| geneid | 84162 |
|---|---|
| ensemblid | ENSG00000138688.17 |
| hgncid | 26953 |
| symbol | BLTP1 |
| name | bridge-like lipid transfer protein family member 1 |
| refseq_nuc | NM_001384125.1 |
| refseq_prot | NP_001371054.1 |
| ensembl_nuc | ENST00000679879.1 |
| ensembl_prot | ENSP00000505357.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 122152331 |
| end | 122362752 |
| strand | + |
| ver | v1.2 |
| region | chr4:122152331-122362752 |
| region5000 | chr4:122147331-122367752 |
| regionname0 | BLTP1_chr4_122152331_122362752 |
| regionname5000 | BLTP1_chr4_122147331_122367752 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 5093 | 269 | 61 | 44 | 121 | 13 | 28 | 96 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0002 | 0/0 | 5093 | 21 | 0 | 2 | 19 | 0 | 0 | 11 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0003 | 0/0 | 5093 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0004 | 0/0 | 5093 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0005 | 0/0 | 5093 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0006 | 0/0 | 5093 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0007 | 0/0 | 5093 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0008 | 0/0 | 5093 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0009 | 0/0 | 5093 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0010 | 0/0 | 5093 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0011 | 0/0 | 750 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0012 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0013 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0014 | 0/0 | 5093 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0015 | 0/0 | 1968 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0016 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0017 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0018 | 0/0 | 5093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0019 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 15282 | 106 | 35 | 13 | 47 | 2 | 8 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0002 | 0/0 | 15282 | 74 | 3 | 19 | 39 | 2 | 11 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0003 | 0/1 | 15282 | 34 | 0 | 4 | 21 | 4 | 4 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0004 | 0/0 | 15282 | 20 | 0 | 2 | 18 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0005 | 0/0 | 15282 | 15 | 7 | 3 | 0 | 1 | 4 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0006 | 0/0 | 15282 | 14 | 13 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0007 | 0/0 | 15282 | 12 | 11 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0008 | 0/0 | 15282 | 4 | 0 | 2 | 0 | 1 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0009 | 0/0 | 15282 | 4 | 0 | 0 | 4 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0010 | 0/0 | 15282 | 4 | 0 | 3 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0011 | 0/0 | 15282 | 3 | 3 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0012 | 0/0 | 15282 | 3 | 3 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0013 | 0/0 | 15282 | 3 | 1 | 2 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0014 | 0/0 | 15282 | 3 | 2 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0015 | 0/0 | 15282 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0016 | 0/0 | 15282 | 2 | 0 | 0 | 2 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0017 | 0/0 | 15282 | 2 | 1 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0018 | 0/0 | 15282 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0019 | 0/0 | 15282 | 2 | 0 | 0 | 0 | 2 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0020 | 0/0 | 15282 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0021 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0022 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0023 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0024 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0025 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0026 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0027 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0028 | 0/0 | 15271 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0029 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0030 | 0/0 | 15282 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0031 | 0/0 | 15282 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0032 | 0/0 | 15282 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0033 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0034 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0035 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0036 | 0/0 | 15282 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0037 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0038 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0039 | 0/0 | 15282 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0040 | 0/0 | 15531 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0041 | 0/0 | 15531 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0042 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0043 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0044 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| c0045 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 881 | 321 | 79 | 55 | 141 | 14 | 30 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0002 | 0/0 | 885 | 6 | 6 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0003 | 0/0 | 881 | 2 | 1 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0004 | 0/0 | 881 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0005 | 0/0 | 881 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0006 | 0/0 | 881 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0007 | 0/0 | 881 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0008 | 0/0 | 881 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0009 | 0/0 | 881 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| t0010 | 0/0 | 881 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 15282 | 106 | 35 | 13 | 47 | 2 | 8 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0002 | 0/0 | 15282 | 74 | 3 | 19 | 39 | 2 | 11 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0003 | 0/1 | 15282 | 34 | 0 | 4 | 21 | 4 | 4 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0005 | 0/0 | 15282 | 15 | 7 | 3 | 0 | 1 | 4 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0007 | 0/0 | 15282 | 12 | 11 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0008 | 0/0 | 15282 | 4 | 0 | 2 | 0 | 1 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0009 | 0/0 | 15282 | 4 | 0 | 0 | 4 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0015 | 0/0 | 15282 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0016 | 0/0 | 15282 | 2 | 0 | 0 | 2 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0017 | 0/0 | 15282 | 2 | 1 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0019 | 0/0 | 15282 | 2 | 0 | 0 | 0 | 2 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0023 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0024 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0025 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0026 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0027 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0029 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0032 | 0/0 | 15282 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0033 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0034 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0036 | 0/0 | 15282 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0037 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0038 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0002c0004 | 0/0 | 15282 | 20 | 0 | 2 | 18 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0002c0043 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0003c0006 | 0/0 | 15282 | 14 | 13 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0004c0013 | 0/0 | 15282 | 3 | 1 | 2 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0004c0031 | 0/0 | 15282 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0005c0010 | 0/0 | 15282 | 4 | 0 | 3 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0006c0014 | 0/0 | 15282 | 3 | 2 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0007c0012 | 0/0 | 15282 | 3 | 3 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0008c0018 | 0/0 | 15282 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0008c0021 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0009c0011 | 0/0 | 15282 | 3 | 3 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0010c0020 | 0/0 | 15282 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0011c0040 | 0/0 | 15531 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0011c0041 | 0/0 | 15531 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0012c0042 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0013c0044 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0014c0030 | 0/0 | 15282 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0015c0028 | 0/0 | 15271 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0016c0022 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0017c0035 | 0/0 | 15282 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0018c0039 | 0/0 | 15282 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0019c0045 | 0/0 | 15282 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 16162 | 102 | 32 | 12 | 47 | 2 | 8 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0001t0003 | 0/0 | 16162 | 2 | 1 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0001t0004 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0001t0009 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0002t0001 | 0/0 | 16162 | 73 | 3 | 19 | 38 | 2 | 11 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0002t0008 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0003t0001 | 0/1 | 16162 | 33 | 0 | 4 | 20 | 4 | 4 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0003t0006 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0005t0001 | 0/0 | 16162 | 9 | 1 | 3 | 0 | 1 | 4 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0005t0002 | 0/0 | 16166 | 6 | 6 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0007t0001 | 0/0 | 16162 | 12 | 11 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0008t0001 | 0/0 | 16162 | 4 | 0 | 2 | 0 | 1 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0009t0001 | 0/0 | 16162 | 4 | 0 | 0 | 4 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0015t0001 | 0/0 | 16162 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0016t0001 | 0/0 | 16162 | 2 | 0 | 0 | 2 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0017t0001 | 0/0 | 16162 | 2 | 1 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0019t0001 | 0/0 | 16162 | 2 | 0 | 0 | 0 | 2 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0023t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0024t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0025t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0026t0001 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0027t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0029t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0032t0001 | 0/0 | 16162 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0033t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0034t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0036t0001 | 0/0 | 16162 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0037t0001 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0001c0038t0005 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0002c0004t0001 | 0/0 | 16162 | 20 | 0 | 2 | 18 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0002c0043t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0003c0006t0001 | 0/0 | 16162 | 14 | 13 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0004c0013t0001 | 0/0 | 16162 | 3 | 1 | 2 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0004c0031t0001 | 0/0 | 16162 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0005c0010t0001 | 0/0 | 16162 | 4 | 0 | 3 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0006c0014t0001 | 0/0 | 16162 | 3 | 2 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0007c0012t0001 | 0/0 | 16162 | 3 | 3 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0008c0018t0001 | 0/0 | 16162 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0008c0021t0010 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0009c0011t0001 | 0/0 | 16162 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0009c0011t0007 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0010c0020t0001 | 0/0 | 16162 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0011c0040t0001 | 0/0 | 16411 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0011c0041t0001 | 0/0 | 16411 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0012c0042t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0013c0044t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0014c0030t0001 | 0/0 | 16162 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0015c0028t0001 | 0/0 | 16151 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0016c0022t0001 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0017c0035t0001 | 0/0 | 16162 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0018c0039t0001 | 0/0 | 16162 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| a0019c0045t0001 | 0/0 | 16162 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | copy fasta | chr4 | 122147331 | 122367752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0001t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0002t0008g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0003t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0005t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0007t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0008t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0008t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0008t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0009t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0009t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0009t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0009t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0015t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0015t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0016t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0016t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0017t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0017t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0019t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0023t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0024t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0025t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0026t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0027t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0029t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0032t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0033t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0034t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0036t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0037t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0001c0038t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0002c0043t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0003c0006t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0004c0013t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0004c0013t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0004c0013t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0004c0031t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0005c0010t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0005c0010t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0005c0010t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0005c0010t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0006c0014t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0006c0014t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0006c0014t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0007c0012t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0007c0012t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0007c0012t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0008c0018t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0008c0018t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0008c0021t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0009c0011t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0009c0011t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0009c0011t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0010c0020t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0010c0020t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0011c0040t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0011c0041t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0012c0042t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0013c0044t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0014c0030t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0015c0028t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0016c0022t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0017c0035t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0018c0039t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| a0019c0045t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0231 | EUR | GBR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00099 | hp2 | a0005 | c0010 | t0001 | g0305 | EUR | GBR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0034 | EUR | GBR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00280 | hp1 | a0001 | c0036 | t0001 | g0320 | EUR | FIN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0178 | EUR | FIN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0195 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00558 | hp1 | a0002 | c0004 | t0001 | g0127 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00558 | hp2 | a0001 | c0033 | t0001 | g0052 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0177 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00639 | hp1 | a0001 | c0007 | t0001 | g0243 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0194 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00673 | hp2 | a0002 | c0004 | t0001 | g0158 | EAS | CHS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00733 | hp1 | a0018 | c0039 | t0001 | g0233 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00735 | hp1 | a0001 | c0017 | t0001 | g0295 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00738 | hp2 | a0011 | c0040 | t0001 | g0248 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0199 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01069 | hp2 | a0001 | c0032 | t0001 | g0176 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01074 | hp1 | a0005 | c0010 | t0001 | g0297 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0213 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01081 | hp2 | a0004 | c0031 | t0001 | g0197 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0203 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01106 | hp1 | a0005 | c0010 | t0001 | g0319 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0106 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01168 | hp2 | a0002 | c0004 | t0001 | g0149 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0234 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01175 | hp2 | a0005 | c0010 | t0001 | g0307 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01243 | hp2 | a0006 | c0014 | t0001 | g0117 | AMR | PUR | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01256 | hp2 | a0001 | c0008 | t0001 | g0164 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01257 | hp2 | a0001 | c0005 | t0001 | g0107 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01258 | hp1 | a0001 | c0008 | t0001 | g0165 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0108 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01361 | hp1 | a0004 | c0013 | t0001 | g0226 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01361 | hp2 | a0003 | c0006 | t0001 | g0011 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0237 | EUR | IBS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01515 | hp2 | a0001 | c0019 | t0001 | g0003 | EUR | IBS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01517 | hp1 | a0001 | c0019 | t0001 | g0003 | EUR | IBS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01517 | hp2 | a0001 | c0008 | t0001 | g0075 | EUR | IBS | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01884 | hp2 | a0003 | c0006 | t0001 | g0044 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0138 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02055 | hp1 | a0001 | c0005 | t0002 | g0007 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02055 | hp2 | a0003 | c0006 | t0001 | g0048 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02071 | hp2 | a0002 | c0004 | t0001 | g0148 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02074 | hp2 | a0002 | c0004 | t0001 | g0154 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02129 | hp1 | a0019 | c0045 | t0001 | g0212 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02132 | hp1 | a0001 | c0003 | t0006 | g0196 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0327 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02145 | hp2 | a0006 | c0014 | t0001 | g0144 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | CDX | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02155 | hp2 | a0002 | c0004 | t0001 | g0128 | EAS | CDX | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | CDX | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02165 | hp2 | a0002 | c0004 | t0001 | g0049 | EAS | CDX | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02257 | hp1 | a0001 | c0007 | t0001 | g0157 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02280 | hp2 | a0003 | c0006 | t0001 | g0010 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0245 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02523 | hp2 | a0002 | c0004 | t0001 | g0139 | EAS | KHV | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02572 | hp1 | a0009 | c0011 | t0001 | g0112 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02572 | hp2 | a0003 | c0006 | t0001 | g0012 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02615 | hp2 | a0003 | c0006 | t0001 | g0047 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02622 | hp1 | a0001 | c0007 | t0001 | g0241 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02622 | hp2 | a0003 | c0006 | t0001 | g0040 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02647 | hp1 | a0001 | c0037 | t0001 | g0103 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02647 | hp2 | a0001 | c0015 | t0001 | g0078 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02717 | hp2 | a0001 | c0005 | t0002 | g0001 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02809 | hp1 | a0007 | c0012 | t0001 | g0315 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02809 | hp2 | a0010 | c0020 | t0001 | g0104 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02818 | hp2 | a0001 | c0005 | t0002 | g0005 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02886 | hp2 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02895 | hp1 | a0001 | c0007 | t0001 | g0240 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02895 | hp2 | a0009 | c0011 | t0001 | g0045 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02897 | hp1 | a0001 | c0017 | t0001 | g0303 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0239 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02922 | hp2 | a0003 | c0006 | t0001 | g0009 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02965 | hp1 | a0008 | c0018 | t0001 | g0115 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0242 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02976 | hp1 | a0001 | c0015 | t0001 | g0079 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03041 | hp2 | a0003 | c0006 | t0001 | g0041 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03098 | hp2 | a0009 | c0011 | t0007 | g0039 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03139 | hp2 | a0003 | c0006 | t0001 | g0038 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03225 | hp1 | a0001 | c0026 | t0001 | g0080 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03453 | hp1 | a0008 | c0021 | t0010 | g0116 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03486 | hp1 | a0001 | c0005 | t0002 | g0006 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03490 | hp1 | a0001 | c0005 | t0001 | g0110 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03492 | hp2 | a0001 | c0005 | t0001 | g0109 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03516 | hp1 | a0010 | c0020 | t0001 | g0180 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03516 | hp2 | a0016 | c0022 | t0001 | g0113 | AFR | ESN | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0284 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03579 | hp1 | a0003 | c0006 | t0001 | g0042 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03688 | hp1 | a0001 | c0008 | t0001 | g0098 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0191 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0200 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0201 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04115 | hp1 | a0014 | c0030 | t0001 | g0202 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04115 | hp2 | a0001 | c0005 | t0001 | g0173 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0193 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0105 | SAS | STU | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18747 | hp1 | a0001 | c0009 | t0001 | g0081 | EAS | CHB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18906 | hp1 | a0008 | c0018 | t0001 | g0114 | AFR | YRI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18906 | hp2 | a0001 | c0007 | t0001 | g0244 | AFR | YRI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18942 | hp1 | a0002 | c0004 | t0001 | g0137 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18943 | hp1 | a0002 | c0004 | t0001 | g0150 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18950 | hp2 | a0001 | c0002 | t0008 | g0294 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18952 | hp2 | a0002 | c0004 | t0001 | g0153 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18974 | hp2 | a0015 | c0028 | t0001 | g0058 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18979 | hp1 | a0002 | c0004 | t0001 | g0151 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18981 | hp2 | a0001 | c0027 | t0001 | g0072 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18984 | hp1 | a0002 | c0004 | t0001 | g0130 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18986 | hp2 | a0002 | c0004 | t0001 | g0134 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18992 | hp1 | a0001 | c0016 | t0001 | g0028 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18993 | hp2 | a0002 | c0004 | t0001 | g0131 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0275 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18998 | hp2 | a0001 | c0024 | t0001 | g0163 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19000 | hp1 | a0001 | c0038 | t0005 | g0285 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19000 | hp2 | a0001 | c0025 | t0001 | g0022 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19005 | hp1 | a0001 | c0009 | t0001 | g0083 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19010 | hp2 | a0013 | c0044 | t0001 | g0133 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19011 | hp2 | a0002 | c0043 | t0001 | g0132 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19030 | hp2 | a0003 | c0006 | t0001 | g0046 | AFR | LWK | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19043 | hp1 | a0006 | c0014 | t0001 | g0118 | AFR | LWK | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19054 | hp2 | a0012 | c0042 | t0001 | g0152 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19056 | hp2 | a0002 | c0004 | t0001 | g0129 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19062 | hp1 | a0001 | c0034 | t0001 | g0286 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19062 | hp2 | a0001 | c0029 | t0001 | g0032 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19064 | hp1 | a0001 | c0009 | t0001 | g0082 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19065 | hp2 | a0001 | c0009 | t0001 | g0168 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19066 | hp2 | a0001 | c0016 | t0001 | g0029 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19079 | hp2 | a0001 | c0023 | t0001 | g0249 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19086 | hp2 | a0002 | c0004 | t0001 | g0136 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19088 | hp1 | a0002 | c0004 | t0001 | g0135 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19240 | hp1 | a0007 | c0012 | t0001 | g0313 | AFR | YRI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA19240 | hp2 | a0003 | c0006 | t0001 | g0043 | AFR | YRI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ASW | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ASW | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0206 | EUR | TSI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | TSI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20805 | hp1 | a0001 | c0005 | t0001 | g0111 | EUR | TSI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | GIH | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20905 | hp2 | a0011 | c0041 | t0001 | g0246 | SAS | GIH | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG01123 | hp2 | a0004 | c0013 | t0001 | g0227 | AMR | CLM | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0140 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02559 | hp1 | a0007 | c0012 | t0001 | g0316 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG02559 | hp2 | a0001 | c0005 | t0002 | g0001 | AFR | ACB | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG03471 | hp2 | a0017 | c0035 | t0001 | g0142 | AFR | MSL | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG06807 | hp1 | a0001 | c0007 | t0001 | g0238 | AFR | USA | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| HG06807 | hp2 | a0001 | c0005 | t0002 | g0004 | AFR | USA | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20300 | hp1 | a0004 | c0013 | t0001 | g0198 | AFR | USA | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0247 | AFR | USA | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | LWK | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0283 | AFR | LWK | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0192 | REF | REF | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0126 | REF | REF | BLTP1_chr4_122147331_122367752 | BLTP1 | chr4 | 122147331 | 122367752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122187460
|
C | G | 1 | a0019 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.575C>G | p.Pro192Arg | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 8/88 | 950/16162 | 575/15282 | 192/5093 | chr4 | 122187460 | ||
| chr4:122192273
|
A | G | 5 | a0002a0006a0010others(2): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
missense_variant | MODERATE | c.946A>G | p.Ser316Gly | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/88 | 1321/16162 | 946/15282 | 316/5093 | chr4 | 122192273 | ||
| chr4:122192366
|
G | A | 1 | a0009 | 3 | HG02572.hp1 HG02895.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1039G>A | p.Ala347Thr | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/88 | 1414/16162 | 1039/15282 | 347/5093 | chr4 | 122192366 | ||
| chr4:122209324
|
G | A | 1 | a0007 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.1918G>A | p.Val640Ile | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 18/88 | 2293/16162 | 1918/15282 | 640/5093 | chr4 | 122209324 | ||
| chr4:122219365
|
T | A | 1 | a0012 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.2273T>A | p.Met758Lys | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/88 | 2648/16162 | 2273/15282 | 758/5093 | chr4 | 122219365 | ||
| chr4:122229131
|
T | C | 1 | a0005 | 4 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
missense_variant | MODERATE | c.2933T>C | p.Ile978Thr | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 25/88 | 3308/16162 | 2933/15282 | 978/5093 | chr4 | 122229131 | ||
| chr4:122229133
|
C | T | 1 | a0010 | 2 | HG02809.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2935C>T | p.Pro979Ser | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 25/88 | 3310/16162 | 2935/15282 | 979/5093 | chr4 | 122229133 | ||
| chr4:122238094
|
A | T | 1 | a0013 | 1 | NA19010.hp2 | missense_variant&splice_region_variant | MODERATE | c.3577A>T | p.Asn1193Tyr | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/88 | 3952/16162 | 3577/15282 | 1193/5093 | chr4 | 122238094 | ||
| chr4:122239527
|
A | G | 1 | a0011 | 2 | HG00738.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.3845A>G | p.Glu1282Gly | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/88 | 4220/16162 | 3845/15282 | 1282/5093 | chr4 | 122239527 | ||
| chr4:122247165
|
G | A | 1 | a0014 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.5320G>A | p.Val1774Ile | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/88 | 5695/16162 | 5320/15282 | 1774/5093 | chr4 | 122247165 | ||
| chr4:122250504
|
T | A | 1 | a0004 | 4 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(1): Show |
missense_variant | MODERATE | c.5853T>A | p.Asp1951Glu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/88 | 6228/16162 | 5853/15282 | 1951/5093 | chr4 | 122250504 | ||
| chr4:122250531
|
CCCTTCCT others(4): Show |
C | 1 | a0015 | 1 | NA18974.hp2 | frameshift_variant | HIGH | c.5882_5892delCTTCCT others(5): Show |
p.Pro1961fs | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/88 | 6257/16162 | 5882/15282 | 1961/5093 | INFO_REALIGN_3_PRIME | chr4 | 122250531 | |
| chr4:122258745
|
C | T | 1 | a0018 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.6664C>T | p.Arg2222Trp | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/88 | 7039/16162 | 6664/15282 | 2222/5093 | chr4 | 122258745 | ||
| chr4:122316369
|
A | C | 1 | a0016 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.10561A>C | p.Ser3521Arg | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 62/88 | 10936/16162 | 10561/15282 | 3521/5093 | chr4 | 122316369 | ||
| chr4:122316445
|
G | A | 1 | a0017 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.10637G>A | p.Arg3546His | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 62/88 | 11012/16162 | 10637/15282 | 3546/5093 | chr4 | 122316445 | ||
| chr4:122328203
|
C | A | 3 | a0008a0016a0017 | 5 | HG02965.hp1 HG03453.hp1 HG03471.hp2 others(2): Show |
missense_variant | MODERATE | c.11359C>A | p.Pro3787Thr | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/88 | 11734/16162 | 11359/15282 | 3787/5093 | chr4 | 122328203 | ||
| chr4:122328307
|
A | C | 1 | a0006 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.11463A>C | p.Glu3821Asp | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/88 | 11838/16162 | 11463/15282 | 3821/5093 | chr4 | 122328307 | ||
| chr4:122347704
|
A | G | 5 | a0002a0006a0010others(2): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
missense_variant | MODERATE | c.13318A>G | p.Thr4440Ala | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/88 | 13693/16162 | 13318/15282 | 4440/5093 | chr4 | 122347704 | ||
| chr4:122355846
|
A | G | 2 | a0003a0009 | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
missense_variant | MODERATE | c.14620A>G | p.Thr4874Ala | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/88 | 14995/16162 | 14620/15282 | 4874/5093 | chr4 | 122355846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122186208
|
A | G | 1 | a0006c0014 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.531A>G | p.Gln177Gln | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 7/88 | 906/16162 | 531/15282 | 177/5093 | chr4 | 122186208 | ||
| chr4:122187927
|
G | A | 2 | a0008c0021a0016c0022 | 2 | HG03453.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.660G>A | p.Pro220Pro | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/88 | 1035/16162 | 660/15282 | 220/5093 | chr4 | 122187927 | ||
| chr4:122192239
|
G | A | 2 | a0008c0021a0016c0022 | 2 | HG03453.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.912G>A | p.Pro304Pro | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/88 | 1287/16162 | 912/15282 | 304/5093 | chr4 | 122192239 | ||
| chr4:122209872
|
T | C | 1 | a0001c0023 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.1986T>C | p.Tyr662Tyr | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 19/88 | 2361/16162 | 1986/15282 | 662/5093 | chr4 | 122209872 | ||
| chr4:122219447
|
A | T | 2 | a0008c0021a0016c0022 | 2 | HG03453.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.2355A>T | p.Gly785Gly | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/88 | 2730/16162 | 2355/15282 | 785/5093 | chr4 | 122219447 | ||
| chr4:122224596
|
T | A | 11 | a0001c0002a0001c0008a0001c0009others(8): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.2712T>A | p.Pro904Pro | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/88 | 3087/16162 | 2712/15282 | 904/5093 | chr4 | 122224596 | ||
| chr4:122229972
|
A | G | 1 | a0001c0029 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.3084A>G | p.Gln1028Gln | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/88 | 3459/16162 | 3084/15282 | 1028/5093 | chr4 | 122229972 | ||
| chr4:122238222
|
G | A | 1 | a0001c0024 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.3705G>A | p.Glu1235Glu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/88 | 4080/16162 | 3705/15282 | 1235/5093 | chr4 | 122238222 | ||
| chr4:122240176
|
C | T | 2 | a0003c0006a0009c0011 | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.4494C>T | p.Pro1498Pro | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/88 | 4869/16162 | 4494/15282 | 1498/5093 | chr4 | 122240176 | ||
| chr4:122243860
|
G | A | 1 | a0001c0025 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.4749G>A | p.Pro1583Pro | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/88 | 5124/16162 | 4749/15282 | 1583/5093 | chr4 | 122243860 | ||
| chr4:122247206
|
A | G | 3 | a0001c0007a0011c0040a0011c0041 | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
synonymous_variant | LOW | c.5361A>G | p.Ser1787Ser | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/88 | 5736/16162 | 5361/15282 | 1787/5093 | chr4 | 122247206 | ||
| chr4:122250435
|
T | C | 2 | a0001c0015a0001c0026 | 3 | HG02647.hp2 HG02976.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.5784T>C | p.Gly1928Gly | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/88 | 6159/16162 | 5784/15282 | 1928/5093 | chr4 | 122250435 | ||
| chr4:122254890
|
T | C | 1 | a0001c0017 | 2 | HG00735.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.6160T>C | p.Leu2054Leu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 39/88 | 6535/16162 | 6160/15282 | 2054/5093 | chr4 | 122254890 | ||
| chr4:122255220
|
A | G | 5 | a0001c0007a0003c0006a0009c0011others(2): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
synonymous_variant | LOW | c.6315A>G | p.Leu2105Leu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/88 | 6690/16162 | 6315/15282 | 2105/5093 | chr4 | 122255220 | ||
| chr4:122255223
|
T | C | 1 | a0001c0032 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.6318T>C | p.Cys2106Cys | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/88 | 6693/16162 | 6318/15282 | 2106/5093 | chr4 | 122255223 | ||
| chr4:122257419
|
T | C | 1 | a0001c0008 | 4 | HG01256.hp2 HG01258.hp1 HG01517.hp2 others(1): Show |
synonymous_variant | LOW | c.6543T>C | p.Asp2181Asp | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/88 | 6918/16162 | 6543/15282 | 2181/5093 | chr4 | 122257419 | ||
| chr4:122271165
|
G | T | 1 | a0001c0038 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.7641G>T | p.Arg2547Arg | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 47/88 | 8016/16162 | 7641/15282 | 2547/5093 | chr4 | 122271165 | ||
| chr4:122271228
|
T | C | 12 | a0001c0002a0001c0008a0001c0009others(9): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
synonymous_variant | LOW | c.7704T>C | p.Asp2568Asp | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 47/88 | 8079/16162 | 7704/15282 | 2568/5093 | chr4 | 122271228 | ||
| chr4:122279970
|
G | A | 2 | a0003c0006a0009c0011 | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.8787G>A | p.Gln2929Gln | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/88 | 9162/16162 | 8787/15282 | 2929/5093 | chr4 | 122279970 | ||
| chr4:122286575
|
T | C | 1 | a0001c0034 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.9072T>C | p.Asn3024Asn | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/88 | 9447/16162 | 9072/15282 | 3024/5093 | chr4 | 122286575 | ||
| chr4:122305894
|
T | C | 1 | a0001c0027 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.9690T>C | p.Gly3230Gly | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/88 | 10065/16162 | 9690/15282 | 3230/5093 | chr4 | 122305894 | ||
| chr4:122307977
|
C | T | 12 | a0001c0002a0001c0008a0001c0009others(9): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
synonymous_variant | LOW | c.9870C>T | p.Ala3290Ala | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/88 | 10245/16162 | 9870/15282 | 3290/5093 | chr4 | 122307977 | ||
| chr4:122316419
|
A | G | 1 | a0011c0041 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.10611A>G | p.Leu3537Leu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 62/88 | 10986/16162 | 10611/15282 | 3537/5093 | chr4 | 122316419 | ||
| chr4:122318189
|
A | G | 1 | a0001c0016 | 2 | NA18992.hp1 NA19066.hp2 |
synonymous_variant | LOW | c.10914A>G | p.Gln3638Gln | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/88 | 11289/16162 | 10914/15282 | 3638/5093 | chr4 | 122318189 | ||
| chr4:122328274
|
G | A | 1 | a0001c0036 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.11430G>A | p.Leu3810Leu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/88 | 11805/16162 | 11430/15282 | 3810/5093 | chr4 | 122328274 | ||
| chr4:122346705
|
T | C | 1 | a0001c0009 | 4 | NA18747.hp1 NA19005.hp1 NA19064.hp1 others(1): Show |
synonymous_variant | LOW | c.13080T>C | p.Tyr4360Tyr | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/88 | 13455/16162 | 13080/15282 | 4360/5093 | chr4 | 122346705 | ||
| chr4:122350013
|
A | G | 1 | a0001c0037 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.14052A>G | p.Pro4684Pro | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/88 | 14427/16162 | 14052/15282 | 4684/5093 | chr4 | 122350013 | ||
| chr4:122350034
|
G | A | 2 | a0003c0006a0009c0011 | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.14073G>A | p.Lys4691Lys | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/88 | 14448/16162 | 14073/15282 | 4691/5093 | chr4 | 122350034 | ||
| chr4:122355806
|
G | A | 6 | a0001c0005a0001c0019a0008c0018others(3): Show | 22 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
synonymous_variant | LOW | c.14580G>A | p.Leu4860Leu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/88 | 14955/16162 | 14580/15282 | 4860/5093 | chr4 | 122355806 | ||
| chr4:122355866
|
G | A | 1 | a0001c0019 | 2 | HG01515.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.14640G>A | p.Leu4880Leu | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/88 | 15015/16162 | 14640/15282 | 4880/5093 | chr4 | 122355866 | ||
| chr4:122359705
|
T | C | 5 | a0001c0003a0001c0023a0001c0032others(2): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
synonymous_variant | LOW | c.15048T>C | p.His5016His | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/88 | 15423/16162 | 15048/15282 | 5016/5093 | chr4 | 122359705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122152359
|
C | T | 1 | a0008c0021t0010 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-347C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/88 | 18289 | chr4 | 122152359 | |||||
| chr4:122152371
|
C | T | 1 | a0001c0001t0003 | 2 | HG01884.hp1 HG01978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-335C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/88 | 18277 | chr4 | 122152371 | |||||
| chr4:122152389
|
C | A | 1 | a0001c0001t0004 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-317C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/88 | 18259 | chr4 | 122152389 | |||||
| chr4:122152395
|
C | T | 1 | a0001c0001t0004 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-311C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/88 | chr4 | 122152395 | ||||||
| chr4:122152407
|
T | C | 1 | a0001c0038t0005 | 1 | NA19000.hp1 | 5_prime_UTR_variant | MODIFIER | c.-299T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/88 | 18241 | chr4 | 122152407 | |||||
| chr4:122152504
|
C | T | 1 | a0001c0001t0009 | 1 | HG02145.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-202C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/88 | chr4 | 122152504 | ||||||
| chr4:122362281
|
G | T | 1 | a0001c0002t0008 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 88/88 | 34 | chr4 | 122362281 | |||||
| chr4:122362446
|
A | G | 1 | a0009c0011t0007 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 88/88 | 199 | chr4 | 122362446 | |||||
| chr4:122362465
|
A | ATAAC | 1 | a0001c0005t0002 | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*220_*223dupAACT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 88/88 | 224 | INFO_REALIGN_3_PRIME | chr4 | 122362465 | ||||
| chr4:122362664
|
T | C | 1 | a0001c0003t0006 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 88/88 | 417 | chr4 | 122362664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122152654
|
A | G | 12 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(9): Show | 12 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-122+70A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122152654 | ||||||
| chr4:122152784
|
C | CT | 39 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.-122+201dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122152784 | |||||
| chr4:122152806
|
A | T | 1 | a0001c0002t0008g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-122+222A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122152806 | ||||||
| chr4:122152854
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-122+270G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122152854 | ||||||
| chr4:122153066
|
A | G | 1 | a0001c0003t0001g0292 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-122+482A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122153066 | ||||||
| chr4:122153159
|
G | GT | 96 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0181others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-122+595dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122153159 | |||||
| chr4:122153159
|
G | GTT | 36 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(33): Show | 36 | HG00423.hp1 HG01884.hp1 HG01978.hp1 others(33): Show |
intron_variant | MODIFIER | c.-122+594_-122+595d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122153159 | |||||
| chr4:122153159
|
G | GTTT | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(4): Show | 7 | HG02004.hp2 HG02056.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122+593_-122+595d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122153159 | |||||
| chr4:122153159
|
GT | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(32): Show | 35 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.-122+595delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122153159 | |||||
| chr4:122153159
|
GTT | G | 6 | a0001c0002t0001g0008a0003c0006t0001g0009a0003c0006t0001g0010others(3): Show | 6 | HG01168.hp1 HG01361.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122+594_-122+595d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122153159 | |||||
| chr4:122153159
|
GTTT | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122+593_-122+595d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | INFO_REALIGN_3_PRIME | chr4 | 122153159 | |||||
| chr4:122153189
|
T | C | 1 | a0001c0002t0001g0014 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-122+605T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122153189 | ||||||
| chr4:122153493
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-121-532A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122153493 | ||||||
| chr4:122153686
|
A | G | 1 | a0001c0023t0001g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-121-339A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122153686 | ||||||
| chr4:122153749
|
A | T | 1 | a0002c0004t0001g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-121-276A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122153749 | ||||||
| chr4:122153861
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-121-164A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 1/87 | chr4 | 122153861 | ||||||
| chr4:122154162
|
C | CT | 83 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-34+81dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
C | CTT | 58 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0207others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-34+80_-34+81dupTT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
C | CTTT | 9 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0310others(6): Show | 9 | HG01175.hp1 HG01256.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+79_-34+81dupTT others(1): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
C | CTTTT | 9 | a0001c0001t0001g0312a0001c0001t0001g0314a0001c0007t0001g0157others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+78_-34+81dupTT others(2): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
C | CTTTTTT | 6 | a0003c0006t0001g0046a0003c0006t0001g0047a0003c0006t0001g0048others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+76_-34+81dupTT others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
CT | C | 24 | a0001c0001t0001g0102a0001c0001t0001g0159a0001c0001t0001g0172others(21): Show | 25 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-34+81delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
CTTT | C | 15 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(12): Show | 15 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34+79_-34+81delTT others(1): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
CTTTT | C | 70 | a0001c0002t0001g0008a0001c0002t0001g0014a0001c0002t0001g0015others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34+78_-34+81delTT others(2): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154162
|
CTTTTT | C | 7 | a0001c0002t0001g0002a0001c0002t0001g0050a0001c0002t0001g0051others(4): Show | 8 | HG00558.hp2 HG01169.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+77_-34+81delTT others(3): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122154162 | |||||
| chr4:122154166
|
T | G | 1 | a0002c0004t0001g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-34+54T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154166 | ||||||
| chr4:122154202
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+90G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154202 | ||||||
| chr4:122154215
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-34+103G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154215 | ||||||
| chr4:122154238
|
C | A | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-34+126C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154238 | ||||||
| chr4:122154244
|
T | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+132T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154244 | ||||||
| chr4:122154578
|
G | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+466G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154578 | ||||||
| chr4:122154599
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+487C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154599 | ||||||
| chr4:122154630
|
T | C | 1 | a0003c0006t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34+518T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154630 | ||||||
| chr4:122154639
|
C | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+527C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154639 | ||||||
| chr4:122154640
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-34+528G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154640 | ||||||
| chr4:122154648
|
C | T | 27 | a0001c0002t0001g0093a0001c0002t0001g0101a0002c0004t0001g0049others(24): Show | 27 | HG00558.hp1 HG00673.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-34+536C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154648 | ||||||
| chr4:122154689
|
T | C | 6 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0017others(3): Show | 6 | HG00408.hp2 NA18960.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+577T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154689 | ||||||
| chr4:122154728
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0330a0001c0001t0001g0331 | 3 | HG01192.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-34+616C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154728 | ||||||
| chr4:122154729
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-34+617G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154729 | ||||||
| chr4:122154733
|
G | T | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-34+621G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154733 | ||||||
| chr4:122154741
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+629G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154741 | ||||||
| chr4:122154765
|
G | A | 11 | a0001c0002t0001g0050a0001c0002t0001g0051a0001c0002t0001g0057others(8): Show | 11 | HG01169.hp2 HG01975.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+653G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154765 | ||||||
| chr4:122154789
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+677A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154789 | ||||||
| chr4:122154852
|
A | G | 42 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0003t0001g0177others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.-34+740A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122154852 | ||||||
| chr4:122155056
|
G | A | 1 | a0002c0004t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-34+944G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155056 | ||||||
| chr4:122155089
|
G | A | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-34+977G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155089 | ||||||
| chr4:122155206
|
G | A | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.-34+1094G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155206 | ||||||
| chr4:122155214
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-34+1102A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155214 | ||||||
| chr4:122155230
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34+1118A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155230 | ||||||
| chr4:122155249
|
T | TAAA | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+1138_-34+1140d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122155249 | |||||
| chr4:122155324
|
A | AT | 9 | a0001c0001t0001g0272a0001c0001t0001g0281a0001c0001t0001g0291others(6): Show | 9 | HG00140.hp2 HG00735.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+1228dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122155324 | |||||
| chr4:122155324
|
AT | A | 29 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(26): Show | 31 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+1228delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122155324 | |||||
| chr4:122155361
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-34+1249C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155361 | ||||||
| chr4:122155413
|
T | G | 60 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(57): Show | 60 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-34+1301T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155413 | ||||||
| chr4:122155448
|
C | T | 1 | a0008c0021t0010g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-34+1336C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155448 | ||||||
| chr4:122155449
|
G | A | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+1337G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155449 | ||||||
| chr4:122155521
|
A | C | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-34+1409A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155521 | ||||||
| chr4:122155604
|
G | A | 30 | a0001c0001t0001g0141a0001c0001t0001g0155a0002c0004t0001g0049others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+1492G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155604 | ||||||
| chr4:122155614
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+1502G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155614 | ||||||
| chr4:122155685
|
G | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34+1573G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155685 | ||||||
| chr4:122155740
|
A | G | 106 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-34+1628A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155740 | ||||||
| chr4:122155954
|
G | A | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-34+1842G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155954 | ||||||
| chr4:122155980
|
A | G | 1 | a0003c0006t0001g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-34+1868A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122155980 | ||||||
| chr4:122156053
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-34+1941T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156053 | ||||||
| chr4:122156177
|
G | A | 1 | a0001c0003t0001g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-34+2065G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156177 | ||||||
| chr4:122156179
|
G | C | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.-34+2067G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156179 | ||||||
| chr4:122156251
|
G | A | 1 | a0001c0003t0001g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-34+2139G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156251 | ||||||
| chr4:122156720
|
C | A | 12 | a0003c0006t0001g0038a0003c0006t0001g0040a0003c0006t0001g0041others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34+2608C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156720 | ||||||
| chr4:122156722
|
T | C | 1 | a0001c0002t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-34+2610T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156722 | ||||||
| chr4:122156796
|
A | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 8 | HG01081.hp1 HG02129.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+2684A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156796 | ||||||
| chr4:122156851
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-34+2739G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156851 | ||||||
| chr4:122156893
|
G | T | 1 | a0005c0010t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-34+2781G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156893 | ||||||
| chr4:122156937
|
A | G | 2 | a0009c0011t0001g0112a0009c0011t0007g0039 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-34+2825A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156937 | ||||||
| chr4:122156957
|
T | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+2845T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122156957 | ||||||
| chr4:122157057
|
G | GGGA | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+2956_-34+2958d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122157057 | |||||
| chr4:122157149
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-34+3037C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157149 | ||||||
| chr4:122157208
|
G | A | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-34+3096G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157208 | ||||||
| chr4:122157510
|
G | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34+3398G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157510 | ||||||
| chr4:122157557
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+3445A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157557 | ||||||
| chr4:122157632
|
C | G | 1 | a0001c0003t0001g0237 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-34+3520C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157632 | ||||||
| chr4:122157694
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-34+3582A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157694 | ||||||
| chr4:122157778
|
C | T | 3 | a0001c0001t0001g0310a0001c0001t0001g0314a0001c0001t0001g0321 | 3 | HG03669.hp1 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-34+3666C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157778 | ||||||
| chr4:122157852
|
C | T | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | NA18955.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+3740C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157852 | ||||||
| chr4:122157910
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+3798G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157910 | ||||||
| chr4:122157979
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-34+3867T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122157979 | ||||||
| chr4:122158285
|
A | G | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+4173A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158285 | ||||||
| chr4:122158337
|
A | G | 7 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(4): Show | 7 | NA18947.hp2 NA18955.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+4225A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158337 | ||||||
| chr4:122158370
|
C | T | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+4258C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158370 | ||||||
| chr4:122158440
|
C | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+4328C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158440 | ||||||
| chr4:122158567
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+4455A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158567 | ||||||
| chr4:122158568
|
C | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34+4456C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158568 | ||||||
| chr4:122158687
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-34+4575C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158687 | ||||||
| chr4:122158688
|
G | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34+4576G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158688 | ||||||
| chr4:122158821
|
C | T | 1 | a0001c0005t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-34+4709C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122158821 | ||||||
| chr4:122159206
|
G | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-34+5094G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159206 | ||||||
| chr4:122159416
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-34+5304C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159416 | ||||||
| chr4:122159461
|
C | CA | 35 | a0001c0002t0001g0015a0001c0002t0001g0162a0001c0007t0001g0157others(32): Show | 35 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-34+5363dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122159461 | |||||
| chr4:122159462
|
A | C | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34+5350A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159462 | ||||||
| chr4:122159477
|
TTTTTA | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+5371_-34+5375d others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122159477 | |||||
| chr4:122159481
|
T | C | 1 | a0001c0002t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-34+5369T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159481 | ||||||
| chr4:122159528
|
T | A | 1 | a0001c0023t0001g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-34+5416T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159528 | ||||||
| chr4:122159563
|
G | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+5451G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159563 | ||||||
| chr4:122159594
|
TAATA | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+5485_-34+5488d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122159594 | |||||
| chr4:122159846
|
A | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-34+5734A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122159846 | ||||||
| chr4:122160129
|
T | C | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-34+6017T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160129 | ||||||
| chr4:122160136
|
C | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+6024C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160136 | ||||||
| chr4:122160140
|
C | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-34+6028C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160140 | ||||||
| chr4:122160305
|
C | G | 143 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(140): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-34+6193C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160305 | ||||||
| chr4:122160328
|
C | G | 1 | a0001c0001t0001g0291 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-34+6216C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160328 | ||||||
| chr4:122160525
|
C | G | 1 | a0006c0014t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-34+6413C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160525 | ||||||
| chr4:122160544
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-34+6432C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160544 | ||||||
| chr4:122160569
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-34+6457G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160569 | ||||||
| chr4:122160661
|
T | C | 3 | a0009c0011t0001g0045a0009c0011t0001g0112a0009c0011t0007g0039 | 3 | HG02572.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-34+6549T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160661 | ||||||
| chr4:122160703
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-34+6591T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160703 | ||||||
| chr4:122160793
|
A | G | 1 | a0001c0005t0001g0173 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-34+6681A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160793 | ||||||
| chr4:122160798
|
C | G | 1 | a0001c0003t0001g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-34+6686C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160798 | ||||||
| chr4:122160889
|
GA | G | 10 | a0001c0001t0001g0156a0001c0001t0001g0325a0001c0001t0001g0326others(7): Show | 10 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+6778delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122160889 | ||||||
| chr4:122161265
|
T | A | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34+7153T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122161265 | ||||||
| chr4:122161704
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-34+7592C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122161704 | ||||||
| chr4:122161800
|
G | A | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-34+7688G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122161800 | ||||||
| chr4:122161826
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34+7714G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122161826 | ||||||
| chr4:122161846
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-34+7734G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122161846 | ||||||
| chr4:122161902
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-34+7790G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122161902 | ||||||
| chr4:122162117
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+8005A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162117 | ||||||
| chr4:122162140
|
T | G | 1 | a0001c0003t0001g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-34+8028T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162140 | ||||||
| chr4:122162391
|
G | GAT | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-33-8221_-33-8220d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122162391 | |||||
| chr4:122162412
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-33-8203A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162412 | ||||||
| chr4:122162608
|
C | T | 1 | a0011c0040t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-33-8007C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162608 | ||||||
| chr4:122162732
|
C | CA | 8 | a0001c0001t0001g0222a0001c0002t0001g0020a0001c0002t0001g0021others(5): Show | 8 | HG00621.hp1 HG01099.hp1 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-7881dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122162732 | |||||
| chr4:122162734
|
AC | A | 14 | a0001c0002t0001g0161a0001c0009t0001g0081a0001c0009t0001g0082others(11): Show | 14 | HG01884.hp2 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33-7880delC | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162734 | ||||||
| chr4:122162735
|
C | A | 80 | a0001c0001t0001g0222a0001c0002t0001g0002a0001c0002t0001g0008others(77): Show | 81 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-33-7880C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162735 | ||||||
| chr4:122162735
|
C | CA | 31 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(28): Show | 32 | HG01106.hp2 HG01192.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.-33-7870dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122162735 | |||||
| chr4:122162735
|
CA | C | 107 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-33-7870delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122162735 | |||||
| chr4:122162738
|
A | C | 7 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(4): Show | 8 | HG00738.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-7877A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162738 | ||||||
| chr4:122162741
|
A | C | 1 | a0001c0005t0002g0007 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-33-7874A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162741 | ||||||
| chr4:122162924
|
C | A | 1 | a0001c0003t0001g0273 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-33-7691C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122162924 | ||||||
| chr4:122163333
|
C | T | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-33-7282C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163333 | ||||||
| chr4:122163417
|
C | T | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-33-7198C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163417 | ||||||
| chr4:122163440
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-7175G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163440 | ||||||
| chr4:122163453
|
G | A | 2 | a0001c0008t0001g0164a0001c0008t0001g0165 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-33-7162G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163453 | ||||||
| chr4:122163699
|
A | G | 8 | a0001c0002t0001g0051a0001c0002t0001g0059a0001c0002t0001g0060others(5): Show | 8 | HG01169.hp2 HG01975.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-6916A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163699 | ||||||
| chr4:122163719
|
G | A | 30 | a0001c0001t0001g0141a0001c0001t0001g0155a0002c0004t0001g0049others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33-6896G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163719 | ||||||
| chr4:122163726
|
G | A | 1 | a0003c0006t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33-6889G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163726 | ||||||
| chr4:122163738
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-33-6877A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163738 | ||||||
| chr4:122163844
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-33-6771G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122163844 | ||||||
| chr4:122164026
|
A | G | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-33-6589A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164026 | ||||||
| chr4:122164527
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-6088A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164527 | ||||||
| chr4:122164631
|
T | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33-5984T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164631 | ||||||
| chr4:122164759
|
AT | A | 13 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(10): Show | 13 | HG00609.hp2 HG00735.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-5845delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122164759 | |||||
| chr4:122164763
|
T | TA | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33-5852_-33-5851i others(3): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164763 | ||||||
| chr4:122164765
|
T | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-5850T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164765 | ||||||
| chr4:122164781
|
A | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-5834A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164781 | ||||||
| chr4:122164819
|
A | G | 1 | a0001c0003t0001g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-33-5796A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122164819 | ||||||
| chr4:122165001
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-33-5614G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165001 | ||||||
| chr4:122165122
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33-5493C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165122 | ||||||
| chr4:122165167
|
C | T | 33 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33-5448C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165167 | ||||||
| chr4:122165246
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-5369C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165246 | ||||||
| chr4:122165342
|
G | A | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33-5273G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165342 | ||||||
| chr4:122165522
|
G | A | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-5093G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165522 | ||||||
| chr4:122165534
|
G | C | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-5081G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165534 | ||||||
| chr4:122165544
|
C | T | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-5071C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165544 | ||||||
| chr4:122165559
|
T | A | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-5056T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165559 | ||||||
| chr4:122165562
|
T | A | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-5053T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165562 | ||||||
| chr4:122165569
|
A | G | 137 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-33-5046A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165569 | ||||||
| chr4:122165594
|
A | G | 279 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-33-5021A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165594 | ||||||
| chr4:122165631
|
G | C | 141 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-33-4984G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165631 | ||||||
| chr4:122165642
|
C | T | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-33-4973C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165642 | ||||||
| chr4:122165661
|
G | A | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-4954G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165661 | ||||||
| chr4:122165683
|
T | C | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-4932T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165683 | ||||||
| chr4:122165720
|
G | C | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-4895G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165720 | ||||||
| chr4:122165735
|
T | A | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33-4880T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165735 | ||||||
| chr4:122165742
|
T | C | 136 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-33-4873T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165742 | ||||||
| chr4:122165774
|
G | A | 3 | a0001c0007t0001g0239a0001c0007t0001g0240a0001c0007t0001g0241 | 3 | HG02622.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-33-4841G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165774 | ||||||
| chr4:122165886
|
T | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-4729T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165886 | ||||||
| chr4:122165899
|
C | T | 3 | a0002c0004t0001g0128a0002c0004t0001g0139a0002c0004t0001g0148 | 3 | HG02071.hp2 HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-33-4716C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165899 | ||||||
| chr4:122165946
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-33-4669T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165946 | ||||||
| chr4:122165966
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-33-4649G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122165966 | ||||||
| chr4:122166070
|
T | G | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-4545T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166070 | ||||||
| chr4:122166095
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0210 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-33-4520A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166095 | ||||||
| chr4:122166148
|
C | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-4467C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166148 | ||||||
| chr4:122166149
|
A | G | 143 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(140): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-33-4466A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166149 | ||||||
| chr4:122166213
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-4402C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166213 | ||||||
| chr4:122166224
|
T | G | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.-33-4391T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166224 | ||||||
| chr4:122166274
|
T | G | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-33-4341T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166274 | ||||||
| chr4:122166287
|
C | A | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-33-4328C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166287 | ||||||
| chr4:122166306
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-4309C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166306 | ||||||
| chr4:122166342
|
A | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-4273A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166342 | ||||||
| chr4:122166391
|
C | T | 4 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142others(1): Show | 4 | HG00733.hp1 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-4224C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166391 | ||||||
| chr4:122166423
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33-4192A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166423 | ||||||
| chr4:122166444
|
G | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-4171G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166444 | ||||||
| chr4:122166467
|
G | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33-4148G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166467 | ||||||
| chr4:122166504
|
C | G | 1 | a0001c0001t0001g0317 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-33-4111C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166504 | ||||||
| chr4:122166505
|
C | G | 32 | a0001c0001t0001g0317a0001c0007t0001g0157a0001c0007t0001g0238others(29): Show | 32 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.-33-4110C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166505 | ||||||
| chr4:122166511
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-33-4104G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166511 | ||||||
| chr4:122166609
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33-4006G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166609 | ||||||
| chr4:122166688
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33-3927G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166688 | ||||||
| chr4:122166756
|
G | A | 11 | a0003c0006t0001g0038a0003c0006t0001g0040a0003c0006t0001g0041others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-3859G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166756 | ||||||
| chr4:122166802
|
T | C | 137 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-33-3813T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166802 | ||||||
| chr4:122166813
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-33-3802A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166813 | ||||||
| chr4:122166815
|
T | C | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-33-3800T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166815 | ||||||
| chr4:122166913
|
C | T | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.-33-3702C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122166913 | ||||||
| chr4:122167119
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33-3496T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167119 | ||||||
| chr4:122167152
|
C | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33-3463C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167152 | ||||||
| chr4:122167263
|
T | A | 1 | a0001c0003t0001g0282 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-33-3352T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167263 | ||||||
| chr4:122167558
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0036 | 2 | HG00423.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-33-3057G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167558 | ||||||
| chr4:122167735
|
A | G | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-33-2880A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167735 | ||||||
| chr4:122167776
|
T | C | 1 | a0001c0017t0001g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-33-2839T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167776 | ||||||
| chr4:122167806
|
G | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-2809G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167806 | ||||||
| chr4:122167807
|
C | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-2808C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122167807 | ||||||
| chr4:122168188
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-33-2427T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122168188 | ||||||
| chr4:122168214
|
G | A | 2 | a0001c0003t0001g0192a0001c0003t0001g0194 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-33-2401G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122168214 | ||||||
| chr4:122168252
|
A | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-2363A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122168252 | ||||||
| chr4:122168603
|
G | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0120 | 3 | HG01123.hp1 HG01346.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-33-2012G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122168603 | ||||||
| chr4:122168722
|
A | G | 3 | a0001c0005t0001g0109a0001c0005t0001g0110a0001c0019t0001g0003 | 4 | HG01515.hp2 HG01517.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-1893A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122168722 | ||||||
| chr4:122168776
|
G | A | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-1839G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122168776 | ||||||
| chr4:122169060
|
G | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33-1555G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169060 | ||||||
| chr4:122169078
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01175.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-33-1537G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169078 | ||||||
| chr4:122169083
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-33-1532G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169083 | ||||||
| chr4:122169513
|
A | G | 4 | a0005c0010t0001g0297a0005c0010t0001g0305a0005c0010t0001g0307others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-1102A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169513 | ||||||
| chr4:122169665
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33-950A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169665 | ||||||
| chr4:122169894
|
G | A | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33-721G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169894 | ||||||
| chr4:122169947
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33-668A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169947 | ||||||
| chr4:122169998
|
G | C | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33-617G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122169998 | ||||||
| chr4:122170032
|
C | T | 1 | a0002c0004t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-33-583C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122170032 | ||||||
| chr4:122170033
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-582G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122170033 | ||||||
| chr4:122170289
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-33-326C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122170289 | ||||||
| chr4:122170305
|
C | CA | 10 | a0001c0001t0001g0172a0001c0001t0001g0306a0001c0001t0001g0321others(7): Show | 10 | HG00423.hp2 HG00741.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33-287dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122170305 | |||||
| chr4:122170305
|
CA | C | 129 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0145others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-33-287delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122170305 | |||||
| chr4:122170305
|
CAA | C | 6 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0265others(3): Show | 6 | HG02886.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-288_-33-287del others(2): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122170305 | |||||
| chr4:122170305
|
CAAAA | C | 11 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-290_-33-287del others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122170305 | |||||
| chr4:122170305
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0002t0001g0056a0001c0002t0001g0084a0001c0002t0001g0085others(4): Show | 7 | HG01074.hp2 HG01192.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-296_-33-287del others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122170305 | |||||
| chr4:122170305
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0001g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-33-297_-33-287del others(11): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | INFO_REALIGN_3_PRIME | chr4 | 122170305 | |||||
| chr4:122170339
|
A | T | 1 | a0001c0002t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-33-276A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122170339 | ||||||
| chr4:122170360
|
A | C | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-33-255A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122170360 | ||||||
| chr4:122170523
|
C | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-92C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 2/87 | chr4 | 122170523 | ||||||
| chr4:122170913
|
T | C | 1 | a0003c0006t0001g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+169T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122170913 | ||||||
| chr4:122171036
|
T | C | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+292T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171036 | ||||||
| chr4:122171217
|
A | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.97+473A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171217 | ||||||
| chr4:122171296
|
G | A | 143 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(140): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.97+552G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171296 | ||||||
| chr4:122171641
|
GT | G | 311 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.97+916delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | INFO_REALIGN_3_PRIME | chr4 | 122171641 | |||||
| chr4:122171647
|
T | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+903T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171647 | ||||||
| chr4:122171799
|
G | GA | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1062dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | INFO_REALIGN_3_PRIME | chr4 | 122171799 | |||||
| chr4:122171830
|
T | C | 12 | a0003c0006t0001g0038a0003c0006t0001g0040a0003c0006t0001g0041others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+1086T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171830 | ||||||
| chr4:122171871
|
G | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1127G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171871 | ||||||
| chr4:122171873
|
G | A | 1 | a0001c0019t0001g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.97+1129G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171873 | ||||||
| chr4:122171896
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-1140A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122171896 | ||||||
| chr4:122172064
|
A | T | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.98-972A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172064 | ||||||
| chr4:122172095
|
A | T | 49 | a0001c0001t0001g0220a0001c0002t0001g0171a0001c0005t0001g0105others(46): Show | 50 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.98-941A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172095 | ||||||
| chr4:122172121
|
T | C | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.98-915T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172121 | ||||||
| chr4:122172145
|
A | C | 1 | a0012c0042t0001g0152 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.98-891A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172145 | ||||||
| chr4:122172150
|
G | T | 12 | a0003c0006t0001g0038a0003c0006t0001g0040a0003c0006t0001g0041others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-886G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172150 | ||||||
| chr4:122172161
|
T | G | 1 | a0011c0040t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.98-875T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172161 | ||||||
| chr4:122172318
|
A | G | 1 | a0001c0002t0001g0054 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.98-718A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172318 | ||||||
| chr4:122172532
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.98-504A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172532 | ||||||
| chr4:122172540
|
T | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-496T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172540 | ||||||
| chr4:122172632
|
A | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.98-404A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172632 | ||||||
| chr4:122172862
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.98-174C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 3/87 | chr4 | 122172862 | ||||||
| chr4:122173545
|
G | A | 4 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0016t0001g0028others(1): Show | 4 | NA18966.hp2 NA18992.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+393G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122173545 | ||||||
| chr4:122173627
|
C | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+475C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122173627 | ||||||
| chr4:122173911
|
A | G | 1 | a0001c0002t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.215-663A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122173911 | ||||||
| chr4:122174037
|
T | C | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-537T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174037 | ||||||
| chr4:122174045
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.215-529A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174045 | ||||||
| chr4:122174195
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.215-379C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174195 | ||||||
| chr4:122174243
|
A | T | 143 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(140): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.215-331A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174243 | ||||||
| chr4:122174374
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-200A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174374 | ||||||
| chr4:122174523
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.215-51C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174523 | ||||||
| chr4:122174548
|
C | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.215-26C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 4/87 | chr4 | 122174548 | ||||||
| chr4:122174685
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.293+33G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122174685 | ||||||
| chr4:122174734
|
G | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.293+82G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122174734 | ||||||
| chr4:122174788
|
T | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.293+136T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122174788 | ||||||
| chr4:122174812
|
A | G | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.293+160A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122174812 | ||||||
| chr4:122174952
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.293+300C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122174952 | ||||||
| chr4:122174953
|
G | A | 1 | a0001c0002t0001g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293+301G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122174953 | ||||||
| chr4:122175035
|
G | A | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.293+383G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175035 | ||||||
| chr4:122175117
|
C | A | 1 | a0001c0002t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.293+465C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175117 | ||||||
| chr4:122175331
|
T | C | 143 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(140): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.294-519T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175331 | ||||||
| chr4:122175387
|
TA | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.294-459delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | INFO_REALIGN_3_PRIME | chr4 | 122175387 | |||||
| chr4:122175520
|
A | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.294-330A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175520 | ||||||
| chr4:122175534
|
C | T | 5 | a0001c0001t0001g0222a0001c0005t0002g0001a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.294-316C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175534 | ||||||
| chr4:122175535
|
G | A | 1 | a0018c0039t0001g0233 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.294-315G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175535 | ||||||
| chr4:122175669
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0036 | 2 | HG00423.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.294-181C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175669 | ||||||
| chr4:122175683
|
C | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.294-167C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 5/87 | chr4 | 122175683 | ||||||
| chr4:122175950
|
A | G | 1 | a0002c0004t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358+36A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122175950 | ||||||
| chr4:122176029
|
C | T | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.358+115C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176029 | ||||||
| chr4:122176302
|
C | CA | 20 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(17): Show | 20 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.358+398dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122176302 | |||||
| chr4:122176504
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.358+590C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176504 | ||||||
| chr4:122176520
|
A | G | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02647.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.358+606A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176520 | ||||||
| chr4:122176533
|
T | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.358+619T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176533 | ||||||
| chr4:122176591
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358+677T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176591 | ||||||
| chr4:122176781
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.358+867C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176781 | ||||||
| chr4:122176892
|
T | G | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.358+978T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122176892 | ||||||
| chr4:122177039
|
T | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.358+1125T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177039 | ||||||
| chr4:122177107
|
A | G | 1 | a0001c0003t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.358+1193A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177107 | ||||||
| chr4:122177210
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358+1296A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177210 | ||||||
| chr4:122177322
|
C | G | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.358+1408C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177322 | ||||||
| chr4:122177406
|
A | G | 1 | a0001c0002t0001g0087 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.358+1492A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177406 | ||||||
| chr4:122177684
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+1770A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177684 | ||||||
| chr4:122177808
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358+1894C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177808 | ||||||
| chr4:122177914
|
C | A | 1 | a0002c0004t0001g0129 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.358+2000C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177914 | ||||||
| chr4:122177976
|
G | A | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+2062G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122177976 | ||||||
| chr4:122178010
|
C | T | 2 | a0001c0002t0001g0066a0001c0002t0001g0077 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.358+2096C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122178010 | ||||||
| chr4:122178099
|
A | G | 2 | a0002c0004t0001g0135a0002c0004t0001g0136 | 2 | NA19086.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.358+2185A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122178099 | ||||||
| chr4:122178582
|
A | C | 1 | a0001c0029t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.358+2668A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122178582 | ||||||
| chr4:122178807
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.358+2893C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122178807 | ||||||
| chr4:122178949
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358+3035G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122178949 | ||||||
| chr4:122179049
|
T | C | 1 | a0001c0029t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.358+3135T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179049 | ||||||
| chr4:122179476
|
A | G | 1 | a0001c0003t0001g0292 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.358+3562A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179476 | ||||||
| chr4:122179585
|
G | A | 38 | a0001c0001t0001g0143a0001c0001t0001g0250a0001c0001t0001g0251others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.358+3671G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179585 | ||||||
| chr4:122179611
|
T | A | 2 | a0003c0006t0001g0038a0003c0006t0001g0046 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.358+3697T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179611 | ||||||
| chr4:122179654
|
A | G | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.358+3740A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179654 | ||||||
| chr4:122179667
|
A | G | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.358+3753A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179667 | ||||||
| chr4:122179797
|
G | A | 1 | a0016c0022t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358+3883G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179797 | ||||||
| chr4:122179836
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.358+3922C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179836 | ||||||
| chr4:122179882
|
G | C | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.358+3968G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179882 | ||||||
| chr4:122179956
|
T | C | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4042T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122179956 | ||||||
| chr4:122180025
|
TAC | T | 157 | a0001c0001t0001g0121a0001c0001t0001g0143a0001c0001t0001g0156others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.358+4129_358+4130d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122180025 | |||||
| chr4:122180039
|
C | CACACACA others(1): Show |
7 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(4): Show | 8 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+4130_358+4131i others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122180039 | |||||
| chr4:122180039
|
CACACAT | C | 3 | a0001c0002t0001g0055a0001c0007t0001g0241a0003c0006t0001g0042 | 3 | HG02622.hp1 HG03579.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.358+4131_358+4136d others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122180039 | |||||
| chr4:122180041
|
C | CAT | 4 | a0007c0012t0001g0313a0008c0018t0001g0114a0008c0018t0001g0115others(1): Show | 4 | HG02965.hp1 HG03471.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4128_358+4129i others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122180041 | |||||
| chr4:122180041
|
CACAT | C | 143 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(140): Show | 144 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.358+4131_358+4134d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122180041 | |||||
| chr4:122180043
|
C | T | 6 | a0001c0001t0001g0145a0001c0003t0006g0196a0001c0005t0002g0001others(3): Show | 7 | HG02055.hp1 HG02132.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+4129C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180043 | ||||||
| chr4:122180045
|
T | C | 20 | a0001c0001t0001g0145a0001c0003t0006g0196a0001c0005t0001g0105others(17): Show | 22 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.358+4131T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180045 | ||||||
| chr4:122180045
|
T | TAC | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4158_358+4159d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122180045 | |||||
| chr4:122180047
|
C | T | 142 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(139): Show | 143 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.358+4133C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180047 | ||||||
| chr4:122180049
|
C | T | 2 | a0001c0002t0001g0055a0001c0007t0001g0241 | 2 | HG02622.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.358+4135C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180049 | ||||||
| chr4:122180051
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.358+4137C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180051 | ||||||
| chr4:122180504
|
T | C | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+4590T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180504 | ||||||
| chr4:122180509
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.358+4595A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180509 | ||||||
| chr4:122180565
|
C | T | 5 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0016t0001g0028others(2): Show | 5 | NA18966.hp2 NA18992.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+4651C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180565 | ||||||
| chr4:122180860
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.358+4946G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122180860 | ||||||
| chr4:122181019
|
G | T | 1 | a0009c0011t0001g0045 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.359-5017G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181019 | ||||||
| chr4:122181176
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-4860A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181176 | ||||||
| chr4:122181290
|
C | T | 1 | a0001c0007t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.359-4746C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181290 | ||||||
| chr4:122181296
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-4740G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181296 | ||||||
| chr4:122181442
|
C | T | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.359-4594C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181442 | ||||||
| chr4:122181706
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.359-4330A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181706 | ||||||
| chr4:122181765
|
T | C | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.359-4271T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181765 | ||||||
| chr4:122181811
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.359-4225G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181811 | ||||||
| chr4:122181980
|
A | G | 1 | a0001c0002t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.359-4056A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122181980 | ||||||
| chr4:122182401
|
A | G | 1 | a0001c0003t0001g0232 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.359-3635A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122182401 | ||||||
| chr4:122182490
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.359-3546C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122182490 | ||||||
| chr4:122182953
|
A | AC | 40 | a0001c0001t0001g0221a0001c0003t0001g0177a0001c0003t0001g0178others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.359-3082dupC | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122182953 | |||||
| chr4:122183090
|
C | T | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.359-2946C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122183090 | ||||||
| chr4:122183335
|
C | CA | 268 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.359-2685dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122183335 | |||||
| chr4:122183335
|
C | CAA | 27 | a0001c0001t0001g0186a0001c0001t0001g0250a0001c0001t0001g0254others(24): Show | 28 | HG00423.hp1 HG00558.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.359-2686_359-2685d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122183335 | |||||
| chr4:122183372
|
A | G | 1 | a0001c0009t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.359-2664A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122183372 | ||||||
| chr4:122183635
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.359-2401A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122183635 | ||||||
| chr4:122183802
|
CCTT | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-2228_359-2226d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122183802 | |||||
| chr4:122183868
|
A | C | 3 | a0001c0002t0001g0076a0001c0002t0001g0097a0001c0002t0001g0161 | 3 | NA18957.hp1 NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.359-2168A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122183868 | ||||||
| chr4:122184089
|
G | A | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-1947G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184089 | ||||||
| chr4:122184139
|
G | A | 1 | a0002c0004t0001g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.359-1897G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184139 | ||||||
| chr4:122184236
|
C | T | 1 | a0001c0003t0001g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.359-1800C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184236 | ||||||
| chr4:122184318
|
A | G | 1 | a0001c0007t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.359-1718A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184318 | ||||||
| chr4:122184415
|
G | A | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359-1621G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184415 | ||||||
| chr4:122184466
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.359-1570G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184466 | ||||||
| chr4:122184500
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.359-1536A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184500 | ||||||
| chr4:122184639
|
C | CA | 13 | a0001c0001t0001g0321a0003c0006t0001g0038a0003c0006t0001g0040others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.359-1388dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | INFO_REALIGN_3_PRIME | chr4 | 122184639 | |||||
| chr4:122184803
|
C | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-1233C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184803 | ||||||
| chr4:122184803
|
C | T | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.359-1233C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184803 | ||||||
| chr4:122184927
|
C | T | 320 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.359-1109C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122184927 | ||||||
| chr4:122185067
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-969T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185067 | ||||||
| chr4:122185159
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.359-877T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185159 | ||||||
| chr4:122185193
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.359-843G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185193 | ||||||
| chr4:122185303
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0219 | 2 | HG01975.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.359-733G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185303 | ||||||
| chr4:122185504
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.359-532A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185504 | ||||||
| chr4:122185555
|
A | G | 3 | a0002c0004t0001g0128a0002c0004t0001g0139a0002c0004t0001g0148 | 3 | HG02071.hp2 HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.359-481A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185555 | ||||||
| chr4:122185577
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.359-459G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185577 | ||||||
| chr4:122185701
|
A | T | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.359-335A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185701 | ||||||
| chr4:122185721
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.359-315G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185721 | ||||||
| chr4:122185749
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.359-287G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185749 | ||||||
| chr4:122185795
|
A | G | 5 | a0001c0001t0004g0175a0001c0002t0001g0014a0001c0002t0001g0024others(2): Show | 5 | HG00423.hp2 HG02132.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-241A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185795 | ||||||
| chr4:122185849
|
C | T | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.359-187C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 6/87 | chr4 | 122185849 | ||||||
| chr4:122186627
|
T | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.545+405T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 7/87 | chr4 | 122186627 | ||||||
| chr4:122186961
|
G | T | 1 | a0001c0007t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.546-470G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 7/87 | chr4 | 122186961 | ||||||
| chr4:122187013
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.546-418G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 7/87 | chr4 | 122187013 | ||||||
| chr4:122187103
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.546-328G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 7/87 | chr4 | 122187103 | ||||||
| chr4:122187234
|
A | G | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.546-197A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 7/87 | chr4 | 122187234 | ||||||
| chr4:122187607
|
G | A | 320 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.627+95G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 8/87 | chr4 | 122187607 | ||||||
| chr4:122187864
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.628-31A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 8/87 | chr4 | 122187864 | ||||||
| chr4:122187883
|
T | A | 1 | a0001c0002t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.628-12T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 8/87 | chr4 | 122187883 | ||||||
| chr4:122188180
|
A | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.821+92A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188180 | ||||||
| chr4:122188555
|
C | T | 19 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(16): Show | 19 | HG00558.hp1 HG00673.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.821+467C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188555 | ||||||
| chr4:122188607
|
AT | A | 29 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0005t0001g0105others(26): Show | 30 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.821+532delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | INFO_REALIGN_3_PRIME | chr4 | 122188607 | |||||
| chr4:122188612
|
T | G | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.821+524T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188612 | ||||||
| chr4:122188683
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.821+595C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188683 | ||||||
| chr4:122188741
|
A | G | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.821+653A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188741 | ||||||
| chr4:122188818
|
T | G | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.821+730T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188818 | ||||||
| chr4:122188906
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.821+818A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188906 | ||||||
| chr4:122188960
|
C | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.821+872C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188960 | ||||||
| chr4:122188997
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.821+909G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122188997 | ||||||
| chr4:122189171
|
C | CTTGT | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.822-827_822-826ins others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | INFO_REALIGN_3_PRIME | chr4 | 122189171 | |||||
| chr4:122189350
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-650A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189350 | ||||||
| chr4:122189419
|
C | T | 5 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00609.hp2 HG02523.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.822-581C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189419 | ||||||
| chr4:122189422
|
T | C | 1 | a0003c0006t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.822-578T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189422 | ||||||
| chr4:122189501
|
A | G | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.822-499A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189501 | ||||||
| chr4:122189709
|
T | G | 1 | a0001c0002t0001g0097 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.822-291T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189709 | ||||||
| chr4:122189801
|
A | G | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.822-199A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189801 | ||||||
| chr4:122189920
|
T | C | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.822-80T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189920 | ||||||
| chr4:122189942
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.822-58T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 9/87 | chr4 | 122189942 | ||||||
| chr4:122190139
|
C | T | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.901+60C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190139 | ||||||
| chr4:122190154
|
T | G | 4 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0046others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+75T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190154 | ||||||
| chr4:122190199
|
C | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.901+120C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190199 | ||||||
| chr4:122190201
|
A | G | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.901+122A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190201 | ||||||
| chr4:122190282
|
GAT | G | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.901+204_901+205del others(2): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190282 | ||||||
| chr4:122190483
|
C | G | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.901+404C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190483 | ||||||
| chr4:122190496
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.901+417A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190496 | ||||||
| chr4:122190714
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.901+635G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190714 | ||||||
| chr4:122190763
|
T | C | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.901+684T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190763 | ||||||
| chr4:122190960
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0281 | 3 | NA18947.hp1 NA18960.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.901+881A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122190960 | ||||||
| chr4:122191056
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0068 | 2 | HG00597.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.901+977G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191056 | ||||||
| chr4:122191367
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.902-862T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191367 | ||||||
| chr4:122191438
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.902-791T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191438 | ||||||
| chr4:122191517
|
G | A | 1 | a0001c0002t0008g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.902-712G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191517 | ||||||
| chr4:122191626
|
T | C | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.902-603T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191626 | ||||||
| chr4:122191684
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.902-545G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191684 | ||||||
| chr4:122191765
|
C | T | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.902-464C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191765 | ||||||
| chr4:122191798
|
A | G | 1 | a0003c0006t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.902-431A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191798 | ||||||
| chr4:122191867
|
A | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0120 | 3 | HG01123.hp1 HG01346.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.902-362A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191867 | ||||||
| chr4:122191868
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.902-361A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122191868 | ||||||
| chr4:122192197
|
A | G | 40 | a0001c0001t0001g0221a0001c0003t0001g0177a0001c0003t0001g0178others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.902-32A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 10/87 | chr4 | 122192197 | ||||||
| chr4:122192405
|
T | G | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1052+26T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122192405 | ||||||
| chr4:122192576
|
G | A | 2 | a0001c0002t0001g0016a0001c0002t0001g0035 | 2 | NA18968.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1052+197G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122192576 | ||||||
| chr4:122192597
|
C | T | 2 | a0001c0009t0001g0081a0001c0009t0001g0168 | 2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1052+218C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122192597 | ||||||
| chr4:122192822
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0259 | 2 | NA18941.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1052+443G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122192822 | ||||||
| chr4:122192927
|
C | G | 1 | a0001c0007t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1052+548C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122192927 | ||||||
| chr4:122192989
|
A | G | 1 | a0001c0019t0001g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1052+610A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122192989 | ||||||
| chr4:122193102
|
C | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0097a0001c0002t0001g0161 | 3 | NA18957.hp1 NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1052+723C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193102 | ||||||
| chr4:122193461
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1052+1082A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193461 | ||||||
| chr4:122193467
|
A | G | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1052+1088A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193467 | ||||||
| chr4:122193507
|
A | AT | 12 | a0003c0006t0001g0038a0003c0006t0001g0040a0003c0006t0001g0041others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1052+1132dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | INFO_REALIGN_3_PRIME | chr4 | 122193507 | |||||
| chr4:122193558
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1052+1179C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193558 | ||||||
| chr4:122193746
|
G | T | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1052+1367G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193746 | ||||||
| chr4:122193850
|
A | G | 1 | a0007c0012t0001g0313 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1052+1471A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193850 | ||||||
| chr4:122193901
|
C | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1052+1522C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193901 | ||||||
| chr4:122193948
|
C | T | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1052+1569C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193948 | ||||||
| chr4:122193956
|
G | C | 3 | a0009c0011t0001g0045a0009c0011t0001g0112a0009c0011t0007g0039 | 3 | HG02572.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1052+1577G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122193956 | ||||||
| chr4:122194023
|
C | T | 5 | a0001c0002t0001g0031a0001c0005t0002g0001a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1052+1644C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194023 | ||||||
| chr4:122194117
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1052+1738C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194117 | ||||||
| chr4:122194205
|
C | T | 4 | a0001c0001t0001g0270a0008c0018t0001g0114a0008c0018t0001g0115others(1): Show | 4 | HG02965.hp1 HG03471.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+1826C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194205 | ||||||
| chr4:122194347
|
A | G | 8 | a0001c0001t0001g0306a0001c0001t0001g0309a0001c0001t0001g0310others(5): Show | 8 | HG00280.hp1 HG01256.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1052+1968A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194347 | ||||||
| chr4:122194395
|
A | C | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1052+2016A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194395 | ||||||
| chr4:122194421
|
T | C | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1052+2042T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194421 | ||||||
| chr4:122194453
|
G | A | 4 | a0004c0013t0001g0198a0004c0013t0001g0226a0004c0013t0001g0227others(1): Show | 4 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+2074G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194453 | ||||||
| chr4:122194825
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1053-1810C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122194825 | ||||||
| chr4:122195022
|
C | T | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1053-1613C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195022 | ||||||
| chr4:122195197
|
A | G | 1 | a0007c0012t0001g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1053-1438A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195197 | ||||||
| chr4:122195264
|
A | G | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053-1371A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195264 | ||||||
| chr4:122195431
|
A | AT | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1053-1193dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | INFO_REALIGN_3_PRIME | chr4 | 122195431 | |||||
| chr4:122195619
|
G | C | 142 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(139): Show | 145 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1053-1016G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195619 | ||||||
| chr4:122195707
|
T | G | 106 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0174others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1053-928T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195707 | ||||||
| chr4:122195840
|
T | C | 105 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1053-795T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195840 | ||||||
| chr4:122195927
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1053-708C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195927 | ||||||
| chr4:122195978
|
A | G | 1 | a0001c0002t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1053-657A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122195978 | ||||||
| chr4:122196007
|
C | T | 1 | a0001c0019t0001g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1053-628C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122196007 | ||||||
| chr4:122196023
|
A | G | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1053-612A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122196023 | ||||||
| chr4:122196046
|
A | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1053-589A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122196046 | ||||||
| chr4:122196144
|
T | C | 1 | a0002c0004t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1053-491T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122196144 | ||||||
| chr4:122196396
|
G | A | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1053-239G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122196396 | ||||||
| chr4:122196432
|
C | CT | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG02071.hp1 NA18940.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-201dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | INFO_REALIGN_3_PRIME | chr4 | 122196432 | |||||
| chr4:122196574
|
T | C | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1053-61T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 11/87 | chr4 | 122196574 | ||||||
| chr4:122196800
|
T | C | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+9T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 12/87 | chr4 | 122196800 | ||||||
| chr4:122197587
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1288+313G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122197587 | ||||||
| chr4:122197587
|
G | GT | 11 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1288+321dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | INFO_REALIGN_3_PRIME | chr4 | 122197587 | |||||
| chr4:122197624
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1288+350G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122197624 | ||||||
| chr4:122197708
|
A | T | 2 | a0001c0002t0001g0167a0001c0002t0001g0169 | 2 | HG00735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1288+434A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122197708 | ||||||
| chr4:122197712
|
C | T | 1 | a0002c0004t0001g0127 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1288+438C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122197712 | ||||||
| chr4:122197802
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+528T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122197802 | ||||||
| chr4:122198146
|
A | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1288+872A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198146 | ||||||
| chr4:122198211
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288+937C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198211 | ||||||
| chr4:122198271
|
A | G | 1 | a0011c0040t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1288+997A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198271 | ||||||
| chr4:122198584
|
A | G | 4 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0046others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-775A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198584 | ||||||
| chr4:122198738
|
G | A | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-621G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198738 | ||||||
| chr4:122198762
|
A | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1289-597A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198762 | ||||||
| chr4:122198772
|
T | A | 4 | a0001c0002t0001g0066a0001c0002t0001g0069a0001c0002t0001g0070others(1): Show | 4 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-587T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198772 | ||||||
| chr4:122198834
|
A | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1289-525A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122198834 | ||||||
| chr4:122199240
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1289-119G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 13/87 | chr4 | 122199240 | ||||||
| chr4:122199459
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380+9G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122199459 | ||||||
| chr4:122199582
|
A | G | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1380+132A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122199582 | ||||||
| chr4:122199756
|
G | A | 1 | a0004c0031t0001g0197 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1380+306G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122199756 | ||||||
| chr4:122199797
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1380+347C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122199797 | ||||||
| chr4:122199798
|
G | A | 2 | a0001c0002t0001g0095a0015c0028t0001g0058 | 2 | NA18940.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1380+348G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122199798 | ||||||
| chr4:122199935
|
G | T | 1 | a0003c0006t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1380+485G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122199935 | ||||||
| chr4:122200120
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1380+670T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200120 | ||||||
| chr4:122200297
|
G | A | 1 | a0003c0006t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1381-712G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200297 | ||||||
| chr4:122200340
|
G | A | 62 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1381-669G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200340 | ||||||
| chr4:122200344
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0182 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1381-665G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200344 | ||||||
| chr4:122200452
|
T | C | 5 | a0001c0001t0001g0308a0005c0010t0001g0297a0005c0010t0001g0305others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-557T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200452 | ||||||
| chr4:122200463
|
C | T | 1 | a0003c0006t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1381-546C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200463 | ||||||
| chr4:122200574
|
G | A | 1 | a0002c0004t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1381-435G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200574 | ||||||
| chr4:122200578
|
C | CAAAACA | 2 | a0001c0005t0002g0001a0001c0005t0002g0006 | 3 | HG02559.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1381-426_1381-421d others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200578 | |||||
| chr4:122200583
|
C | CA | 13 | a0001c0001t0001g0121a0001c0001t0001g0187a0001c0001t0001g0296others(10): Show | 13 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-407dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200583 | |||||
| chr4:122200583
|
C | CAAAAA | 29 | a0001c0005t0001g0105a0001c0005t0001g0107a0001c0005t0001g0108others(26): Show | 30 | HG00639.hp1 HG00738.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1381-411_1381-407d others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200583 | |||||
| chr4:122200583
|
C | CAAAAAA | 15 | a0001c0002t0001g0030a0001c0005t0001g0106a0001c0005t0001g0173others(12): Show | 15 | HG00558.hp2 HG01106.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1381-412_1381-407d others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200583 | |||||
| chr4:122200583
|
C | CAAAAAAA | 74 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0015others(71): Show | 75 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1381-413_1381-407d others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200583 | |||||
| chr4:122200583
|
C | CAAAAAAA others(1): Show |
15 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0023others(12): Show | 15 | HG00597.hp1 HG00735.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1381-414_1381-407d others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200583 | |||||
| chr4:122200588
|
A | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1381-421A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200588 | ||||||
| chr4:122200592
|
A | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1381-417A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200592 | ||||||
| chr4:122200719
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1381-290C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | chr4 | 122200719 | ||||||
| chr4:122200991
|
CTAACA | C | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1381-16_1381-12del others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 14/87 | INFO_REALIGN_3_PRIME | chr4 | 122200991 | |||||
| chr4:122201191
|
GTTTTAC | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1498+71_1498+76del others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122201191 | |||||
| chr4:122201204
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1498+78A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201204 | ||||||
| chr4:122201222
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1498+96A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201222 | ||||||
| chr4:122201285
|
T | C | 43 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0156others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1498+159T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201285 | ||||||
| chr4:122201506
|
A | G | 37 | a0001c0001t0001g0143a0001c0001t0001g0250a0001c0001t0001g0251others(34): Show | 37 | HG00423.hp1 HG01255.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1498+380A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201506 | ||||||
| chr4:122201528
|
C | T | 2 | a0001c0002t0001g0085a0001c0002t0001g0162 | 2 | HG03490.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1498+402C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201528 | ||||||
| chr4:122201563
|
G | A | 1 | a0001c0005t0001g0173 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1498+437G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201563 | ||||||
| chr4:122201701
|
A | G | 1 | a0018c0039t0001g0233 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1498+575A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201701 | ||||||
| chr4:122201752
|
T | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA18951.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1498+626T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201752 | ||||||
| chr4:122201843
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1498+717C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201843 | ||||||
| chr4:122201872
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1498+746G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201872 | ||||||
| chr4:122201977
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1498+851T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122201977 | ||||||
| chr4:122202028
|
A | G | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1498+902A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202028 | ||||||
| chr4:122202270
|
A | G | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1498+1144A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202270 | ||||||
| chr4:122202320
|
T | G | 3 | a0001c0005t0001g0106a0001c0005t0001g0107a0001c0005t0001g0108 | 3 | HG01106.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1498+1194T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202320 | ||||||
| chr4:122202406
|
A | G | 7 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0328others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498+1280A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202406 | ||||||
| chr4:122202458
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1498+1332T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202458 | ||||||
| chr4:122202496
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1498+1370A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202496 | ||||||
| chr4:122202580
|
G | C | 1 | a0001c0007t0001g0247 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1498+1454G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202580 | ||||||
| chr4:122202609
|
A | G | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1498+1483A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202609 | ||||||
| chr4:122202617
|
C | A | 1 | a0001c0002t0001g0014 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+1491C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202617 | ||||||
| chr4:122202622
|
A | G | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498+1496A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202622 | ||||||
| chr4:122202735
|
A | G | 1 | a0002c0004t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1498+1609A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202735 | ||||||
| chr4:122202959
|
G | A | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1498+1833G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202959 | ||||||
| chr4:122202994
|
T | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498+1868T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202994 | ||||||
| chr4:122202997
|
G | A | 320 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1498+1871G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122202997 | ||||||
| chr4:122203035
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1498+1909A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203035 | ||||||
| chr4:122203172
|
C | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1498+2046C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203172 | ||||||
| chr4:122203204
|
G | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1498+2078G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203204 | ||||||
| chr4:122203384
|
TAAG | T | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1498+2259_1498+226 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203384 | ||||||
| chr4:122203442
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1498+2316T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203442 | ||||||
| chr4:122203488
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1498+2362T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203488 | ||||||
| chr4:122203573
|
G | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1498+2447G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203573 | ||||||
| chr4:122203760
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0314others(1): Show | 4 | HG03669.hp1 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1498+2634T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203760 | ||||||
| chr4:122203801
|
C | CG | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498+2676dupG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122203801 | |||||
| chr4:122203821
|
A | G | 5 | a0001c0002t0001g0171a0001c0008t0001g0075a0001c0008t0001g0098others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+2695A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122203821 | ||||||
| chr4:122204027
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1498+2901A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122204027 | ||||||
| chr4:122204077
|
A | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1498+2951A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122204077 | ||||||
| chr4:122204370
|
A | AT | 107 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0174others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1499-2736dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122204370 | |||||
| chr4:122204553
|
CTGTT | C | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1499-2554_1499-255 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122204553 | |||||
| chr4:122204568
|
G | A | 13 | a0001c0002t0001g0016a0001c0002t0001g0035a0001c0002t0001g0050others(10): Show | 13 | HG01169.hp2 HG01975.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1499-2542G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122204568 | ||||||
| chr4:122204806
|
C | G | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1499-2304C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122204806 | ||||||
| chr4:122205055
|
CAA | C | 3 | a0001c0003t0001g0178a0001c0003t0001g0231a0001c0003t0001g0237 | 3 | HG00099.hp1 HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1499-2054_1499-205 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205055 | ||||||
| chr4:122205066
|
A | C | 1 | a0002c0004t0001g0151 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1499-2044A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205066 | ||||||
| chr4:122205237
|
T | A | 1 | a0001c0019t0001g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1499-1873T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205237 | ||||||
| chr4:122205295
|
C | A | 107 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0174others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1499-1815C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205295 | ||||||
| chr4:122205451
|
G | A | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1499-1659G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205451 | ||||||
| chr4:122205499
|
T | TTC | 22 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0328others(19): Show | 23 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1499-1585_1499-158 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205499 | |||||
| chr4:122205499
|
T | TTCTC | 11 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(8): Show | 11 | HG00639.hp1 HG00735.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1499-1587_1499-158 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205499 | |||||
| chr4:122205499
|
TTC | T | 103 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(100): Show | 104 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1499-1585_1499-158 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205499 | |||||
| chr4:122205571
|
CCT | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1499-1522_1499-152 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205571 | |||||
| chr4:122205629
|
GT | G | 6 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499-1478delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205629 | |||||
| chr4:122205641
|
TTC | T | 319 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(316): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1499-1449_1499-144 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205641 | |||||
| chr4:122205643
|
C | T | 1 | a0001c0007t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1499-1467C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205643 | ||||||
| chr4:122205678
|
G | C | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1499-1432G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205678 | ||||||
| chr4:122205699
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1499-1411A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205699 | ||||||
| chr4:122205774
|
T | C | 1 | a0001c0002t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1499-1336T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205774 | ||||||
| chr4:122205785
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1499-1325T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205785 | ||||||
| chr4:122205785
|
T | TAC | 62 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(59): Show | 63 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1499-1294_1499-129 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
T | TACAC | 61 | a0001c0001t0001g0302a0001c0002t0001g0002a0001c0002t0001g0016others(58): Show | 62 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1499-1296_1499-129 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
T | TACACAC | 34 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065others(31): Show | 35 | HG00621.hp1 HG00673.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.1499-1298_1499-129 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
T | TACACACA others(1): Show |
7 | a0001c0005t0001g0140a0002c0004t0001g0127a0002c0004t0001g0137others(4): Show | 7 | HG00558.hp1 HG02109.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1499-1300_1499-129 others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
T | TACACACA others(3): Show |
6 | a0001c0005t0001g0107a0001c0005t0001g0108a0002c0004t0001g0151others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1302_1499-129 others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
T | TACACACA others(5): Show |
1 | a0002c0043t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1499-1304_1499-129 others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
TAC | T | 119 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1499-1294_1499-129 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205785
|
TACAC | T | 5 | a0001c0001t0001g0266a0002c0004t0001g0128a0002c0004t0001g0134others(2): Show | 5 | HG00423.hp1 HG02071.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-1296_1499-129 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | INFO_REALIGN_3_PRIME | chr4 | 122205785 | |||||
| chr4:122205789
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1499-1321C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205789 | ||||||
| chr4:122205923
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1499-1187G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205923 | ||||||
| chr4:122205946
|
G | A | 1 | a0002c0004t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1499-1164G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205946 | ||||||
| chr4:122205967
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1499-1143T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122205967 | ||||||
| chr4:122206049
|
A | G | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1499-1061A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122206049 | ||||||
| chr4:122206259
|
T | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1499-851T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122206259 | ||||||
| chr4:122206368
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1499-742A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122206368 | ||||||
| chr4:122206570
|
A | G | 320 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1499-540A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122206570 | ||||||
| chr4:122206691
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1499-419G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122206691 | ||||||
| chr4:122206865
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1499-245C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 15/87 | chr4 | 122206865 | ||||||
| chr4:122207424
|
G | A | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1655-117G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 16/87 | chr4 | 122207424 | ||||||
| chr4:122207514
|
C | CT | 105 | a0001c0001t0001g0250a0001c0001t0001g0256a0001c0001t0001g0296others(102): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1655-10dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 16/87 | INFO_REALIGN_3_PRIME | chr4 | 122207514 | |||||
| chr4:122207514
|
C | CTT | 8 | a0001c0007t0001g0238a0001c0007t0001g0240a0001c0007t0001g0241others(5): Show | 8 | HG00639.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1655-11_1655-10dup others(2): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 16/87 | INFO_REALIGN_3_PRIME | chr4 | 122207514 | |||||
| chr4:122207688
|
T | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1752+50T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122207688 | ||||||
| chr4:122207746
|
T | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1752+108T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122207746 | ||||||
| chr4:122208499
|
A | C | 1 | a0016c0022t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1753-660A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122208499 | ||||||
| chr4:122208706
|
C | G | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1753-453C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122208706 | ||||||
| chr4:122208750
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1753-409A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122208750 | ||||||
| chr4:122208940
|
G | C | 1 | a0001c0033t0001g0052 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1753-219G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122208940 | ||||||
| chr4:122208985
|
TA | T | 186 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1753-155delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | INFO_REALIGN_3_PRIME | chr4 | 122208985 | |||||
| chr4:122208985
|
TAA | T | 51 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0259others(48): Show | 51 | HG00558.hp1 HG00673.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.1753-156_1753-155d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | INFO_REALIGN_3_PRIME | chr4 | 122208985 | |||||
| chr4:122208987
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1753-172A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122208987 | ||||||
| chr4:122209059
|
C | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1753-100C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122209059 | ||||||
| chr4:122209092
|
CGTAA | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1753-63_1753-60del others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | INFO_REALIGN_3_PRIME | chr4 | 122209092 | |||||
| chr4:122209137
|
G | A | 4 | a0001c0009t0001g0081a0001c0009t0001g0082a0001c0009t0001g0083others(1): Show | 4 | NA18747.hp1 NA19005.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-22G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 17/87 | chr4 | 122209137 | ||||||
| chr4:122209399
|
C | T | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1931+62C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 18/87 | chr4 | 122209399 | ||||||
| chr4:122209442
|
C | T | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1931+105C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 18/87 | chr4 | 122209442 | ||||||
| chr4:122209697
|
A | G | 1 | a0003c0006t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1932-121A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 18/87 | chr4 | 122209697 | ||||||
| chr4:122209731
|
A | G | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1932-87A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 18/87 | chr4 | 122209731 | ||||||
| chr4:122209785
|
C | T | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1932-33C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 18/87 | chr4 | 122209785 | ||||||
| chr4:122210093
|
G | A | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.2038+169G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 19/87 | chr4 | 122210093 | ||||||
| chr4:122210349
|
A | G | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2038+425A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 19/87 | chr4 | 122210349 | ||||||
| chr4:122210549
|
G | A | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.2039-338G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 19/87 | chr4 | 122210549 | ||||||
| chr4:122210608
|
C | T | 1 | a0001c0007t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2039-279C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 19/87 | chr4 | 122210608 | ||||||
| chr4:122211056
|
T | TCTCTATG others(242): Show |
2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2247+201_2247+202i others(251): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122211056 | |||||
| chr4:122211177
|
A | C | 1 | a0002c0004t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2247+82A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211177 | ||||||
| chr4:122211337
|
A | G | 105 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2247+242A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211337 | ||||||
| chr4:122211505
|
C | A | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2247+410C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211505 | ||||||
| chr4:122211561
|
A | T | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2247+466A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211561 | ||||||
| chr4:122211577
|
G | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2247+482G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211577 | ||||||
| chr4:122211707
|
T | A | 1 | a0001c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2247+612T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211707 | ||||||
| chr4:122211793
|
A | C | 1 | a0001c0002t0001g0034 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2247+698A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211793 | ||||||
| chr4:122211905
|
A | G | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2247+810A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122211905 | ||||||
| chr4:122212002
|
C | T | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2247+907C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122212002 | ||||||
| chr4:122212023
|
C | G | 64 | a0001c0002t0001g0002a0001c0002t0001g0016a0001c0002t0001g0035others(61): Show | 65 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2247+928C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122212023 | ||||||
| chr4:122212226
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2247+1131A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122212226 | ||||||
| chr4:122212385
|
C | T | 1 | a0018c0039t0001g0233 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2247+1290C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122212385 | ||||||
| chr4:122212617
|
C | CA | 11 | a0001c0007t0001g0157a0001c0007t0001g0244a0001c0007t0001g0245others(8): Show | 11 | HG01361.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2247+1532dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122212617 | |||||
| chr4:122212617
|
C | CAA | 8 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(5): Show | 8 | HG00639.hp1 HG00738.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2247+1531_2247+153 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122212617 | |||||
| chr4:122212619
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2247+1524A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122212619 | ||||||
| chr4:122212898
|
CA | C | 105 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2247+1806delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122212898 | |||||
| chr4:122212983
|
C | T | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2247+1888C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122212983 | ||||||
| chr4:122213003
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2247+1908G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122213003 | ||||||
| chr4:122213015
|
A | G | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2247+1920A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122213015 | ||||||
| chr4:122213042
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2247+1947G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122213042 | ||||||
| chr4:122213120
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0314others(1): Show | 4 | HG03669.hp1 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+2025A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122213120 | ||||||
| chr4:122213601
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2247+2506A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122213601 | ||||||
| chr4:122213828
|
T | C | 3 | a0004c0013t0001g0198a0004c0013t0001g0226a0004c0013t0001g0227 | 3 | HG01123.hp2 HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2247+2733T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122213828 | ||||||
| chr4:122214265
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2247+3170T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122214265 | ||||||
| chr4:122214321
|
A | G | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2247+3226A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122214321 | ||||||
| chr4:122214433
|
A | C | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2247+3338A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122214433 | ||||||
| chr4:122214593
|
AT | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2247+3511delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122214593 | |||||
| chr4:122214616
|
C | CTT | 36 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0003t0001g0177others(33): Show | 36 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2247+3546_2247+354 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122214616 | |||||
| chr4:122214616
|
CT | C | 24 | a0001c0001t0001g0102a0001c0001t0001g0207a0001c0001t0001g0215others(21): Show | 24 | HG00597.hp1 HG00621.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2247+3547delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122214616 | |||||
| chr4:122214616
|
CTT | C | 234 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(231): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2247+3546_2247+354 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122214616 | |||||
| chr4:122214616
|
CTTT | C | 20 | a0001c0001t0001g0328a0001c0008t0001g0164a0002c0004t0001g0129others(17): Show | 20 | HG01169.hp1 HG01256.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2247+3545_2247+354 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122214616 | |||||
| chr4:122214616
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2247+3535_2247+354 others(17): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122214616 | |||||
| chr4:122214701
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247+3606C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122214701 | ||||||
| chr4:122214708
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2247+3613C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122214708 | ||||||
| chr4:122214808
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2247+3713C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122214808 | ||||||
| chr4:122215206
|
G | A | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2247+4111G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215206 | ||||||
| chr4:122215208
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2247+4113A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215208 | ||||||
| chr4:122215361
|
A | T | 56 | a0001c0001t0001g0143a0001c0001t0001g0181a0001c0001t0001g0183others(53): Show | 56 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.2248-3979A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215361 | ||||||
| chr4:122215521
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2248-3819G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215521 | ||||||
| chr4:122215528
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2248-3812A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215528 | ||||||
| chr4:122215628
|
G | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2248-3712G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215628 | ||||||
| chr4:122215684
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2248-3656T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215684 | ||||||
| chr4:122215815
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2248-3525G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215815 | ||||||
| chr4:122215834
|
A | AC | 19 | a0001c0005t0001g0111a0001c0038t0005g0285a0002c0004t0001g0131others(16): Show | 19 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2248-3498dupC | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122215834 | |||||
| chr4:122215834
|
A | G | 1 | a0011c0040t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2248-3506A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215834 | ||||||
| chr4:122215837
|
C | CCCG | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2248-3501_2248-350 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122215837 | |||||
| chr4:122215838
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2248-3502C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215838 | ||||||
| chr4:122215900
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2248-3440A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215900 | ||||||
| chr4:122215982
|
A | G | 1 | a0001c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2248-3358A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122215982 | ||||||
| chr4:122216055
|
A | ATG | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2248-3271_2248-327 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216055 | |||||
| chr4:122216069
|
G | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2248-3271G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216069 | ||||||
| chr4:122216079
|
T | TTGTC | 17 | a0001c0001t0001g0304a0001c0001t0001g0311a0001c0001t0001g0314others(14): Show | 17 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2248-3255_2248-325 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216079 | |||||
| chr4:122216079
|
T | TTGTCTGT others(1): Show |
3 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0331 | 3 | HG02280.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2248-3259_2248-325 others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216079 | |||||
| chr4:122216085
|
G | GTCTA | 11 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0092others(8): Show | 11 | HG00408.hp2 HG01255.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.2248-3198_2248-319 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
G | GTCTATCT others(1): Show |
4 | a0001c0002t0001g0024a0001c0003t0001g0275a0001c0027t0001g0072others(1): Show | 4 | HG02040.hp1 HG02132.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248-3202_2248-319 others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
G | GTCTGTCT others(1): Show |
3 | a0001c0001t0001g0306a0001c0001t0004g0175a0003c0006t0001g0040 | 3 | HG01257.hp1 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2248-3252_2248-325 others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
GTCTA | G | 74 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.2248-3198_2248-319 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
GTCTATCT others(1): Show |
G | 28 | a0001c0001t0001g0102a0001c0001t0001g0124a0001c0001t0001g0182others(25): Show | 29 | HG00140.hp1 HG00621.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.2248-3202_2248-319 others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
GTCTATCT others(5): Show |
G | 27 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0125others(24): Show | 27 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2248-3206_2248-319 others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
GTCTATCT others(9): Show |
G | 47 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0189others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.2248-3210_2248-319 others(20): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216085
|
GTCTATCT others(13): Show |
G | 5 | a0001c0001t0001g0207a0001c0005t0002g0001a0001c0005t0002g0005others(2): Show | 6 | HG01346.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2248-3214_2248-319 others(24): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122216085 | |||||
| chr4:122216089
|
A | G | 39 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(36): Show | 39 | HG00609.hp2 HG01192.hp1 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.2248-3251A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216089 | ||||||
| chr4:122216093
|
A | G | 17 | a0001c0001t0001g0156a0001c0001t0001g0299a0001c0001t0001g0308others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2248-3247A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216093 | ||||||
| chr4:122216097
|
A | G | 3 | a0001c0007t0001g0157a0001c0007t0001g0242a0001c0007t0001g0244 | 3 | HG02257.hp1 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2248-3243A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216097 | ||||||
| chr4:122216101
|
A | G | 2 | a0001c0017t0001g0303a0011c0040t0001g0248 | 2 | HG00738.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2248-3239A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216101 | ||||||
| chr4:122216137
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2248-3203A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216137 | ||||||
| chr4:122216218
|
G | A | 2 | a0001c0001t0001g0220a0001c0032t0001g0176 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2248-3122G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216218 | ||||||
| chr4:122216533
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2248-2807G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216533 | ||||||
| chr4:122216577
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2248-2763A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216577 | ||||||
| chr4:122216851
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2248-2489A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216851 | ||||||
| chr4:122216976
|
T | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2248-2364T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122216976 | ||||||
| chr4:122217101
|
A | G | 1 | a0001c0019t0001g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2248-2239A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217101 | ||||||
| chr4:122217211
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2248-2129G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217211 | ||||||
| chr4:122217248
|
A | G | 1 | a0001c0016t0001g0028 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2248-2092A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217248 | ||||||
| chr4:122217367
|
AT | A | 6 | a0001c0001t0001g0187a0006c0014t0001g0117a0008c0021t0010g0116others(3): Show | 6 | HG00738.hp2 HG01243.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2248-1961delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122217367 | |||||
| chr4:122217568
|
A | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2248-1772A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217568 | ||||||
| chr4:122217758
|
A | G | 93 | a0001c0001t0001g0312a0001c0002t0001g0002a0001c0002t0001g0008others(90): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2248-1582A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217758 | ||||||
| chr4:122217767
|
A | G | 4 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0046others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248-1573A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217767 | ||||||
| chr4:122217774
|
T | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2248-1566T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217774 | ||||||
| chr4:122217806
|
G | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2248-1534G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217806 | ||||||
| chr4:122217946
|
T | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2248-1394T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122217946 | ||||||
| chr4:122218018
|
C | T | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.2248-1322C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218018 | ||||||
| chr4:122218166
|
C | G | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2248-1174C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218166 | ||||||
| chr4:122218202
|
G | A | 1 | a0001c0016t0001g0029 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2248-1138G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218202 | ||||||
| chr4:122218496
|
A | G | 1 | a0001c0002t0001g0030 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2248-844A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218496 | ||||||
| chr4:122218503
|
G | T | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2248-837G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218503 | ||||||
| chr4:122218539
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2248-801G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218539 | ||||||
| chr4:122218695
|
G | GA | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2248-639dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | INFO_REALIGN_3_PRIME | chr4 | 122218695 | |||||
| chr4:122218705
|
A | T | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.2248-635A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218705 | ||||||
| chr4:122218839
|
A | G | 1 | a0001c0026t0001g0080 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2248-501A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122218839 | ||||||
| chr4:122219135
|
A | G | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.2248-205A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122219135 | ||||||
| chr4:122219279
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2248-61A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122219279 | ||||||
| chr4:122219315
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2248-25A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 20/87 | chr4 | 122219315 | ||||||
| chr4:122219584
|
G | C | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2475+17G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122219584 | ||||||
| chr4:122219820
|
G | A | 1 | a0001c0029t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2475+253G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122219820 | ||||||
| chr4:122219840
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2475+273G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122219840 | ||||||
| chr4:122219899
|
T | C | 40 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0003t0001g0177others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.2475+332T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122219899 | ||||||
| chr4:122219915
|
T | C | 12 | a0001c0001t0003g0260a0001c0001t0003g0278a0001c0005t0001g0105others(9): Show | 13 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2475+348T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122219915 | ||||||
| chr4:122220010
|
C | T | 1 | a0003c0006t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2476-323C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122220010 | ||||||
| chr4:122220105
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2476-228G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122220105 | ||||||
| chr4:122220138
|
C | T | 1 | a0002c0043t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2476-195C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122220138 | ||||||
| chr4:122220150
|
G | A | 1 | a0006c0014t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2476-183G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122220150 | ||||||
| chr4:122220265
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2476-68T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 21/87 | chr4 | 122220265 | ||||||
| chr4:122221115
|
T | C | 3 | a0001c0003t0001g0178a0001c0003t0001g0231a0001c0003t0001g0237 | 3 | HG00099.hp1 HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2613+645T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122221115 | ||||||
| chr4:122221149
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2613+679G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122221149 | ||||||
| chr4:122221209
|
T | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2613+739T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122221209 | ||||||
| chr4:122221913
|
A | G | 1 | a0008c0021t0010g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2613+1443A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122221913 | ||||||
| chr4:122221988
|
T | TG | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2613+1519dupG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | INFO_REALIGN_3_PRIME | chr4 | 122221988 | |||||
| chr4:122222046
|
A | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2613+1576A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222046 | ||||||
| chr4:122222065
|
C | T | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.2613+1595C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222065 | ||||||
| chr4:122222087
|
A | C | 1 | a0001c0002t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2613+1617A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222087 | ||||||
| chr4:122222126
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2613+1656G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222126 | ||||||
| chr4:122222192
|
A | G | 1 | a0001c0002t0008g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2613+1722A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222192 | ||||||
| chr4:122222203
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2613+1733G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222203 | ||||||
| chr4:122222390
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2613+1920T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222390 | ||||||
| chr4:122222444
|
T | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2613+1974T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222444 | ||||||
| chr4:122222476
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2613+2006C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222476 | ||||||
| chr4:122222496
|
G | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2614-2002G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222496 | ||||||
| chr4:122222508
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2614-1990A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222508 | ||||||
| chr4:122222519
|
G | C | 2 | a0006c0014t0001g0117a0006c0014t0001g0144 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2614-1979G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222519 | ||||||
| chr4:122222557
|
G | T | 2 | a0006c0014t0001g0117a0006c0014t0001g0144 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2614-1941G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222557 | ||||||
| chr4:122222656
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2614-1842C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222656 | ||||||
| chr4:122222767
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2614-1731T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222767 | ||||||
| chr4:122222815
|
A | G | 1 | a0014c0030t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2614-1683A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222815 | ||||||
| chr4:122222906
|
A | G | 64 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(61): Show | 64 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2614-1592A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222906 | ||||||
| chr4:122222927
|
C | G | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2614-1571C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222927 | ||||||
| chr4:122222939
|
A | T | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.2614-1559A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122222939 | ||||||
| chr4:122223067
|
G | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2614-1431G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223067 | ||||||
| chr4:122223115
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2614-1383A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223115 | ||||||
| chr4:122223254
|
T | A | 1 | a0001c0002t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2614-1244T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223254 | ||||||
| chr4:122223310
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2614-1188G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223310 | ||||||
| chr4:122223747
|
A | G | 1 | a0001c0002t0001g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2614-751A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223747 | ||||||
| chr4:122223871
|
T | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2614-627T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223871 | ||||||
| chr4:122223889
|
G | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2614-609G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223889 | ||||||
| chr4:122223900
|
C | T | 1 | a0001c0009t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2614-598C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223900 | ||||||
| chr4:122223901
|
C | T | 1 | a0001c0009t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2614-597C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122223901 | ||||||
| chr4:122224182
|
G | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2614-316G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122224182 | ||||||
| chr4:122224182
|
G | T | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2614-316G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122224182 | ||||||
| chr4:122224298
|
T | TC | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2614-199dupC | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | INFO_REALIGN_3_PRIME | chr4 | 122224298 | |||||
| chr4:122224344
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2614-154G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 22/87 | chr4 | 122224344 | ||||||
| chr4:122225070
|
T | G | 105 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2793+393T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122225070 | ||||||
| chr4:122225373
|
G | A | 1 | a0001c0003t0001g0275 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2793+696G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122225373 | ||||||
| chr4:122225584
|
G | A | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2793+907G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122225584 | ||||||
| chr4:122225701
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2794-1006T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122225701 | ||||||
| chr4:122225807
|
A | C | 1 | a0001c0025t0001g0022 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2794-900A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122225807 | ||||||
| chr4:122225973
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2794-734A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122225973 | ||||||
| chr4:122226075
|
A | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2794-632A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122226075 | ||||||
| chr4:122226366
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2794-341T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122226366 | ||||||
| chr4:122226415
|
CCTT | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2794-291_2794-289d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 23/87 | chr4 | 122226415 | ||||||
| chr4:122226921
|
A | G | 1 | a0001c0007t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2922+86A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122226921 | ||||||
| chr4:122226983
|
C | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2922+148C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122226983 | ||||||
| chr4:122227041
|
AAAG | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2922+209_2922+211d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | INFO_REALIGN_3_PRIME | chr4 | 122227041 | |||||
| chr4:122227058
|
A | G | 1 | a0003c0006t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2922+223A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227058 | ||||||
| chr4:122227222
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2922+387C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227222 | ||||||
| chr4:122227387
|
C | G | 1 | a0002c0004t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2922+552C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227387 | ||||||
| chr4:122227482
|
A | T | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2922+647A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227482 | ||||||
| chr4:122227680
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2922+845A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227680 | ||||||
| chr4:122227814
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2922+979C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227814 | ||||||
| chr4:122227855
|
G | A | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2922+1020G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227855 | ||||||
| chr4:122227916
|
AT | A | 7 | a0001c0002t0001g0074a0001c0005t0002g0001a0001c0005t0002g0004others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2922+1096delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | INFO_REALIGN_3_PRIME | chr4 | 122227916 | |||||
| chr4:122227999
|
C | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2923-1122C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122227999 | ||||||
| chr4:122228038
|
C | T | 4 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0046others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2923-1083C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228038 | ||||||
| chr4:122228051
|
C | G | 1 | a0001c0002t0001g0015 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2923-1070C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228051 | ||||||
| chr4:122228238
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2923-883T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228238 | ||||||
| chr4:122228418
|
A | G | 1 | a0009c0011t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2923-703A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228418 | ||||||
| chr4:122228456
|
A | G | 1 | a0002c0004t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2923-665A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228456 | ||||||
| chr4:122228690
|
C | T | 1 | a0001c0007t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2923-431C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228690 | ||||||
| chr4:122228700
|
T | TTG | 3 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0306 | 3 | HG00140.hp1 HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2923-404_2923-403d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | INFO_REALIGN_3_PRIME | chr4 | 122228700 | |||||
| chr4:122228700
|
TTGTG | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2923-406_2923-403d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | INFO_REALIGN_3_PRIME | chr4 | 122228700 | |||||
| chr4:122228700
|
TTGTGTG | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2923-408_2923-403d others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | INFO_REALIGN_3_PRIME | chr4 | 122228700 | |||||
| chr4:122228829
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2923-292C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228829 | ||||||
| chr4:122228933
|
A | G | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2923-188A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122228933 | ||||||
| chr4:122229097
|
A | G | 4 | a0001c0005t0001g0106a0001c0005t0001g0107a0001c0005t0001g0108others(1): Show | 4 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2923-24A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 24/87 | chr4 | 122229097 | ||||||
| chr4:122229508
|
A | G | 325 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.3042+268A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 25/87 | chr4 | 122229508 | ||||||
| chr4:122229548
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3042+308T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 25/87 | chr4 | 122229548 | ||||||
| chr4:122229707
|
C | G | 2 | a0001c0003t0001g0192a0001c0003t0001g0194 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3043-224C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 25/87 | chr4 | 122229707 | ||||||
| chr4:122229765
|
T | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3043-166T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 25/87 | chr4 | 122229765 | ||||||
| chr4:122230615
|
A | G | 1 | a0001c0002t0001g0002 | 2 | NA18975.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3323+404A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122230615 | ||||||
| chr4:122230644
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3323+433A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122230644 | ||||||
| chr4:122230830
|
A | G | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.3323+619A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122230830 | ||||||
| chr4:122231177
|
AAGGG | A | 4 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0046others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3323+969_3323+972d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | INFO_REALIGN_3_PRIME | chr4 | 122231177 | |||||
| chr4:122231304
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3323+1093A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231304 | ||||||
| chr4:122231539
|
GTTTGT | G | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.3323+1332_3323+133 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | INFO_REALIGN_3_PRIME | chr4 | 122231539 | |||||
| chr4:122231613
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3323+1402C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231613 | ||||||
| chr4:122231621
|
A | G | 2 | a0008c0018t0001g0114a0008c0018t0001g0115 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3323+1410A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231621 | ||||||
| chr4:122231694
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.3323+1483A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231694 | ||||||
| chr4:122231726
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3323+1515G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231726 | ||||||
| chr4:122231783
|
T | G | 9 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(6): Show | 9 | HG00280.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.3323+1572T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231783 | ||||||
| chr4:122231836
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3323+1625A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231836 | ||||||
| chr4:122231970
|
T | C | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3323+1759T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122231970 | ||||||
| chr4:122232047
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3323+1836T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232047 | ||||||
| chr4:122232118
|
G | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3323+1907G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232118 | ||||||
| chr4:122232287
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3323+2076G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232287 | ||||||
| chr4:122232473
|
T | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.3323+2262T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232473 | ||||||
| chr4:122232486
|
A | G | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.3323+2275A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232486 | ||||||
| chr4:122232564
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3324-2209G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232564 | ||||||
| chr4:122232829
|
T | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.3324-1944T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122232829 | ||||||
| chr4:122233686
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3324-1087T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122233686 | ||||||
| chr4:122233691
|
T | C | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3324-1082T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122233691 | ||||||
| chr4:122234063
|
A | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3324-710A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122234063 | ||||||
| chr4:122234212
|
C | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3324-561C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122234212 | ||||||
| chr4:122234235
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3324-538G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122234235 | ||||||
| chr4:122234304
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3324-469G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 26/87 | chr4 | 122234304 | ||||||
| chr4:122235357
|
A | G | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.3574+334A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235357 | ||||||
| chr4:122235527
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3574+504C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235527 | ||||||
| chr4:122235531
|
C | T | 1 | a0002c0004t0001g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3574+508C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235531 | ||||||
| chr4:122235533
|
T | C | 3 | a0001c0002t0001g0054a0001c0002t0001g0060a0001c0003t0001g0232 | 3 | HG02129.hp2 HG02300.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.3574+510T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235533 | ||||||
| chr4:122235543
|
C | T | 1 | a0001c0007t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3574+520C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235543 | ||||||
| chr4:122235544
|
A | G | 1 | a0001c0005t0001g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3574+521A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235544 | ||||||
| chr4:122235572
|
A | G | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3574+549A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235572 | ||||||
| chr4:122235602
|
A | G | 19 | a0001c0003t0001g0178a0001c0003t0001g0231a0001c0003t0001g0237others(16): Show | 20 | HG00099.hp1 HG00280.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.3574+579A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235602 | ||||||
| chr4:122235661
|
C | T | 1 | a0001c0003t0001g0225 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3574+638C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235661 | ||||||
| chr4:122235673
|
C | T | 3 | a0001c0003t0001g0193a0001c0003t0001g0201a0014c0030t0001g0202 | 3 | HG03834.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3574+650C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235673 | ||||||
| chr4:122235729
|
C | T | 2 | a0003c0006t0001g0042a0003c0006t0001g0043 | 2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3574+706C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235729 | ||||||
| chr4:122235782
|
G | A | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3574+759G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235782 | ||||||
| chr4:122235791
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3574+768C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235791 | ||||||
| chr4:122235802
|
C | T | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3574+779C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235802 | ||||||
| chr4:122235811
|
GA | G | 26 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(23): Show | 26 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.3574+800delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122235811 | |||||
| chr4:122235835
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3574+812G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235835 | ||||||
| chr4:122235909
|
A | C | 93 | a0001c0001t0001g0258a0001c0002t0001g0002a0001c0002t0001g0008others(90): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.3574+886A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122235909 | ||||||
| chr4:122236338
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3574+1315A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236338 | ||||||
| chr4:122236561
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3575-1531G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236561 | ||||||
| chr4:122236578
|
A | C | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3575-1514A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236578 | ||||||
| chr4:122236590
|
C | T | 1 | a0001c0003t0001g0194 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3575-1502C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236590 | ||||||
| chr4:122236691
|
A | AATATT | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3575-1400_3575-139 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122236691 | |||||
| chr4:122236876
|
AACCCCT | A | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3575-1213_3575-120 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122236876 | |||||
| chr4:122236885
|
A | G | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3575-1207A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236885 | ||||||
| chr4:122236888
|
C | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3575-1204C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236888 | ||||||
| chr4:122236938
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3575-1154A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236938 | ||||||
| chr4:122236986
|
A | G | 40 | a0001c0001t0001g0221a0001c0003t0001g0177a0001c0003t0001g0178others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.3575-1106A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122236986 | ||||||
| chr4:122237254
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3575-838G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237254 | ||||||
| chr4:122237340
|
G | A | 1 | a0001c0007t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3575-752G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237340 | ||||||
| chr4:122237348
|
G | C | 1 | a0001c0003t0001g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3575-744G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237348 | ||||||
| chr4:122237451
|
A | G | 1 | a0001c0003t0001g0231 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3575-641A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237451 | ||||||
| chr4:122237477
|
G | C | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3575-615G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237477 | ||||||
| chr4:122237554
|
T | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3575-538T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237554 | ||||||
| chr4:122237712
|
G | A | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3575-380G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122237712 | ||||||
| chr4:122237981
|
C | CA | 210 | a0001c0001t0001g0119a0001c0001t0001g0141a0001c0001t0001g0143others(207): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3575-91dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122237981 | |||||
| chr4:122237981
|
C | CAA | 37 | a0001c0001t0001g0121a0001c0001t0001g0174a0001c0001t0001g0252others(34): Show | 38 | HG00423.hp2 HG00738.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.3575-92_3575-91dup others(2): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122237981 | |||||
| chr4:122237981
|
C | CAAA | 12 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(9): Show | 12 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3575-93_3575-91dup others(3): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122237981 | |||||
| chr4:122237981
|
C | CAAAAAA | 11 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(8): Show | 11 | HG01361.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3575-96_3575-91dup others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | INFO_REALIGN_3_PRIME | chr4 | 122237981 | |||||
| chr4:122238075
|
A | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3575-17A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 27/87 | chr4 | 122238075 | ||||||
| chr4:122238357
|
A | G | 1 | a0002c0004t0001g0129 | 1 | NA19056.hp2 | splice_region_variant&intron_variant | LOW | c.3833+7A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122238357 | ||||||
| chr4:122238395
|
A | G | 1 | a0001c0002t0001g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3833+45A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122238395 | ||||||
| chr4:122238428
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3833+78T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122238428 | ||||||
| chr4:122238561
|
G | C | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3833+211G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122238561 | ||||||
| chr4:122239041
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3834-475T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122239041 | ||||||
| chr4:122239062
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3834-454C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122239062 | ||||||
| chr4:122239209
|
G | A | 1 | a0001c0003t0001g0273 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3834-307G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122239209 | ||||||
| chr4:122239455
|
G | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA18951.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3834-61G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122239455 | ||||||
| chr4:122239491
|
G | A | 11 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3834-25G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 28/87 | chr4 | 122239491 | ||||||
| chr4:122240422
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4671+69T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122240422 | ||||||
| chr4:122240464
|
A | G | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.4671+111A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122240464 | ||||||
| chr4:122240626
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4671+273A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122240626 | ||||||
| chr4:122240690
|
T | C | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4671+337T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122240690 | ||||||
| chr4:122240799
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4671+446A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122240799 | ||||||
| chr4:122240808
|
G | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4671+455G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122240808 | ||||||
| chr4:122241047
|
C | A | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.4671+694C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241047 | ||||||
| chr4:122241198
|
A | T | 2 | a0002c0004t0001g0149a0002c0004t0001g0234 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4671+845A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241198 | ||||||
| chr4:122241364
|
C | T | 1 | a0004c0013t0001g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4671+1011C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241364 | ||||||
| chr4:122241609
|
A | G | 1 | a0001c0002t0001g0068 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4671+1256A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241609 | ||||||
| chr4:122241635
|
G | A | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.4671+1282G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241635 | ||||||
| chr4:122241687
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.4672-1311G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241687 | ||||||
| chr4:122241830
|
AGGATAGA others(64): Show |
A | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0289 | 3 | NA18951.hp2 NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.4672-1167_4672-109 others(75): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241830 | ||||||
| chr4:122241860
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4672-1138A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241860 | ||||||
| chr4:122241905
|
T | TA | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0289 | 3 | NA18951.hp2 NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.4672-1093_4672-109 others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122241905 | ||||||
| chr4:122242017
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01175.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.4672-981G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242017 | ||||||
| chr4:122242119
|
A | G | 25 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(22): Show | 25 | HG00280.hp1 HG01175.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.4672-879A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242119 | ||||||
| chr4:122242403
|
T | C | 1 | a0001c0027t0001g0072 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4672-595T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242403 | ||||||
| chr4:122242407
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4672-591A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242407 | ||||||
| chr4:122242473
|
G | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.4672-525G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242473 | ||||||
| chr4:122242482
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4672-516A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242482 | ||||||
| chr4:122242615
|
C | T | 2 | a0001c0009t0001g0081a0001c0009t0001g0168 | 2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4672-383C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242615 | ||||||
| chr4:122242622
|
A | G | 4 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0016t0001g0028others(1): Show | 4 | NA18966.hp2 NA18992.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.4672-376A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242622 | ||||||
| chr4:122242741
|
A | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4672-257A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242741 | ||||||
| chr4:122242757
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4672-241T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242757 | ||||||
| chr4:122242891
|
A | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.4672-107A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 29/87 | chr4 | 122242891 | ||||||
| chr4:122243618
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4743-236G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 30/87 | chr4 | 122243618 | ||||||
| chr4:122243620
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4743-234A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 30/87 | chr4 | 122243620 | ||||||
| chr4:122243645
|
A | G | 69 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.4743-209A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 30/87 | chr4 | 122243645 | ||||||
| chr4:122243672
|
G | T | 1 | a0001c0007t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4743-182G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 30/87 | chr4 | 122243672 | ||||||
| chr4:122244031
|
T | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.4916+4T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244031 | ||||||
| chr4:122244068
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4916+41A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244068 | ||||||
| chr4:122244086
|
G | A | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4916+59G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244086 | ||||||
| chr4:122244108
|
G | A | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4916+81G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244108 | ||||||
| chr4:122244119
|
T | A | 5 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00609.hp2 HG02523.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.4916+92T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244119 | ||||||
| chr4:122244128
|
T | C | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4916+101T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244128 | ||||||
| chr4:122244135
|
T | C | 1 | a0005c0010t0001g0297 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4916+108T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244135 | ||||||
| chr4:122244146
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4916+119T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244146 | ||||||
| chr4:122244188
|
A | AAAAATG | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4916+167_4916+172d others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | INFO_REALIGN_3_PRIME | chr4 | 122244188 | |||||
| chr4:122244213
|
T | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4916+186T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244213 | ||||||
| chr4:122244258
|
G | A | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.4916+231G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244258 | ||||||
| chr4:122244486
|
T | G | 1 | a0001c0025t0001g0022 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4916+459T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244486 | ||||||
| chr4:122244752
|
C | T | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.4917-268C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244752 | ||||||
| chr4:122244938
|
T | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.4917-82T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 31/87 | chr4 | 122244938 | ||||||
| chr4:122245144
|
A | G | 1 | a0001c0025t0001g0022 | 1 | NA19000.hp2 | splice_region_variant&intron_variant | LOW | c.5037+4A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122245144 | ||||||
| chr4:122245168
|
A | C | 1 | a0001c0003t0001g0232 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5037+28A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122245168 | ||||||
| chr4:122245262
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5037+122G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122245262 | ||||||
| chr4:122245694
|
A | G | 1 | a0015c0028t0001g0058 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.5038-458A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122245694 | ||||||
| chr4:122245704
|
A | T | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5038-448A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122245704 | ||||||
| chr4:122245738
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5038-414T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122245738 | ||||||
| chr4:122246084
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5038-68G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122246084 | ||||||
| chr4:122246120
|
T | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.5038-32T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122246120 | ||||||
| chr4:122246127
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5038-25A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 32/87 | chr4 | 122246127 | ||||||
| chr4:122246320
|
A | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.5184+22A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 33/87 | chr4 | 122246320 | ||||||
| chr4:122246417
|
G | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5184+119G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 33/87 | chr4 | 122246417 | ||||||
| chr4:122246532
|
ATT | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5185-148_5185-147d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 33/87 | INFO_REALIGN_3_PRIME | chr4 | 122246532 | |||||
| chr4:122246617
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5185-66G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 33/87 | chr4 | 122246617 | ||||||
| chr4:122246966
|
CAT | C | 28 | a0001c0002t0001g0008a0001c0002t0001g0014a0001c0002t0001g0015others(25): Show | 28 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.5312+159_5312+160d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 34/87 | INFO_REALIGN_3_PRIME | chr4 | 122246966 | |||||
| chr4:122247008
|
C | T | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5313-150C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 34/87 | chr4 | 122247008 | ||||||
| chr4:122247368
|
A | G | 1 | a0001c0003t0001g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.5512+11A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122247368 | ||||||
| chr4:122247596
|
CTTCTATT others(8): Show |
C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.5512+255_5512+269d others(17): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | INFO_REALIGN_3_PRIME | chr4 | 122247596 | |||||
| chr4:122247615
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5512+258T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122247615 | ||||||
| chr4:122247641
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5512+284A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122247641 | ||||||
| chr4:122247652
|
C | T | 1 | a0001c0007t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5512+295C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122247652 | ||||||
| chr4:122247776
|
C | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5512+419C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122247776 | ||||||
| chr4:122247869
|
C | A | 4 | a0005c0010t0001g0297a0005c0010t0001g0305a0005c0010t0001g0307others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.5512+512C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122247869 | ||||||
| chr4:122248031
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5512+674G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248031 | ||||||
| chr4:122248083
|
C | A | 1 | a0001c0003t0001g0225 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5512+726C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248083 | ||||||
| chr4:122248229
|
G | A | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5512+872G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248229 | ||||||
| chr4:122248258
|
C | T | 1 | a0001c0002t0001g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5512+901C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248258 | ||||||
| chr4:122248270
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | NA18974.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.5512+913C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248270 | ||||||
| chr4:122248271
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5512+914G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248271 | ||||||
| chr4:122248279
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.5512+922C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248279 | ||||||
| chr4:122248322
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5512+965T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248322 | ||||||
| chr4:122248452
|
A | G | 57 | a0001c0001t0001g0143a0001c0001t0001g0181a0001c0001t0001g0183others(54): Show | 57 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.5513-1033A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248452 | ||||||
| chr4:122248459
|
C | G | 1 | a0002c0004t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5513-1026C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248459 | ||||||
| chr4:122248499
|
G | A | 2 | a0002c0004t0001g0129a0002c0004t0001g0154 | 2 | HG02074.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.5513-986G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248499 | ||||||
| chr4:122248513
|
G | T | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5513-972G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248513 | ||||||
| chr4:122248540
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0219 | 2 | HG01975.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.5513-945G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248540 | ||||||
| chr4:122248711
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.5513-774A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122248711 | ||||||
| chr4:122249085
|
A | G | 2 | a0001c0002t0001g0088a0001c0002t0001g0100 | 2 | NA18994.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.5513-400A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122249085 | ||||||
| chr4:122249102
|
G | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5513-383G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122249102 | ||||||
| chr4:122249294
|
A | G | 1 | a0002c0004t0001g0134 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5513-191A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122249294 | ||||||
| chr4:122249337
|
T | C | 1 | a0004c0013t0001g0227 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.5513-148T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122249337 | ||||||
| chr4:122249440
|
G | C | 1 | a0001c0003t0001g0290 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5513-45G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 35/87 | chr4 | 122249440 | ||||||
| chr4:122249811
|
G | T | 2 | a0003c0006t0001g0038a0003c0006t0001g0046 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5710+129G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122249811 | ||||||
| chr4:122249821
|
C | A | 1 | a0015c0028t0001g0058 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.5710+139C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122249821 | ||||||
| chr4:122249921
|
G | A | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5710+239G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122249921 | ||||||
| chr4:122249998
|
G | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5710+316G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122249998 | ||||||
| chr4:122250018
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5710+336A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122250018 | ||||||
| chr4:122250063
|
G | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5711-299G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122250063 | ||||||
| chr4:122250163
|
T | C | 9 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(6): Show | 9 | HG00280.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.5711-199T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122250163 | ||||||
| chr4:122250323
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5711-39T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 36/87 | chr4 | 122250323 | ||||||
| chr4:122250755
|
C | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5922+182C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122250755 | ||||||
| chr4:122250795
|
T | G | 1 | a0001c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.5922+222T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122250795 | ||||||
| chr4:122250849
|
A | G | 1 | a0001c0001t0009g0327 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5922+276A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122250849 | ||||||
| chr4:122250924
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5922+351T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122250924 | ||||||
| chr4:122251076
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5922+503T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251076 | ||||||
| chr4:122251089
|
T | G | 143 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(140): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.5922+516T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251089 | ||||||
| chr4:122251105
|
G | A | 13 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(10): Show | 13 | HG01361.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.5922+532G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251105 | ||||||
| chr4:122251218
|
G | GTAATA | 40 | a0001c0001t0001g0221a0001c0003t0001g0177a0001c0003t0001g0178others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.5922+646_5922+650d others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | INFO_REALIGN_3_PRIME | chr4 | 122251218 | |||||
| chr4:122251249
|
T | C | 5 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00609.hp2 HG02523.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.5922+676T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251249 | ||||||
| chr4:122251263
|
A | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5922+690A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251263 | ||||||
| chr4:122251421
|
C | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.5922+848C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251421 | ||||||
| chr4:122251953
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5922+1380T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122251953 | ||||||
| chr4:122252008
|
A | G | 1 | a0002c0004t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5922+1435A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252008 | ||||||
| chr4:122252141
|
A | G | 7 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5922+1568A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252141 | ||||||
| chr4:122252158
|
A | G | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5922+1585A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252158 | ||||||
| chr4:122252211
|
C | G | 1 | a0001c0017t0001g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5922+1638C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252211 | ||||||
| chr4:122252717
|
C | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5923-1478C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252717 | ||||||
| chr4:122252784
|
A | AATCAGCT others(39): Show |
2 | a0002c0004t0001g0129a0002c0004t0001g0154 | 2 | HG02074.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.5923-1411_5923-141 others(50): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252784 | ||||||
| chr4:122252805
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5923-1390C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252805 | ||||||
| chr4:122252840
|
C | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5923-1355C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252840 | ||||||
| chr4:122252883
|
C | A | 4 | a0003c0006t0001g0009a0003c0006t0001g0011a0003c0006t0001g0013others(1): Show | 4 | HG01361.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5923-1312C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252883 | ||||||
| chr4:122252946
|
G | A | 1 | a0002c0004t0001g0134 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5923-1249G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252946 | ||||||
| chr4:122252992
|
A | C | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5923-1203A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122252992 | ||||||
| chr4:122253079
|
T | G | 2 | a0001c0002t0001g0053a0001c0002t0001g0054 | 2 | HG02129.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.5923-1116T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253079 | ||||||
| chr4:122253095
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.5923-1100A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253095 | ||||||
| chr4:122253184
|
TG | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5923-1008delG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | INFO_REALIGN_3_PRIME | chr4 | 122253184 | |||||
| chr4:122253318
|
CCA | C | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5923-876_5923-875d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253318 | ||||||
| chr4:122253324
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5923-871A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253324 | ||||||
| chr4:122253506
|
A | C | 1 | a0008c0021t0010g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5923-689A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253506 | ||||||
| chr4:122253649
|
A | T | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.5923-546A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253649 | ||||||
| chr4:122253777
|
T | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5923-418T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253777 | ||||||
| chr4:122253924
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0219 | 2 | HG01975.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.5923-271C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253924 | ||||||
| chr4:122253968
|
C | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.5923-227C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122253968 | ||||||
| chr4:122254036
|
A | G | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5923-159A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122254036 | ||||||
| chr4:122254097
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5923-98A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 37/87 | chr4 | 122254097 | ||||||
| chr4:122254437
|
T | C | 1 | a0008c0021t0010g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6074+91T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 38/87 | chr4 | 122254437 | ||||||
| chr4:122254636
|
A | AT | 325 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.6075-161dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 38/87 | INFO_REALIGN_3_PRIME | chr4 | 122254636 | |||||
| chr4:122254745
|
G | A | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.6075-60G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 38/87 | chr4 | 122254745 | ||||||
| chr4:122255293
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6378+10T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122255293 | ||||||
| chr4:122255411
|
C | T | 93 | a0001c0001t0001g0143a0001c0002t0001g0002a0001c0002t0001g0008others(90): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.6378+128C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122255411 | ||||||
| chr4:122255507
|
G | A | 1 | a0003c0006t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6378+224G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122255507 | ||||||
| chr4:122255703
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0182 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.6378+420A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122255703 | ||||||
| chr4:122255764
|
C | T | 3 | a0001c0003t0001g0177a0001c0003t0001g0179a0001c0003t0001g0200 | 3 | HG00621.hp2 HG03831.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6378+481C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122255764 | ||||||
| chr4:122255844
|
G | A | 1 | a0003c0006t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6378+561G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122255844 | ||||||
| chr4:122256098
|
T | C | 1 | a0002c0004t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6378+815T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122256098 | ||||||
| chr4:122256358
|
A | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6379-897A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122256358 | ||||||
| chr4:122256449
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.6379-806G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122256449 | ||||||
| chr4:122256703
|
G | C | 1 | a0001c0005t0002g0007 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6379-552G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122256703 | ||||||
| chr4:122257037
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6379-218A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122257037 | ||||||
| chr4:122257209
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6379-46A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122257209 | ||||||
| chr4:122257214
|
A | G | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02647.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.6379-41A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 40/87 | chr4 | 122257214 | ||||||
| chr4:122257707
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.6619+212T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/87 | chr4 | 122257707 | ||||||
| chr4:122257886
|
T | C | 59 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(56): Show | 59 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.6619+391T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/87 | chr4 | 122257886 | ||||||
| chr4:122258069
|
AT | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6619+578delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/87 | INFO_REALIGN_3_PRIME | chr4 | 122258069 | |||||
| chr4:122258230
|
G | T | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02647.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.6620-471G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/87 | chr4 | 122258230 | ||||||
| chr4:122258261
|
T | C | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.6620-440T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/87 | chr4 | 122258261 | ||||||
| chr4:122258547
|
CTGAG | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.6620-149_6620-146d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 41/87 | INFO_REALIGN_3_PRIME | chr4 | 122258547 | |||||
| chr4:122258875
|
C | T | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.6762+32C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122258875 | ||||||
| chr4:122258910
|
A | G | 4 | a0002c0004t0001g0149a0002c0004t0001g0234a0010c0020t0001g0104others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.6762+67A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122258910 | ||||||
| chr4:122259001
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6762+158T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259001 | ||||||
| chr4:122259209
|
T | G | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6762+366T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259209 | ||||||
| chr4:122259363
|
C | T | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6762+520C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259363 | ||||||
| chr4:122259374
|
G | A | 2 | a0001c0001t0001g0291a0018c0039t0001g0233 | 2 | HG00733.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.6762+531G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259374 | ||||||
| chr4:122259514
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6762+671G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259514 | ||||||
| chr4:122259604
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6762+761A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259604 | ||||||
| chr4:122259858
|
C | CAAA | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.6762+1025_6762+102 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122259858 | |||||
| chr4:122259971
|
C | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.6762+1128C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122259971 | ||||||
| chr4:122260065
|
G | A | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6762+1222G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260065 | ||||||
| chr4:122260203
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6762+1360A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260203 | ||||||
| chr4:122260247
|
T | C | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.6762+1404T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260247 | ||||||
| chr4:122260272
|
T | C | 2 | a0003c0006t0001g0042a0003c0006t0001g0043 | 2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6762+1429T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260272 | ||||||
| chr4:122260320
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.6762+1477A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260320 | ||||||
| chr4:122260469
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6762+1626C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260469 | ||||||
| chr4:122260748
|
T | C | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.6762+1905T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260748 | ||||||
| chr4:122260773
|
C | T | 4 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0016t0001g0028others(1): Show | 4 | NA18966.hp2 NA18992.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.6762+1930C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260773 | ||||||
| chr4:122260928
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6763-1836G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260928 | ||||||
| chr4:122260934
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6763-1830C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122260934 | ||||||
| chr4:122261262
|
CT | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.6763-1495delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122261262 | |||||
| chr4:122261504
|
A | G | 1 | a0001c0027t0001g0072 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6763-1260A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122261504 | ||||||
| chr4:122261554
|
A | C | 1 | a0005c0010t0001g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6763-1210A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122261554 | ||||||
| chr4:122261611
|
C | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.6763-1153C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122261611 | ||||||
| chr4:122261637
|
A | T | 1 | a0001c0001t0003g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6763-1127A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122261637 | ||||||
| chr4:122261741
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.6763-1023C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122261741 | ||||||
| chr4:122262002
|
C | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.6763-762C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262002 | ||||||
| chr4:122262050
|
A | C | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.6763-714A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262050 | ||||||
| chr4:122262148
|
T | TGTGTGTG others(4): Show |
1 | a0001c0029t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.6763-616_6763-615i others(13): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262148 | ||||||
| chr4:122262148
|
T | TTG | 44 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0172others(41): Show | 45 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.6763-578_6763-577d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTG | 43 | a0001c0001t0001g0143a0001c0001t0001g0264a0001c0001t0001g0266others(40): Show | 43 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.6763-580_6763-577d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTG | 50 | a0001c0001t0001g0183a0001c0001t0001g0187a0001c0001t0001g0222others(47): Show | 50 | HG00733.hp1 HG00733.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.6763-582_6763-577d others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTGT others(1): Show |
39 | a0001c0001t0001g0121a0001c0001t0001g0145a0001c0001t0001g0159others(36): Show | 39 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.6763-584_6763-577d others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTGT others(3): Show |
80 | a0001c0001t0001g0155a0001c0001t0001g0207a0001c0001t0001g0216others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.6763-586_6763-577d others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTGT others(5): Show |
25 | a0001c0001t0001g0141a0001c0001t0001g0189a0001c0001t0001g0217others(22): Show | 25 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.6763-588_6763-577d others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTGT others(7): Show |
7 | a0001c0001t0001g0221a0001c0002t0001g0002a0001c0002t0001g0021others(4): Show | 8 | HG01361.hp1 HG02056.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.6763-590_6763-577d others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTGT others(9): Show |
2 | a0001c0002t0001g0020a0001c0002t0001g0037 | 2 | HG01099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.6763-592_6763-577d others(18): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
T | TTGTGTGT others(11): Show |
1 | a0001c0002t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6763-594_6763-577d others(20): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
TTG | T | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG01243.hp2 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.6763-578_6763-577d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
TTGTGTGT others(7): Show |
T | 5 | a0008c0018t0001g0114a0008c0018t0001g0115a0008c0021t0010g0116others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6763-590_6763-577d others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262148
|
TTGTGTGT others(9): Show |
T | 2 | a0002c0004t0001g0130a0002c0004t0001g0131 | 2 | NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.6763-592_6763-577d others(18): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262148 | |||||
| chr4:122262188
|
A | G | 64 | a0001c0002t0001g0002a0001c0002t0001g0016a0001c0002t0001g0035others(61): Show | 65 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.6763-576A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262188 | ||||||
| chr4:122262310
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6763-454A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262310 | ||||||
| chr4:122262333
|
C | A | 4 | a0001c0009t0001g0081a0001c0009t0001g0082a0001c0009t0001g0083others(1): Show | 4 | NA18747.hp1 NA19005.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.6763-431C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262333 | ||||||
| chr4:122262486
|
T | TTAAA | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.6763-277_6763-274d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | INFO_REALIGN_3_PRIME | chr4 | 122262486 | |||||
| chr4:122262588
|
A | C | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.6763-176A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262588 | ||||||
| chr4:122262655
|
T | C | 1 | a0016c0022t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6763-109T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 42/87 | chr4 | 122262655 | ||||||
| chr4:122263010
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.6982+27A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 43/87 | chr4 | 122263010 | ||||||
| chr4:122263130
|
G | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.6982+147G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 43/87 | chr4 | 122263130 | ||||||
| chr4:122263149
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6982+166G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 43/87 | chr4 | 122263149 | ||||||
| chr4:122263256
|
T | C | 186 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.6983-186T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 43/87 | chr4 | 122263256 | ||||||
| chr4:122263672
|
G | A | 40 | a0001c0001t0001g0221a0001c0003t0001g0177a0001c0003t0001g0178others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.7141+72G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 44/87 | chr4 | 122263672 | ||||||
| chr4:122263786
|
G | C | 1 | a0018c0039t0001g0233 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.7141+186G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 44/87 | chr4 | 122263786 | ||||||
| chr4:122264508
|
C | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.7317+81C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264508 | ||||||
| chr4:122264527
|
C | A | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.7317+100C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264527 | ||||||
| chr4:122264567
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7317+140G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264567 | ||||||
| chr4:122264747
|
C | T | 1 | a0001c0036t0001g0320 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7317+320C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264747 | ||||||
| chr4:122264783
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7317+356G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264783 | ||||||
| chr4:122264939
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7317+512A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264939 | ||||||
| chr4:122264989
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.7317+562G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122264989 | ||||||
| chr4:122265094
|
A | G | 4 | a0005c0010t0001g0297a0005c0010t0001g0305a0005c0010t0001g0307others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.7317+667A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265094 | ||||||
| chr4:122265238
|
A | G | 1 | a0018c0039t0001g0233 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.7317+811A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265238 | ||||||
| chr4:122265323
|
T | C | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.7317+896T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265323 | ||||||
| chr4:122265396
|
G | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0019 | 2 | HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.7317+969G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265396 | ||||||
| chr4:122265439
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.7317+1012G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265439 | ||||||
| chr4:122265518
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7317+1091C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265518 | ||||||
| chr4:122265695
|
G | T | 2 | a0001c0003t0001g0230a0001c0003t0001g0232 | 2 | NA18944.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.7318-1088G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265695 | ||||||
| chr4:122265698
|
G | GTTGT | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.7318-1069_7318-106 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | INFO_REALIGN_3_PRIME | chr4 | 122265698 | |||||
| chr4:122265899
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.7318-884G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122265899 | ||||||
| chr4:122266061
|
G | A | 1 | a0002c0004t0001g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.7318-722G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122266061 | ||||||
| chr4:122266239
|
C | G | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.7318-544C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122266239 | ||||||
| chr4:122266438
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7318-345C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122266438 | ||||||
| chr4:122266621
|
A | C | 3 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0120 | 3 | HG01123.hp1 HG01346.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.7318-162A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122266621 | ||||||
| chr4:122266714
|
C | T | 142 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(139): Show | 145 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.7318-69C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 45/87 | chr4 | 122266714 | ||||||
| chr4:122267051
|
A | AT | 38 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0190others(35): Show | 38 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.7493+118dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATT | 6 | a0001c0003t0001g0195a0001c0003t0001g0204a0001c0003t0001g0236others(3): Show | 6 | HG00408.hp1 HG02071.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.7493+117_7493+118d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTT | 7 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0108others(4): Show | 8 | HG01106.hp2 HG01258.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.7493+115_7493+118d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT | 6 | a0003c0006t0001g0040a0003c0006t0001g0041a0003c0006t0001g0044others(3): Show | 6 | HG01123.hp2 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.7493+112_7493+118d others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(1): Show |
6 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0013others(3): Show | 6 | HG02280.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.7493+111_7493+118d others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(2): Show |
8 | a0001c0003t0001g0223a0001c0032t0001g0176a0003c0006t0001g0011others(5): Show | 8 | HG01069.hp2 HG01361.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.7493+110_7493+118d others(11): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(3): Show |
5 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0282others(2): Show | 5 | HG00733.hp1 HG03453.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.7493+109_7493+118d others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0017t0001g0295 | 3 | HG00735.hp1 HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.7493+108_7493+118d others(13): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(5): Show |
5 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(2): Show | 5 | HG00099.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.7493+107_7493+118d others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(6): Show |
13 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0328others(10): Show | 13 | HG01074.hp1 HG01106.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.7493+106_7493+118d others(15): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(7): Show |
13 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0304others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.7493+105_7493+118d others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(8): Show |
10 | a0001c0001t0001g0145a0001c0001t0001g0299a0001c0001t0001g0308others(7): Show | 10 | HG01175.hp1 HG02615.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.7493+104_7493+118d others(17): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0311a0001c0001t0001g0321 | 2 | HG02738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7493+103_7493+118d others(18): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(10): Show |
1 | a0001c0037t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7493+102_7493+118d others(19): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(11): Show |
6 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG02809.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.7493+101_7493+118d others(20): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0123a0001c0003t0006g0196a0006c0014t0001g0117others(1): Show | 4 | HG01243.hp2 HG02132.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.7493+100_7493+118d others(21): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(13): Show |
6 | a0001c0001t0001g0222a0001c0003t0001g0191a0001c0003t0001g0194others(3): Show | 6 | HG00639.hp2 HG02559.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.7493+99_7493+118du others(21): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(14): Show |
3 | a0001c0001t0001g0159a0001c0003t0001g0203a0006c0014t0001g0144 | 3 | HG01099.hp2 HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7493+98_7493+118du others(22): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(15): Show |
4 | a0001c0001t0001g0102a0001c0003t0001g0199a0001c0003t0001g0206others(1): Show | 4 | HG00741.hp2 HG03540.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.7493+97_7493+118du others(23): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(18): Show |
1 | a0001c0003t0001g0292 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.7493+94_7493+118du others(26): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(20): Show |
2 | a0001c0003t0001g0177a0001c0003t0001g0192 | 2 | HG00621.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.7493+118_7493+119i others(29): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7493+118_7493+119i others(30): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(22): Show |
1 | a0001c0001t0001g0317 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.7493+118_7493+119i others(31): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(24): Show |
2 | a0001c0001t0001g0221a0001c0001t0001g0302 | 2 | HG02056.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.7493+118_7493+119i others(33): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(25): Show |
1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.7493+118_7493+119i others(34): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(26): Show |
2 | a0001c0001t0001g0301a0001c0001t0001g0318 | 2 | NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.7493+118_7493+119i others(35): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
A | ATTTTTTT others(31): Show |
1 | a0001c0017t0001g0303 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.7493+118_7493+119i others(40): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
AT | A | 82 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.7493+118delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267051
|
ATT | A | 7 | a0001c0002t0001g0068a0001c0002t0001g0086a0001c0005t0002g0001others(4): Show | 8 | HG01074.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.7493+117_7493+118d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122267051 | |||||
| chr4:122267057
|
T | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.7493+99T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267057 | ||||||
| chr4:122267147
|
C | T | 28 | a0001c0002t0001g0008a0001c0002t0001g0014a0001c0002t0001g0015others(25): Show | 28 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.7493+189C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267147 | ||||||
| chr4:122267151
|
C | T | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.7493+193C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267151 | ||||||
| chr4:122267294
|
C | G | 41 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.7493+336C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267294 | ||||||
| chr4:122267346
|
A | G | 107 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0174others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.7493+388A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267346 | ||||||
| chr4:122267531
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7493+573G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267531 | ||||||
| chr4:122267874
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.7493+916A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267874 | ||||||
| chr4:122267996
|
C | G | 30 | a0001c0001t0001g0141a0001c0001t0001g0155a0002c0004t0001g0049others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.7493+1038C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122267996 | ||||||
| chr4:122268040
|
A | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.7493+1082A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268040 | ||||||
| chr4:122268100
|
C | T | 1 | a0001c0003t0001g0292 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.7493+1142C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268100 | ||||||
| chr4:122268196
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7493+1238A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268196 | ||||||
| chr4:122268294
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.7493+1336G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268294 | ||||||
| chr4:122268306
|
C | CCTT | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.7493+1349_7493+135 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122268306 | |||||
| chr4:122268578
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7493+1620A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268578 | ||||||
| chr4:122268757
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7493+1799G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268757 | ||||||
| chr4:122268772
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.7493+1814C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268772 | ||||||
| chr4:122268794
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.7493+1836T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268794 | ||||||
| chr4:122268806
|
A | G | 1 | a0001c0002t0001g0074 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7493+1848A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268806 | ||||||
| chr4:122268874
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7493+1916A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122268874 | ||||||
| chr4:122269350
|
C | G | 11 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.7494-1668C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269350 | ||||||
| chr4:122269475
|
G | A | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.7494-1543G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269475 | ||||||
| chr4:122269494
|
A | G | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.7494-1524A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269494 | ||||||
| chr4:122269582
|
G | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.7494-1436G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269582 | ||||||
| chr4:122269614
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7494-1404A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269614 | ||||||
| chr4:122269746
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7494-1272C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269746 | ||||||
| chr4:122269794
|
T | C | 2 | a0001c0002t0001g0088a0001c0002t0001g0100 | 2 | NA18994.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.7494-1224T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269794 | ||||||
| chr4:122269937
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0314others(1): Show | 4 | HG03669.hp1 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.7494-1081T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269937 | ||||||
| chr4:122269987
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7494-1031C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122269987 | ||||||
| chr4:122270034
|
A | G | 3 | a0001c0002t0001g0024a0001c0002t0001g0026a0001c0002t0001g0036 | 3 | HG00423.hp2 HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.7494-984A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270034 | ||||||
| chr4:122270057
|
C | G | 1 | a0001c0002t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.7494-961C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270057 | ||||||
| chr4:122270119
|
G | A | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | NA18955.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.7494-899G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270119 | ||||||
| chr4:122270166
|
G | T | 1 | a0001c0002t0001g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.7494-852G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270166 | ||||||
| chr4:122270316
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7494-702C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270316 | ||||||
| chr4:122270355
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.7494-663C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270355 | ||||||
| chr4:122270635
|
C | CA | 31 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(28): Show | 32 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.7494-382dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122270635 | |||||
| chr4:122270636
|
A | AC | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.7494-382_7494-381i others(3): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | chr4 | 122270636 | ||||||
| chr4:122270646
|
A | AG | 96 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(93): Show | 98 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.7494-365dupG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 46/87 | INFO_REALIGN_3_PRIME | chr4 | 122270646 | |||||
| chr4:122272091
|
A | G | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.8201-69A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 47/87 | chr4 | 122272091 | ||||||
| chr4:122272124
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8201-36G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 47/87 | chr4 | 122272124 | ||||||
| chr4:122272413
|
T | C | 1 | a0001c0027t0001g0072 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.8446+8T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122272413 | ||||||
| chr4:122272507
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.8446+102A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122272507 | ||||||
| chr4:122272533
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.8446+128C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122272533 | ||||||
| chr4:122272715
|
A | G | 225 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(222): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.8446+310A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122272715 | ||||||
| chr4:122273106
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.8446+701T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273106 | ||||||
| chr4:122273114
|
G | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.8446+709G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273114 | ||||||
| chr4:122273119
|
G | A | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.8446+714G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273119 | ||||||
| chr4:122273272
|
G | A | 1 | a0001c0003t0006g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.8446+867G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273272 | ||||||
| chr4:122273282
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8446+877C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273282 | ||||||
| chr4:122273299
|
A | G | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.8446+894A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273299 | ||||||
| chr4:122273306
|
A | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.8446+901A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273306 | ||||||
| chr4:122273588
|
C | T | 2 | a0002c0004t0001g0135a0002c0004t0001g0136 | 2 | NA19086.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.8447-755C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273588 | ||||||
| chr4:122273740
|
C | T | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8447-603C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273740 | ||||||
| chr4:122273801
|
T | C | 1 | a0001c0002t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.8447-542T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273801 | ||||||
| chr4:122273852
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8447-491A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273852 | ||||||
| chr4:122273888
|
T | C | 1 | a0001c0003t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.8447-455T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273888 | ||||||
| chr4:122273889
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.8447-454T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273889 | ||||||
| chr4:122273949
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8447-394A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122273949 | ||||||
| chr4:122274281
|
T | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.8447-62T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 48/87 | chr4 | 122274281 | ||||||
| chr4:122274527
|
A | G | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.8540+91A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122274527 | ||||||
| chr4:122274552
|
T | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.8540+116T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122274552 | ||||||
| chr4:122274703
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.8540+267G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122274703 | ||||||
| chr4:122274856
|
AT | A | 3 | a0001c0005t0001g0106a0001c0005t0001g0107a0001c0005t0001g0108 | 3 | HG01106.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.8540+421delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122274856 | ||||||
| chr4:122274904
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.8540+468A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122274904 | ||||||
| chr4:122275031
|
C | T | 1 | a0001c0037t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8540+595C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122275031 | ||||||
| chr4:122275139
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.8540+703G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122275139 | ||||||
| chr4:122275202
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.8540+766G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122275202 | ||||||
| chr4:122275229
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.8541-743T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122275229 | ||||||
| chr4:122275244
|
G | A | 4 | a0004c0013t0001g0198a0004c0013t0001g0226a0004c0013t0001g0227others(1): Show | 4 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.8541-728G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122275244 | ||||||
| chr4:122275427
|
G | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.8541-545G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 49/87 | chr4 | 122275427 | ||||||
| chr4:122276888
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.8591+866G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122276888 | ||||||
| chr4:122276980
|
T | TTAATG | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.8591+960_8591+961i others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | INFO_REALIGN_3_PRIME | chr4 | 122276980 | |||||
| chr4:122277280
|
A | G | 184 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(181): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.8591+1258A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122277280 | ||||||
| chr4:122277484
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.8591+1462C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122277484 | ||||||
| chr4:122277722
|
T | G | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.8591+1700T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122277722 | ||||||
| chr4:122277763
|
T | A | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.8591+1741T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122277763 | ||||||
| chr4:122277766
|
T | C | 1 | a0001c0001t0001g0317 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.8591+1744T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122277766 | ||||||
| chr4:122278212
|
C | A | 5 | a0003c0006t0001g0040a0003c0006t0001g0042a0003c0006t0001g0043others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.8592-1563C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122278212 | ||||||
| chr4:122278253
|
AT | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.8592-1520delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | INFO_REALIGN_3_PRIME | chr4 | 122278253 | |||||
| chr4:122278736
|
A | G | 1 | a0005c0010t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.8592-1039A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122278736 | ||||||
| chr4:122278860
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.8592-915G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122278860 | ||||||
| chr4:122278866
|
A | G | 4 | a0001c0002t0001g0008a0001c0002t0001g0019a0001c0002t0001g0020others(1): Show | 4 | HG01099.hp1 HG01168.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.8592-909A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122278866 | ||||||
| chr4:122279026
|
A | G | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8592-749A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122279026 | ||||||
| chr4:122279438
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.8592-337A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122279438 | ||||||
| chr4:122279482
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0119 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.8592-293T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122279482 | ||||||
| chr4:122279540
|
T | C | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.8592-235T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122279540 | ||||||
| chr4:122279638
|
T | C | 5 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0073others(2): Show | 5 | HG00597.hp1 NA18944.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.8592-137T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122279638 | ||||||
| chr4:122279749
|
T | C | 3 | a0006c0014t0001g0117a0006c0014t0001g0118a0006c0014t0001g0144 | 3 | HG01243.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8592-26T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 50/87 | chr4 | 122279749 | ||||||
| chr4:122280110
|
G | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.8798+129G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280110 | ||||||
| chr4:122280134
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.8798+153A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280134 | ||||||
| chr4:122280156
|
A | T | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.8798+175A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280156 | ||||||
| chr4:122280180
|
G | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.8798+199G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280180 | ||||||
| chr4:122280241
|
G | T | 1 | a0001c0003t0001g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.8798+260G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280241 | ||||||
| chr4:122280250
|
G | C | 25 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.8798+269G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280250 | ||||||
| chr4:122280446
|
T | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.8798+465T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280446 | ||||||
| chr4:122280568
|
C | T | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.8798+587C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280568 | ||||||
| chr4:122280578
|
G | A | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.8798+597G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280578 | ||||||
| chr4:122280588
|
G | A | 1 | a0001c0036t0001g0320 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.8798+607G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280588 | ||||||
| chr4:122280662
|
T | TA | 16 | a0001c0001t0001g0184a0001c0001t0001g0208a0001c0001t0001g0324others(13): Show | 16 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.8798+701dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | INFO_REALIGN_3_PRIME | chr4 | 122280662 | |||||
| chr4:122280662
|
TA | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0141a0001c0001t0001g0155others(3): Show | 6 | HG00558.hp2 HG02040.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.8798+701delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | INFO_REALIGN_3_PRIME | chr4 | 122280662 | |||||
| chr4:122280680
|
A | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.8798+699A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280680 | ||||||
| chr4:122280820
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.8799-716T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280820 | ||||||
| chr4:122280947
|
A | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.8799-589A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122280947 | ||||||
| chr4:122281060
|
C | A | 1 | a0006c0014t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.8799-476C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122281060 | ||||||
| chr4:122281080
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.8799-456A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122281080 | ||||||
| chr4:122281149
|
T | C | 1 | a0002c0004t0001g0131 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.8799-387T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122281149 | ||||||
| chr4:122281152
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8799-384T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122281152 | ||||||
| chr4:122281343
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.8799-193T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 51/87 | chr4 | 122281343 | ||||||
| chr4:122281829
|
T | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9037+55T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122281829 | ||||||
| chr4:122281926
|
A | G | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9037+152A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122281926 | ||||||
| chr4:122281943
|
C | T | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.9037+169C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122281943 | ||||||
| chr4:122282093
|
G | T | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.9037+319G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122282093 | ||||||
| chr4:122282105
|
A | G | 1 | a0002c0004t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.9037+331A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122282105 | ||||||
| chr4:122282412
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01175.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.9037+638C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122282412 | ||||||
| chr4:122282418
|
G | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9037+644G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122282418 | ||||||
| chr4:122282641
|
C | CA | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9037+876dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | INFO_REALIGN_3_PRIME | chr4 | 122282641 | |||||
| chr4:122282745
|
C | G | 1 | a0001c0007t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9037+971C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122282745 | ||||||
| chr4:122282982
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.9037+1208A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122282982 | ||||||
| chr4:122283240
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9037+1466A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283240 | ||||||
| chr4:122283242
|
AGTATATA others(13): Show |
A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9037+1500_9037+151 others(24): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | INFO_REALIGN_3_PRIME | chr4 | 122283242 | |||||
| chr4:122283280
|
A | G | 1 | a0005c0010t0001g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.9037+1506A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283280 | ||||||
| chr4:122283416
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9037+1642A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283416 | ||||||
| chr4:122283448
|
CCTGA | C | 13 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(10): Show | 14 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.9037+1677_9037+168 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | INFO_REALIGN_3_PRIME | chr4 | 122283448 | |||||
| chr4:122283534
|
C | T | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.9037+1760C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283534 | ||||||
| chr4:122283570
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9037+1796G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283570 | ||||||
| chr4:122283785
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.9037+2011C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283785 | ||||||
| chr4:122283988
|
A | G | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9037+2214A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122283988 | ||||||
| chr4:122284208
|
T | C | 3 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0314 | 3 | HG03669.hp1 HG03688.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.9038-2333T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284208 | ||||||
| chr4:122284376
|
C | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9038-2165C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284376 | ||||||
| chr4:122284588
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9038-1953G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284588 | ||||||
| chr4:122284593
|
C | CTTACATA others(8): Show |
14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9038-1948_9038-194 others(19): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284593 | ||||||
| chr4:122284597
|
A | AT | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9038-1944_9038-194 others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284597 | ||||||
| chr4:122284624
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.9038-1917T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284624 | ||||||
| chr4:122284636
|
A | T | 1 | a0003c0006t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.9038-1905A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284636 | ||||||
| chr4:122284848
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9038-1693A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284848 | ||||||
| chr4:122284855
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9038-1686A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122284855 | ||||||
| chr4:122285139
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9038-1402C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122285139 | ||||||
| chr4:122285559
|
C | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.9038-982C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122285559 | ||||||
| chr4:122286038
|
G | A | 1 | a0001c0002t0001g0053 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.9038-503G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122286038 | ||||||
| chr4:122286078
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0219 | 2 | HG01975.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.9038-463C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122286078 | ||||||
| chr4:122286105
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9038-436T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122286105 | ||||||
| chr4:122286242
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.9038-299A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 52/87 | chr4 | 122286242 | ||||||
| chr4:122287106
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9282+321C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287106 | ||||||
| chr4:122287194
|
G | A | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9282+409G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287194 | ||||||
| chr4:122287287
|
A | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.9282+502A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287287 | ||||||
| chr4:122287467
|
C | G | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.9282+682C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287467 | ||||||
| chr4:122287806
|
C | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9282+1021C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287806 | ||||||
| chr4:122287956
|
C | T | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02647.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9283-1131C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287956 | ||||||
| chr4:122287984
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.9283-1103A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287984 | ||||||
| chr4:122287992
|
G | C | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | NA18955.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.9283-1095G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287992 | ||||||
| chr4:122287995
|
A | G | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.9283-1092A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122287995 | ||||||
| chr4:122288078
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9283-1009A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288078 | ||||||
| chr4:122288092
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0037 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.9283-995T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288092 | ||||||
| chr4:122288204
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9283-883G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288204 | ||||||
| chr4:122288528
|
C | T | 2 | a0001c0003t0001g0192a0001c0003t0001g0194 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.9283-559C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288528 | ||||||
| chr4:122288608
|
C | T | 1 | a0006c0014t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9283-479C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288608 | ||||||
| chr4:122288609
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9283-478G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288609 | ||||||
| chr4:122288634
|
A | G | 5 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00609.hp2 HG02523.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.9283-453A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288634 | ||||||
| chr4:122288651
|
CTAAA | C | 171 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(168): Show | 172 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.9283-394_9283-391d others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | INFO_REALIGN_3_PRIME | chr4 | 122288651 | |||||
| chr4:122288651
|
CTAAATAA others(1): Show |
C | 20 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(17): Show | 21 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.9283-398_9283-391d others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | INFO_REALIGN_3_PRIME | chr4 | 122288651 | |||||
| chr4:122288651
|
CTAAATAA others(5): Show |
C | 19 | a0001c0001t0001g0298a0001c0001t0001g0304a0003c0006t0001g0009others(16): Show | 19 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.9283-402_9283-391d others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | INFO_REALIGN_3_PRIME | chr4 | 122288651 | |||||
| chr4:122288651
|
CTAAATAA others(9): Show |
C | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.9283-406_9283-391d others(18): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | INFO_REALIGN_3_PRIME | chr4 | 122288651 | |||||
| chr4:122288702
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9283-385T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288702 | ||||||
| chr4:122288741
|
G | A | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.9283-346G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288741 | ||||||
| chr4:122288742
|
C | T | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.9283-345C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288742 | ||||||
| chr4:122288767
|
A | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9283-320A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288767 | ||||||
| chr4:122288872
|
A | C | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.9283-215A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122288872 | ||||||
| chr4:122289004
|
T | C | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.9283-83T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122289004 | ||||||
| chr4:122289048
|
A | G | 1 | a0001c0002t0001g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.9283-39A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 53/87 | chr4 | 122289048 | ||||||
| chr4:122289214
|
T | C | 1 | a0015c0028t0001g0058 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.9388+22T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289214 | ||||||
| chr4:122289258
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.9388+66C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289258 | ||||||
| chr4:122289288
|
C | T | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.9388+96C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289288 | ||||||
| chr4:122289348
|
C | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9388+156C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289348 | ||||||
| chr4:122289450
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9388+258G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289450 | ||||||
| chr4:122289638
|
A | C | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.9388+446A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289638 | ||||||
| chr4:122289781
|
A | G | 3 | a0001c0002t0001g0076a0001c0002t0001g0097a0001c0002t0001g0161 | 3 | NA18957.hp1 NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.9388+589A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289781 | ||||||
| chr4:122289875
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9388+683G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289875 | ||||||
| chr4:122289915
|
A | G | 332 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(329): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.9388+723A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289915 | ||||||
| chr4:122289990
|
A | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9388+798A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122289990 | ||||||
| chr4:122290021
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9388+829G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290021 | ||||||
| chr4:122290041
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9388+849A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290041 | ||||||
| chr4:122290510
|
A | G | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.9388+1318A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290510 | ||||||
| chr4:122290559
|
G | A | 20 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(17): Show | 20 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.9388+1367G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290559 | ||||||
| chr4:122290585
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9388+1393A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290585 | ||||||
| chr4:122290680
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.9388+1488G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290680 | ||||||
| chr4:122290755
|
C | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9388+1563C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290755 | ||||||
| chr4:122290756
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.9388+1564C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290756 | ||||||
| chr4:122290768
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9388+1576T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290768 | ||||||
| chr4:122290782
|
G | A | 1 | a0001c0009t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.9388+1590G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290782 | ||||||
| chr4:122290786
|
C | CA | 44 | a0001c0001t0001g0156a0001c0001t0001g0172a0001c0001t0001g0296others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.9388+1617dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290786 | |||||
| chr4:122290786
|
C | CAA | 26 | a0001c0001t0001g0299a0001c0001t0001g0323a0001c0001t0001g0324others(23): Show | 26 | HG00558.hp1 HG00735.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.9388+1616_9388+161 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290786 | |||||
| chr4:122290786
|
CAAA | C | 13 | a0001c0007t0001g0238a0001c0007t0001g0240a0001c0007t0001g0241others(10): Show | 13 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.9388+1615_9388+161 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290786 | |||||
| chr4:122290805
|
AAAAAT | A | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.9388+1615_9388+161 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290805 | |||||
| chr4:122290808
|
A | AT | 6 | a0001c0001t0001g0159a0001c0001t0001g0218a0001c0001t0001g0258others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.9388+1616_9388+161 others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290808 | ||||||
| chr4:122290808
|
A | ATAT | 3 | a0001c0001t0001g0251a0001c0001t0001g0289a0001c0001t0003g0260 | 3 | HG01884.hp1 HG01993.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.9388+1616_9388+161 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290808 | ||||||
| chr4:122290808
|
A | T | 1 | a0001c0003t0001g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.9388+1616A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290808 | ||||||
| chr4:122290810
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9388+1618T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290810 | ||||||
| chr4:122290810
|
T | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0289a0001c0001t0003g0260 | 3 | HG01884.hp1 HG01993.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.9388+1618T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290810 | ||||||
| chr4:122290812
|
T | C | 22 | a0001c0001t0001g0159a0001c0001t0001g0189a0001c0001t0001g0209others(19): Show | 23 | HG00597.hp2 HG00673.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.9388+1620T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290812 | ||||||
| chr4:122290812
|
T | TAC | 57 | a0001c0001t0001g0121a0001c0001t0001g0143a0001c0001t0001g0174others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.9388+1656_9388+165 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
T | TACAC | 12 | a0001c0001t0001g0124a0001c0001t0001g0217a0001c0001t0001g0221others(9): Show | 12 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.9388+1654_9388+165 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
T | TACACAC | 8 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0184others(5): Show | 8 | HG02074.hp1 HG02486.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.9388+1652_9388+165 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.9388+1648_9388+165 others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
T | TATACACA others(3): Show |
1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9388+1621_9388+162 others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
TAC | T | 96 | a0001c0001t0004g0175a0001c0002t0001g0002a0001c0002t0001g0008others(93): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.9388+1656_9388+165 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
TACACAC | T | 9 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0007t0001g0238others(6): Show | 9 | HG00639.hp1 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.9388+1652_9388+165 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290812
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9388+1646_9388+165 others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122290812 | |||||
| chr4:122290814
|
C | T | 16 | a0001c0007t0001g0284a0003c0006t0001g0012a0003c0006t0001g0038others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.9388+1622C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290814 | ||||||
| chr4:122290850
|
T | C | 1 | a0001c0003t0001g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.9388+1658T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290850 | ||||||
| chr4:122290859
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.9388+1667A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290859 | ||||||
| chr4:122290864
|
T | C | 2 | a0001c0001t0001g0329a0001c0001t0009g0327 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.9388+1672T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290864 | ||||||
| chr4:122290880
|
A | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9388+1688A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290880 | ||||||
| chr4:122290940
|
C | A | 3 | a0003c0006t0001g0012a0009c0011t0001g0045a0009c0011t0007g0039 | 3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.9388+1748C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122290940 | ||||||
| chr4:122291130
|
T | A | 1 | a0001c0003t0001g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.9388+1938T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291130 | ||||||
| chr4:122291305
|
G | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9388+2113G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291305 | ||||||
| chr4:122291307
|
C | T | 1 | a0001c0038t0005g0285 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.9388+2115C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291307 | ||||||
| chr4:122291372
|
T | G | 1 | a0001c0001t0001g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.9388+2180T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291372 | ||||||
| chr4:122291513
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9388+2321T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291513 | ||||||
| chr4:122291541
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9388+2349A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291541 | ||||||
| chr4:122291697
|
G | C | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.9388+2505G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291697 | ||||||
| chr4:122291835
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9388+2643T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122291835 | ||||||
| chr4:122291966
|
G | GT | 52 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0190others(49): Show | 52 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.9388+2797dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122291966 | |||||
| chr4:122291966
|
G | GTT | 10 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0007t0001g0157others(7): Show | 10 | HG00738.hp2 HG02074.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.9388+2796_9388+279 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122291966 | |||||
| chr4:122291966
|
GT | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(7): Show | 10 | HG01069.hp2 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.9388+2797delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122291966 | |||||
| chr4:122292073
|
C | T | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.9388+2881C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292073 | ||||||
| chr4:122292105
|
G | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.9388+2913G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292105 | ||||||
| chr4:122292214
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.9388+3022G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292214 | ||||||
| chr4:122292247
|
C | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9388+3055C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292247 | ||||||
| chr4:122292314
|
A | G | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.9388+3122A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292314 | ||||||
| chr4:122292455
|
A | G | 2 | a0001c0003t0001g0192a0001c0003t0001g0194 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.9388+3263A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292455 | ||||||
| chr4:122292565
|
C | T | 4 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0169others(1): Show | 4 | HG00735.hp2 HG02148.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.9388+3373C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292565 | ||||||
| chr4:122292791
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.9388+3599C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292791 | ||||||
| chr4:122292796
|
T | C | 3 | a0001c0003t0001g0193a0001c0003t0001g0201a0014c0030t0001g0202 | 3 | HG03834.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.9388+3604T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292796 | ||||||
| chr4:122292812
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.9388+3620A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292812 | ||||||
| chr4:122292913
|
G | T | 1 | a0001c0009t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.9388+3721G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122292913 | ||||||
| chr4:122292958
|
C | CA | 30 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(27): Show | 30 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.9388+3777dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122292958 | |||||
| chr4:122293068
|
G | A | 1 | a0001c0017t0001g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.9388+3876G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293068 | ||||||
| chr4:122293122
|
T | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.9388+3930T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293122 | ||||||
| chr4:122293178
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.9388+3986C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293178 | ||||||
| chr4:122293269
|
C | G | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.9388+4077C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293269 | ||||||
| chr4:122293435
|
C | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9388+4243C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293435 | ||||||
| chr4:122293479
|
A | C | 46 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(43): Show | 47 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.9388+4287A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293479 | ||||||
| chr4:122293680
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9388+4488A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293680 | ||||||
| chr4:122293825
|
C | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9388+4633C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122293825 | ||||||
| chr4:122294026
|
C | T | 1 | a0001c0003t0001g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.9388+4834C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294026 | ||||||
| chr4:122294035
|
C | G | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.9388+4843C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294035 | ||||||
| chr4:122294226
|
C | T | 106 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0174others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.9388+5034C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294226 | ||||||
| chr4:122294301
|
A | G | 64 | a0001c0002t0001g0002a0001c0002t0001g0016a0001c0002t0001g0035others(61): Show | 65 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.9388+5109A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294301 | ||||||
| chr4:122294356
|
T | C | 1 | a0001c0002t0001g0055 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.9388+5164T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294356 | ||||||
| chr4:122294634
|
A | T | 1 | a0001c0002t0001g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.9388+5442A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294634 | ||||||
| chr4:122294643
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.9388+5451C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294643 | ||||||
| chr4:122294687
|
A | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG02071.hp1 NA18940.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.9388+5495A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294687 | ||||||
| chr4:122294993
|
G | C | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.9388+5801G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122294993 | ||||||
| chr4:122295114
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9388+5922A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295114 | ||||||
| chr4:122295275
|
ACT | A | 40 | a0001c0003t0001g0177a0001c0003t0001g0178a0001c0003t0001g0179others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.9389-6023_9389-602 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122295275 | |||||
| chr4:122295281
|
C | A | 1 | a0001c0001t0001g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.9389-6019C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295281 | ||||||
| chr4:122295430
|
C | T | 1 | a0002c0004t0001g0134 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.9389-5870C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295430 | ||||||
| chr4:122295434
|
C | T | 1 | a0001c0002t0001g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.9389-5866C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295434 | ||||||
| chr4:122295456
|
A | C | 1 | a0009c0011t0007g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389-5844A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295456 | ||||||
| chr4:122295493
|
A | G | 1 | a0011c0040t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.9389-5807A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295493 | ||||||
| chr4:122295976
|
G | A | 10 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(7): Show | 10 | HG00639.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.9389-5324G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122295976 | ||||||
| chr4:122296000
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9389-5300G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296000 | ||||||
| chr4:122296092
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.9389-5208C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296092 | ||||||
| chr4:122296410
|
A | G | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.9389-4890A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296410 | ||||||
| chr4:122296668
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9389-4632A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296668 | ||||||
| chr4:122296821
|
A | G | 2 | a0001c0005t0001g0109a0001c0005t0001g0110 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.9389-4479A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296821 | ||||||
| chr4:122296926
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9389-4374G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296926 | ||||||
| chr4:122296979
|
C | G | 1 | a0001c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.9389-4321C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296979 | ||||||
| chr4:122296993
|
T | A | 1 | a0001c0007t0001g0245 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.9389-4307T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122296993 | ||||||
| chr4:122297155
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.9389-4145T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297155 | ||||||
| chr4:122297158
|
A | G | 9 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(6): Show | 9 | HG00280.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.9389-4142A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297158 | ||||||
| chr4:122297280
|
C | T | 32 | a0001c0002t0001g0166a0001c0007t0001g0157a0001c0007t0001g0238others(29): Show | 32 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.9389-4020C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297280 | ||||||
| chr4:122297537
|
C | T | 3 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092 | 3 | NA18947.hp2 NA18955.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.9389-3763C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297537 | ||||||
| chr4:122297790
|
A | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.9389-3510A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297790 | ||||||
| chr4:122297843
|
T | A | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.9389-3457T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297843 | ||||||
| chr4:122297845
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.9389-3455G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297845 | ||||||
| chr4:122297848
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.9389-3452G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122297848 | ||||||
| chr4:122298067
|
AAAAG | A | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0314others(1): Show | 4 | HG03669.hp1 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.9389-3229_9389-322 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122298067 | |||||
| chr4:122298111
|
C | G | 1 | a0001c0001t0001g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9389-3189C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298111 | ||||||
| chr4:122298137
|
A | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0120 | 3 | HG01123.hp1 HG01346.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.9389-3163A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298137 | ||||||
| chr4:122298181
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9389-3119A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298181 | ||||||
| chr4:122298215
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9389-3085T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298215 | ||||||
| chr4:122298258
|
TTG | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9389-3038_9389-303 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122298258 | |||||
| chr4:122298293
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9389-3007A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298293 | ||||||
| chr4:122298518
|
T | A | 1 | a0003c0006t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9389-2782T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298518 | ||||||
| chr4:122298639
|
T | TTACTTCT others(13): Show |
325 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.9389-2660_9389-264 others(24): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122298639 | |||||
| chr4:122298992
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.9389-2308C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298992 | ||||||
| chr4:122298996
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9389-2304T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122298996 | ||||||
| chr4:122299010
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9389-2290G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122299010 | ||||||
| chr4:122299089
|
TTTAA | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9389-2207_9389-220 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122299089 | |||||
| chr4:122299714
|
G | T | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.9389-1586G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122299714 | ||||||
| chr4:122300034
|
C | G | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9389-1266C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122300034 | ||||||
| chr4:122300074
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.9389-1226C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122300074 | ||||||
| chr4:122300410
|
G | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9389-890G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122300410 | ||||||
| chr4:122300500
|
A | G | 1 | a0001c0003t0001g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.9389-800A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122300500 | ||||||
| chr4:122300695
|
T | C | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0318 | 3 | HG00609.hp2 NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.9389-605T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122300695 | ||||||
| chr4:122300918
|
CA | C | 43 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(40): Show | 44 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.9389-367delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122300918 | |||||
| chr4:122301030
|
G | T | 2 | a0003c0006t0001g0013a0009c0011t0001g0112 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.9389-270G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122301030 | ||||||
| chr4:122301242
|
A | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.9389-58A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | chr4 | 122301242 | ||||||
| chr4:122301262
|
T | TA | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9389-27dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122301262 | |||||
| chr4:122301262
|
TA | T | 122 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(119): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.9389-27delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 54/87 | INFO_REALIGN_3_PRIME | chr4 | 122301262 | |||||
| chr4:122301730
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.9486+333C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122301730 | ||||||
| chr4:122301974
|
A | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9486+577A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122301974 | ||||||
| chr4:122301977
|
A | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.9486+580A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122301977 | ||||||
| chr4:122302071
|
A | T | 1 | a0001c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.9486+674A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302071 | ||||||
| chr4:122302207
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.9486+810T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302207 | ||||||
| chr4:122302256
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.9486+859C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302256 | ||||||
| chr4:122302320
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.9486+923C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302320 | ||||||
| chr4:122302747
|
A | T | 1 | a0001c0017t0001g0303 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.9486+1350A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302747 | ||||||
| chr4:122302825
|
G | A | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9486+1428G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302825 | ||||||
| chr4:122302867
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.9486+1470C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302867 | ||||||
| chr4:122302869
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9486+1472A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302869 | ||||||
| chr4:122302877
|
T | C | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.9486+1480T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122302877 | ||||||
| chr4:122303015
|
C | T | 4 | a0005c0010t0001g0297a0005c0010t0001g0305a0005c0010t0001g0307others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.9486+1618C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122303015 | ||||||
| chr4:122303068
|
A | G | 1 | a0003c0006t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.9486+1671A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122303068 | ||||||
| chr4:122303139
|
G | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9487-1659G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122303139 | ||||||
| chr4:122303304
|
G | A | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9487-1494G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122303304 | ||||||
| chr4:122303510
|
T | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9487-1288T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122303510 | ||||||
| chr4:122303704
|
G | A | 1 | a0002c0004t0001g0131 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.9487-1094G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122303704 | ||||||
| chr4:122304200
|
A | G | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.9487-598A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122304200 | ||||||
| chr4:122304507
|
A | G | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9487-291A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122304507 | ||||||
| chr4:122304660
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0155a0002c0004t0001g0128 | 3 | HG02155.hp2 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.9487-138A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 55/87 | chr4 | 122304660 | ||||||
| chr4:122305220
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9672+237G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | chr4 | 122305220 | ||||||
| chr4:122305228
|
T | C | 93 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(90): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.9672+245T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | chr4 | 122305228 | ||||||
| chr4:122305279
|
T | A | 1 | a0002c0004t0001g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.9672+296T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | chr4 | 122305279 | ||||||
| chr4:122305721
|
G | GT | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9673-153dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | INFO_REALIGN_3_PRIME | chr4 | 122305721 | |||||
| chr4:122305746
|
A | G | 1 | a0007c0012t0001g0313 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.9673-131A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | chr4 | 122305746 | ||||||
| chr4:122305755
|
C | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.9673-122C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | chr4 | 122305755 | ||||||
| chr4:122305841
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9673-36T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 56/87 | chr4 | 122305841 | ||||||
| chr4:122306227
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9841+182T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122306227 | ||||||
| chr4:122306541
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.9841+496G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122306541 | ||||||
| chr4:122306616
|
C | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.9841+571C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122306616 | ||||||
| chr4:122306652
|
G | A | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9841+607G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122306652 | ||||||
| chr4:122306652
|
G | C | 31 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(28): Show | 31 | HG00639.hp1 HG00738.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.9841+607G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122306652 | ||||||
| chr4:122306958
|
T | C | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.9841+913T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122306958 | ||||||
| chr4:122307010
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0291 | 2 | NA18943.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.9842-939A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307010 | ||||||
| chr4:122307075
|
TG | T | 108 | a0001c0001t0001g0121a0001c0001t0001g0143a0001c0001t0001g0159others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.9842-871delG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | INFO_REALIGN_3_PRIME | chr4 | 122307075 | |||||
| chr4:122307100
|
G | A | 3 | a0001c0002t0001g0002a0001c0002t0001g0055a0001c0033t0001g0052 | 4 | HG00558.hp2 NA18975.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.9842-849G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307100 | ||||||
| chr4:122307113
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9842-836T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307113 | ||||||
| chr4:122307667
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.9842-282T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307667 | ||||||
| chr4:122307677
|
T | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0019 | 2 | HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.9842-272T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307677 | ||||||
| chr4:122307724
|
C | G | 1 | a0003c0006t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.9842-225C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307724 | ||||||
| chr4:122307757
|
T | C | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | NA18955.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.9842-192T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307757 | ||||||
| chr4:122307933
|
T | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.9842-16T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 57/87 | chr4 | 122307933 | ||||||
| chr4:122308238
|
A | T | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.10053+78A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122308238 | ||||||
| chr4:122308245
|
A | G | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.10053+85A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122308245 | ||||||
| chr4:122308296
|
A | G | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.10053+136A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122308296 | ||||||
| chr4:122308398
|
C | A | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.10053+238C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122308398 | ||||||
| chr4:122308740
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.10054-526C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122308740 | ||||||
| chr4:122309171
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10054-95G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122309171 | ||||||
| chr4:122309224
|
T | G | 1 | a0001c0002t0001g0055 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.10054-42T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 58/87 | chr4 | 122309224 | ||||||
| chr4:122309599
|
C | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.10252+135C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122309599 | ||||||
| chr4:122309637
|
A | C | 1 | a0001c0002t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.10252+173A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122309637 | ||||||
| chr4:122309638
|
G | T | 1 | a0001c0002t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.10252+174G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122309638 | ||||||
| chr4:122309639
|
T | C | 1 | a0001c0002t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.10252+175T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122309639 | ||||||
| chr4:122309793
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10252+329A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122309793 | ||||||
| chr4:122309978
|
G | A | 24 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.10252+514G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122309978 | ||||||
| chr4:122310347
|
G | T | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.10252+883G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122310347 | ||||||
| chr4:122310453
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.10252+989T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122310453 | ||||||
| chr4:122310554
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10252+1090G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122310554 | ||||||
| chr4:122310554
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.10252+1090G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122310554 | ||||||
| chr4:122310758
|
A | C | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.10252+1294A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122310758 | ||||||
| chr4:122310822
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.10252+1358A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122310822 | ||||||
| chr4:122311186
|
G | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10252+1722G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122311186 | ||||||
| chr4:122311474
|
A | G | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.10252+2010A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122311474 | ||||||
| chr4:122311832
|
C | T | 2 | a0002c0004t0001g0129a0002c0004t0001g0154 | 2 | HG02074.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.10253-1796C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122311832 | ||||||
| chr4:122312005
|
A | G | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.10253-1623A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312005 | ||||||
| chr4:122312052
|
T | C | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.10253-1576T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312052 | ||||||
| chr4:122312154
|
G | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.10253-1474G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312154 | ||||||
| chr4:122312498
|
A | G | 16 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.10253-1130A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312498 | ||||||
| chr4:122312613
|
A | AGGTACTA others(3): Show |
39 | a0001c0002t0001g0002a0001c0002t0001g0016a0001c0002t0001g0035others(36): Show | 40 | HG00558.hp2 HG00597.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.10253-1014_10253-1 others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | INFO_REALIGN_3_PRIME | chr4 | 122312613 | |||||
| chr4:122312651
|
A | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10253-977A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312651 | ||||||
| chr4:122312778
|
A | G | 1 | a0001c0003t0001g0201 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.10253-850A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312778 | ||||||
| chr4:122312856
|
A | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.10253-772A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122312856 | ||||||
| chr4:122313026
|
G | A | 4 | a0005c0010t0001g0297a0005c0010t0001g0305a0005c0010t0001g0307others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.10253-602G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122313026 | ||||||
| chr4:122313223
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10253-405A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122313223 | ||||||
| chr4:122313450
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.10253-178C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122313450 | ||||||
| chr4:122313605
|
T | C | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.10253-23T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 59/87 | chr4 | 122313605 | ||||||
| chr4:122313790
|
A | T | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.10312+103A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122313790 | ||||||
| chr4:122313855
|
G | C | 24 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.10312+168G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122313855 | ||||||
| chr4:122313861
|
T | TTA | 18 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(15): Show | 19 | HG00639.hp1 HG00738.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.10312+189_10312+19 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | INFO_REALIGN_3_PRIME | chr4 | 122313861 | |||||
| chr4:122313861
|
T | TTATA | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.10312+187_10312+19 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | INFO_REALIGN_3_PRIME | chr4 | 122313861 | |||||
| chr4:122313861
|
T | TTATATAT others(1): Show |
3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10312+183_10312+19 others(12): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | INFO_REALIGN_3_PRIME | chr4 | 122313861 | |||||
| chr4:122313861
|
TTA | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.10312+189_10312+19 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | INFO_REALIGN_3_PRIME | chr4 | 122313861 | |||||
| chr4:122313913
|
G | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0318 | 2 | NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.10312+226G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122313913 | ||||||
| chr4:122314015
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.10312+328A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314015 | ||||||
| chr4:122314039
|
G | A | 24 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.10312+352G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314039 | ||||||
| chr4:122314222
|
C | T | 1 | a0001c0008t0001g0075 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.10312+535C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314222 | ||||||
| chr4:122314262
|
A | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.10312+575A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314262 | ||||||
| chr4:122314428
|
A | G | 42 | a0001c0001t0001g0222a0001c0003t0001g0177a0001c0003t0001g0178others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.10312+741A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314428 | ||||||
| chr4:122314644
|
C | T | 1 | a0001c0002t0001g0017 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.10313-818C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314644 | ||||||
| chr4:122314692
|
C | T | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.10313-770C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314692 | ||||||
| chr4:122314980
|
C | A | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10313-482C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314980 | ||||||
| chr4:122314981
|
C | G | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10313-481C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122314981 | ||||||
| chr4:122315062
|
T | A | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.10313-400T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 60/87 | chr4 | 122315062 | ||||||
| chr4:122315702
|
C | G | 1 | a0001c0002t0001g0087 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.10539+14C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 61/87 | chr4 | 122315702 | ||||||
| chr4:122315787
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.10539+99T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 61/87 | chr4 | 122315787 | ||||||
| chr4:122316175
|
A | G | 93 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(90): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.10540-173A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 61/87 | chr4 | 122316175 | ||||||
| chr4:122316183
|
T | C | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.10540-165T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 61/87 | chr4 | 122316183 | ||||||
| chr4:122316191
|
CA | C | 3 | a0004c0013t0001g0198a0004c0013t0001g0226a0004c0013t0001g0227 | 3 | HG01123.hp2 HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.10540-155delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 61/87 | INFO_REALIGN_3_PRIME | chr4 | 122316191 | |||||
| chr4:122316549
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp1 | splice_donor_variant&intron_variant | HIGH | c.10740+1G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 62/87 | chr4 | 122316549 | ||||||
| chr4:122316656
|
G | A | 2 | a0001c0003t0001g0192a0001c0003t0001g0194 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.10741-76G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 62/87 | chr4 | 122316656 | ||||||
| chr4:122317079
|
C | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.10871+217C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317079 | ||||||
| chr4:122317098
|
G | A | 4 | a0001c0002t0001g0066a0001c0002t0001g0069a0001c0002t0001g0070others(1): Show | 4 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.10871+236G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317098 | ||||||
| chr4:122317247
|
G | A | 3 | a0001c0003t0001g0228a0001c0003t0001g0229a0001c0003t0001g0274 | 3 | HG00673.hp1 NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.10871+385G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317247 | ||||||
| chr4:122317274
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10871+412G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317274 | ||||||
| chr4:122317332
|
CA | C | 28 | a0001c0001t0001g0187a0001c0001t0001g0300a0001c0001t0001g0301others(25): Show | 29 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.10871+482delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | INFO_REALIGN_3_PRIME | chr4 | 122317332 | |||||
| chr4:122317506
|
G | A | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.10872-641G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317506 | ||||||
| chr4:122317514
|
T | C | 93 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(90): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.10872-633T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317514 | ||||||
| chr4:122317649
|
T | A | 1 | a0001c0032t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.10872-498T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317649 | ||||||
| chr4:122317809
|
T | G | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.10872-338T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 63/87 | chr4 | 122317809 | ||||||
| chr4:122318433
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.10995+163C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318433 | ||||||
| chr4:122318434
|
G | A | 6 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284others(3): Show | 6 | HG02257.hp1 HG02965.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.10995+164G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318434 | ||||||
| chr4:122318557
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.10995+287T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318557 | ||||||
| chr4:122318633
|
G | C | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.10995+363G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318633 | ||||||
| chr4:122318737
|
G | A | 1 | a0003c0006t0001g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.10995+467G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318737 | ||||||
| chr4:122318746
|
A | G | 1 | a0001c0005t0002g0006 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10995+476A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318746 | ||||||
| chr4:122318842
|
C | T | 1 | a0012c0042t0001g0152 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10995+572C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122318842 | ||||||
| chr4:122319276
|
CT | C | 6 | a0001c0001t0001g0187a0001c0002t0001g0016a0001c0002t0001g0035others(3): Show | 6 | HG02165.hp1 NA18941.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.10995+1014delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122319276 | |||||
| chr4:122319464
|
G | A | 37 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.10995+1194G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319464 | ||||||
| chr4:122319539
|
A | AT | 10 | a0001c0001t0001g0102a0001c0001t0001g0277a0001c0001t0001g0314others(7): Show | 10 | HG00280.hp1 HG01978.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.10995+1289dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122319539 | |||||
| chr4:122319539
|
AT | A | 17 | a0001c0001t0001g0145a0001c0001t0001g0183a0001c0001t0001g0317others(14): Show | 17 | HG00558.hp1 HG00639.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.10995+1289delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122319539 | |||||
| chr4:122319539
|
ATT | A | 100 | a0001c0001t0001g0304a0001c0002t0001g0002a0001c0002t0001g0008others(97): Show | 102 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.10995+1288_10995+1 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122319539 | |||||
| chr4:122319635
|
G | A | 10 | a0001c0005t0001g0106a0001c0005t0001g0107a0001c0005t0001g0108others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.10995+1365G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319635 | ||||||
| chr4:122319729
|
C | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10995+1459C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319729 | ||||||
| chr4:122319760
|
T | C | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.10995+1490T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319760 | ||||||
| chr4:122319804
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.10995+1534G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319804 | ||||||
| chr4:122319892
|
G | C | 12 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(9): Show | 12 | HG00280.hp1 HG01175.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.10995+1622G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319892 | ||||||
| chr4:122319900
|
T | C | 1 | a0007c0012t0001g0313 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10995+1630T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122319900 | ||||||
| chr4:122320051
|
A | G | 1 | a0001c0002t0001g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.10995+1781A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320051 | ||||||
| chr4:122320097
|
A | T | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.10995+1827A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320097 | ||||||
| chr4:122320198
|
G | C | 3 | a0001c0003t0001g0193a0001c0003t0001g0201a0014c0030t0001g0202 | 3 | HG03834.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.10995+1928G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320198 | ||||||
| chr4:122320538
|
T | G | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.10995+2268T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320538 | ||||||
| chr4:122320580
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.10995+2310G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320580 | ||||||
| chr4:122320643
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.10995+2373C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320643 | ||||||
| chr4:122320871
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.10995+2601C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320871 | ||||||
| chr4:122320917
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.10995+2647G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122320917 | ||||||
| chr4:122320989
|
CT | C | 8 | a0001c0001t0001g0215a0001c0001t0001g0250a0001c0001t0001g0280others(5): Show | 8 | HG00639.hp2 HG01099.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.10995+2735delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122320989 | |||||
| chr4:122321038
|
T | G | 148 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(145): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.10995+2768T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321038 | ||||||
| chr4:122321077
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10995+2807A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321077 | ||||||
| chr4:122321276
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.10995+3006C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321276 | ||||||
| chr4:122321364
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.10996-3063C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321364 | ||||||
| chr4:122321389
|
TAAGCATA others(6): Show |
T | 1 | a0001c0002t0001g0068 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.10996-3035_10996-3 others(19): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321389 | |||||
| chr4:122321407
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10996-3020C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321407 | ||||||
| chr4:122321542
|
T | C | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.10996-2885T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321542 | ||||||
| chr4:122321606
|
C | A | 1 | a0006c0014t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.10996-2821C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321606 | ||||||
| chr4:122321733
|
T | C | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.10996-2694T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321733 | ||||||
| chr4:122321839
|
T | TG | 324 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.10996-2585dupG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321839 | |||||
| chr4:122321978
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0215 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.10996-2449_10996-2 others(27): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321978 | ||||||
| chr4:122321979
|
A | AT | 7 | a0001c0001t0001g0304a0001c0003t0001g0232a0001c0005t0001g0106others(4): Show | 7 | HG01106.hp2 HG01258.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.10996-2412dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTT | 10 | a0001c0001t0001g0296a0001c0001t0001g0299a0003c0006t0001g0010others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.10996-2414_10996-2 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTT | 7 | a0001c0001t0001g0298a0001c0003t0001g0193a0001c0003t0001g0201others(4): Show | 7 | HG01361.hp2 HG02040.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.10996-2415_10996-2 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(3): Show |
2 | a0001c0037t0001g0103a0018c0039t0001g0233 | 2 | HG00733.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.10996-2421_10996-2 others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0159others(1): Show | 4 | HG03098.hp1 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.10996-2422_10996-2 others(17): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(6): Show |
12 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0001g0262others(9): Show | 12 | HG01069.hp2 HG01975.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.10996-2424_10996-2 others(19): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(7): Show |
21 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0182others(18): Show | 21 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.10996-2425_10996-2 others(20): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(8): Show |
16 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0261others(13): Show | 16 | HG00673.hp1 HG01099.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.10996-2426_10996-2 others(21): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(9): Show |
10 | a0001c0001t0001g0250a0001c0001t0001g0256a0001c0003t0001g0177others(7): Show | 10 | HG00621.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.10996-2427_10996-2 others(22): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(10): Show |
8 | a0001c0001t0001g0187a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | HG01884.hp1 HG02074.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.10996-2428_10996-2 others(23): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(11): Show |
10 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0181others(7): Show | 10 | HG00673.hp2 HG01081.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.10996-2429_10996-2 others(24): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(12): Show |
9 | a0001c0001t0001g0216a0001c0001t0001g0255a0001c0001t0001g0258others(6): Show | 9 | HG00099.hp1 HG00609.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.10996-2430_10996-2 others(25): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(13): Show |
4 | a0001c0001t0001g0217a0001c0001t0003g0278a0001c0003t0001g0178others(1): Show | 4 | HG00280.hp2 HG01978.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.10996-2431_10996-2 others(26): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0218 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.10996-2432_10996-2 others(27): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(15): Show |
1 | a0014c0030t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.10996-2433_10996-2 others(28): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(16): Show |
3 | a0001c0001t0001g0259a0001c0001t0001g0264a0002c0004t0001g0127 | 3 | HG00558.hp1 NA18941.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.10996-2434_10996-2 others(29): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(17): Show |
2 | a0001c0001t0001g0184a0001c0003t0001g0228 | 2 | HG02074.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.10996-2435_10996-2 others(30): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(18): Show |
2 | a0001c0001t0001g0190a0002c0004t0001g0130 | 2 | NA18984.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.10996-2436_10996-2 others(31): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(19): Show |
1 | a0001c0001t0001g0185 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.10996-2437_10996-2 others(32): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(20): Show |
1 | a0001c0003t0001g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.10996-2438_10996-2 others(33): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | ATTTTTTT others(28): Show |
1 | a0001c0001t0001g0208 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.10996-2446_10996-2 others(41): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
A | T | 1 | a0001c0001t0001g0215 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.10996-2448A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122321979 | ||||||
| chr4:122321979
|
AT | A | 19 | a0001c0001t0001g0146a0001c0001t0001g0266a0001c0001t0001g0302others(16): Show | 19 | HG00280.hp1 HG00423.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.10996-2412delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATT | A | 22 | a0001c0001t0001g0156a0001c0001t0001g0300a0001c0001t0001g0301others(19): Show | 23 | HG00609.hp2 HG00735.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.10996-2413_10996-2 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTT | A | 10 | a0001c0001t0001g0291a0001c0001t0001g0312a0001c0003t0001g0213others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.10996-2414_10996-2 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.10996-2421_10996-2 others(16): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.10996-2422_10996-2 others(17): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10996-2423_10996-2 others(18): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(7): Show |
A | 15 | a0001c0001t0001g0145a0001c0001t0001g0188a0001c0001t0001g0207others(12): Show | 15 | HG00738.hp2 HG01346.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.10996-2425_10996-2 others(20): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(8): Show |
A | 89 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(86): Show | 90 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.10996-2426_10996-2 others(21): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(9): Show |
A | 4 | a0001c0002t0001g0053a0001c0002t0001g0063a0001c0002t0001g0076others(1): Show | 4 | HG03704.hp2 NA18957.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.10996-2427_10996-2 others(22): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(13): Show |
A | 1 | a0009c0011t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.10996-2431_10996-2 others(26): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122321979
|
ATTTTTTT others(14): Show |
A | 1 | a0001c0001t0001g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.10996-2432_10996-2 others(27): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122321979 | |||||
| chr4:122322271
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.10996-2156C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122322271 | ||||||
| chr4:122322439
|
A | ATC | 188 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(185): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.10996-1987_10996-1 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122322439 | |||||
| chr4:122322487
|
C | G | 4 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0016t0001g0028others(1): Show | 4 | NA18966.hp2 NA18992.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.10996-1940C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122322487 | ||||||
| chr4:122322534
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.10996-1893C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122322534 | ||||||
| chr4:122322605
|
A | ATGTCTGG others(5): Show |
1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.10996-1822_10996-1 others(18): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122322605 | ||||||
| chr4:122322628
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.10996-1799A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122322628 | ||||||
| chr4:122322910
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.10996-1517A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122322910 | ||||||
| chr4:122323026
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.10996-1401A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122323026 | ||||||
| chr4:122323044
|
C | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.10996-1383C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122323044 | ||||||
| chr4:122323215
|
CTT | C | 34 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0272others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.10996-1210_10996-1 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122323215 | |||||
| chr4:122323225
|
T | A | 1 | a0001c0003t0001g0273 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.10996-1202T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122323225 | ||||||
| chr4:122323440
|
CT | C | 37 | a0001c0001t0001g0218a0001c0001t0001g0304a0001c0002t0001g0162others(34): Show | 38 | HG01106.hp2 HG01243.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.10996-972delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122323440 | |||||
| chr4:122323747
|
ATTAC | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.10996-677_10996-67 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | INFO_REALIGN_3_PRIME | chr4 | 122323747 | |||||
| chr4:122324033
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.10996-394G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122324033 | ||||||
| chr4:122324310
|
C | T | 5 | a0008c0018t0001g0114a0008c0018t0001g0115a0008c0021t0010g0116others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.10996-117C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 64/87 | chr4 | 122324310 | ||||||
| chr4:122324566
|
T | A | 1 | a0003c0006t0001g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.11105+30T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 65/87 | chr4 | 122324566 | ||||||
| chr4:122324872
|
C | CTAG | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.11105+340_11105+34 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 65/87 | INFO_REALIGN_3_PRIME | chr4 | 122324872 | |||||
| chr4:122324953
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11106-277T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 65/87 | chr4 | 122324953 | ||||||
| chr4:122325003
|
G | A | 1 | a0001c0007t0001g0247 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.11106-227G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 65/87 | chr4 | 122325003 | ||||||
| chr4:122325030
|
A | T | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.11106-200A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 65/87 | chr4 | 122325030 | ||||||
| chr4:122325395
|
C | T | 1 | a0001c0002t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.11196+75C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 66/87 | chr4 | 122325395 | ||||||
| chr4:122325432
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.11196+112A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 66/87 | chr4 | 122325432 | ||||||
| chr4:122325553
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11196+233A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 66/87 | chr4 | 122325553 | ||||||
| chr4:122325616
|
A | G | 5 | a0001c0002t0001g0051a0001c0002t0001g0059a0001c0002t0001g0060others(2): Show | 5 | HG01169.hp2 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.11197-239A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 66/87 | chr4 | 122325616 | ||||||
| chr4:122325816
|
G | GT | 11 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(8): Show | 12 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.11197-25dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 66/87 | INFO_REALIGN_3_PRIME | chr4 | 122325816 | |||||
| chr4:122325837
|
C | G | 2 | a0001c0007t0001g0244a0001c0007t0001g0245 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.11197-18C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 66/87 | chr4 | 122325837 | ||||||
| chr4:122325991
|
T | C | 1 | a0005c0010t0001g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.11259+74T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122325991 | ||||||
| chr4:122326079
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11259+162T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122326079 | ||||||
| chr4:122326647
|
T | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11259+730T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122326647 | ||||||
| chr4:122326792
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.11259+875A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122326792 | ||||||
| chr4:122326793
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.11259+876T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122326793 | ||||||
| chr4:122326795
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.11259+878G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122326795 | ||||||
| chr4:122327048
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.11260-1056A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327048 | ||||||
| chr4:122327093
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.11260-1011A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327093 | ||||||
| chr4:122327099
|
G | GTGTTT | 193 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0122others(190): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.11260-974_11260-97 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327099 | |||||
| chr4:122327099
|
G | GTGTTTTG others(3): Show |
80 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0188others(77): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.11260-979_11260-97 others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327099 | |||||
| chr4:122327099
|
G | GTGTTTTG others(8): Show |
30 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0317others(27): Show | 30 | HG00558.hp1 HG00639.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.11260-984_11260-97 others(19): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327099 | |||||
| chr4:122327099
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.11260-1005G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327099 | ||||||
| chr4:122327242
|
CCCCATG | C | 37 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.11260-860_11260-85 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327242 | |||||
| chr4:122327250
|
A | T | 37 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.11260-854A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327250 | ||||||
| chr4:122327328
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11260-776A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327328 | ||||||
| chr4:122327419
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11260-685T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327419 | ||||||
| chr4:122327441
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.11260-663T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327441 | ||||||
| chr4:122327442
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.11260-662A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327442 | ||||||
| chr4:122327447
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.11260-657T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327447 | ||||||
| chr4:122327521
|
ATACAGCA others(4): Show |
A | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.11260-581_11260-57 others(15): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327521 | |||||
| chr4:122327601
|
A | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11260-503A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327601 | ||||||
| chr4:122327607
|
A | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.11260-497A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327607 | ||||||
| chr4:122327649
|
TTTTAAAA others(25): Show |
T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11260-421_11260-39 others(36): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327649 | |||||
| chr4:122327856
|
AAT | A | 106 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(103): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.11260-243_11260-24 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | INFO_REALIGN_3_PRIME | chr4 | 122327856 | |||||
| chr4:122327895
|
T | C | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.11260-209T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122327895 | ||||||
| chr4:122328081
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.11260-23A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 67/87 | chr4 | 122328081 | ||||||
| chr4:122328617
|
G | C | 1 | a0001c0002t0001g0093 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.11513+260G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122328617 | ||||||
| chr4:122328636
|
G | A | 1 | a0001c0003t0001g0290 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.11513+279G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122328636 | ||||||
| chr4:122329163
|
T | C | 2 | a0003c0006t0001g0038a0003c0006t0001g0046 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.11513+806T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329163 | ||||||
| chr4:122329229
|
A | C | 41 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(38): Show | 43 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(40): Show |
intron_variant | MODIFIER | c.11513+872A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329229 | ||||||
| chr4:122329230
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11513+873G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329230 | ||||||
| chr4:122329345
|
A | G | 1 | a0001c0036t0001g0320 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.11513+988A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329345 | ||||||
| chr4:122329358
|
T | A | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.11513+1001T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329358 | ||||||
| chr4:122329373
|
A | G | 1 | a0001c0007t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.11513+1016A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329373 | ||||||
| chr4:122329375
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11513+1018A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329375 | ||||||
| chr4:122329413
|
T | A | 3 | a0001c0005t0001g0109a0001c0005t0001g0110a0001c0019t0001g0003 | 4 | HG01515.hp2 HG01517.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.11513+1056T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329413 | ||||||
| chr4:122329443
|
C | T | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.11513+1086C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329443 | ||||||
| chr4:122329488
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.11513+1131T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329488 | ||||||
| chr4:122329498
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.11513+1141G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329498 | ||||||
| chr4:122329701
|
T | TA | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.11513+1345dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | INFO_REALIGN_3_PRIME | chr4 | 122329701 | |||||
| chr4:122329796
|
C | T | 320 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.11513+1439C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329796 | ||||||
| chr4:122329830
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11513+1473T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329830 | ||||||
| chr4:122329873
|
C | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.11514-1453C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329873 | ||||||
| chr4:122329879
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11514-1447A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122329879 | ||||||
| chr4:122330060
|
G | A | 1 | a0002c0004t0001g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.11514-1266G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330060 | ||||||
| chr4:122330153
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.11514-1173C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330153 | ||||||
| chr4:122330216
|
C | T | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.11514-1110C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330216 | ||||||
| chr4:122330289
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.11514-1037T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330289 | ||||||
| chr4:122330338
|
C | T | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.11514-988C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330338 | ||||||
| chr4:122330452
|
TTTTGG | T | 30 | a0001c0001t0001g0141a0001c0001t0001g0155a0002c0004t0001g0049others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.11514-869_11514-86 others(9): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | INFO_REALIGN_3_PRIME | chr4 | 122330452 | |||||
| chr4:122330552
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.11514-774A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330552 | ||||||
| chr4:122330685
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.11514-641T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330685 | ||||||
| chr4:122330693
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11514-633T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330693 | ||||||
| chr4:122330839
|
GGT | G | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.11514-484_11514-48 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | INFO_REALIGN_3_PRIME | chr4 | 122330839 | |||||
| chr4:122330846
|
AG | A | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.11514-479delG | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330846 | ||||||
| chr4:122330848
|
T | A | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.11514-478T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330848 | ||||||
| chr4:122330978
|
T | G | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.11514-348T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122330978 | ||||||
| chr4:122331053
|
A | G | 2 | a0001c0017t0001g0295a0001c0017t0001g0303 | 2 | HG00735.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.11514-273A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122331053 | ||||||
| chr4:122331249
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.11514-77A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122331249 | ||||||
| chr4:122331283
|
T | C | 2 | a0001c0001t0001g0214a0004c0031t0001g0197 | 2 | HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.11514-43T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122331283 | ||||||
| chr4:122331299
|
T | C | 1 | a0001c0002t0001g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.11514-27T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 68/87 | chr4 | 122331299 | ||||||
| chr4:122331625
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11729+84T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122331625 | ||||||
| chr4:122331706
|
T | C | 1 | a0002c0004t0001g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.11729+165T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122331706 | ||||||
| chr4:122331918
|
G | T | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11729+377G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122331918 | ||||||
| chr4:122332065
|
T | A | 1 | a0003c0006t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.11729+524T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332065 | ||||||
| chr4:122332091
|
TA | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.11729+558delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | INFO_REALIGN_3_PRIME | chr4 | 122332091 | |||||
| chr4:122332115
|
G | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11729+574G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332115 | ||||||
| chr4:122332181
|
G | A | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.11729+640G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332181 | ||||||
| chr4:122332260
|
T | C | 4 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0169others(1): Show | 4 | HG00735.hp2 HG02148.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.11729+719T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332260 | ||||||
| chr4:122332418
|
G | A | 1 | a0001c0005t0001g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.11729+877G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332418 | ||||||
| chr4:122332629
|
C | CT | 134 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0145others(131): Show | 134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.11730-986dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | INFO_REALIGN_3_PRIME | chr4 | 122332629 | |||||
| chr4:122332629
|
C | CTT | 114 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.11730-987_11730-98 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | INFO_REALIGN_3_PRIME | chr4 | 122332629 | |||||
| chr4:122332629
|
C | CTTT | 71 | a0001c0001t0001g0221a0001c0001t0001g0264a0001c0001t0001g0300others(68): Show | 72 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.11730-988_11730-98 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | INFO_REALIGN_3_PRIME | chr4 | 122332629 | |||||
| chr4:122332720
|
T | C | 1 | a0014c0030t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.11730-909T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332720 | ||||||
| chr4:122332768
|
C | T | 6 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.11730-861C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332768 | ||||||
| chr4:122332851
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.11730-778A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332851 | ||||||
| chr4:122332951
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.11730-678G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332951 | ||||||
| chr4:122332953
|
T | C | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.11730-676T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332953 | ||||||
| chr4:122332965
|
A | C | 63 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.11730-664A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332965 | ||||||
| chr4:122332991
|
T | C | 3 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092 | 3 | NA18947.hp2 NA18955.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.11730-638T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122332991 | ||||||
| chr4:122333013
|
G | C | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.11730-616G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333013 | ||||||
| chr4:122333085
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.11730-544A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333085 | ||||||
| chr4:122333092
|
C | T | 92 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.11730-537C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333092 | ||||||
| chr4:122333241
|
C | T | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.11730-388C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333241 | ||||||
| chr4:122333274
|
G | A | 42 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0183others(39): Show | 42 | HG00423.hp1 HG00558.hp2 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.11730-355G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333274 | ||||||
| chr4:122333302
|
G | C | 42 | a0001c0001t0001g0222a0001c0003t0001g0177a0001c0003t0001g0178others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.11730-327G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333302 | ||||||
| chr4:122333441
|
G | C | 1 | a0001c0005t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.11730-188G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333441 | ||||||
| chr4:122333466
|
T | G | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | NA18955.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.11730-163T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | chr4 | 122333466 | ||||||
| chr4:122333606
|
TAAG | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.11730-20_11730-18d others(5): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 69/87 | INFO_REALIGN_3_PRIME | chr4 | 122333606 | |||||
| chr4:122334164
|
G | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.11911-180G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 70/87 | chr4 | 122334164 | ||||||
| chr4:122334164
|
G | T | 5 | a0002c0004t0001g0049a0002c0004t0001g0128a0002c0004t0001g0134others(2): Show | 5 | HG02071.hp2 HG02155.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.11911-180G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 70/87 | chr4 | 122334164 | ||||||
| chr4:122334560
|
T | C | 3 | a0001c0003t0001g0195a0001c0003t0001g0204a0001c0003t0001g0275 | 3 | HG00408.hp1 NA18994.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.12112+15T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122334560 | ||||||
| chr4:122334594
|
G | T | 1 | a0001c0002t0001g0034 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.12112+49G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122334594 | ||||||
| chr4:122334667
|
A | T | 1 | a0003c0006t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12112+122A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122334667 | ||||||
| chr4:122334967
|
C | T | 10 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(7): Show | 11 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.12112+422C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122334967 | ||||||
| chr4:122335010
|
T | C | 59 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(56): Show | 61 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.12112+465T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335010 | ||||||
| chr4:122335012
|
T | C | 8 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299others(5): Show | 8 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.12112+467T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335012 | ||||||
| chr4:122335145
|
C | G | 10 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(7): Show | 11 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.12112+600C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335145 | ||||||
| chr4:122335421
|
G | A | 2 | a0002c0004t0001g0151a0002c0043t0001g0132 | 2 | NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.12113-771G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335421 | ||||||
| chr4:122335466
|
C | G | 24 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.12113-726C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335466 | ||||||
| chr4:122335612
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.12113-580C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335612 | ||||||
| chr4:122335811
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.12113-381C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122335811 | ||||||
| chr4:122336018
|
G | A | 1 | a0001c0002t0001g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.12113-174G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 71/87 | chr4 | 122336018 | ||||||
| chr4:122336409
|
T | C | 24 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.12274+56T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | chr4 | 122336409 | ||||||
| chr4:122336449
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.12274+96A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | chr4 | 122336449 | ||||||
| chr4:122336535
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.12274+182G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | chr4 | 122336535 | ||||||
| chr4:122336560
|
C | G | 2 | a0011c0040t0001g0248a0011c0041t0001g0246 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.12274+207C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | chr4 | 122336560 | ||||||
| chr4:122336593
|
A | ATT | 329 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.12274+241_12274+24 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | INFO_REALIGN_3_PRIME | chr4 | 122336593 | |||||
| chr4:122336658
|
T | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | HG00408.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.12275-223T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | chr4 | 122336658 | ||||||
| chr4:122336776
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.12275-105G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 72/87 | chr4 | 122336776 | ||||||
| chr4:122337228
|
C | G | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.12414+208C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122337228 | ||||||
| chr4:122337388
|
A | G | 1 | a0002c0004t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.12414+368A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122337388 | ||||||
| chr4:122337410
|
A | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.12414+390A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122337410 | ||||||
| chr4:122337587
|
T | C | 1 | a0001c0002t0001g0087 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.12414+567T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122337587 | ||||||
| chr4:122338099
|
T | G | 2 | a0001c0005t0002g0001a0001c0005t0002g0006 | 3 | HG02559.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.12414+1079T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338099 | ||||||
| chr4:122338138
|
ATGAGGGT others(1): Show |
A | 28 | a0002c0004t0001g0049a0002c0004t0001g0127a0002c0004t0001g0128others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.12415-1060_12415-1 others(14): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | INFO_REALIGN_3_PRIME | chr4 | 122338138 | |||||
| chr4:122338150
|
G | C | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | NA18955.hp1 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.12415-1057G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338150 | ||||||
| chr4:122338333
|
C | T | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.12415-874C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338333 | ||||||
| chr4:122338334
|
G | A | 1 | a0001c0005t0002g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.12415-873G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338334 | ||||||
| chr4:122338340
|
G | A | 5 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00609.hp2 HG02523.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.12415-867G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338340 | ||||||
| chr4:122338492
|
A | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.12415-715A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338492 | ||||||
| chr4:122338628
|
C | A | 1 | a0001c0002t0001g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.12415-579C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338628 | ||||||
| chr4:122338760
|
C | T | 2 | a0001c0017t0001g0295a0001c0017t0001g0303 | 2 | HG00735.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.12415-447C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338760 | ||||||
| chr4:122338885
|
T | C | 16 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(13): Show | 16 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.12415-322T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338885 | ||||||
| chr4:122338896
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.12415-311T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338896 | ||||||
| chr4:122338983
|
G | A | 1 | a0001c0027t0001g0072 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.12415-224G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 73/87 | chr4 | 122338983 | ||||||
| chr4:122339613
|
G | A | 323 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0141others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.12616+205G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122339613 | ||||||
| chr4:122339629
|
C | G | 1 | a0002c0004t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.12616+221C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122339629 | ||||||
| chr4:122339858
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.12616+450A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122339858 | ||||||
| chr4:122339907
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12616+499A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122339907 | ||||||
| chr4:122340064
|
G | C | 1 | a0001c0002t0001g0055 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.12616+656G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340064 | ||||||
| chr4:122340067
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0314others(1): Show | 4 | HG03669.hp1 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.12616+659T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340067 | ||||||
| chr4:122340120
|
C | T | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.12616+712C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340120 | ||||||
| chr4:122340186
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0119 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.12616+778G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340186 | ||||||
| chr4:122340298
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.12616+890A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340298 | ||||||
| chr4:122340299
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.12616+891A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340299 | ||||||
| chr4:122340375
|
A | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.12616+967A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340375 | ||||||
| chr4:122340493
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.12616+1085T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340493 | ||||||
| chr4:122340561
|
A | T | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.12616+1153A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340561 | ||||||
| chr4:122340627
|
T | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.12616+1219T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340627 | ||||||
| chr4:122340857
|
G | GA | 38 | a0001c0001t0001g0143a0001c0001t0001g0221a0001c0001t0001g0250others(35): Show | 38 | HG00423.hp1 HG01255.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.12616+1453dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | INFO_REALIGN_3_PRIME | chr4 | 122340857 | |||||
| chr4:122340903
|
A | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0068 | 2 | HG00597.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.12616+1495A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340903 | ||||||
| chr4:122340909
|
C | T | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.12616+1501C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340909 | ||||||
| chr4:122340933
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.12616+1525A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340933 | ||||||
| chr4:122340990
|
ATT | A | 5 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG01081.hp1 HG01081.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.12616+1584_12616+1 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | INFO_REALIGN_3_PRIME | chr4 | 122340990 | |||||
| chr4:122340993
|
T | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG01081.hp2 HG02300.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.12616+1585T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122340993 | ||||||
| chr4:122341070
|
G | T | 10 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(7): Show | 11 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.12616+1662G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341070 | ||||||
| chr4:122341318
|
C | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.12616+1910C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341318 | ||||||
| chr4:122341349
|
T | G | 1 | a0001c0002t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.12616+1941T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341349 | ||||||
| chr4:122341528
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.12617-1882A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341528 | ||||||
| chr4:122341572
|
A | T | 1 | a0001c0008t0001g0075 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.12617-1838A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341572 | ||||||
| chr4:122341734
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.12617-1676T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341734 | ||||||
| chr4:122341805
|
T | C | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.12617-1605T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341805 | ||||||
| chr4:122341875
|
C | T | 4 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | HG00621.hp1 NA18998.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.12617-1535C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122341875 | ||||||
| chr4:122342291
|
T | C | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.12617-1119T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122342291 | ||||||
| chr4:122342338
|
T | TTTTA | 3 | a0001c0001t0001g0207a0001c0001t0001g0289a0001c0023t0001g0249 | 3 | HG01346.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.12617-1048_12617-1 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | INFO_REALIGN_3_PRIME | chr4 | 122342338 | |||||
| chr4:122342362
|
ATTTT | A | 10 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(7): Show | 11 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.12617-1040_12617-1 others(10): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | INFO_REALIGN_3_PRIME | chr4 | 122342362 | |||||
| chr4:122342366
|
T | A | 308 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.12617-1044T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122342366 | ||||||
| chr4:122342370
|
T | A | 1 | a0001c0003t0001g0194 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.12617-1040T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122342370 | ||||||
| chr4:122342516
|
C | T | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.12617-894C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122342516 | ||||||
| chr4:122342544
|
T | G | 1 | a0001c0003t0001g0201 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.12617-866T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122342544 | ||||||
| chr4:122342954
|
C | CT | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.12617-455dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | INFO_REALIGN_3_PRIME | chr4 | 122342954 | |||||
| chr4:122342977
|
C | T | 1 | a0003c0006t0001g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.12617-433C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122342977 | ||||||
| chr4:122343026
|
C | G | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.12617-384C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122343026 | ||||||
| chr4:122343038
|
T | G | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.12617-372T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122343038 | ||||||
| chr4:122343067
|
C | A | 4 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0026others(1): Show | 4 | HG00423.hp2 HG02132.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.12617-343C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122343067 | ||||||
| chr4:122343330
|
T | C | 106 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.12617-80T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 74/87 | chr4 | 122343330 | ||||||
| chr4:122343650
|
A | T | 1 | a0002c0004t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.12817+40A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 75/87 | chr4 | 122343650 | ||||||
| chr4:122343693
|
C | T | 2 | a0001c0002t0001g0053a0001c0002t0001g0054 | 2 | HG02129.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.12817+83C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 75/87 | chr4 | 122343693 | ||||||
| chr4:122343834
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.12817+224C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 75/87 | chr4 | 122343834 | ||||||
| chr4:122343934
|
G | A | 40 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.12817+324G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 75/87 | chr4 | 122343934 | ||||||
| chr4:122344186
|
G | A | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.12818-196G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 75/87 | chr4 | 122344186 | ||||||
| chr4:122344736
|
T | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.12997+175T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122344736 | ||||||
| chr4:122345077
|
A | G | 3 | a0003c0006t0001g0040a0003c0006t0001g0042a0003c0006t0001g0043 | 3 | HG02622.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.12997+516A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345077 | ||||||
| chr4:122345107
|
G | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.12997+546G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345107 | ||||||
| chr4:122345366
|
A | T | 1 | a0001c0005t0001g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.12997+805A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345366 | ||||||
| chr4:122345481
|
A | C | 1 | a0001c0036t0001g0320 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12997+920A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345481 | ||||||
| chr4:122345482
|
G | GTGAACAT others(26): Show |
1 | a0018c0039t0001g0233 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.12997+939_12997+97 others(37): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | INFO_REALIGN_3_PRIME | chr4 | 122345482 | |||||
| chr4:122345590
|
G | C | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.12997+1029G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345590 | ||||||
| chr4:122345597
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.12998-1026G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345597 | ||||||
| chr4:122345637
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.12998-986T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345637 | ||||||
| chr4:122345776
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.12998-847G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345776 | ||||||
| chr4:122345860
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.12998-763A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122345860 | ||||||
| chr4:122346113
|
T | C | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.12998-510T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122346113 | ||||||
| chr4:122346125
|
A | C | 1 | a0001c0002t0001g0073 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.12998-498A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122346125 | ||||||
| chr4:122346172
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.12998-451C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122346172 | ||||||
| chr4:122346177
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.12998-446G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122346177 | ||||||
| chr4:122346357
|
G | C | 1 | a0001c0005t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.12998-266G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | chr4 | 122346357 | ||||||
| chr4:122346527
|
A | ATAATTCA others(6): Show |
1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.12998-91_12998-79d others(15): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 76/87 | INFO_REALIGN_3_PRIME | chr4 | 122346527 | |||||
| chr4:122346781
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.13135+21T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/87 | chr4 | 122346781 | ||||||
| chr4:122346799
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.13135+39C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/87 | chr4 | 122346799 | ||||||
| chr4:122347124
|
C | T | 10 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(7): Show | 11 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.13135+364C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/87 | chr4 | 122347124 | ||||||
| chr4:122347247
|
G | A | 1 | a0011c0041t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.13136-275G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/87 | chr4 | 122347247 | ||||||
| chr4:122347416
|
A | G | 5 | a0008c0018t0001g0114a0008c0018t0001g0115a0008c0021t0010g0116others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.13136-106A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/87 | chr4 | 122347416 | ||||||
| chr4:122347467
|
G | A | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.13136-55G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 77/87 | chr4 | 122347467 | ||||||
| chr4:122347835
|
T | C | 1 | a0001c0003t0001g0273 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.13393+56T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122347835 | ||||||
| chr4:122347899
|
C | CA | 34 | a0001c0001t0001g0184a0001c0001t0001g0207a0001c0001t0001g0289others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.13393+137dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | INFO_REALIGN_3_PRIME | chr4 | 122347899 | |||||
| chr4:122347899
|
CA | C | 52 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0301others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.13393+137delA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | INFO_REALIGN_3_PRIME | chr4 | 122347899 | |||||
| chr4:122347901
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.13393+122A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122347901 | ||||||
| chr4:122347934
|
A | C | 4 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0073others(1): Show | 4 | HG00597.hp1 NA18944.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.13393+155A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122347934 | ||||||
| chr4:122348096
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.13393+317C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122348096 | ||||||
| chr4:122348203
|
G | T | 3 | a0001c0003t0001g0228a0001c0003t0001g0229a0001c0003t0001g0274 | 3 | HG00673.hp1 NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.13394-364G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122348203 | ||||||
| chr4:122348349
|
T | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.13394-218T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122348349 | ||||||
| chr4:122348530
|
A | T | 3 | a0007c0012t0001g0313a0007c0012t0001g0315a0007c0012t0001g0316 | 3 | HG02559.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.13394-37A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 78/87 | chr4 | 122348530 | ||||||
| chr4:122348827
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.13544+110A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 79/87 | chr4 | 122348827 | ||||||
| chr4:122348837
|
C | T | 1 | a0011c0040t0001g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.13544+120C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 79/87 | chr4 | 122348837 | ||||||
| chr4:122348946
|
G | T | 106 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(103): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.13545-212G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 79/87 | chr4 | 122348946 | ||||||
| chr4:122349059
|
C | G | 3 | a0001c0002t0001g0015a0001c0002t0001g0017a0001c0002t0001g0018 | 3 | HG00408.hp2 NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.13545-99C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 79/87 | chr4 | 122349059 | ||||||
| chr4:122349412
|
G | T | 1 | a0001c0001t0001g0314 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.13703-38G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 80/87 | chr4 | 122349412 | ||||||
| chr4:122349721
|
C | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.13895+79C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 81/87 | chr4 | 122349721 | ||||||
| chr4:122349779
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.13896-78C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 81/87 | chr4 | 122349779 | ||||||
| chr4:122349780
|
G | A | 12 | a0003c0006t0001g0012a0003c0006t0001g0038a0003c0006t0001g0040others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.13896-77G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 81/87 | chr4 | 122349780 | ||||||
| chr4:122349820
|
G | A | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.13896-37G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 81/87 | chr4 | 122349820 | ||||||
| chr4:122350122
|
T | A | 1 | a0001c0003t0006g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.14113+48T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350122 | ||||||
| chr4:122350151
|
T | C | 1 | a0003c0006t0001g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.14113+77T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350151 | ||||||
| chr4:122350405
|
G | A | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.14113+331G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350405 | ||||||
| chr4:122350440
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.14113+366T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350440 | ||||||
| chr4:122350471
|
G | A | 1 | a0002c0004t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.14113+397G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350471 | ||||||
| chr4:122350513
|
G | C | 106 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.14113+439G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350513 | ||||||
| chr4:122350651
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.14113+577T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350651 | ||||||
| chr4:122350715
|
A | G | 1 | a0001c0024t0001g0163 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.14113+641A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350715 | ||||||
| chr4:122350773
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14113+699C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350773 | ||||||
| chr4:122350963
|
C | T | 1 | a0001c0002t0001g0027 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.14113+889C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122350963 | ||||||
| chr4:122351236
|
G | C | 2 | a0010c0020t0001g0104a0010c0020t0001g0180 | 2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.14113+1162G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122351236 | ||||||
| chr4:122351242
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.14113+1168A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122351242 | ||||||
| chr4:122351354
|
CTG | C | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.14113+1282_14113+1 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | INFO_REALIGN_3_PRIME | chr4 | 122351354 | |||||
| chr4:122351531
|
C | A | 1 | a0001c0001t0001g0322 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14114-1373C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122351531 | ||||||
| chr4:122351729
|
A | G | 324 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.14114-1175A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122351729 | ||||||
| chr4:122351925
|
C | A | 7 | a0001c0007t0001g0238a0001c0007t0001g0239a0001c0007t0001g0240others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.14114-979C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122351925 | ||||||
| chr4:122352349
|
GT | G | 16 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(13): Show | 16 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.14114-550delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | INFO_REALIGN_3_PRIME | chr4 | 122352349 | |||||
| chr4:122352355
|
C | CT | 37 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0185others(34): Show | 37 | HG00735.hp1 HG01069.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.14114-527dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | INFO_REALIGN_3_PRIME | chr4 | 122352355 | |||||
| chr4:122352355
|
CT | C | 13 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG00099.hp2 HG00558.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.14114-527delT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | INFO_REALIGN_3_PRIME | chr4 | 122352355 | |||||
| chr4:122352356
|
T | C | 16 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(13): Show | 16 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.14114-548T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122352356 | ||||||
| chr4:122352362
|
T | G | 16 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(13): Show | 16 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.14114-542T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122352362 | ||||||
| chr4:122352377
|
T | G | 1 | a0002c0004t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.14114-527T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122352377 | ||||||
| chr4:122352606
|
C | T | 17 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0256others(14): Show | 17 | HG00423.hp1 HG01884.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.14114-298C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122352606 | ||||||
| chr4:122352611
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(2): Show | 5 | HG00280.hp1 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.14114-293C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 82/87 | chr4 | 122352611 | ||||||
| chr4:122353235
|
A | G | 1 | a0001c0003t0001g0292 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.14365+80A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 83/87 | chr4 | 122353235 | ||||||
| chr4:122353388
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.14365+233A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 83/87 | chr4 | 122353388 | ||||||
| chr4:122353435
|
G | A | 1 | a0015c0028t0001g0058 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.14365+280G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 83/87 | chr4 | 122353435 | ||||||
| chr4:122353518
|
T | C | 13 | a0001c0001t0001g0156a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.14366-296T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 83/87 | chr4 | 122353518 | ||||||
| chr4:122353651
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.14366-163A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 83/87 | chr4 | 122353651 | ||||||
| chr4:122354217
|
T | C | 1 | a0004c0013t0001g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.14569+200T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354217 | ||||||
| chr4:122354279
|
A | T | 91 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0014others(88): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.14569+262A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354279 | ||||||
| chr4:122354283
|
T | C | 5 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00609.hp2 HG02523.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.14569+266T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354283 | ||||||
| chr4:122354305
|
G | T | 1 | a0001c0002t0001g0033 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.14569+288G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354305 | ||||||
| chr4:122354381
|
A | G | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.14569+364A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354381 | ||||||
| chr4:122354400
|
C | T | 6 | a0001c0003t0001g0178a0001c0003t0001g0192a0001c0003t0001g0194others(3): Show | 6 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.14569+383C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354400 | ||||||
| chr4:122354476
|
G | GT | 288 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0121others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.14569+470dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122354476 | |||||
| chr4:122354476
|
G | GTT | 15 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(12): Show | 16 | HG01243.hp2 HG01361.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.14569+469_14569+47 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122354476 | |||||
| chr4:122354476
|
G | GTTT | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.14569+468_14569+47 others(7): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122354476 | |||||
| chr4:122354476
|
G | GTTTT | 6 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG02922.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.14569+467_14569+47 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122354476 | |||||
| chr4:122354647
|
T | TA | 17 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.14569+635dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122354647 | |||||
| chr4:122354669
|
C | CT | 14 | a0001c0001t0001g0145a0001c0002t0001g0017a0001c0002t0001g0018others(11): Show | 15 | HG00408.hp2 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.14569+667dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122354669 | |||||
| chr4:122354827
|
C | T | 2 | a0008c0021t0010g0116a0016c0022t0001g0113 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.14569+810C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354827 | ||||||
| chr4:122354839
|
G | C | 1 | a0001c0007t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.14569+822G>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354839 | ||||||
| chr4:122354920
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.14570-876C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122354920 | ||||||
| chr4:122355046
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.14570-750T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355046 | ||||||
| chr4:122355125
|
A | G | 2 | a0001c0002t0001g0033a0001c0003t0001g0193 | 2 | HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.14570-671A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355125 | ||||||
| chr4:122355155
|
G | A | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.14570-641G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355155 | ||||||
| chr4:122355185
|
C | G | 1 | a0001c0002t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14570-611C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355185 | ||||||
| chr4:122355242
|
C | T | 136 | a0001c0001t0001g0145a0001c0002t0001g0002a0001c0002t0001g0008others(133): Show | 139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.14570-554C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355242 | ||||||
| chr4:122355265
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.14570-531T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355265 | ||||||
| chr4:122355347
|
A | T | 1 | a0001c0001t0001g0300 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.14570-449A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355347 | ||||||
| chr4:122355427
|
C | T | 1 | a0001c0002t0001g0100 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.14570-369C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355427 | ||||||
| chr4:122355539
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14570-257A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355539 | ||||||
| chr4:122355596
|
C | CATATGTA others(23): Show |
5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.14570-187_14570-15 others(34): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | INFO_REALIGN_3_PRIME | chr4 | 122355596 | |||||
| chr4:122355625
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14570-171G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 84/87 | chr4 | 122355625 | ||||||
| chr4:122356037
|
C | G | 6 | a0001c0001t0001g0251a0001c0001t0001g0261a0001c0001t0001g0293others(3): Show | 6 | HG01884.hp1 HG01978.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.14764+47C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | chr4 | 122356037 | ||||||
| chr4:122356043
|
A | T | 1 | a0001c0002t0001g0014 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.14764+53A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | chr4 | 122356043 | ||||||
| chr4:122356071
|
G | GT | 9 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(6): Show | 9 | HG00280.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.14764+82dupT | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | INFO_REALIGN_3_PRIME | chr4 | 122356071 | |||||
| chr4:122356101
|
C | A | 1 | a0001c0002t0001g0171 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.14764+111C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | chr4 | 122356101 | ||||||
| chr4:122356121
|
T | C | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.14764+131T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | chr4 | 122356121 | ||||||
| chr4:122356462
|
A | T | 1 | a0001c0002t0008g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.14765-159A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | chr4 | 122356462 | ||||||
| chr4:122356507
|
T | C | 2 | a0001c0002t0001g0085a0001c0002t0001g0162 | 2 | HG03490.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.14765-114T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 85/87 | chr4 | 122356507 | ||||||
| chr4:122356960
|
A | G | 3 | a0001c0007t0001g0157a0001c0007t0001g0283a0001c0007t0001g0284 | 3 | HG02257.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.14899+205A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122356960 | ||||||
| chr4:122357305
|
G | A | 1 | a0001c0016t0001g0029 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.14899+550G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122357305 | ||||||
| chr4:122357405
|
A | G | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.14899+650A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122357405 | ||||||
| chr4:122357568
|
C | CA | 15 | a0001c0001t0001g0121a0001c0001t0001g0311a0001c0005t0001g0105others(12): Show | 16 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.14899+830dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | INFO_REALIGN_3_PRIME | chr4 | 122357568 | |||||
| chr4:122357625
|
T | C | 2 | a0001c0001t0001g0302a0001c0001t0001g0317 | 2 | HG02523.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.14899+870T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122357625 | ||||||
| chr4:122357816
|
T | C | 327 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0122others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.14899+1061T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122357816 | ||||||
| chr4:122357885
|
C | T | 4 | a0001c0001t0001g0289a0004c0013t0001g0198a0004c0013t0001g0226others(1): Show | 4 | HG01123.hp2 HG01361.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.14899+1130C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122357885 | ||||||
| chr4:122358096
|
C | T | 2 | a0007c0012t0001g0315a0007c0012t0001g0316 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.14899+1341C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358096 | ||||||
| chr4:122358102
|
A | G | 4 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | HG00621.hp1 NA18998.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.14899+1347A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358102 | ||||||
| chr4:122358206
|
T | C | 4 | a0001c0005t0002g0001a0001c0005t0002g0005a0001c0005t0002g0006others(1): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.14900-1351T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358206 | ||||||
| chr4:122358360
|
C | G | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.14900-1197C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358360 | ||||||
| chr4:122358479
|
G | A | 4 | a0001c0002t0001g0066a0001c0002t0001g0069a0001c0002t0001g0070others(1): Show | 4 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.14900-1078G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358479 | ||||||
| chr4:122358951
|
A | C | 55 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(52): Show | 57 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.14900-606A>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358951 | ||||||
| chr4:122358970
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.14900-587C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122358970 | ||||||
| chr4:122359039
|
A | T | 1 | a0001c0037t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.14900-518A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122359039 | ||||||
| chr4:122359077
|
T | TA | 15 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(12): Show | 16 | HG02055.hp1 HG02071.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.14900-469dupA | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | INFO_REALIGN_3_PRIME | chr4 | 122359077 | |||||
| chr4:122359077
|
T | TAA | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.14900-470_14900-46 others(6): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | INFO_REALIGN_3_PRIME | chr4 | 122359077 | |||||
| chr4:122359089
|
C | A | 1 | a0008c0021t0010g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.14900-468C>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122359089 | ||||||
| chr4:122359135
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0182 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.14900-422C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122359135 | ||||||
| chr4:122359177
|
T | G | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.14900-380T>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122359177 | ||||||
| chr4:122359548
|
T | C | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.14900-9T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 86/87 | chr4 | 122359548 | ||||||
| chr4:122359904
|
G | A | 1 | a0006c0014t0001g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15065+182G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122359904 | ||||||
| chr4:122360138
|
T | C | 28 | a0001c0002t0001g0008a0001c0002t0001g0014a0001c0002t0001g0015others(25): Show | 28 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.15065+416T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360138 | ||||||
| chr4:122360360
|
T | C | 14 | a0001c0007t0001g0157a0001c0007t0001g0238a0001c0007t0001g0239others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.15065+638T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360360 | ||||||
| chr4:122360602
|
A | G | 1 | a0001c0007t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15065+880A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360602 | ||||||
| chr4:122360660
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG01255.hp1 HG02004.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.15065+938A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360660 | ||||||
| chr4:122360812
|
T | TAA | 42 | a0001c0001t0001g0156a0001c0001t0001g0296a0001c0001t0001g0298others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.15065+1092_15065+1 others(8): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | INFO_REALIGN_3_PRIME | chr4 | 122360812 | |||||
| chr4:122360820
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0037t0001g0103 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.15065+1098A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360820 | ||||||
| chr4:122360822
|
T | A | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.15065+1100T>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360822 | ||||||
| chr4:122360866
|
T | C | 14 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(11): Show | 15 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.15065+1144T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122360866 | ||||||
| chr4:122361170
|
C | G | 1 | a0001c0002t0001g0014 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.15066-861C>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361170 | ||||||
| chr4:122361214
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG01361.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.15066-817A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361214 | ||||||
| chr4:122361269
|
T | C | 5 | a0001c0005t0002g0001a0001c0005t0002g0004a0001c0005t0002g0005others(2): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.15066-762T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361269 | ||||||
| chr4:122361382
|
A | T | 3 | a0008c0018t0001g0114a0008c0018t0001g0115a0017c0035t0001g0142 | 3 | HG02965.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.15066-649A>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361382 | ||||||
| chr4:122361518
|
T | C | 1 | a0001c0002t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.15066-513T>C | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361518 | ||||||
| chr4:122361599
|
C | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.15066-432C>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361599 | ||||||
| chr4:122361600
|
G | A | 2 | a0001c0002t0001g0093a0001c0002t0001g0101 | 2 | HG01069.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.15066-431G>A | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361600 | ||||||
| chr4:122361617
|
G | T | 10 | a0001c0005t0001g0105a0001c0005t0001g0106a0001c0005t0001g0107others(7): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.15066-414G>T | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361617 | ||||||
| chr4:122361823
|
A | G | 1 | a0002c0004t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.15066-208A>G | BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | chr4 | 122361823 | ||||||
| chr4:122362008
|
AAT | A | 97 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0181others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.15066-21_15066-20d others(4): Show |
BLTP1 | ENSG00000138688.17 | transcript | ENST00000679879.1 | protein_coding | 87/87 | INFO_REALIGN_3_PRIME | chr4 | 122362008 |