a0001c0001t0003g0001others(169): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.-13-4971delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr15 | 69250805 | |||||
| chr15:69251199
|
T | G | 1 | a0001c0001t0001g0306 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-13-4595T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251199 | ||||||
| chr15:69251225
|
G | C | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-4569G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251225 | ||||||
| chr15:69251277
|
C | T | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-4517C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251277 | ||||||
| chr15:69251474
|
T | C | 1 | a0002c0002t0002g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-13-4320T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251474 | ||||||
| chr15:69251528
|
T | A | 1 | a0001c0001t0003g0173 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-13-4266T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251528 | ||||||
| chr15:69251529
|
A | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-4265A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251529 | ||||||
| chr15:69251624
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-13-4170A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251624 | ||||||
| chr15:69251682
|
T | G | 51 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0145others(48): Show | 54 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-13-4112T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251682 | ||||||
| chr15:69251683
|
T | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-4111T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251683 | ||||||
| chr15:69251733
|
G | C | 1 | a0002c0002t0002g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-13-4061G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251733 | ||||||
| chr15:69251750
|
C | T | 1 | a0002c0002t0002g0332 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-13-4044C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251750 | ||||||
| chr15:69251766
|
A | G | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-4028A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251766 | ||||||
| chr15:69251895
|
A | G | 1 | a0003c0004t0002g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-13-3899A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251895 | ||||||
| chr15:69251984
|
C | A | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-3810C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69251984 | ||||||
| chr15:69252260
|
A | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG02572.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-13-3534A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69252260 | ||||||
| chr15:69252282
|
G | C | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-3512G>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69252282 | ||||||
| chr15:69252695
|
T | A | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-13-3099T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69252695 | ||||||
| chr15:69252767
|
A | G | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-3027A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69252767 | ||||||
| chr15:69252881
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-2913G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69252881 | ||||||
| chr15:69253078
|
A | G | 1 | a0001c0001t0003g0176 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-13-2716A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69253078 | ||||||
| chr15:69253175
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-13-2619G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69253175 | ||||||
| chr15:69253416
|
A | T | 1 | a0001c0001t0003g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-13-2378A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69253416 | ||||||
| chr15:69253600
|
A | T | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-2194A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69253600 | ||||||
| chr15:69253603
|
A | G | 1 | a0001c0001t0003g0181 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-13-2191A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69253603 | ||||||
| chr15:69253768
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-13-2026G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69253768 | ||||||
| chr15:69254176
|
C | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-1618C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254176 | ||||||
| chr15:69254181
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-1613C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254181 | ||||||
| chr15:69254194
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-13-1600C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254194 | ||||||
| chr15:69254643
|
T | G | 1 | a0002c0002t0002g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-13-1151T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254643 | ||||||
| chr15:69254681
|
G | A | 2 | a0005c0007t0002g0094a0005c0007t0002g0095 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-1113G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254681 | ||||||
| chr15:69254755
|
C | A | 2 | a0001c0003t0014g0131a0001c0003t0014g0136 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-13-1039C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254755 | ||||||
| chr15:69254757
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13-1037A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254757 | ||||||
| chr15:69254764
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-1030A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254764 | ||||||
| chr15:69254767
|
T | C | 1 | a0003c0004t0002g0080 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-13-1027T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254767 | ||||||
| chr15:69254782
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-13-1012C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254782 | ||||||
| chr15:69254790
|
C | T | 3 | a0002c0002t0002g0026a0002c0002t0002g0044a0002c0002t0002g0090 | 3 | NA18970.hp2 NA18979.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-13-1004C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254790 | ||||||
| chr15:69254823
|
A | T | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13-971A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254823 | ||||||
| chr15:69254876
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13-918G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254876 | ||||||
| chr15:69254943
|
A | G | 2 | a0002c0002t0002g0002a0002c0002t0002g0124 | 3 | HG00140.hp2 HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-13-851A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69254943 | ||||||
| chr15:69255066
|
A | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-728A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69255066 | ||||||
| chr15:69255457
|
A | G | 7 | a0002c0002t0002g0026a0004c0005t0007g0012a0004c0005t0007g0013others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-337A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69255457 | ||||||
| chr15:69255525
|
A | T | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13-269A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 2/4 | chr15 | 69255525 | ||||||
| chr15:69256683
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.586+291G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69256683 | ||||||
| chr15:69256749
|
C | T | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+357C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69256749 | ||||||
| chr15:69256822
|
C | A | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.586+430C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69256822 | ||||||
| chr15:69256838
|
T | C | 2 | a0002c0002t0002g0002a0002c0002t0002g0124 | 3 | HG00140.hp2 HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.586+446T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69256838 | ||||||
| chr15:69257103
|
G | A | 3 | a0001c0001t0001g0303a0001c0001t0001g0308a0001c0001t0001g0310 | 3 | HG02523.hp2 NA18991.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.586+711G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257103 | ||||||
| chr15:69257144
|
G | A | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+752G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257144 | ||||||
| chr15:69257269
|
T | G | 1 | a0001c0001t0001g0299 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.586+877T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257269 | ||||||
| chr15:69257341
|
T | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.586+949T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257341 | ||||||
| chr15:69257423
|
C | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+1031C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257423 | ||||||
| chr15:69257745
|
C | G | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+1353C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257745 | ||||||
| chr15:69257886
|
G | A | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.586+1494G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257886 | ||||||
| chr15:69257967
|
G | A | 1 | a0002c0002t0002g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.586+1575G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69257967 | ||||||
| chr15:69258044
|
T | C | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+1652T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258044 | ||||||
| chr15:69258146
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0023g0212 | 2 | NA18950.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.586+1754C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258146 | ||||||
| chr15:69258153
|
T | C | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 204 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.586+1761T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258153 | ||||||
| chr15:69258247
|
AT | A | 15 | a0001c0001t0003g0132a0001c0003t0005g0003a0001c0003t0005g0137others(12): Show | 16 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.586+1858delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr15 | 69258247 | |||||
| chr15:69258324
|
ATC | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.586+1936_586+1937d others(4): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr15 | 69258324 | |||||
| chr15:69258597
|
G | A | 9 | a0001c0001t0001g0226a0001c0001t0001g0264a0001c0001t0001g0287others(6): Show | 9 | HG00408.hp2 HG02015.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+2205G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258597 | ||||||
| chr15:69258660
|
T | A | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.586+2268T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258660 | ||||||
| chr15:69258708
|
C | A | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+2316C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258708 | ||||||
| chr15:69258771
|
A | G | 2 | a0005c0007t0002g0094a0005c0007t0002g0095 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.587-2316A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258771 | ||||||
| chr15:69258831
|
T | C | 102 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0018others(99): Show | 103 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.587-2256T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69258831 | ||||||
| chr15:69259037
|
A | G | 1 | a0001c0003t0006g0135 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.587-2050A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259037 | ||||||
| chr15:69259282
|
T | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.587-1805T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259282 | ||||||
| chr15:69259359
|
C | A | 1 | a0001c0001t0001g0250 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.587-1728C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259359 | ||||||
| chr15:69259378
|
C | A | 9 | a0002c0002t0002g0002a0002c0002t0002g0017a0002c0002t0002g0118others(6): Show | 10 | HG00140.hp2 HG00280.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-1709C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259378 | ||||||
| chr15:69259793
|
A | G | 20 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(17): Show | 21 | HG02258.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.587-1294A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259793 | ||||||
| chr15:69259856
|
G | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0030others(32): Show | 36 | HG00408.hp2 HG00597.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.587-1231G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259856 | ||||||
| chr15:69259979
|
C | T | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.587-1108C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259979 | ||||||
| chr15:69259980
|
G | A | 1 | a0002c0002t0002g0329 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.587-1107G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69259980 | ||||||
| chr15:69260045
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0030 | 2 | HG00597.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.587-1042A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260045 | ||||||
| chr15:69260066
|
T | G | 19 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0151others(16): Show | 19 | HG00438.hp1 NA18939.hp2 NA18942.hp1 others(16): Show |
intron_variant | MODIFIER | c.587-1021T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260066 | ||||||
| chr15:69260168
|
T | C | 4 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0300others(1): Show | 4 | NA18960.hp1 NA19005.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-919T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260168 | ||||||
| chr15:69260190
|
A | C | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-897A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260190 | ||||||
| chr15:69260231
|
T | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.587-856T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260231 | ||||||
| chr15:69260251
|
G | GT | 9 | a0002c0002t0002g0039a0002c0002t0002g0044a0002c0002t0002g0048others(6): Show | 9 | HG01346.hp1 HG02145.hp1 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.587-836_587-835ins others(1): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260251 | ||||||
| chr15:69260251
|
G | GTT | 3 | a0002c0002t0002g0026a0002c0002t0002g0032a0002c0002t0002g0076 | 3 | NA18979.hp1 NA19006.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.587-836_587-835ins others(2): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260251 | ||||||
| chr15:69260252
|
G | GCTT | 10 | a0001c0003t0005g0003a0001c0003t0005g0139a0001c0003t0005g0140others(7): Show | 11 | HG02630.hp2 HG02922.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-835_587-834ins others(3): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260252 | ||||||
| chr15:69260252
|
G | GCTTT | 4 | a0001c0003t0005g0137a0001c0003t0014g0131a0001c0003t0014g0136others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-835_587-834ins others(4): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260252 | ||||||
| chr15:69260252
|
G | GT | 42 | a0001c0001t0003g0001a0001c0001t0003g0147a0001c0001t0003g0148others(39): Show | 44 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.587-810dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr15 | 69260252 | |||||
| chr15:69260252
|
G | T | 37 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0021others(34): Show | 37 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.587-835G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260252 | ||||||
| chr15:69260252
|
GT | G | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(101): Show | 107 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.587-810delT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr15 | 69260252 | |||||
| chr15:69260253
|
T | C | 2 | a0004c0005t0013g0015a0004c0005t0013g0016 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.587-834T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260253 | ||||||
| chr15:69260254
|
T | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-833T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260254 | ||||||
| chr15:69260416
|
C | A | 1 | a0001c0001t0003g0189 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.587-671C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260416 | ||||||
| chr15:69260455
|
T | C | 11 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-632T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260455 | ||||||
| chr15:69260773
|
A | C | 4 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(1): Show | 4 | HG02809.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-314A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260773 | ||||||
| chr15:69260783
|
A | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.587-304A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260783 | ||||||
| chr15:69260961
|
T | C | 1 | a0001c0003t0006g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.587-126T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69260961 | ||||||
| chr15:69261021
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.587-66A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 3/4 | chr15 | 69261021 | ||||||
| chr15:69261389
|
C | A | 69 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(66): Show | 72 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.829+60C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69261389 | ||||||
| chr15:69261389
|
C | T | 1 | a0002c0002t0002g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.829+60C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69261389 | ||||||
| chr15:69261588
|
G | A | 2 | a0001c0003t0006g0326a0001c0003t0016g0327 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.829+259G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69261588 | ||||||
| chr15:69261736
|
T | A | 11 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(8): Show | 12 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.829+407T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69261736 | ||||||
| chr15:69262084
|
T | G | 1 | a0002c0002t0010g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.829+755T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69262084 | ||||||
| chr15:69262354
|
T | G | 5 | a0002c0002t0002g0024a0002c0002t0002g0039a0002c0002t0002g0040others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.829+1025T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69262354 | ||||||
| chr15:69262740
|
T | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0260 | 2 | NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.829+1411T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69262740 | ||||||
| chr15:69262780
|
G | A | 3 | a0001c0003t0006g0134a0001c0003t0006g0326a0001c0003t0016g0327 | 3 | HG03098.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829+1451G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69262780 | ||||||
| chr15:69263025
|
A | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0244 | 2 | HG00280.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.829+1696A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263025 | ||||||
| chr15:69263280
|
A | G | 1 | a0001c0003t0026g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.829+1951A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263280 | ||||||
| chr15:69263284
|
G | T | 3 | a0002c0002t0002g0111a0002c0002t0009g0105a0002c0002t0009g0106 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829+1955G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263284 | ||||||
| chr15:69263426
|
T | C | 9 | a0001c0003t0014g0131a0001c0003t0014g0136a0001c0003t0026g0143others(6): Show | 9 | HG02258.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.829+2097T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263426 | ||||||
| chr15:69263491
|
T | G | 69 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(66): Show | 72 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.829+2162T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263491 | ||||||
| chr15:69263836
|
TTTGTTGG others(61): Show |
T | 1 | a0002c0002t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.829+2509_829+2576d others(70): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr15 | 69263836 | |||||
| chr15:69263854
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.829+2525T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263854 | ||||||
| chr15:69263933
|
T | C | 3 | a0001c0003t0006g0134a0001c0003t0006g0326a0001c0003t0016g0327 | 3 | HG03098.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829+2604T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69263933 | ||||||
| chr15:69264072
|
T | C | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+2743T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264072 | ||||||
| chr15:69264110
|
T | A | 78 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(75): Show | 81 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.829+2781T>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264110 | ||||||
| chr15:69264150
|
A | G | 2 | a0002c0002t0002g0027a0002c0002t0002g0049 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.829+2821A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264150 | ||||||
| chr15:69264165
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.829+2836T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264165 | ||||||
| chr15:69264224
|
A | G | 333 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(330): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.829+2895A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264224 | ||||||
| chr15:69264245
|
C | A | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.829+2916C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264245 | ||||||
| chr15:69264485
|
G | A | 3 | a0002c0002t0002g0027a0002c0002t0002g0037a0002c0002t0002g0049 | 3 | HG02257.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.829+3156G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264485 | ||||||
| chr15:69264504
|
T | G | 1 | a0002c0002t0010g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.829+3175T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264504 | ||||||
| chr15:69264511
|
A | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.829+3182A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264511 | ||||||
| chr15:69264533
|
C | T | 2 | a0003c0004t0002g0008a0003c0004t0002g0083 | 2 | NA18985.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.829+3204C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264533 | ||||||
| chr15:69264644
|
A | G | 69 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(66): Show | 72 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.829+3315A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264644 | ||||||
| chr15:69264847
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0284 | 2 | NA18952.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.830-3373A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264847 | ||||||
| chr15:69264870
|
G | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0284 | 2 | NA18952.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.830-3350G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69264870 | ||||||
| chr15:69265054
|
T | G | 89 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(86): Show | 93 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.830-3166T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69265054 | ||||||
| chr15:69265130
|
TA | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-3087delA | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr15 | 69265130 | |||||
| chr15:69265701
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0276 | 2 | HG00738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.830-2519T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69265701 | ||||||
| chr15:69265752
|
C | T | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-2468C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69265752 | ||||||
| chr15:69265798
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.830-2422G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69265798 | ||||||
| chr15:69265844
|
C | T | 331 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.830-2376C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69265844 | ||||||
| chr15:69266061
|
G | A | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-2159G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266061 | ||||||
| chr15:69266147
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.830-2073A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266147 | ||||||
| chr15:69266335
|
C | CT | 8 | a0001c0001t0001g0238a0001c0001t0001g0259a0001c0001t0001g0314others(5): Show | 8 | HG00621.hp1 HG02071.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.830-1874dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr15 | 69266335 | |||||
| chr15:69266441
|
G | A | 5 | a0002c0002t0002g0024a0002c0002t0002g0039a0002c0002t0002g0040others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-1779G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266441 | ||||||
| chr15:69266458
|
C | G | 5 | a0001c0001t0003g0004a0001c0001t0003g0161a0001c0001t0003g0174others(2): Show | 6 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-1762C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266458 | ||||||
| chr15:69266494
|
T | C | 13 | a0001c0001t0003g0168a0001c0003t0006g0138a0002c0002t0002g0130others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.830-1726T>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266494 | ||||||
| chr15:69266542
|
T | G | 4 | a0002c0002t0002g0086a0002c0002t0002g0087a0002c0002t0002g0088others(1): Show | 4 | NA18961.hp1 NA18995.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.830-1678T>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266542 | ||||||
| chr15:69266583
|
G | A | 6 | a0004c0005t0007g0012a0004c0005t0007g0013a0004c0005t0007g0014others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-1637G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266583 | ||||||
| chr15:69266715
|
C | A | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.830-1505C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266715 | ||||||
| chr15:69266764
|
C | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.830-1456C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266764 | ||||||
| chr15:69266879
|
A | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.830-1341A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266879 | ||||||
| chr15:69266911
|
C | T | 2 | a0002c0002t0002g0057a0002c0002t0002g0231 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.830-1309C>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69266911 | ||||||
| chr15:69267001
|
G | T | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 217 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.830-1219G>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267001 | ||||||
| chr15:69267045
|
TTTG | T | 105 | a0001c0001t0003g0196a0002c0002t0002g0002a0002c0002t0002g0017others(102): Show | 106 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.830-1169_830-1167d others(5): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr15 | 69267045 | |||||
| chr15:69267057
|
A | C | 1 | a0002c0002t0002g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1163A>C | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267057 | ||||||
| chr15:69267158
|
A | G | 14 | a0001c0003t0005g0003a0001c0003t0005g0137a0001c0003t0005g0139others(11): Show | 15 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.830-1062A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267158 | ||||||
| chr15:69267742
|
A | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0091others(79): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.830-478A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267742 | ||||||
| chr15:69267776
|
A | T | 2 | a0002c0002t0010g0010a0002c0002t0010g0011 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.830-444A>T | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267776 | ||||||
| chr15:69267807
|
C | G | 3 | a0001c0001t0001g0303a0001c0001t0001g0308a0001c0001t0001g0310 | 3 | HG02523.hp2 NA18991.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.830-413C>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267807 | ||||||
| chr15:69267843
|
C | CT | 70 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0009others(67): Show | 73 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.830-363dupT | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr15 | 69267843 | |||||
| chr15:69267843
|
C | CTT | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 144 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.830-364_830-363dup others(2): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr15 | 69267843 | |||||
| chr15:69267942
|
A | G | 5 | a0002c0002t0002g0024a0002c0002t0002g0039a0002c0002t0002g0040others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-278A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69267942 | ||||||
| chr15:69268012
|
A | G | 3 | a0001c0001t0001g0298a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | NA18960.hp1 NA19005.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.830-208A>G | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69268012 | ||||||
| chr15:69268047
|
C | A | 1 | a0001c0001t0001g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.830-173C>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69268047 | ||||||
| chr15:69268127
|
G | A | 11 | a0002c0002t0002g0130a0002c0002t0004g0104a0002c0002t0004g0107others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.830-93G>A | GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 4/4 | chr15 | 69268127 |