| geneid | 3360 |
|---|---|
| ensemblid | ENSG00000164270.19 |
| hgncid | 5299 |
| symbol | HTR4 |
| name | 5-hydroxytryptamine receptor 4 |
| refseq_nuc | NM_000870.7 |
| refseq_prot | NP_000861.1 |
| ensembl_nuc | ENST00000377888.8 |
| ensembl_prot | ENSP00000367120.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 148481547 |
| end | 148654527 |
| strand | - |
| ver | v1.2 |
| region | chr5:148481547-148654527 |
| region5000 | chr5:148476547-148659527 |
| regionname0 | HTR4_chr5_148481547_148654527 |
| regionname5000 | HTR4_chr5_148476547_148659527 |
| 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 | 388 | 304 | 84 | 37 | 141 | 10 | 30 | 105 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0002 | 0/0 | 388 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0003 | 0/0 | 388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0004 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1167 | 290 | 74 | 36 | 141 | 10 | 27 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0002 | 0/0 | 1167 | 8 | 8 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0003 | 0/0 | 1167 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0004 | 0/0 | 1167 | 2 | 0 | 1 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0005 | 0/0 | 1167 | 2 | 1 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0006 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0007 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0008 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| c0009 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| 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 | 2170 | 117 | 41 | 17 | 39 | 4 | 14 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0002 | 0/0 | 2170 | 67 | 3 | 6 | 49 | 4 | 5 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0003 | 0/0 | 2170 | 39 | 17 | 1 | 16 | 1 | 4 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0004 | 0/0 | 2170 | 20 | 0 | 0 | 20 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0005 | 0/0 | 2170 | 16 | 1 | 7 | 4 | 0 | 4 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0006 | 0/0 | 2170 | 10 | 2 | 3 | 3 | 0 | 2 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0007 | 0/0 | 2170 | 9 | 0 | 0 | 8 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0008 | 0/0 | 2170 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0009 | 0/0 | 2170 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0010 | 0/0 | 2170 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0011 | 0/0 | 2170 | 3 | 2 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0012 | 0/0 | 2170 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0013 | 0/0 | 2170 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0014 | 0/0 | 2170 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0015 | 0/0 | 2170 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0016 | 0/0 | 2170 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0017 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0018 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0019 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0020 | 0/0 | 2170 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0021 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0022 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0023 | 0/0 | 2170 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0024 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0025 | 0/0 | 2170 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0026 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| t0027 | 0/0 | 2170 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1167 | 290 | 74 | 36 | 141 | 10 | 27 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0002 | 0/0 | 1167 | 8 | 8 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0004 | 0/0 | 1167 | 2 | 0 | 1 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0005 | 0/0 | 1167 | 2 | 1 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0006 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0008 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0002c0003 | 0/0 | 1167 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0003c0009 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0004c0007 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3336 | 112 | 38 | 16 | 39 | 4 | 13 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0002 | 0/0 | 3336 | 66 | 3 | 6 | 48 | 4 | 5 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0003 | 0/0 | 3336 | 34 | 13 | 1 | 16 | 1 | 3 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0004 | 0/0 | 3336 | 20 | 0 | 0 | 20 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0005 | 0/0 | 3336 | 14 | 0 | 7 | 4 | 0 | 3 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0006 | 0/0 | 3336 | 10 | 2 | 3 | 3 | 0 | 2 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0007 | 0/0 | 3336 | 9 | 0 | 0 | 8 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0008 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0009 | 0/0 | 3336 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0010 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0011 | 0/0 | 3336 | 3 | 2 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0012 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0014 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0015 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0016 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0017 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0018 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0020 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0021 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0023 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0024 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0025 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0001t0026 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0002t0001 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0002t0003 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0002t0008 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0004t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0004t0003 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0005t0005 | 0/0 | 3336 | 2 | 1 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0006t0003 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0001c0008t0001 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0002c0003t0013 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0002c0003t0019 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0002c0003t0022 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0003c0009t0027 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| a0004c0007t0002 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | copy fasta | chr5 | 148476547 | 148659527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0010g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0015g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0017g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0018g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0020g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0021g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0023g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0025g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0001t0026g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0002t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0004t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0005t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0005t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0006t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0001c0008t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0002c0003t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0002c0003t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0002c0003t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0002c0003t0022g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0003c0009t0027g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| a0004c0007t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0025 | g0301 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0121 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | FIN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00438 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00544 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01243 | hp1 | a0003 | c0009 | t0027 | g0310 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0240 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0232 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01496 | hp1 | a0001 | c0001 | t0023 | g0143 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01496 | hp2 | a0001 | c0001 | t0011 | g0108 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | IBS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01884 | hp1 | a0001 | c0001 | t0026 | g0186 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0109 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0139 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0012 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02055 | hp2 | a0002 | c0003 | t0013 | g0197 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0039 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0085 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CDX | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0144 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02300 | hp2 | a0001 | c0004 | t0001 | g0262 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02451 | hp1 | a0001 | c0001 | t0024 | g0153 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0208 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0086 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02683 | hp1 | a0001 | c0008 | t0001 | g0158 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0151 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0138 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02735 | hp2 | a0001 | c0005 | t0005 | g0141 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0091 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0081 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02922 | hp1 | a0001 | c0002 | t0008 | g0134 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02965 | hp1 | a0002 | c0003 | t0013 | g0193 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0176 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03041 | hp1 | a0001 | c0006 | t0003 | g0112 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03209 | hp1 | a0002 | c0003 | t0022 | g0101 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0133 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03225 | hp2 | a0002 | c0003 | t0019 | g0120 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0265 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0145 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0058 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03927 | hp1 | a0001 | c0004 | t0003 | g0115 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0132 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18962 | hp2 | a0004 | c0007 | t0002 | g0026 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18964 | hp2 | a0001 | c0001 | t0007 | g0052 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0083 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19043 | hp2 | a0001 | c0001 | t0017 | g0082 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19074 | hp2 | a0001 | c0001 | t0020 | g0125 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0213 | AFR | ASW | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | TSI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | GIH | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG02559 | hp2 | a0001 | c0005 | t0005 | g0146 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0099 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | USA | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0249 | REF | REF | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0283 | REF | REF | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:148483255
|
C | T | 1 | a0002 | 4 | HG02055.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.1115G>A | p.Cys372Tyr | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1628/3336 | 1115/1167 | 372/388 | chr5 | 148483255 | ||
| chr5:148483280
|
A | G | 1 | a0004 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.1090T>C | p.Cys364Arg | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1603/3336 | 1090/1167 | 364/388 | chr5 | 148483280 | ||
| chr5:148550218
|
G | A | 1 | a0003 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.71C>T | p.Thr24Met | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/7 | 584/3336 | 71/1167 | 24/388 | chr5 | 148550218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:148509464
|
A | G | 1 | a0001c0002 | 8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.1068T>C | p.His356His | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1581/3336 | 1068/1167 | 356/388 | chr5 | 148509464 | ||
| chr5:148509548
|
G | A | 1 | a0001c0006 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.984C>T | p.Cys328Cys | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1497/3336 | 984/1167 | 328/388 | chr5 | 148509548 | ||
| chr5:148509590
|
G | A | 1 | a0001c0008 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.942C>T | p.Phe314Phe | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1455/3336 | 942/1167 | 314/388 | chr5 | 148509590 | ||
| chr5:148509785
|
A | G | 3 | a0001c0004a0001c0006a0003c0009 | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.747T>C | p.His249His | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1260/3336 | 747/1167 | 249/388 | chr5 | 148509785 | ||
| chr5:148550177
|
G | A | 1 | a0001c0005 | 2 | HG02559.hp2 HG02735.hp2 |
synonymous_variant | LOW | c.112C>T | p.Leu38Leu | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/7 | 625/3336 | 112/1167 | 38/388 | chr5 | 148550177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:148481738
|
A | G | 1 | a0001c0001t0015 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1465 | chr5 | 148481738 | |||||
| chr5:148482152
|
G | T | 1 | a0001c0001t0025 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1051C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1051 | chr5 | 148482152 | |||||
| chr5:148482193
|
G | C | 6 | a0001c0001t0006a0001c0001t0007a0001c0001t0011others(3): Show | 25 | HG00438.hp1 HG00544.hp2 HG01257.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1010C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1010 | chr5 | 148482193 | |||||
| chr5:148482204
|
G | A | 3 | a0002c0003t0013a0002c0003t0019a0002c0003t0022 | 4 | HG02055.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*999C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 999 | chr5 | 148482204 | |||||
| chr5:148482404
|
T | C | 3 | a0001c0001t0004a0001c0001t0016a0001c0001t0020 | 22 | HG00544.hp1 HG02074.hp2 NA18943.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 799 | chr5 | 148482404 | |||||
| chr5:148482442
|
A | G | 3 | a0001c0001t0012a0001c0001t0017a0001c0001t0018 | 4 | HG01884.hp2 HG02647.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 761 | chr5 | 148482442 | |||||
| chr5:148482609
|
C | G | 1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 594 | chr5 | 148482609 | |||||
| chr5:148482724
|
G | A | 1 | a0001c0001t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 479 | chr5 | 148482724 | |||||
| chr5:148483072
|
C | A | 1 | a0001c0001t0026 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 131 | chr5 | 148483072 | |||||
| chr5:148483098
|
G | A | 1 | a0002c0003t0022 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 105 | chr5 | 148483098 | |||||
| chr5:148654084
|
G | A | 2 | a0001c0001t0008a0001c0002t0008 | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | chr5 | 148654084 | ||||||
| chr5:148654188
|
G | C | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-174C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17174 | chr5 | 148654188 | |||||
| chr5:148654296
|
C | T | 2 | a0001c0001t0009a0001c0001t0024 | 5 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-282G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17282 | chr5 | 148654296 | |||||
| chr5:148654328
|
C | T | 3 | a0001c0001t0005a0001c0001t0023a0001c0005t0005 | 17 | HG01071.hp1 HG01074.hp2 HG01257.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-314G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17314 | chr5 | 148654328 | |||||
| chr5:148654421
|
C | G | 2 | a0001c0001t0010a0001c0001t0017 | 4 | HG02896.hp1 HG02897.hp1 NA19030.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-407G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17407 | chr5 | 148654421 | |||||
| chr5:148654434
|
G | A | 1 | a0003c0009t0027 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-420C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17420 | chr5 | 148654434 | |||||
| chr5:148654450
|
A | G | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(17): Show | 134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
5_prime_UTR_variant | MODIFIER | c.-436T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17436 | chr5 | 148654450 | |||||
| chr5:148654477
|
C | G | 5 | a0001c0001t0002a0001c0001t0007a0001c0001t0015others(2): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-463G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17463 | chr5 | 148654477 | |||||
| chr5:148654482
|
C | G | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-468G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17468 | chr5 | 148654482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:148483471
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0184others(100): Show | 103 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1077-178T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483471 | ||||||
| chr5:148483523
|
T | A | 3 | a0001c0001t0001g0296a0001c0001t0005g0149a0001c0001t0005g0150 | 3 | HG01071.hp1 HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1077-230A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483523 | ||||||
| chr5:148483536
|
C | T | 1 | a0002c0003t0019g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1077-243G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483536 | ||||||
| chr5:148483555
|
C | T | 4 | a0001c0001t0012g0208a0001c0001t0012g0213a0001c0001t0017g0082others(1): Show | 4 | HG01884.hp2 HG02647.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-262G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483555 | ||||||
| chr5:148483797
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0191a0001c0001t0001g0194 | 3 | HG01891.hp1 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-504A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483797 | ||||||
| chr5:148483934
|
ATTAT | A | 216 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0172others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1077-645_1077-642d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | ||||||
| chr5:148483934
|
ATTATTTA others(1): Show |
A | 26 | a0001c0001t0001g0160a0001c0001t0001g0184a0001c0001t0001g0185others(23): Show | 26 | HG00099.hp2 HG01243.hp1 HG02148.hp1 others(23): Show |
intron_variant | MODIFIER | c.1077-649_1077-642d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | ||||||
| chr5:148483934
|
ATTATTTA others(5): Show |
A | 21 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0209others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1077-653_1077-642d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | ||||||
| chr5:148483934
|
ATTATTTA others(9): Show |
A | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0253others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-657_1077-642d others(18): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | ||||||
| chr5:148483934
|
ATTATTTA others(17): Show |
A | 26 | a0001c0001t0004g0157a0001c0001t0004g0162a0001c0001t0004g0165others(23): Show | 26 | HG00544.hp1 HG02055.hp2 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1077-665_1077-642d others(26): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | ||||||
| chr5:148484023
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1077-730C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484023 | ||||||
| chr5:148484091
|
G | T | 1 | a0001c0001t0014g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1077-798C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484091 | ||||||
| chr5:148484234
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1077-941T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484234 | ||||||
| chr5:148484271
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0260a0001c0001t0003g0123 | 3 | NA18974.hp2 NA19006.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1077-978G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484271 | ||||||
| chr5:148484289
|
T | C | 4 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0228others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-996A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484289 | ||||||
| chr5:148484320
|
G | A | 1 | a0001c0001t0016g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1077-1027C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484320 | ||||||
| chr5:148484415
|
A | G | 1 | a0001c0001t0004g0308 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1077-1122T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484415 | ||||||
| chr5:148484547
|
T | A | 22 | a0001c0001t0004g0157a0001c0001t0004g0162a0001c0001t0004g0165others(19): Show | 22 | HG00544.hp1 HG02074.hp2 NA18943.hp1 others(19): Show |
intron_variant | MODIFIER | c.1077-1254A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484547 | ||||||
| chr5:148484603
|
T | C | 22 | a0001c0001t0004g0157a0001c0001t0004g0162a0001c0001t0004g0165others(19): Show | 22 | HG00544.hp1 HG02074.hp2 NA18943.hp1 others(19): Show |
intron_variant | MODIFIER | c.1077-1310A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484603 | ||||||
| chr5:148484609
|
C | G | 1 | a0001c0001t0003g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1077-1316G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484609 | ||||||
| chr5:148484842
|
C | G | 1 | a0001c0002t0008g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1077-1549G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484842 | ||||||
| chr5:148484873
|
C | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-1580G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484873 | ||||||
| chr5:148485074
|
G | A | 3 | a0001c0001t0005g0144a0001c0001t0005g0147a0001c0001t0005g0148 | 3 | HG01952.hp1 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1077-1781C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485074 | ||||||
| chr5:148485496
|
G | C | 131 | a0001c0001t0001g0160a0001c0001t0001g0173a0001c0001t0001g0174others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1077-2203C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485496 | ||||||
| chr5:148485527
|
G | C | 2 | a0001c0001t0002g0043a0001c0001t0005g0139 | 2 | HG01516.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1077-2234C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485527 | ||||||
| chr5:148485565
|
C | T | 17 | a0001c0001t0001g0280a0001c0001t0002g0033a0001c0001t0002g0065others(14): Show | 17 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.1077-2272G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485565 | ||||||
| chr5:148485947
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1077-2654C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485947 | ||||||
| chr5:148486127
|
C | G | 1 | a0001c0001t0002g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1077-2834G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486127 | ||||||
| chr5:148486129
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1077-2836G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486129 | ||||||
| chr5:148486142
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-2849C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486142 | ||||||
| chr5:148486319
|
T | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0184a0001c0001t0001g0185others(102): Show | 105 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1077-3026A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486319 | ||||||
| chr5:148486339
|
C | T | 7 | a0001c0001t0002g0002a0001c0001t0002g0051a0001c0001t0003g0117others(4): Show | 7 | HG02080.hp1 NA18941.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-3046G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486339 | ||||||
| chr5:148486393
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1077-3100C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486393 | ||||||
| chr5:148486437
|
C | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-3144G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486437 | ||||||
| chr5:148486442
|
A | G | 3 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0290 | 3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1077-3149T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486442 | ||||||
| chr5:148486483
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1077-3190C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486483 | ||||||
| chr5:148486692
|
C | A | 1 | a0002c0003t0013g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1077-3399G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486692 | ||||||
| chr5:148486781
|
T | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1077-3488A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486781 | ||||||
| chr5:148486926
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1077-3633G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486926 | ||||||
| chr5:148487102
|
CT | C | 173 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1077-3810delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487102 | ||||||
| chr5:148487144
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1077-3851C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487144 | ||||||
| chr5:148487168
|
GTT | G | 3 | a0001c0001t0003g0092a0001c0001t0009g0156a0001c0001t0012g0213 | 3 | HG02717.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077-3877_1077-387 others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487168 | ||||||
| chr5:148487215
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0288a0001c0001t0004g0244others(1): Show | 4 | NA18943.hp1 NA18945.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-3922C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487215 | ||||||
| chr5:148487232
|
T | A | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077-3939A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487232 | ||||||
| chr5:148487239
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1077-3946T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487239 | ||||||
| chr5:148487347
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077-4054C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487347 | ||||||
| chr5:148487391
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0006g0176 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1077-4098T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487391 | ||||||
| chr5:148487576
|
C | G | 174 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1077-4283G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487576 | ||||||
| chr5:148487673
|
C | CAGAGAGT others(53): Show |
1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077-4381_1077-438 others(64): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487673 | ||||||
| chr5:148487673
|
CAGAGAGC others(23): Show |
C | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-4410_1077-438 others(34): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487673 | ||||||
| chr5:148487916
|
G | T | 167 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1077-4623C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487916 | ||||||
| chr5:148487974
|
G | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-4681C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487974 | ||||||
| chr5:148488206
|
T | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1077-4913A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488206 | ||||||
| chr5:148488221
|
T | C | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-4928A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488221 | ||||||
| chr5:148488284
|
G | T | 62 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077-4991C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488284 | ||||||
| chr5:148488375
|
G | A | 62 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077-5082C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488375 | ||||||
| chr5:148488461
|
T | C | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-5168A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488461 | ||||||
| chr5:148488464
|
T | C | 5 | a0001c0001t0002g0004a0001c0001t0003g0093a0001c0001t0003g0094others(2): Show | 5 | HG00423.hp2 HG00544.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-5171A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488464 | ||||||
| chr5:148488539
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077-5246G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488539 | ||||||
| chr5:148488573
|
A | G | 102 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0189others(99): Show | 102 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077-5280T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488573 | ||||||
| chr5:148488592
|
G | A | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-5299C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488592 | ||||||
| chr5:148488693
|
G | A | 6 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(3): Show | 6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-5400C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488693 | ||||||
| chr5:148488824
|
C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0243 | 2 | NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1077-5531G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488824 | ||||||
| chr5:148488853
|
C | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-5560G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488853 | ||||||
| chr5:148488856
|
A | C | 1 | a0001c0001t0003g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1077-5563T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488856 | ||||||
| chr5:148488902
|
T | C | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-5609A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488902 | ||||||
| chr5:148488950
|
G | A | 15 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1077-5657C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488950 | ||||||
| chr5:148488979
|
C | T | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-5686G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488979 | ||||||
| chr5:148489008
|
CAG | C | 9 | a0001c0001t0001g0195a0001c0001t0001g0215a0001c0001t0001g0264others(6): Show | 9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1077-5717_1077-571 others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489008 | ||||||
| chr5:148489056
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1077-5763C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489056 | ||||||
| chr5:148489276
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-5983T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489276 | ||||||
| chr5:148489308
|
A | T | 101 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0189others(98): Show | 101 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1077-6015T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489308 | ||||||
| chr5:148489380
|
A | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1077-6087T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489380 | ||||||
| chr5:148489432
|
G | T | 6 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(3): Show | 6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-6139C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489432 | ||||||
| chr5:148489557
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1077-6264A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489557 | ||||||
| chr5:148489845
|
C | T | 67 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1077-6552G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489845 | ||||||
| chr5:148489846
|
T | G | 69 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1077-6553A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489846 | ||||||
| chr5:148489946
|
A | G | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-6653T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489946 | ||||||
| chr5:148490146
|
T | TATGTATA | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077-6854_1077-685 others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490146 | ||||||
| chr5:148490317
|
C | T | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077-7024G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490317 | ||||||
| chr5:148490413
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0292 | 2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1077-7120C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490413 | ||||||
| chr5:148490433
|
T | C | 63 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1077-7140A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490433 | ||||||
| chr5:148490514
|
A | T | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077-7221T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490514 | ||||||
| chr5:148490528
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1077-7235G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490528 | ||||||
| chr5:148490554
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1077-7261C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490554 | ||||||
| chr5:148490946
|
G | T | 1 | a0001c0001t0003g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1077-7653C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490946 | ||||||
| chr5:148491201
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1077-7908C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491201 | ||||||
| chr5:148491249
|
C | T | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1077-7956G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491249 | ||||||
| chr5:148491317
|
T | TA | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-8025dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491317 | ||||||
| chr5:148491319
|
T | A | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-8026A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491319 | ||||||
| chr5:148491320
|
A | T | 6 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(3): Show | 6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-8027T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491320 | ||||||
| chr5:148491322
|
A | T | 6 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(3): Show | 6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-8029T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491322 | ||||||
| chr5:148491324
|
T | A | 73 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1077-8031A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491324 | ||||||
| chr5:148491326
|
T | A | 71 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1077-8033A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491326 | ||||||
| chr5:148491328
|
T | A | 64 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1077-8035A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491328 | ||||||
| chr5:148491355
|
A | G | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-8062T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491355 | ||||||
| chr5:148491574
|
G | A | 164 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1077-8281C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491574 | ||||||
| chr5:148491576
|
C | A | 164 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1077-8283G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491576 | ||||||
| chr5:148491636
|
A | T | 166 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1077-8343T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491636 | ||||||
| chr5:148491656
|
C | T | 71 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1077-8363G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491656 | ||||||
| chr5:148491828
|
A | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-8535T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491828 | ||||||
| chr5:148491856
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1077-8563G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491856 | ||||||
| chr5:148491911
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0002g0018 | 2 | HG02258.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1077-8618G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491911 | ||||||
| chr5:148491927
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1077-8634T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491927 | ||||||
| chr5:148491945
|
A | G | 163 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-8652T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491945 | ||||||
| chr5:148491948
|
A | G | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1077-8655T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491948 | ||||||
| chr5:148492144
|
C | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0291a0001c0001t0002g0075others(1): Show | 4 | NA18945.hp1 NA18949.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-8851G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492144 | ||||||
| chr5:148492176
|
C | T | 66 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1077-8883G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492176 | ||||||
| chr5:148492187
|
C | A | 1 | a0001c0001t0007g0073 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1077-8894G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492187 | ||||||
| chr5:148492243
|
A | G | 64 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1077-8950T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492243 | ||||||
| chr5:148492357
|
T | C | 12 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(9): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1077-9064A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492357 | ||||||
| chr5:148492403
|
G | A | 163 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-9110C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492403 | ||||||
| chr5:148492533
|
G | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-9240C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492533 | ||||||
| chr5:148492591
|
T | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-9298A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492591 | ||||||
| chr5:148492849
|
C | T | 3 | a0001c0001t0003g0092a0001c0001t0009g0156a0001c0001t0012g0213 | 3 | HG02717.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077-9556G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492849 | ||||||
| chr5:148492902
|
G | A | 163 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-9609C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492902 | ||||||
| chr5:148493003
|
G | T | 163 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-9710C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493003 | ||||||
| chr5:148493046
|
G | C | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-9753C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493046 | ||||||
| chr5:148493350
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1077-10057C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493350 | ||||||
| chr5:148493659
|
C | T | 1 | a0001c0001t0005g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1077-10366G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493659 | ||||||
| chr5:148493751
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1077-10458C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493751 | ||||||
| chr5:148493796
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1077-10503C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493796 | ||||||
| chr5:148493831
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-10538G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493831 | ||||||
| chr5:148493834
|
T | C | 163 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-10541A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493834 | ||||||
| chr5:148493941
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0005g0137 | 2 | HG02027.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1077-10648A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493941 | ||||||
| chr5:148494097
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1077-10804T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494097 | ||||||
| chr5:148494150
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1077-10857A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494150 | ||||||
| chr5:148494187
|
T | C | 168 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1077-10894A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494187 | ||||||
| chr5:148494206
|
G | A | 6 | a0001c0001t0001g0284a0001c0001t0002g0011a0001c0001t0002g0013others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-10913C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494206 | ||||||
| chr5:148494270
|
G | A | 1 | a0001c0001t0006g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1077-10977C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494270 | ||||||
| chr5:148494989
|
G | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-11696C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494989 | ||||||
| chr5:148494993
|
G | A | 163 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-11700C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494993 | ||||||
| chr5:148495056
|
A | G | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-11763T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495056 | ||||||
| chr5:148495125
|
G | A | 177 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1077-11832C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495125 | ||||||
| chr5:148495160
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077-11867A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495160 | ||||||
| chr5:148495297
|
A | G | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(3): Show | 6 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-12004T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495297 | ||||||
| chr5:148495347
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1077-12054C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495347 | ||||||
| chr5:148495498
|
C | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-12205G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495498 | ||||||
| chr5:148495518
|
G | A | 92 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0189others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1077-12225C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495518 | ||||||
| chr5:148495578
|
G | A | 176 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(173): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1077-12285C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495578 | ||||||
| chr5:148495706
|
T | A | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-12413A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495706 | ||||||
| chr5:148495907
|
G | T | 1 | a0001c0002t0001g0200 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1077-12614C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495907 | ||||||
| chr5:148495912
|
C | T | 3 | a0001c0001t0003g0092a0001c0001t0009g0156a0001c0001t0012g0213 | 3 | HG02717.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077-12619G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495912 | ||||||
| chr5:148496026
|
G | A | 2 | a0001c0002t0001g0200a0001c0002t0003g0086 | 2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1077-12733C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496026 | ||||||
| chr5:148496049
|
G | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1077-12756C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496049 | ||||||
| chr5:148496188
|
A | G | 100 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0189others(97): Show | 100 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1077-12895T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496188 | ||||||
| chr5:148496226
|
C | T | 3 | a0001c0001t0002g0035a0001c0001t0007g0038a0001c0001t0007g0061 | 3 | NA18949.hp1 NA19075.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1077-12933G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496226 | ||||||
| chr5:148496517
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1076+12939T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496517 | ||||||
| chr5:148496664
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1076+12792A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496664 | ||||||
| chr5:148496693
|
G | C | 1 | a0001c0001t0017g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076+12763C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496693 | ||||||
| chr5:148496763
|
G | A | 7 | a0001c0001t0001g0270a0001c0001t0001g0299a0001c0001t0003g0118others(4): Show | 7 | HG00544.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+12693C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496763 | ||||||
| chr5:148496893
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+12563C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496893 | ||||||
| chr5:148496926
|
C | T | 11 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(8): Show | 11 | HG00673.hp1 HG01074.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1076+12530G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496926 | ||||||
| chr5:148496948
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+12508T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496948 | ||||||
| chr5:148497126
|
CA | C | 9 | a0001c0001t0001g0195a0001c0001t0001g0215a0001c0001t0001g0264others(6): Show | 9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076+12329delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497126 | ||||||
| chr5:148497137
|
AT | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+12318delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497137 | ||||||
| chr5:148497165
|
T | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+12291A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497165 | ||||||
| chr5:148497288
|
G | T | 1 | a0001c0001t0003g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1076+12168C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497288 | ||||||
| chr5:148497421
|
A | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+12035T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497421 | ||||||
| chr5:148497562
|
A | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+11894T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497562 | ||||||
| chr5:148497753
|
T | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+11703A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497753 | ||||||
| chr5:148497807
|
C | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+11649G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497807 | ||||||
| chr5:148497887
|
T | C | 22 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1076+11569A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497887 | ||||||
| chr5:148498013
|
T | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+11443A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498013 | ||||||
| chr5:148498092
|
T | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0062 | 2 | NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1076+11364A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498092 | ||||||
| chr5:148498118
|
A | T | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1076+11338T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498118 | ||||||
| chr5:148498161
|
G | A | 167 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1076+11295C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498161 | ||||||
| chr5:148498358
|
T | C | 1 | a0001c0001t0002g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1076+11098A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498358 | ||||||
| chr5:148498432
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0295 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1076+11024G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498432 | ||||||
| chr5:148498462
|
C | G | 8 | a0001c0002t0001g0159a0001c0002t0001g0161a0001c0002t0001g0200others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1076+10994G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498462 | ||||||
| chr5:148498564
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1076+10892G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498564 | ||||||
| chr5:148498577
|
C | G | 3 | a0001c0004t0001g0262a0001c0004t0003g0115a0003c0009t0027g0310 | 3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+10879G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498577 | ||||||
| chr5:148498643
|
G | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10813C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498643 | ||||||
| chr5:148498802
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10654G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498802 | ||||||
| chr5:148498970
|
A | T | 1 | a0001c0001t0003g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1076+10486T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498970 | ||||||
| chr5:148499029
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+10427C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499029 | ||||||
| chr5:148499109
|
G | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10347C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499109 | ||||||
| chr5:148499168
|
T | C | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+10288A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499168 | ||||||
| chr5:148499212
|
T | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076+10244A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499212 | ||||||
| chr5:148499252
|
A | T | 1 | a0001c0001t0002g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1076+10204T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499252 | ||||||
| chr5:148499260
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+10196T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499260 | ||||||
| chr5:148499321
|
G | T | 3 | a0001c0001t0004g0247a0001c0001t0004g0287a0001c0001t0006g0282 | 3 | NA18991.hp2 NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1076+10135C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499321 | ||||||
| chr5:148499427
|
A | AATTT | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10025_1076+10 others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499427 | ||||||
| chr5:148499711
|
G | A | 167 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1076+9745C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499711 | ||||||
| chr5:148499756
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1076+9700C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499756 | ||||||
| chr5:148499853
|
A | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1076+9603T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499853 | ||||||
| chr5:148499893
|
T | C | 63 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1076+9563A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499893 | ||||||
| chr5:148500501
|
C | A | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+8955G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500501 | ||||||
| chr5:148500610
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+8846T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500610 | ||||||
| chr5:148500618
|
A | G | 194 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0178others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1076+8838T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500618 | ||||||
| chr5:148500919
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+8537C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500919 | ||||||
| chr5:148500941
|
T | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0032 | 2 | HG02135.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1076+8515A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500941 | ||||||
| chr5:148501016
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1076+8440A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501016 | ||||||
| chr5:148501159
|
T | C | 1 | a0001c0001t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1076+8297A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501159 | ||||||
| chr5:148501211
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1076+8245G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501211 | ||||||
| chr5:148501530
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1076+7926C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501530 | ||||||
| chr5:148501534
|
A | G | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+7922T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501534 | ||||||
| chr5:148501688
|
A | G | 92 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0189others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1076+7768T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501688 | ||||||
| chr5:148501691
|
A | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+7765T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501691 | ||||||
| chr5:148501900
|
A | G | 1 | a0001c0001t0003g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1076+7556T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501900 | ||||||
| chr5:148501921
|
A | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+7535T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501921 | ||||||
| chr5:148501989
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+7467C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501989 | ||||||
| chr5:148502388
|
T | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+7068A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502388 | ||||||
| chr5:148502402
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0295 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1076+7054G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502402 | ||||||
| chr5:148502468
|
A | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+6988T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502468 | ||||||
| chr5:148502516
|
A | AC | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+6939dupG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502516 | ||||||
| chr5:148502566
|
C | T | 100 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0189others(97): Show | 100 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1076+6890G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502566 | ||||||
| chr5:148502593
|
TC | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+6862delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502593 | ||||||
| chr5:148502907
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+6549T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502907 | ||||||
| chr5:148503006
|
C | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+6450G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503006 | ||||||
| chr5:148503220
|
A | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+6236T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503220 | ||||||
| chr5:148503313
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1076+6143G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503313 | ||||||
| chr5:148503315
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1076+6141T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503315 | ||||||
| chr5:148503319
|
G | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+6137C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503319 | ||||||
| chr5:148503326
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0007g0003 | 2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.1076+6130C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503326 | ||||||
| chr5:148503330
|
C | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+6126G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503330 | ||||||
| chr5:148503332
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1076+6124T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503332 | ||||||
| chr5:148503512
|
C | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+5944G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503512 | ||||||
| chr5:148503563
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1076+5893C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503563 | ||||||
| chr5:148503584
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1076+5872G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503584 | ||||||
| chr5:148503672
|
G | T | 1 | a0001c0001t0024g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1076+5784C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503672 | ||||||
| chr5:148503674
|
G | A | 5 | a0001c0001t0003g0107a0001c0001t0006g0217a0001c0001t0011g0108others(2): Show | 5 | HG01243.hp1 HG01496.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+5782C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503674 | ||||||
| chr5:148503731
|
C | T | 176 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(173): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1076+5725G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503731 | ||||||
| chr5:148503843
|
C | G | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1076+5613G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503843 | ||||||
| chr5:148503862
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+5594T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503862 | ||||||
| chr5:148503976
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1076+5480C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503976 | ||||||
| chr5:148504237
|
G | T | 63 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1076+5219C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504237 | ||||||
| chr5:148504389
|
G | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+5067C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504389 | ||||||
| chr5:148504487
|
T | C | 1 | a0001c0001t0003g0092 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1076+4969A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504487 | ||||||
| chr5:148504570
|
C | T | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4886G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504570 | ||||||
| chr5:148504615
|
C | T | 7 | a0001c0001t0001g0270a0001c0001t0001g0299a0001c0001t0003g0118others(4): Show | 7 | HG00544.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+4841G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504615 | ||||||
| chr5:148504642
|
T | C | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+4814A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504642 | ||||||
| chr5:148504741
|
C | G | 2 | a0001c0001t0001g0305a0001c0001t0003g0114 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1076+4715G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504741 | ||||||
| chr5:148504741
|
C | T | 1 | a0001c0001t0003g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1076+4715G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504741 | ||||||
| chr5:148504788
|
G | A | 3 | a0001c0004t0001g0262a0001c0004t0003g0115a0003c0009t0027g0310 | 3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+4668C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504788 | ||||||
| chr5:148504792
|
T | C | 36 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0177others(33): Show | 36 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1076+4664A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504792 | ||||||
| chr5:148504820
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+4636G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504820 | ||||||
| chr5:148504841
|
T | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+4615A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504841 | ||||||
| chr5:148504863
|
C | T | 166 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+4593G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504863 | ||||||
| chr5:148504871
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1076+4585G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504871 | ||||||
| chr5:148504872
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1076+4584C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504872 | ||||||
| chr5:148505048
|
G | A | 1 | a0001c0005t0005g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1076+4408C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505048 | ||||||
| chr5:148505105
|
C | T | 166 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+4351G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505105 | ||||||
| chr5:148505235
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0295 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1076+4221G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505235 | ||||||
| chr5:148505417
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+4039G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505417 | ||||||
| chr5:148505427
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+4029C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505427 | ||||||
| chr5:148505496
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0192 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1076+3960G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505496 | ||||||
| chr5:148505505
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0192 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1076+3951C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505505 | ||||||
| chr5:148505540
|
A | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+3916T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505540 | ||||||
| chr5:148505623
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0212a0001c0001t0001g0220others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+3833G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505623 | ||||||
| chr5:148505628
|
C | T | 7 | a0001c0002t0001g0159a0001c0002t0001g0161a0001c0002t0001g0200others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+3828G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505628 | ||||||
| chr5:148505645
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1076+3811A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505645 | ||||||
| chr5:148505663
|
A | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0062 | 2 | NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1076+3793T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505663 | ||||||
| chr5:148505731
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1076+3725T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505731 | ||||||
| chr5:148505911
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0292 | 2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1076+3545T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505911 | ||||||
| chr5:148505929
|
G | A | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+3527C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505929 | ||||||
| chr5:148505930
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1076+3526G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505930 | ||||||
| chr5:148505953
|
G | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+3503C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505953 | ||||||
| chr5:148505955
|
A | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+3501T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505955 | ||||||
| chr5:148506002
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+3454G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506002 | ||||||
| chr5:148506098
|
G | A | 1 | a0001c0001t0020g0125 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1076+3358C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506098 | ||||||
| chr5:148506108
|
A | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1076+3348T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506108 | ||||||
| chr5:148506129
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+3327G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506129 | ||||||
| chr5:148506160
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1076+3296A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506160 | ||||||
| chr5:148506239
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1076+3217A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506239 | ||||||
| chr5:148506340
|
G | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+3116C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506340 | ||||||
| chr5:148506360
|
T | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+3096A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506360 | ||||||
| chr5:148506419
|
C | T | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+3037G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506419 | ||||||
| chr5:148506434
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+3022C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506434 | ||||||
| chr5:148506442
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1076+3014G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506442 | ||||||
| chr5:148506448
|
G | A | 166 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+3008C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506448 | ||||||
| chr5:148506454
|
T | G | 61 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1076+3002A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506454 | ||||||
| chr5:148506486
|
C | T | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+2970G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506486 | ||||||
| chr5:148506496
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1076+2960G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506496 | ||||||
| chr5:148506545
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0180 | 3 | NA18994.hp1 NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1076+2911G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506545 | ||||||
| chr5:148506594
|
G | A | 166 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+2862C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506594 | ||||||
| chr5:148506608
|
T | G | 4 | a0001c0001t0001g0182a0001c0001t0002g0036a0001c0001t0002g0053others(1): Show | 4 | HG02738.hp2 NA18951.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+2848A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506608 | ||||||
| chr5:148506702
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1076+2754T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506702 | ||||||
| chr5:148506804
|
C | G | 166 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+2652G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506804 | ||||||
| chr5:148506994
|
T | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+2462A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506994 | ||||||
| chr5:148507040
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+2416G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507040 | ||||||
| chr5:148507113
|
T | G | 1 | a0001c0001t0001g0256 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1076+2343A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507113 | ||||||
| chr5:148507138
|
T | C | 22 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1076+2318A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507138 | ||||||
| chr5:148507202
|
G | A | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1076+2254C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507202 | ||||||
| chr5:148507213
|
C | T | 193 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1076+2243G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507213 | ||||||
| chr5:148507267
|
C | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+2189G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507267 | ||||||
| chr5:148507384
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+2072C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507384 | ||||||
| chr5:148507388
|
G | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+2068C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507388 | ||||||
| chr5:148507478
|
G | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+1978C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507478 | ||||||
| chr5:148507488
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+1968G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507488 | ||||||
| chr5:148507489
|
G | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076+1967C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507489 | ||||||
| chr5:148507504
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+1952G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507504 | ||||||
| chr5:148507577
|
CA | C | 180 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(177): Show | 180 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1076+1878delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507577 | ||||||
| chr5:148507907
|
A | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+1549T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507907 | ||||||
| chr5:148508025
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1076+1431A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508025 | ||||||
| chr5:148508122
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1076+1334T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508122 | ||||||
| chr5:148508186
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+1270C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508186 | ||||||
| chr5:148508314
|
T | C | 3 | a0001c0004t0001g0262a0001c0004t0003g0115a0003c0009t0027g0310 | 3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+1142A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508314 | ||||||
| chr5:148508409
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1076+1047T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508409 | ||||||
| chr5:148508533
|
A | G | 2 | a0001c0001t0007g0041a0001c0001t0007g0073 | 2 | NA18957.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1076+923T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508533 | ||||||
| chr5:148508536
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1076+920C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508536 | ||||||
| chr5:148508708
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1076+748T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508708 | ||||||
| chr5:148508710
|
T | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+746A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508710 | ||||||
| chr5:148508801
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1076+655A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508801 | ||||||
| chr5:148508802
|
A | G | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1076+654T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508802 | ||||||
| chr5:148508921
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+535C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508921 | ||||||
| chr5:148509032
|
A | G | 1 | a0001c0001t0007g0031 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1076+424T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509032 | ||||||
| chr5:148509104
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+352G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509104 | ||||||
| chr5:148509185
|
T | A | 1 | a0001c0001t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1076+271A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509185 | ||||||
| chr5:148509202
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1076+254C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509202 | ||||||
| chr5:148509276
|
TCCAGAGC others(12): Show |
T | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1076+161_1076+179d others(21): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509276 | ||||||
| chr5:148510060
|
A | G | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.508-36T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510060 | ||||||
| chr5:148510114
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-90C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510114 | ||||||
| chr5:148510139
|
A | G | 37 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0184others(34): Show | 37 | HG00738.hp2 HG01167.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.508-115T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510139 | ||||||
| chr5:148510180
|
A | G | 99 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(96): Show | 99 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.508-156T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510180 | ||||||
| chr5:148510494
|
A | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-470T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510494 | ||||||
| chr5:148510561
|
C | T | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.508-537G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510561 | ||||||
| chr5:148510693
|
T | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-669A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510693 | ||||||
| chr5:148510697
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-673G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510697 | ||||||
| chr5:148510722
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-698G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510722 | ||||||
| chr5:148510727
|
G | A | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-703C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510727 | ||||||
| chr5:148510790
|
ATAACACA others(3): Show |
A | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.508-776_508-767del others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510790 | ||||||
| chr5:148510941
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.508-917A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510941 | ||||||
| chr5:148510982
|
C | A | 5 | a0001c0001t0001g0248a0001c0001t0006g0223a0001c0001t0006g0232others(2): Show | 5 | HG01257.hp1 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-958G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510982 | ||||||
| chr5:148511173
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1149G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511173 | ||||||
| chr5:148511174
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.508-1150C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511174 | ||||||
| chr5:148511198
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1174C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511198 | ||||||
| chr5:148511347
|
C | T | 1 | a0001c0001t0002g0006 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.508-1323G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511347 | ||||||
| chr5:148511437
|
C | CTTTAA | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1418_508-1414d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511437 | ||||||
| chr5:148511619
|
T | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-1595A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TGTGTGTG others(6): Show |
2 | a0001c0001t0002g0047a0001c0001t0005g0138 | 2 | HG02698.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.508-1596_508-1595i others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTG | 36 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(33): Show | 36 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.508-1597_508-1596d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTG | 14 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0187others(11): Show | 14 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-1599_508-1596d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTGTG | 8 | a0001c0001t0001g0163a0001c0001t0001g0215a0001c0001t0001g0264others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-1601_508-1596d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0005g0145 | 3 | HG02976.hp2 HG03669.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.508-1603_508-1596d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTGTGT others(3): Show |
11 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0309others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-1605_508-1596d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTGTGT others(5): Show |
25 | a0001c0001t0001g0185a0001c0001t0001g0242a0001c0001t0001g0306others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.508-1607_508-1596d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTGTGT others(7): Show |
21 | a0001c0001t0001g0202a0001c0001t0001g0241a0001c0001t0001g0260others(18): Show | 21 | HG00408.hp1 HG02056.hp1 HG02895.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-1609_508-1596d others(16): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0263a0001c0001t0002g0037a0001c0001t0002g0050others(1): Show | 4 | HG00621.hp2 HG03225.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1611_508-1596d others(18): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
TTG | T | 5 | a0001c0001t0001g0239a0001c0001t0001g0248a0001c0001t0002g0033others(2): Show | 5 | HG02132.hp2 HG02735.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-1597_508-1596d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511619
|
TTGTG | T | 3 | a0001c0001t0001g0181a0001c0001t0002g0045a0001c0001t0003g0089 | 3 | HG02056.hp2 NA18522.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.508-1599_508-1596d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | ||||||
| chr5:148511646
|
T | C | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-1622A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511646 | ||||||
| chr5:148511647
|
G | GTGTGTGT others(5): Show |
1 | a0001c0002t0003g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508-1635_508-1624d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511647 | ||||||
| chr5:148511701
|
G | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-1677C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511701 | ||||||
| chr5:148511846
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.508-1822A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511846 | ||||||
| chr5:148511851
|
G | A | 22 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-1827C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511851 | ||||||
| chr5:148511976
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.508-1952C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511976 | ||||||
| chr5:148512067
|
C | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-2043G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512067 | ||||||
| chr5:148512072
|
G | A | 1 | a0001c0001t0005g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.508-2048C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512072 | ||||||
| chr5:148512369
|
T | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-2345A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512369 | ||||||
| chr5:148512411
|
T | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-2387A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512411 | ||||||
| chr5:148512441
|
CTCTT | C | 4 | a0001c0001t0003g0107a0001c0001t0006g0217a0001c0001t0011g0108others(1): Show | 4 | HG01496.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-2421_508-2418d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512441 | ||||||
| chr5:148512581
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508-2557G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512581 | ||||||
| chr5:148512619
|
T | C | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.508-2595A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512619 | ||||||
| chr5:148512657
|
G | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-2633C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512657 | ||||||
| chr5:148512661
|
T | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-2637A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512661 | ||||||
| chr5:148512718
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.508-2694C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512718 | ||||||
| chr5:148512826
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.508-2802C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512826 | ||||||
| chr5:148512967
|
C | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-2943G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512967 | ||||||
| chr5:148513011
|
T | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-2987A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513011 | ||||||
| chr5:148513040
|
C | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-3016G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513040 | ||||||
| chr5:148513065
|
T | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(6): Show | 9 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-3041A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513065 | ||||||
| chr5:148513136
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0294 | 2 | HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-3112C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513136 | ||||||
| chr5:148513415
|
C | T | 1 | a0001c0001t0006g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-3391G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513415 | ||||||
| chr5:148513469
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.508-3445C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513469 | ||||||
| chr5:148513685
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.508-3661T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513685 | ||||||
| chr5:148513712
|
T | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3688A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513712 | ||||||
| chr5:148513815
|
C | G | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.508-3791G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513815 | ||||||
| chr5:148513864
|
C | T | 1 | a0001c0001t0002g0005 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.508-3840G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513864 | ||||||
| chr5:148513870
|
C | T | 99 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(96): Show | 99 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.508-3846G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513870 | ||||||
| chr5:148514156
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.508-4132T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514156 | ||||||
| chr5:148514246
|
T | C | 175 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.508-4222A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514246 | ||||||
| chr5:148514566
|
A | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-4542T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514566 | ||||||
| chr5:148514596
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.508-4572A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514596 | ||||||
| chr5:148514679
|
G | A | 22 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-4655C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514679 | ||||||
| chr5:148514760
|
A | C | 1 | a0001c0001t0002g0025 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.508-4736T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514760 | ||||||
| chr5:148514858
|
A | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-4834T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514858 | ||||||
| chr5:148514931
|
C | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0044a0001c0001t0002g0046 | 3 | HG01928.hp2 HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.508-4907G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514931 | ||||||
| chr5:148515073
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.508-5049T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515073 | ||||||
| chr5:148515142
|
G | A | 165 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.508-5118C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515142 | ||||||
| chr5:148515157
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(1): Show | 4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5133G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515157 | ||||||
| chr5:148515316
|
A | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5292T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515316 | ||||||
| chr5:148515385
|
C | T | 300 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(297): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.508-5361G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515385 | ||||||
| chr5:148515389
|
C | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5365G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515389 | ||||||
| chr5:148515487
|
T | G | 60 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.508-5463A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515487 | ||||||
| chr5:148515526
|
A | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(1): Show | 4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5502T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515526 | ||||||
| chr5:148515556
|
G | T | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.508-5532C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515556 | ||||||
| chr5:148515575
|
G | T | 165 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.508-5551C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515575 | ||||||
| chr5:148515690
|
T | A | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.508-5666A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515690 | ||||||
| chr5:148515720
|
C | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-5696G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515720 | ||||||
| chr5:148515754
|
A | AT | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.508-5731dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515754 | ||||||
| chr5:148515791
|
G | A | 1 | a0001c0001t0003g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-5767C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515791 | ||||||
| chr5:148515818
|
G | GT | 3 | a0001c0004t0001g0262a0001c0004t0003g0115a0003c0009t0027g0310 | 3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.508-5795dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515818 | ||||||
| chr5:148515920
|
CTGAA | C | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5900_508-5897d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515920 | ||||||
| chr5:148515931
|
T | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5907A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515931 | ||||||
| chr5:148515985
|
C | CAT | 60 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.508-5963_508-5962d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515985 | ||||||
| chr5:148516059
|
A | T | 1 | a0001c0004t0001g0262 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.508-6035T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516059 | ||||||
| chr5:148516312
|
C | CT | 30 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0182others(27): Show | 30 | HG00741.hp1 HG02145.hp1 HG02572.hp1 others(27): Show |
intron_variant | MODIFIER | c.508-6289dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516312 | ||||||
| chr5:148516312
|
CT | C | 68 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.508-6289delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516312 | ||||||
| chr5:148516312
|
CTT | C | 7 | a0001c0001t0002g0011a0001c0001t0002g0015a0001c0001t0002g0033others(4): Show | 7 | HG00323.hp1 HG02738.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-6290_508-6289d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516312 | ||||||
| chr5:148516345
|
G | A | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6321C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516345 | ||||||
| chr5:148516376
|
A | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-6352T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516376 | ||||||
| chr5:148516389
|
G | A | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-6365C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516389 | ||||||
| chr5:148516422
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.508-6398G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516422 | ||||||
| chr5:148516465
|
A | G | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6441T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516465 | ||||||
| chr5:148516535
|
G | T | 4 | a0001c0004t0001g0262a0001c0004t0003g0115a0001c0006t0003g0112others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6511C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516535 | ||||||
| chr5:148516564
|
C | T | 1 | a0001c0001t0012g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.508-6540G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516564 | ||||||
| chr5:148516597
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-6573G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516597 | ||||||
| chr5:148516598
|
G | A | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.508-6574C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516598 | ||||||
| chr5:148516627
|
C | CT | 10 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(7): Show | 10 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+6565dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | ||||||
| chr5:148516627
|
C | CTT | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+6564_507+6565d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | ||||||
| chr5:148516627
|
C | CTTTTT | 8 | a0001c0002t0001g0159a0001c0002t0001g0161a0001c0002t0001g0200others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+6561_507+6565d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | ||||||
| chr5:148516627
|
C | CTTTTTT | 81 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.507+6560_507+6565d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | ||||||
| chr5:148516664
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+6529G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516664 | ||||||
| chr5:148516745
|
G | A | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.507+6448C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516745 | ||||||
| chr5:148516761
|
T | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+6432A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516761 | ||||||
| chr5:148516971
|
G | A | 63 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.507+6222C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516971 | ||||||
| chr5:148517280
|
C | T | 1 | a0001c0002t0003g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.507+5913G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517280 | ||||||
| chr5:148517391
|
G | A | 11 | a0001c0001t0001g0195a0001c0001t0001g0215a0001c0001t0001g0264others(8): Show | 11 | HG01516.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+5802C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517391 | ||||||
| chr5:148517404
|
A | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0261others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+5789T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517404 | ||||||
| chr5:148517598
|
G | A | 174 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.507+5595C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517598 | ||||||
| chr5:148517635
|
CAAAAA | C | 169 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.507+5553_507+5557d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517635 | ||||||
| chr5:148517746
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+5447C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517746 | ||||||
| chr5:148517767
|
T | C | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.507+5426A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517767 | ||||||
| chr5:148517874
|
A | G | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+5319T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517874 | ||||||
| chr5:148517916
|
C | T | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.507+5277G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517916 | ||||||
| chr5:148518349
|
C | T | 5 | a0001c0001t0003g0107a0001c0001t0006g0217a0001c0001t0011g0108others(2): Show | 5 | HG01496.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+4844G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518349 | ||||||
| chr5:148518471
|
G | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0192 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.507+4722C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518471 | ||||||
| chr5:148518575
|
C | A | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.507+4618G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518575 | ||||||
| chr5:148518585
|
A | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0294 | 2 | HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.507+4608T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518585 | ||||||
| chr5:148518608
|
C | G | 1 | a0001c0001t0006g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.507+4585G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518608 | ||||||
| chr5:148518637
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.507+4556A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518637 | ||||||
| chr5:148518828
|
A | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+4365T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518828 | ||||||
| chr5:148519076
|
T | C | 1 | a0001c0001t0002g0005 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.507+4117A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519076 | ||||||
| chr5:148519126
|
G | A | 63 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.507+4067C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519126 | ||||||
| chr5:148519262
|
G | T | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+3931C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519262 | ||||||
| chr5:148519327
|
C | A | 8 | a0001c0002t0001g0159a0001c0002t0001g0161a0001c0002t0001g0200others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+3866G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519327 | ||||||
| chr5:148519629
|
T | G | 175 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.507+3564A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519629 | ||||||
| chr5:148519669
|
T | C | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0266 | 3 | HG01192.hp1 HG01891.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.507+3524A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519669 | ||||||
| chr5:148519785
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.507+3408G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519785 | ||||||
| chr5:148519826
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.507+3367T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519826 | ||||||
| chr5:148519882
|
G | T | 1 | a0001c0001t0003g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.507+3311C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519882 | ||||||
| chr5:148519962
|
T | A | 10 | a0001c0001t0001g0164a0001c0001t0004g0162a0001c0001t0004g0165others(7): Show | 10 | NA18947.hp2 NA18962.hp1 NA18963.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+3231A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519962 | ||||||
| chr5:148519974
|
A | G | 79 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.507+3219T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519974 | ||||||
| chr5:148520049
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.507+3144A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148520049 | ||||||
| chr5:148520318
|
G | A | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+2875C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148520318 | ||||||
| chr5:148520452
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+2741G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148520452 | ||||||
| chr5:148521121
|
G | A | 4 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+2072C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521121 | ||||||
| chr5:148521376
|
A | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+1817T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521376 | ||||||
| chr5:148521479
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.507+1714A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521479 | ||||||
| chr5:148521578
|
TC | T | 61 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.507+1614delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521578 | ||||||
| chr5:148521630
|
C | T | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+1563G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521630 | ||||||
| chr5:148521938
|
C | A | 2 | a0001c0001t0001g0297a0001c0001t0005g0139 | 2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.507+1255G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521938 | ||||||
| chr5:148522052
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.507+1141C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522052 | ||||||
| chr5:148522109
|
G | A | 2 | a0001c0001t0002g0068a0001c0001t0006g0265 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.507+1084C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522109 | ||||||
| chr5:148522206
|
T | G | 1 | a0001c0001t0002g0054 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.507+987A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522206 | ||||||
| chr5:148522268
|
A | T | 1 | a0001c0001t0002g0055 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.507+925T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522268 | ||||||
| chr5:148522269
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.507+924T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522269 | ||||||
| chr5:148522272
|
A | T | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+921T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522272 | ||||||
| chr5:148522323
|
C | T | 92 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.507+870G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522323 | ||||||
| chr5:148522716
|
C | G | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+477G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522716 | ||||||
| chr5:148522756
|
T | C | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+437A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522756 | ||||||
| chr5:148522765
|
T | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+428A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522765 | ||||||
| chr5:148522824
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.507+369G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522824 | ||||||
| chr5:148522982
|
G | A | 1 | a0001c0001t0003g0124 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.507+211C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522982 | ||||||
| chr5:148523000
|
G | C | 2 | a0001c0001t0001g0297a0001c0001t0005g0139 | 2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.507+193C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148523000 | ||||||
| chr5:148523114
|
C | A | 1 | a0001c0001t0003g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.507+79G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148523114 | ||||||
| chr5:148523140
|
C | A | 95 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+53G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148523140 | ||||||
| chr5:148523375
|
G | C | 2 | a0001c0001t0001g0297a0001c0001t0005g0139 | 2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.354-29C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523375 | ||||||
| chr5:148523409
|
G | A | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.354-63C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523409 | ||||||
| chr5:148523516
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.354-170C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523516 | ||||||
| chr5:148523525
|
G | T | 94 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.354-179C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523525 | ||||||
| chr5:148523553
|
C | G | 1 | a0001c0001t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.354-207G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523553 | ||||||
| chr5:148523648
|
A | C | 5 | a0001c0001t0001g0261a0001c0001t0002g0029a0001c0001t0002g0030others(2): Show | 5 | HG02486.hp2 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.354-302T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523648 | ||||||
| chr5:148523725
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0003g0114 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.354-379G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523725 | ||||||
| chr5:148523769
|
G | T | 2 | a0001c0001t0001g0297a0001c0001t0005g0139 | 2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.354-423C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523769 | ||||||
| chr5:148523844
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0266 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.354-498C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523844 | ||||||
| chr5:148523995
|
G | GT | 92 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.354-650dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523995 | ||||||
| chr5:148524089
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0008g0131a0001c0001t0008g0132others(1): Show | 4 | HG01884.hp2 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-743C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524089 | ||||||
| chr5:148524089
|
G | T | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0257others(3): Show | 6 | HG00597.hp1 HG02155.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-743C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524089 | ||||||
| chr5:148524181
|
A | T | 1 | a0001c0001t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.354-835T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524181 | ||||||
| chr5:148524266
|
T | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.354-920A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524266 | ||||||
| chr5:148524333
|
G | A | 3 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0290 | 3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.354-987C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524333 | ||||||
| chr5:148524678
|
T | C | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.354-1332A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524678 | ||||||
| chr5:148524683
|
A | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-1337T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524683 | ||||||
| chr5:148524885
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.354-1539C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524885 | ||||||
| chr5:148524921
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.354-1575C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524921 | ||||||
| chr5:148524957
|
C | T | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-1611G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524957 | ||||||
| chr5:148524990
|
C | T | 5 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0255others(2): Show | 5 | HG01192.hp1 HG01361.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-1644G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524990 | ||||||
| chr5:148525008
|
T | G | 92 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.354-1662A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525008 | ||||||
| chr5:148525145
|
A | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-1799T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525145 | ||||||
| chr5:148525237
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.354-1891G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525237 | ||||||
| chr5:148525456
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.354-2110C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525456 | ||||||
| chr5:148525518
|
G | A | 61 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.354-2172C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525518 | ||||||
| chr5:148525768
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(1): Show | 4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-2422A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525768 | ||||||
| chr5:148525851
|
G | C | 93 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(90): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.354-2505C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525851 | ||||||
| chr5:148525852
|
G | A | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-2506C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525852 | ||||||
| chr5:148525992
|
C | T | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.354-2646G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525992 | ||||||
| chr5:148526000
|
A | C | 1 | a0001c0001t0003g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.354-2654T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526000 | ||||||
| chr5:148526006
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.354-2660C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526006 | ||||||
| chr5:148526116
|
C | T | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-2770G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526116 | ||||||
| chr5:148526155
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2809C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526155 | ||||||
| chr5:148526442
|
T | C | 89 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-3096A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526442 | ||||||
| chr5:148526766
|
G | C | 3 | a0001c0001t0001g0264a0001c0001t0010g0080a0001c0001t0010g0081 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.354-3420C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526766 | ||||||
| chr5:148526940
|
G | A | 3 | a0001c0001t0002g0037a0001c0001t0002g0072a0001c0001t0002g0074 | 3 | HG00621.hp2 HG02056.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.354-3594C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526940 | ||||||
| chr5:148526949
|
T | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(1): Show | 4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-3603A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526949 | ||||||
| chr5:148527140
|
C | T | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.354-3794G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527140 | ||||||
| chr5:148527338
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.354-3992A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527338 | ||||||
| chr5:148527435
|
T | A | 89 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-4089A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527435 | ||||||
| chr5:148527686
|
CT | C | 75 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-4341delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527686 | ||||||
| chr5:148527713
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-4367G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527713 | ||||||
| chr5:148527726
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.354-4380A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527726 | ||||||
| chr5:148527826
|
C | T | 1 | a0001c0004t0003g0115 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.354-4480G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527826 | ||||||
| chr5:148527930
|
A | G | 1 | a0001c0005t0005g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354-4584T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527930 | ||||||
| chr5:148528016
|
C | A | 2 | a0001c0001t0003g0102a0001c0001t0004g0269 | 2 | HG00558.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.354-4670G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528016 | ||||||
| chr5:148528277
|
G | T | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.354-4931C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528277 | ||||||
| chr5:148528336
|
A | T | 9 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0307others(6): Show | 9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-4990T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528336 | ||||||
| chr5:148528337
|
G | C | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-4991C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528337 | ||||||
| chr5:148528442
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.354-5096G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528442 | ||||||
| chr5:148528543
|
GA | G | 75 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-5198delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528543 | ||||||
| chr5:148528770
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354-5424T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528770 | ||||||
| chr5:148528782
|
T | G | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.354-5436A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528782 | ||||||
| chr5:148528822
|
G | A | 75 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-5476C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528822 | ||||||
| chr5:148528825
|
G | C | 1 | a0001c0001t0001g0248 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.354-5479C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528825 | ||||||
| chr5:148528853
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.354-5507T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528853 | ||||||
| chr5:148529084
|
C | T | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-5738G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529084 | ||||||
| chr5:148529117
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354-5771G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529117 | ||||||
| chr5:148529354
|
C | A | 1 | a0001c0001t0011g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354-6008G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529354 | ||||||
| chr5:148529418
|
G | C | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.354-6072C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529418 | ||||||
| chr5:148529506
|
C | T | 1 | a0001c0001t0011g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354-6160G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529506 | ||||||
| chr5:148529507
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.354-6161C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529507 | ||||||
| chr5:148529517
|
A | T | 9 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0049others(6): Show | 9 | HG00621.hp2 HG02056.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-6171T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529517 | ||||||
| chr5:148529525
|
G | C | 1 | a0001c0001t0002g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.354-6179C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529525 | ||||||
| chr5:148529556
|
C | T | 1 | a0001c0001t0003g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.354-6210G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529556 | ||||||
| chr5:148529647
|
G | T | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.354-6301C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529647 | ||||||
| chr5:148529889
|
G | A | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-6543C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529889 | ||||||
| chr5:148530126
|
A | T | 1 | a0001c0001t0003g0095 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.354-6780T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530126 | ||||||
| chr5:148530176
|
G | A | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.354-6830C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530176 | ||||||
| chr5:148530325
|
G | A | 88 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.354-6979C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530325 | ||||||
| chr5:148530382
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.354-7036C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530382 | ||||||
| chr5:148530534
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.354-7188A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530534 | ||||||
| chr5:148530576
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-7230C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530576 | ||||||
| chr5:148530724
|
C | A | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-7378G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530724 | ||||||
| chr5:148530727
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.354-7381G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530727 | ||||||
| chr5:148531070
|
T | C | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.354-7724A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531070 | ||||||
| chr5:148531297
|
A | G | 100 | a0001c0001t0001g0174a0001c0001t0001g0185a0001c0001t0001g0189others(97): Show | 100 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.354-7951T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531297 | ||||||
| chr5:148531307
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.354-7961C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531307 | ||||||
| chr5:148531510
|
C | G | 16 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 16 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.354-8164G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531510 | ||||||
| chr5:148531607
|
A | G | 4 | a0001c0001t0003g0107a0001c0001t0011g0108a0001c0001t0011g0110others(1): Show | 4 | HG01496.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-8261T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531607 | ||||||
| chr5:148531611
|
A | G | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.354-8265T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531611 | ||||||
| chr5:148531915
|
T | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.354-8569A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531915 | ||||||
| chr5:148532060
|
A | G | 172 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.354-8714T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532060 | ||||||
| chr5:148532120
|
G | A | 1 | a0001c0001t0005g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.354-8774C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532120 | ||||||
| chr5:148532153
|
G | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-8807C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532153 | ||||||
| chr5:148532260
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354-8914G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532260 | ||||||
| chr5:148532309
|
G | A | 88 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.354-8963C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532309 | ||||||
| chr5:148532686
|
C | T | 89 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-9340G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532686 | ||||||
| chr5:148532822
|
C | T | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.354-9476G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532822 | ||||||
| chr5:148532834
|
C | A | 3 | a0001c0001t0003g0118a0001c0001t0004g0298a0001c0001t0004g0300 | 3 | NA18747.hp2 NA18965.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.354-9488G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532834 | ||||||
| chr5:148532993
|
G | A | 9 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0307others(6): Show | 9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-9647C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532993 | ||||||
| chr5:148533074
|
C | T | 2 | a0001c0001t0008g0131a0001c0001t0008g0132 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.354-9728G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533074 | ||||||
| chr5:148533292
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-9946T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533292 | ||||||
| chr5:148533521
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.354-10175A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533521 | ||||||
| chr5:148533636
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-10290C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533636 | ||||||
| chr5:148533650
|
C | T | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.354-10304G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533650 | ||||||
| chr5:148533734
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-10388G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533734 | ||||||
| chr5:148533877
|
ATAT | A | 3 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115 | 3 | HG02300.hp2 HG03139.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.354-10534_354-1053 others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533877 | ||||||
| chr5:148534098
|
C | T | 94 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.354-10752G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534098 | ||||||
| chr5:148534177
|
C | T | 1 | a0001c0001t0003g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.354-10831G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534177 | ||||||
| chr5:148534633
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.354-11287G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534633 | ||||||
| chr5:148534664
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.354-11318C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534664 | ||||||
| chr5:148534717
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.354-11371C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534717 | ||||||
| chr5:148534852
|
G | C | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.354-11506C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534852 | ||||||
| chr5:148534926
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.354-11580G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534926 | ||||||
| chr5:148535084
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.354-11738G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535084 | ||||||
| chr5:148535101
|
C | T | 89 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-11755G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535101 | ||||||
| chr5:148535324
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0304 | 3 | HG00738.hp2 HG02572.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.354-11978C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535324 | ||||||
| chr5:148535364
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.354-12018C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535364 | ||||||
| chr5:148535831
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0015g0012 | 2 | HG01981.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.354-12485C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535831 | ||||||
| chr5:148536082
|
A | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+12586T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536082 | ||||||
| chr5:148536097
|
G | T | 11 | a0001c0001t0001g0164a0001c0001t0001g0268a0001c0001t0004g0162others(8): Show | 11 | HG00558.hp1 NA18947.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.353+12571C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536097 | ||||||
| chr5:148536216
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.353+12452A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536216 | ||||||
| chr5:148536283
|
C | T | 1 | a0001c0001t0006g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.353+12385G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536283 | ||||||
| chr5:148536347
|
C | A | 75 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.353+12321G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536347 | ||||||
| chr5:148536682
|
G | A | 3 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115 | 3 | HG02300.hp2 HG03139.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.353+11986C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536682 | ||||||
| chr5:148536722
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.353+11946G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536722 | ||||||
| chr5:148536744
|
T | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+11924A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536744 | ||||||
| chr5:148536787
|
G | C | 9 | a0001c0001t0001g0206a0001c0001t0001g0214a0001c0001t0001g0248others(6): Show | 9 | HG01257.hp1 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.353+11881C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536787 | ||||||
| chr5:148536835
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.353+11833G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536835 | ||||||
| chr5:148537049
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+11619G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537049 | ||||||
| chr5:148537063
|
C | T | 296 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(293): Show | 296 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.353+11605G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537063 | ||||||
| chr5:148537204
|
T | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.353+11464A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537204 | ||||||
| chr5:148537215
|
G | A | 3 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115 | 3 | HG02300.hp2 HG03139.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.353+11453C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537215 | ||||||
| chr5:148537224
|
A | G | 306 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.353+11444T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537224 | ||||||
| chr5:148537286
|
T | A | 1 | a0001c0001t0002g0025 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.353+11382A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537286 | ||||||
| chr5:148537353
|
C | T | 79 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.353+11315G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537353 | ||||||
| chr5:148537391
|
A | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+11277T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537391 | ||||||
| chr5:148537953
|
T | C | 1 | a0001c0001t0003g0119 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.353+10715A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537953 | ||||||
| chr5:148538106
|
A | G | 3 | a0001c0001t0003g0117a0001c0001t0003g0119a0001c0001t0003g0126 | 3 | NA18981.hp2 NA18983.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.353+10562T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538106 | ||||||
| chr5:148538328
|
C | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+10340G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538328 | ||||||
| chr5:148538354
|
T | C | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.353+10314A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538354 | ||||||
| chr5:148538477
|
C | G | 1 | a0001c0001t0009g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.353+10191G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538477 | ||||||
| chr5:148538486
|
G | A | 1 | a0001c0001t0005g0144 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.353+10182C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538486 | ||||||
| chr5:148538584
|
G | C | 70 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.353+10084C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538584 | ||||||
| chr5:148538631
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.353+10037C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538631 | ||||||
| chr5:148538915
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0005g0136 | 2 | HG02074.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.353+9753G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538915 | ||||||
| chr5:148538955
|
C | T | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+9713G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538955 | ||||||
| chr5:148539010
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.353+9658A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539010 | ||||||
| chr5:148539211
|
T | C | 89 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.353+9457A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539211 | ||||||
| chr5:148539270
|
C | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.353+9398G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539270 | ||||||
| chr5:148539308
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0191a0001c0001t0001g0194others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+9360C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539308 | ||||||
| chr5:148539512
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.353+9156G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539512 | ||||||
| chr5:148539700
|
T | A | 1 | a0001c0001t0007g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.353+8968A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539700 | ||||||
| chr5:148539769
|
G | A | 89 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.353+8899C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539769 | ||||||
| chr5:148539803
|
A | G | 191 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.353+8865T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539803 | ||||||
| chr5:148539930
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.353+8738A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539930 | ||||||
| chr5:148540147
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.353+8521C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540147 | ||||||
| chr5:148540200
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.353+8468T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540200 | ||||||
| chr5:148540211
|
G | A | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.353+8457C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540211 | ||||||
| chr5:148540309
|
C | T | 8 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+8359G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540309 | ||||||
| chr5:148540310
|
G | A | 9 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0307others(6): Show | 9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.353+8358C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540310 | ||||||
| chr5:148540400
|
G | GTATA | 4 | a0001c0001t0001g0218a0001c0001t0002g0023a0001c0001t0004g0279others(1): Show | 4 | HG00609.hp2 HG02559.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+8264_353+8267d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
G | GTATATA | 3 | a0001c0001t0002g0027a0001c0001t0003g0095a0001c0005t0005g0141 | 3 | HG00609.hp1 HG02735.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.353+8262_353+8267d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0270 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.353+8258_353+8267d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTA | G | 72 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0173others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.353+8266_353+8267d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATA | G | 48 | a0001c0001t0001g0160a0001c0001t0001g0182a0001c0001t0001g0188others(45): Show | 48 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.353+8264_353+8267d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATA | G | 57 | a0001c0001t0001g0177a0001c0001t0001g0187a0001c0001t0001g0202others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.353+8262_353+8267d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(1): Show |
G | 23 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0179others(20): Show | 23 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.353+8260_353+8267d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(3): Show |
G | 15 | a0001c0001t0001g0230a0001c0001t0001g0280a0001c0001t0002g0006others(12): Show | 15 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.353+8258_353+8267d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(5): Show |
G | 29 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.353+8256_353+8267d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0002g0043a0001c0006t0003g0112 | 2 | HG01516.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.353+8254_353+8267d others(16): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(13): Show |
G | 1 | a0001c0001t0002g0045 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.353+8248_353+8267d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.353+8246_353+8267d others(24): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540400
|
GTATATAT others(25): Show |
G | 2 | a0001c0001t0001g0290a0003c0009t0027g0310 | 2 | HG01243.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.353+8236_353+8267d others(34): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | ||||||
| chr5:148540402
|
A | G | 3 | a0001c0001t0003g0084a0001c0001t0003g0105a0001c0004t0001g0262 | 3 | HG00673.hp1 HG02300.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.353+8266T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540402 | ||||||
| chr5:148540404
|
A | G | 6 | a0001c0001t0001g0195a0001c0001t0002g0024a0001c0001t0002g0032others(3): Show | 6 | HG02074.hp1 HG02135.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+8264T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540404 | ||||||
| chr5:148540406
|
A | G | 3 | a0001c0001t0001g0201a0001c0001t0002g0016a0001c0001t0005g0139 | 3 | HG01978.hp2 HG02257.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.353+8262T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540406 | ||||||
| chr5:148540408
|
A | G | 6 | a0001c0001t0001g0276a0001c0001t0001g0297a0001c0001t0003g0090others(3): Show | 6 | HG00738.hp1 HG02258.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+8260T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540408 | ||||||
| chr5:148540410
|
A | G | 14 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0231others(11): Show | 14 | HG00140.hp1 HG00423.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.353+8258T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540410 | ||||||
| chr5:148540412
|
A | G | 13 | a0001c0001t0001g0230a0001c0001t0001g0280a0001c0001t0002g0006others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+8256T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540412 | ||||||
| chr5:148540414
|
A | G | 26 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.353+8254T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540414 | ||||||
| chr5:148540416
|
A | G | 2 | a0001c0001t0002g0043a0001c0006t0003g0112 | 2 | HG01516.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.353+8252T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540416 | ||||||
| chr5:148540531
|
A | G | 79 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.353+8137T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540531 | ||||||
| chr5:148540829
|
C | G | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.353+7839G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540829 | ||||||
| chr5:148540919
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.353+7749G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540919 | ||||||
| chr5:148541074
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.353+7594G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541074 | ||||||
| chr5:148541323
|
A | T | 94 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.353+7345T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541323 | ||||||
| chr5:148541378
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+7290G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541378 | ||||||
| chr5:148541635
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.353+7033C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541635 | ||||||
| chr5:148541741
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.353+6927C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541741 | ||||||
| chr5:148541962
|
T | A | 60 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.353+6706A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541962 | ||||||
| chr5:148542433
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.353+6235C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542433 | ||||||
| chr5:148542489
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0291a0001c0001t0002g0075others(1): Show | 4 | NA18945.hp1 NA18949.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+6179C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542489 | ||||||
| chr5:148542499
|
A | T | 70 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.353+6169T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542499 | ||||||
| chr5:148542520
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.353+6148C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542520 | ||||||
| chr5:148542587
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.353+6081T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542587 | ||||||
| chr5:148542617
|
T | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+6051A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542617 | ||||||
| chr5:148542725
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.353+5943T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542725 | ||||||
| chr5:148542790
|
A | G | 90 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+5878T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542790 | ||||||
| chr5:148542870
|
C | G | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.353+5798G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542870 | ||||||
| chr5:148543317
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.353+5351T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543317 | ||||||
| chr5:148543418
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.353+5250G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543418 | ||||||
| chr5:148543551
|
A | G | 191 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.353+5117T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543551 | ||||||
| chr5:148543814
|
A | G | 174 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.353+4854T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543814 | ||||||
| chr5:148544084
|
T | TAAAATGT others(313): Show |
2 | a0001c0001t0004g0271a0001c0001t0014g0001 | 2 | HG00438.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.353+4583_353+4584i others(322): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(314): Show |
1 | a0001c0001t0003g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(323): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(317): Show |
1 | a0001c0001t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353+4583_353+4584i others(326): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(318): Show |
1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(327): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(326): Show |
1 | a0001c0001t0004g0279 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(335): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(327): Show |
4 | a0001c0001t0001g0243a0001c0001t0001g0288a0001c0001t0004g0244others(1): Show | 4 | NA18943.hp1 NA18945.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+4583_353+4584i others(336): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(328): Show |
1 | a0001c0001t0001g0281 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(337): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(329): Show |
1 | a0001c0001t0001g0270 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(338): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(330): Show |
1 | a0001c0001t0004g0298 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(339): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(331): Show |
3 | a0001c0001t0003g0118a0001c0001t0004g0171a0001c0001t0004g0300 | 3 | NA18747.hp2 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.353+4583_353+4584i others(340): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(332): Show |
4 | a0001c0001t0001g0164a0001c0001t0001g0268a0001c0001t0001g0299others(1): Show | 4 | HG00558.hp1 NA18957.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+4583_353+4584i others(341): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(333): Show |
4 | a0001c0001t0004g0162a0001c0001t0004g0165a0001c0001t0004g0166others(1): Show | 4 | NA18964.hp1 NA18991.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+4583_353+4584i others(342): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(334): Show |
2 | a0001c0001t0004g0167a0001c0001t0004g0170 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.353+4583_353+4584i others(343): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(337): Show |
1 | a0001c0001t0020g0125 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(346): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544084
|
T | TAAAATGT others(351): Show |
1 | a0001c0001t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(360): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | ||||||
| chr5:148544201
|
C | T | 3 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0290 | 3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.353+4467G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544201 | ||||||
| chr5:148544278
|
TCTCTCTT others(15): Show |
T | 192 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.353+4368_353+4389d others(24): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544278 | ||||||
| chr5:148544343
|
A | C | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+4325T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544343 | ||||||
| chr5:148544349
|
A | C | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+4319T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544349 | ||||||
| chr5:148544379
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+4289T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544379 | ||||||
| chr5:148544483
|
G | T | 1 | a0001c0001t0002g0037 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.353+4185C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544483 | ||||||
| chr5:148544489
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.353+4179T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544489 | ||||||
| chr5:148544692
|
T | A | 2 | a0001c0001t0001g0277a0001c0001t0025g0301 | 2 | HG00099.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.353+3976A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544692 | ||||||
| chr5:148544849
|
C | T | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.353+3819G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544849 | ||||||
| chr5:148544947
|
G | A | 90 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+3721C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544947 | ||||||
| chr5:148545422
|
A | T | 173 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.353+3246T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545422 | ||||||
| chr5:148545436
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.353+3232G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545436 | ||||||
| chr5:148545573
|
A | C | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+3095T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545573 | ||||||
| chr5:148545628
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.353+3040C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545628 | ||||||
| chr5:148545688
|
G | C | 4 | a0001c0001t0001g0195a0001c0004t0001g0262a0001c0004t0003g0115others(1): Show | 4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+2980C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545688 | ||||||
| chr5:148545700
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.353+2968A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545700 | ||||||
| chr5:148545735
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.353+2933C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545735 | ||||||
| chr5:148545750
|
G | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+2918C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545750 | ||||||
| chr5:148545828
|
A | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+2840T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545828 | ||||||
| chr5:148545899
|
T | C | 1 | a0001c0001t0016g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.353+2769A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545899 | ||||||
| chr5:148545942
|
T | C | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.353+2726A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545942 | ||||||
| chr5:148546000
|
G | C | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+2668C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546000 | ||||||
| chr5:148546236
|
A | G | 2 | a0001c0001t0001g0305a0001c0001t0003g0114 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.353+2432T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546236 | ||||||
| chr5:148546258
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0007g0003 | 2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.353+2410C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546258 | ||||||
| chr5:148546491
|
A | G | 2 | a0001c0005t0005g0141a0001c0005t0005g0146 | 2 | HG02559.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.353+2177T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546491 | ||||||
| chr5:148546589
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+2079G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546589 | ||||||
| chr5:148546638
|
T | A | 8 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(5): Show | 8 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+2030A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546638 | ||||||
| chr5:148546674
|
C | T | 70 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.353+1994G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546674 | ||||||
| chr5:148547112
|
T | G | 3 | a0001c0001t0003g0117a0001c0001t0003g0119a0001c0001t0003g0126 | 3 | NA18981.hp2 NA18983.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.353+1556A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547112 | ||||||
| chr5:148547347
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.353+1321C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547347 | ||||||
| chr5:148547388
|
G | A | 97 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(94): Show | 97 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.353+1280C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547388 | ||||||
| chr5:148547436
|
G | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.353+1232C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547436 | ||||||
| chr5:148547526
|
A | AAAAAT | 100 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.353+1137_353+1141d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | ||||||
| chr5:148547526
|
A | AAAAATAA others(3): Show |
13 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(10): Show | 13 | HG00140.hp1 HG01257.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+1132_353+1141d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | ||||||
| chr5:148547526
|
A | AAAAATAA others(8): Show |
1 | a0001c0001t0003g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.353+1127_353+1141d others(17): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | ||||||
| chr5:148547526
|
A | AAAAATAA others(13): Show |
2 | a0001c0001t0003g0105a0001c0001t0021g0099 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.353+1122_353+1141d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | ||||||
| chr5:148547526
|
A | AAAAATAA others(28): Show |
1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+1107_353+1141d others(37): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | ||||||
| chr5:148547526
|
AAAAAT | A | 12 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0215others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.353+1137_353+1141d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | ||||||
| chr5:148547562
|
A | AAAAT | 90 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+1102_353+1105d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | ||||||
| chr5:148547562
|
A | AAAATAAA others(2): Show |
28 | a0001c0001t0001g0174a0001c0001t0001g0187a0001c0001t0001g0188others(25): Show | 28 | HG00673.hp1 HG00741.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.353+1105_353+1106i others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | ||||||
| chr5:148547562
|
A | AAAATAAA others(7): Show |
38 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(35): Show | 38 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.353+1105_353+1106i others(16): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | ||||||
| chr5:148547562
|
A | AAAATAAA others(12): Show |
8 | a0001c0001t0001g0291a0001c0001t0002g0006a0001c0001t0002g0011others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.353+1105_353+1106i others(21): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | ||||||
| chr5:148547562
|
A | AAAATAAA others(17): Show |
2 | a0001c0001t0001g0195a0001c0001t0001g0227 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.353+1105_353+1106i others(26): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | ||||||
| chr5:148547562
|
A | AAAATAAA others(6): Show |
1 | a0001c0001t0006g0282 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.353+1105_353+1106i others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | ||||||
| chr5:148547566
|
T | TAAAATAA others(14): Show |
1 | a0001c0001t0001g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.353+1101_353+1102i others(23): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547566 | ||||||
| chr5:148547570
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.353+1098A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547570 | ||||||
| chr5:148547668
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+1000C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547668 | ||||||
| chr5:148547688
|
C | T | 97 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(94): Show | 97 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.353+980G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547688 | ||||||
| chr5:148547748
|
A | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+920T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547748 | ||||||
| chr5:148547791
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.353+877C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547791 | ||||||
| chr5:148547816
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.353+852G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547816 | ||||||
| chr5:148547978
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.353+690T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547978 | ||||||
| chr5:148548028
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.353+640T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548028 | ||||||
| chr5:148548094
|
G | T | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+574C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548094 | ||||||
| chr5:148548166
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.353+502T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548166 | ||||||
| chr5:148548336
|
T | C | 97 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(94): Show | 97 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.353+332A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548336 | ||||||
| chr5:148548555
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0007g0038 | 2 | NA19075.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.353+113T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548555 | ||||||
| chr5:148548567
|
T | C | 60 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.353+101A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548567 | ||||||
| chr5:148548662
|
C | T | 96 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0195others(93): Show | 96 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
splice_region_variant&intron_variant | LOW | c.353+6G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548662 | ||||||
| chr5:148549025
|
T | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-157A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549025 | ||||||
| chr5:148549094
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-226C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549094 | ||||||
| chr5:148549118
|
C | T | 61 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.153-250G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549118 | ||||||
| chr5:148549198
|
C | T | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.153-330G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549198 | ||||||
| chr5:148549759
|
G | C | 1 | a0001c0001t0004g0171 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.152+378C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549759 | ||||||
| chr5:148549771
|
CA | C | 42 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.152+365delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549771 | ||||||
| chr5:148549812
|
C | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0065 | 2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.152+325G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549812 | ||||||
| chr5:148549987
|
C | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0228others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+150G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549987 | ||||||
| chr5:148550117
|
G | A | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+20C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148550117 | ||||||
| chr5:148550393
|
G | A | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.27-131C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550393 | ||||||
| chr5:148550435
|
A | G | 4 | a0001c0001t0003g0107a0001c0001t0011g0108a0001c0001t0011g0110others(1): Show | 4 | HG01496.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-173T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550435 | ||||||
| chr5:148550635
|
C | T | 1 | a0001c0001t0001g0249 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.27-373G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550635 | ||||||
| chr5:148550967
|
C | G | 1 | a0001c0001t0001g0206 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27-705G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550967 | ||||||
| chr5:148551013
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0001t0003g0084others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-751C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551013 | ||||||
| chr5:148551032
|
CT | C | 6 | a0001c0001t0002g0022a0001c0001t0002g0033a0001c0001t0002g0065others(3): Show | 6 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-771delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551032 | ||||||
| chr5:148551194
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0288 | 2 | NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.27-932C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551194 | ||||||
| chr5:148551259
|
G | T | 1 | a0001c0001t0003g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.27-997C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551259 | ||||||
| chr5:148551558
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.27-1296A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551558 | ||||||
| chr5:148551802
|
G | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0292 | 3 | HG01167.hp1 HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.27-1540C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551802 | ||||||
| chr5:148551960
|
G | A | 91 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.27-1698C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551960 | ||||||
| chr5:148552094
|
G | A | 1 | a0001c0001t0005g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.27-1832C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552094 | ||||||
| chr5:148552134
|
C | T | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.27-1872G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552134 | ||||||
| chr5:148552180
|
A | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(1): Show | 4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-1918T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552180 | ||||||
| chr5:148552389
|
A | T | 1 | a0001c0001t0004g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.27-2127T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552389 | ||||||
| chr5:148552411
|
C | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0211others(2): Show | 5 | HG01167.hp1 HG01243.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-2149G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552411 | ||||||
| chr5:148552594
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-2332T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552594 | ||||||
| chr5:148552638
|
G | A | 283 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(280): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.27-2376C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552638 | ||||||
| chr5:148552799
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-2537A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552799 | ||||||
| chr5:148553047
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0211a0001c0001t0001g0215others(6): Show | 9 | HG01074.hp1 HG01167.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-2785C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553047 | ||||||
| chr5:148553193
|
G | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0211a0001c0001t0001g0292 | 3 | HG01167.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.27-2931C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553193 | ||||||
| chr5:148553213
|
C | CA | 10 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.27-2952dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553213 | ||||||
| chr5:148553259
|
C | G | 246 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(243): Show | 246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.27-2997G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553259 | ||||||
| chr5:148553333
|
T | C | 6 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0274others(3): Show | 6 | HG01074.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3071A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553333 | ||||||
| chr5:148553440
|
G | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-3178C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553440 | ||||||
| chr5:148553448
|
G | T | 6 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0087others(3): Show | 6 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3186C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553448 | ||||||
| chr5:148553563
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0011g0108a0001c0001t0011g0111 | 3 | HG01496.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.27-3301T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553563 | ||||||
| chr5:148553588
|
T | C | 2 | a0001c0001t0002g0032a0001c0001t0003g0084 | 2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.27-3326A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553588 | ||||||
| chr5:148553624
|
C | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0001t0018g0109others(1): Show | 4 | HG01884.hp2 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-3362G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553624 | ||||||
| chr5:148553703
|
A | C | 105 | a0001c0001t0001g0174a0001c0001t0001g0185a0001c0001t0001g0188others(102): Show | 105 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.27-3441T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553703 | ||||||
| chr5:148553848
|
C | T | 1 | a0002c0003t0013g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.27-3586G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553848 | ||||||
| chr5:148553862
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0211a0001c0001t0001g0215others(6): Show | 9 | HG01074.hp1 HG01167.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-3600G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553862 | ||||||
| chr5:148553885
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.27-3623G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553885 | ||||||
| chr5:148553997
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.27-3735T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553997 | ||||||
| chr5:148554063
|
TTTGTTG | T | 6 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0274others(3): Show | 6 | HG01074.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3807_27-3802del others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554063 | ||||||
| chr5:148554088
|
T | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3826A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554088 | ||||||
| chr5:148554090
|
T | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0242a0001c0001t0002g0055 | 3 | HG00597.hp2 HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.27-3828A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554090 | ||||||
| chr5:148554239
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0009g0154a0002c0003t0019g0120 | 3 | HG02559.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27-3977G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554239 | ||||||
| chr5:148554317
|
C | T | 7 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-4055G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554317 | ||||||
| chr5:148554502
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.27-4240T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554502 | ||||||
| chr5:148554511
|
A | G | 2 | a0001c0001t0003g0119a0001c0001t0003g0126 | 2 | NA18981.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.27-4249T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554511 | ||||||
| chr5:148554569
|
C | T | 1 | a0001c0001t0005g0137 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.27-4307G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554569 | ||||||
| chr5:148554606
|
G | A | 6 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0274others(3): Show | 6 | HG01074.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-4344C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554606 | ||||||
| chr5:148554703
|
A | G | 1 | a0001c0008t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.27-4441T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554703 | ||||||
| chr5:148554752
|
T | C | 8 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(5): Show | 8 | HG00673.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.27-4490A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554752 | ||||||
| chr5:148554982
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.27-4720T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554982 | ||||||
| chr5:148555057
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.27-4795A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555057 | ||||||
| chr5:148555164
|
C | T | 95 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.27-4902G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555164 | ||||||
| chr5:148555463
|
A | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-5201T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555463 | ||||||
| chr5:148555589
|
C | T | 2 | a0001c0001t0002g0032a0001c0001t0003g0084 | 2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.27-5327G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555589 | ||||||
| chr5:148555616
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.27-5354T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555616 | ||||||
| chr5:148555620
|
G | A | 1 | a0001c0002t0003g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.27-5358C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555620 | ||||||
| chr5:148555793
|
A | G | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27-5531T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555793 | ||||||
| chr5:148555946
|
T | TCA | 20 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(17): Show | 20 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.27-5686_27-5685dup others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555946
|
T | TCACA | 4 | a0001c0001t0002g0032a0001c0001t0003g0084a0001c0001t0021g0099others(1): Show | 4 | HG00673.hp1 HG02451.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-5688_27-5685dup others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555946
|
T | TCACACA | 83 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(80): Show | 83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.27-5690_27-5685dup others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555946
|
T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0195a0001c0001t0002g0037a0001c0001t0009g0155others(5): Show | 8 | HG00621.hp2 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-5692_27-5685dup others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555946
|
T | TCACACAC others(3): Show |
1 | a0001c0002t0001g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.27-5694_27-5685dup others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555946
|
T | TCACACAC others(5): Show |
1 | a0001c0002t0008g0133 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.27-5696_27-5685dup others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555946
|
T | TCTCACA | 5 | a0001c0001t0001g0205a0001c0001t0001g0212a0001c0001t0001g0220others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-5685_27-5684ins others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | ||||||
| chr5:148555968
|
ACACT | A | 6 | a0001c0001t0002g0022a0001c0001t0002g0033a0001c0001t0002g0065others(3): Show | 6 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-5710_27-5707del others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555968 | ||||||
| chr5:148555970
|
A | T | 56 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.27-5708T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555970 | ||||||
| chr5:148555972
|
T | A | 2 | a0001c0001t0002g0032a0001c0001t0003g0084 | 2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.27-5710A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555972 | ||||||
| chr5:148556315
|
C | T | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27-6053G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556315 | ||||||
| chr5:148556322
|
A | C | 185 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.27-6060T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556322 | ||||||
| chr5:148556327
|
A | G | 185 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.27-6065T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556327 | ||||||
| chr5:148556557
|
G | A | 94 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.27-6295C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556557 | ||||||
| chr5:148556715
|
T | G | 2 | a0001c0002t0003g0086a0003c0009t0027g0310 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.27-6453A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556715 | ||||||
| chr5:148557047
|
T | C | 3 | a0001c0001t0001g0309a0001c0001t0009g0154a0002c0003t0019g0120 | 3 | HG02559.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27-6785A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557047 | ||||||
| chr5:148557070
|
C | T | 1 | a0001c0002t0008g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.27-6808G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557070 | ||||||
| chr5:148557300
|
G | A | 94 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.27-7038C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557300 | ||||||
| chr5:148557365
|
AT | A | 62 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.27-7104delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557365 | ||||||
| chr5:148557462
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.27-7200G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557462 | ||||||
| chr5:148557562
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27-7300C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557562 | ||||||
| chr5:148557787
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0010g0083 | 2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.27-7525T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557787 | ||||||
| chr5:148557905
|
A | C | 193 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.27-7643T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557905 | ||||||
| chr5:148557921
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0006g0176 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-7659G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557921 | ||||||
| chr5:148558004
|
T | A | 69 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.27-7742A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558004 | ||||||
| chr5:148558070
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-7808T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558070 | ||||||
| chr5:148558179
|
AAC | A | 9 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(6): Show | 9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-7919_27-7918del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558179 | ||||||
| chr5:148558221
|
G | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-7959C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558221 | ||||||
| chr5:148558235
|
T | C | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-7973A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558235 | ||||||
| chr5:148558405
|
C | G | 1 | a0001c0001t0001g0276 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.27-8143G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558405 | ||||||
| chr5:148558556
|
T | C | 6 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-8294A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558556 | ||||||
| chr5:148558593
|
C | T | 1 | a0001c0001t0005g0147 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.27-8331G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558593 | ||||||
| chr5:148558710
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0304 | 2 | HG00738.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.27-8448G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558710 | ||||||
| chr5:148559004
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(12): Show | 15 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-8742G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559004 | ||||||
| chr5:148559289
|
G | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.27-9027C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559289 | ||||||
| chr5:148559292
|
G | A | 1 | a0001c0001t0009g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-9030C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559292 | ||||||
| chr5:148559309
|
G | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0065 | 2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.27-9047C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559309 | ||||||
| chr5:148559399
|
A | G | 160 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.27-9137T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559399 | ||||||
| chr5:148559454
|
T | G | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-9192A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559454 | ||||||
| chr5:148559539
|
T | C | 3 | a0001c0001t0002g0037a0001c0001t0002g0072a0001c0001t0002g0074 | 3 | HG00621.hp2 HG02056.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.27-9277A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559539 | ||||||
| chr5:148559604
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-9342T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559604 | ||||||
| chr5:148559636
|
C | T | 2 | a0001c0001t0008g0131a0001c0001t0008g0132 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-9374G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559636 | ||||||
| chr5:148559642
|
G | A | 2 | a0001c0001t0001g0305a0001c0001t0003g0114 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.27-9380C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559642 | ||||||
| chr5:148559667
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27-9405T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559667 | ||||||
| chr5:148559677
|
C | T | 65 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-9415G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559677 | ||||||
| chr5:148559784
|
C | T | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-9522G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559784 | ||||||
| chr5:148560135
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.27-9873T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560135 | ||||||
| chr5:148560161
|
C | T | 83 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(80): Show | 83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.27-9899G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560161 | ||||||
| chr5:148560196
|
CT | C | 19 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0185others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-9935delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560196 | ||||||
| chr5:148560196
|
CTT | C | 7 | a0001c0001t0001g0243a0001c0001t0001g0259a0001c0001t0001g0281others(4): Show | 7 | HG02080.hp2 NA18943.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-9936_27-9935del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560196 | ||||||
| chr5:148560204
|
TTA | T | 56 | a0001c0001t0001g0172a0001c0001t0001g0201a0001c0001t0001g0204others(53): Show | 56 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.27-9944_27-9943del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560204 | ||||||
| chr5:148560204
|
TTAA | T | 13 | a0001c0001t0001g0230a0001c0001t0001g0284a0001c0001t0001g0297others(10): Show | 13 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.27-9945_27-9943del others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560204 | ||||||
| chr5:148560205
|
T | A | 8 | a0001c0001t0001g0281a0001c0001t0001g0288a0001c0001t0002g0007others(5): Show | 8 | HG02155.hp1 HG02155.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-9943A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | ||||||
| chr5:148560205
|
T | TA | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0268others(8): Show | 11 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.27-9944dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | ||||||
| chr5:148560205
|
TA | T | 30 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0183others(27): Show | 30 | HG00323.hp2 HG00738.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.27-9944delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | ||||||
| chr5:148560205
|
TAA | T | 68 | a0001c0001t0001g0177a0001c0001t0001g0205a0001c0001t0001g0209others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.27-9945_27-9944del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | ||||||
| chr5:148560205
|
TAAA | T | 11 | a0001c0001t0001g0195a0001c0001t0001g0305a0001c0001t0002g0044others(8): Show | 11 | HG01981.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.27-9946_27-9944del others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | ||||||
| chr5:148560205
|
TAAAA | T | 11 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187others(8): Show | 11 | HG00140.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.27-9947_27-9944del others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | ||||||
| chr5:148560207
|
A | T | 2 | a0001c0001t0007g0061a0001c0001t0012g0208 | 2 | HG02647.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.27-9945T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560207 | ||||||
| chr5:148560208
|
A | T | 60 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-9946T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560208 | ||||||
| chr5:148560209
|
A | T | 8 | a0001c0001t0001g0305a0001c0001t0002g0044a0001c0001t0003g0093others(5): Show | 8 | HG01981.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.27-9947T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560209 | ||||||
| chr5:148560210
|
A | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0211a0001c0001t0003g0094 | 3 | HG02970.hp1 HG03579.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.27-9948T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560210 | ||||||
| chr5:148560211
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.27-9949T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560211 | ||||||
| chr5:148560215
|
A | G | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-9953T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560215 | ||||||
| chr5:148560265
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-10003T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560265 | ||||||
| chr5:148560365
|
A | G | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.27-10103T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560365 | ||||||
| chr5:148560479
|
C | T | 97 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0185others(94): Show | 97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.27-10217G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560479 | ||||||
| chr5:148560490
|
C | A | 14 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-10228G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560490 | ||||||
| chr5:148560592
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.27-10330A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560592 | ||||||
| chr5:148560613
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.27-10351T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560613 | ||||||
| chr5:148560699
|
A | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-10437T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560699 | ||||||
| chr5:148561194
|
A | C | 1 | a0001c0001t0002g0024 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.27-10932T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561194 | ||||||
| chr5:148561250
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27-10988T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561250 | ||||||
| chr5:148561482
|
C | G | 2 | a0001c0001t0001g0177a0001c0001t0006g0176 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-11220G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561482 | ||||||
| chr5:148561492
|
G | A | 92 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.27-11230C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561492 | ||||||
| chr5:148561596
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27-11334C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561596 | ||||||
| chr5:148561625
|
A | AT | 7 | a0001c0001t0003g0105a0001c0002t0001g0159a0001c0002t0001g0161others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-11364dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561625 | ||||||
| chr5:148561625
|
AT | A | 23 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0188others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.27-11364delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561625 | ||||||
| chr5:148561783
|
T | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-11521A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561783 | ||||||
| chr5:148561804
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.27-11542G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561804 | ||||||
| chr5:148561833
|
T | A | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27-11571A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561833 | ||||||
| chr5:148561865
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-11603G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561865 | ||||||
| chr5:148561938
|
C | G | 81 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.27-11676G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561938 | ||||||
| chr5:148562035
|
C | T | 2 | a0001c0001t0003g0102a0001c0001t0004g0269 | 2 | HG00558.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.27-11773G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562035 | ||||||
| chr5:148562204
|
T | G | 6 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-11942A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562204 | ||||||
| chr5:148562282
|
G | C | 210 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.27-12020C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562282 | ||||||
| chr5:148562291
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.27-12029G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562291 | ||||||
| chr5:148562437
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.27-12175G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562437 | ||||||
| chr5:148562447
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0065 | 2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.27-12185G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562447 | ||||||
| chr5:148562470
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-12208G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562470 | ||||||
| chr5:148562588
|
A | G | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-12326T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562588 | ||||||
| chr5:148562593
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-12331T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562593 | ||||||
| chr5:148562675
|
T | C | 199 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.27-12413A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562675 | ||||||
| chr5:148562841
|
A | C | 65 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-12579T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562841 | ||||||
| chr5:148562959
|
A | G | 17 | a0001c0001t0001g0173a0001c0001t0001g0182a0001c0001t0002g0002others(14): Show | 17 | HG00408.hp2 HG00558.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-12697T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562959 | ||||||
| chr5:148563187
|
G | A | 2 | a0001c0001t0002g0035a0001c0001t0002g0068 | 2 | HG03831.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.27-12925C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563187 | ||||||
| chr5:148563381
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-13119G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563381 | ||||||
| chr5:148563430
|
T | C | 65 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-13168A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563430 | ||||||
| chr5:148563442
|
C | T | 184 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.27-13180G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563442 | ||||||
| chr5:148563452
|
C | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0295 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.27-13190G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563452 | ||||||
| chr5:148563609
|
C | T | 46 | a0001c0001t0001g0181a0001c0001t0001g0207a0001c0001t0001g0233others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.27-13347G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563609 | ||||||
| chr5:148563924
|
A | ATGAC | 18 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(15): Show | 18 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-13666_27-13663d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563924 | ||||||
| chr5:148563936
|
A | C | 81 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.27-13674T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563936 | ||||||
| chr5:148564159
|
T | C | 2 | a0001c0001t0008g0131a0001c0001t0008g0132 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-13897A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564159 | ||||||
| chr5:148564182
|
A | T | 93 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0185others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.27-13920T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564182 | ||||||
| chr5:148564206
|
T | C | 187 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.27-13944A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564206 | ||||||
| chr5:148564223
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.27-13961C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564223 | ||||||
| chr5:148564349
|
C | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0074 | 2 | HG02056.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.27-14087G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564349 | ||||||
| chr5:148564350
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-14088C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564350 | ||||||
| chr5:148564434
|
C | A | 1 | a0001c0001t0002g0017 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.27-14172G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564434 | ||||||
| chr5:148564798
|
G | A | 1 | a0001c0001t0025g0301 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.27-14536C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564798 | ||||||
| chr5:148564849
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.27-14587G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564849 | ||||||
| chr5:148564924
|
G | A | 187 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.27-14662C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564924 | ||||||
| chr5:148564975
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.27-14713A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564975 | ||||||
| chr5:148565052
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.27-14790C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565052 | ||||||
| chr5:148565108
|
TA | T | 17 | a0001c0001t0001g0187a0001c0001t0001g0205a0001c0001t0001g0211others(14): Show | 17 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.27-14847delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565108 | ||||||
| chr5:148565108
|
TAA | T | 88 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(85): Show | 88 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.27-14848_27-14847d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565108 | ||||||
| chr5:148565278
|
T | C | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-15016A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565278 | ||||||
| chr5:148565298
|
T | A | 1 | a0001c0001t0003g0095 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.27-15036A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565298 | ||||||
| chr5:148565356
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-15094G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565356 | ||||||
| chr5:148565501
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0212a0001c0001t0001g0220others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-15239A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565501 | ||||||
| chr5:148565585
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-15323C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565585 | ||||||
| chr5:148565594
|
T | TG | 309 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.27-15333dupC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565594 | ||||||
| chr5:148565734
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.27-15472C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565734 | ||||||
| chr5:148565744
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.27-15482C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565744 | ||||||
| chr5:148565841
|
C | T | 1 | a0001c0001t0009g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-15579G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565841 | ||||||
| chr5:148565873
|
G | A | 17 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0188others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-15611C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565873 | ||||||
| chr5:148565881
|
T | C | 6 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-15619A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565881 | ||||||
| chr5:148566047
|
A | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-15785T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566047 | ||||||
| chr5:148566278
|
A | C | 1 | a0001c0001t0005g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27-16016T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566278 | ||||||
| chr5:148566717
|
T | C | 1 | a0001c0002t0008g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.27-16455A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566717 | ||||||
| chr5:148566782
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0026g0186 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.27-16520G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566782 | ||||||
| chr5:148566853
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27-16591G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566853 | ||||||
| chr5:148566877
|
T | A | 1 | a0001c0001t0002g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.27-16615A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566877 | ||||||
| chr5:148567398
|
T | C | 14 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-17136A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567398 | ||||||
| chr5:148567463
|
A | G | 83 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(80): Show | 83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.27-17201T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567463 | ||||||
| chr5:148567483
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.27-17221G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567483 | ||||||
| chr5:148567602
|
G | T | 2 | a0001c0001t0008g0131a0001c0001t0008g0132 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-17340C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567602 | ||||||
| chr5:148567650
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-17388C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567650 | ||||||
| chr5:148567659
|
T | G | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.27-17397A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567659 | ||||||
| chr5:148567725
|
C | T | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-17463G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567725 | ||||||
| chr5:148567860
|
T | C | 1 | a0001c0001t0004g0244 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.27-17598A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567860 | ||||||
| chr5:148567904
|
C | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0211a0001c0001t0001g0292 | 3 | HG01167.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.27-17642G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567904 | ||||||
| chr5:148567921
|
G | A | 92 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.27-17659C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567921 | ||||||
| chr5:148567931
|
G | A | 1 | a0002c0003t0013g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.27-17669C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567931 | ||||||
| chr5:148568020
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-17758C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568020 | ||||||
| chr5:148568431
|
T | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(7): Show | 10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-18169A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568431 | ||||||
| chr5:148568441
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0006g0176 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-18179A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568441 | ||||||
| chr5:148568548
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27-18286A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568548 | ||||||
| chr5:148568711
|
A | G | 130 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(127): Show | 130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.27-18449T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568711 | ||||||
| chr5:148568750
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27-18488A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568750 | ||||||
| chr5:148568763
|
G | A | 5 | a0001c0001t0001g0233a0001c0001t0001g0273a0001c0001t0001g0280others(2): Show | 5 | HG00423.hp1 NA18942.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-18501C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568763 | ||||||
| chr5:148568795
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27-18533T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568795 | ||||||
| chr5:148568983
|
G | A | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-18721C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568983 | ||||||
| chr5:148569024
|
T | G | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-18762A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569024 | ||||||
| chr5:148569038
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0211others(6): Show | 9 | HG01167.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-18776T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569038 | ||||||
| chr5:148569077
|
G | GT | 13 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(10): Show | 13 | HG00738.hp2 HG02055.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.27-18816dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569077 | ||||||
| chr5:148569077
|
GT | G | 14 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-18816delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569077 | ||||||
| chr5:148569331
|
G | A | 1 | a0001c0001t0003g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27-19069C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569331 | ||||||
| chr5:148569346
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.27-19084C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569346 | ||||||
| chr5:148569356
|
G | A | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-19094C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569356 | ||||||
| chr5:148569493
|
T | C | 82 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(79): Show | 82 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.27-19231A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569493 | ||||||
| chr5:148569594
|
T | C | 1 | a0001c0001t0007g0038 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.27-19332A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569594 | ||||||
| chr5:148569768
|
T | G | 1 | a0001c0001t0005g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.27-19506A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569768 | ||||||
| chr5:148569815
|
C | A | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-19553G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569815 | ||||||
| chr5:148569829
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.27-19567T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569829 | ||||||
| chr5:148569831
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27-19569G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569831 | ||||||
| chr5:148569886
|
T | C | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-19624A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569886 | ||||||
| chr5:148570048
|
T | C | 116 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(113): Show | 116 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.27-19786A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570048 | ||||||
| chr5:148570408
|
A | G | 112 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(109): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-20146T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570408 | ||||||
| chr5:148570591
|
G | A | 9 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(6): Show | 9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-20329C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570591 | ||||||
| chr5:148570611
|
T | C | 113 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.27-20349A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570611 | ||||||
| chr5:148570833
|
GGTTTTT | G | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-20577_27-20572d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570833 | ||||||
| chr5:148570915
|
A | C | 80 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(77): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.27-20653T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570915 | ||||||
| chr5:148570995
|
G | A | 1 | a0001c0001t0004g0308 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.27-20733C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570995 | ||||||
| chr5:148571515
|
C | T | 9 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(6): Show | 9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-21253G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571515 | ||||||
| chr5:148571616
|
T | G | 1 | a0001c0001t0014g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.27-21354A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571616 | ||||||
| chr5:148571661
|
T | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(7): Show | 10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-21399A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571661 | ||||||
| chr5:148571683
|
T | A | 1 | a0001c0001t0009g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-21421A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571683 | ||||||
| chr5:148571800
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0003g0114 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.27-21538G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571800 | ||||||
| chr5:148571813
|
T | C | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-21551A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571813 | ||||||
| chr5:148571904
|
A | C | 2 | a0001c0001t0001g0284a0001c0001t0015g0012 | 2 | HG01981.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.27-21642T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571904 | ||||||
| chr5:148572289
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.27-22027G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572289 | ||||||
| chr5:148572520
|
T | A | 2 | a0001c0001t0005g0138a0001c0001t0005g0145 | 2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.27-22258A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572520 | ||||||
| chr5:148572634
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27-22372T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572634 | ||||||
| chr5:148572829
|
T | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-22567A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572829 | ||||||
| chr5:148572976
|
T | C | 102 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(99): Show | 102 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.27-22714A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572976 | ||||||
| chr5:148573049
|
C | T | 2 | a0001c0004t0001g0262a0001c0004t0003g0115 | 2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.27-22787G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573049 | ||||||
| chr5:148573158
|
T | A | 1 | a0001c0001t0005g0147 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.27-22896A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573158 | ||||||
| chr5:148573244
|
G | A | 1 | a0001c0002t0008g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.27-22982C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573244 | ||||||
| chr5:148573391
|
T | C | 1 | a0001c0001t0003g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27-23129A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573391 | ||||||
| chr5:148573452
|
C | T | 10 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(7): Show | 10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-23190G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573452 | ||||||
| chr5:148573472
|
G | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0307others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-23210C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573472 | ||||||
| chr5:148573550
|
C | T | 73 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.27-23288G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573550 | ||||||
| chr5:148573561
|
T | C | 8 | a0001c0001t0001g0164a0001c0001t0004g0162a0001c0001t0004g0165others(5): Show | 8 | NA18947.hp2 NA18963.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-23299A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573561 | ||||||
| chr5:148573646
|
A | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-23384T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573646 | ||||||
| chr5:148573684
|
T | C | 91 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(88): Show | 91 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.27-23422A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573684 | ||||||
| chr5:148573704
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-23442T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573704 | ||||||
| chr5:148573808
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.27-23546C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573808 | ||||||
| chr5:148573979
|
C | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0033a0001c0001t0002g0065others(3): Show | 6 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-23717G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573979 | ||||||
| chr5:148573982
|
G | A | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-23720C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573982 | ||||||
| chr5:148574036
|
C | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(8): Show | 11 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.27-23774G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574036 | ||||||
| chr5:148574390
|
G | GCT | 82 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(79): Show | 82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.27-24130_27-24129d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574390 | ||||||
| chr5:148574392
|
T | G | 10 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(7): Show | 10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-24130A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574392 | ||||||
| chr5:148574394
|
T | G | 9 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(6): Show | 9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-24132A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574394 | ||||||
| chr5:148574423
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-24161G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574423 | ||||||
| chr5:148574424
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27-24162C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574424 | ||||||
| chr5:148574463
|
A | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0294 | 2 | HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.27-24201T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574463 | ||||||
| chr5:148574573
|
T | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0211others(6): Show | 9 | HG01167.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-24311A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574573 | ||||||
| chr5:148574616
|
T | C | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-24354A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574616 | ||||||
| chr5:148574623
|
G | C | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-24361C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574623 | ||||||
| chr5:148574660
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-24398A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574660 | ||||||
| chr5:148574683
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-24421G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574683 | ||||||
| chr5:148574717
|
A | G | 112 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(109): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-24455T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574717 | ||||||
| chr5:148574756
|
C | T | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-24494G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574756 | ||||||
| chr5:148574805
|
G | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-24543C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574805 | ||||||
| chr5:148574848
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-24586T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574848 | ||||||
| chr5:148574922
|
A | T | 21 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(18): Show | 21 | HG00673.hp1 HG00738.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.27-24660T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574922 | ||||||
| chr5:148575245
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-24983G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575245 | ||||||
| chr5:148575347
|
AC | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0188others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-25086delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575347 | ||||||
| chr5:148575555
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.27-25293C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575555 | ||||||
| chr5:148575573
|
C | T | 9 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(6): Show | 9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-25311G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575573 | ||||||
| chr5:148575864
|
A | G | 7 | a0001c0001t0001g0201a0001c0001t0001g0211a0001c0001t0003g0097others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-25602T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575864 | ||||||
| chr5:148575887
|
A | T | 1 | a0001c0001t0002g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.27-25625T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575887 | ||||||
| chr5:148576077
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.27-25815G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576077 | ||||||
| chr5:148576098
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.27-25836C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576098 | ||||||
| chr5:148576106
|
G | A | 1 | a0001c0008t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.27-25844C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576106 | ||||||
| chr5:148576110
|
C | CA | 14 | a0001c0001t0001g0180a0001c0001t0001g0246a0001c0001t0001g0250others(11): Show | 14 | HG01361.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.27-25849dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0194others(9): Show | 12 | HG00099.hp2 HG02258.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-25856_27-25849d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
C | CAAAAAAA others(2): Show |
78 | a0001c0001t0001g0174a0001c0001t0001g0191a0001c0001t0001g0195others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.27-25857_27-25849d others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
C | CAAAAAAA others(3): Show |
54 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0210others(51): Show | 54 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.27-25858_27-25849d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0095a0001c0001t0006g0203 | 2 | HG02145.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27-25859_27-25849d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0292a0001c0001t0010g0083 | 2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.27-25860_27-25849d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0187a0001c0001t0001g0211 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.27-25861_27-25849d others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576110
|
CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-25859_27-25849d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | ||||||
| chr5:148576119
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0177a0001c0001t0006g0176 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-25858_27-25857i others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576119 | ||||||
| chr5:148576119
|
A | AAAAAAAA others(2): Show |
7 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0214others(4): Show | 7 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-25858_27-25857i others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576119 | ||||||
| chr5:148576120
|
A | AAAAACAA others(2): Show |
16 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0188others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27-25859_27-25858i others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576120 | ||||||
| chr5:148576128
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0024g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.27-25867_27-25866i others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576128 | ||||||
| chr5:148576128
|
A | AAAAAAAA others(5): Show |
5 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG02257.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-25867_27-25866i others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576128 | ||||||
| chr5:148576134
|
C | A | 3 | a0001c0001t0002g0028a0001c0001t0003g0095a0001c0001t0005g0142 | 3 | HG01978.hp1 NA18986.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27-25872G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576134 | ||||||
| chr5:148576243
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-25981T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576243 | ||||||
| chr5:148576391
|
T | C | 130 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(127): Show | 130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.27-26129A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576391 | ||||||
| chr5:148576491
|
T | A | 195 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.27-26229A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576491 | ||||||
| chr5:148576738
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-26476T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576738 | ||||||
| chr5:148577390
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27128T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577390 | ||||||
| chr5:148577412
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-27150A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577412 | ||||||
| chr5:148577586
|
G | C | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-27324C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577586 | ||||||
| chr5:148577671
|
A | C | 112 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(109): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-27409T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577671 | ||||||
| chr5:148577727
|
A | C | 112 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(109): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-27465T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577727 | ||||||
| chr5:148577755
|
A | G | 112 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(109): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-27493T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577755 | ||||||
| chr5:148577781
|
C | T | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-27519G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577781 | ||||||
| chr5:148577842
|
G | A | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27580C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577842 | ||||||
| chr5:148577843
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27581T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577843 | ||||||
| chr5:148577944
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0009g0152 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27-27682G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577944 | ||||||
| chr5:148578000
|
A | G | 18 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(15): Show | 18 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-27738T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578000 | ||||||
| chr5:148578024
|
T | C | 1 | a0001c0001t0021g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27762A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578024 | ||||||
| chr5:148578067
|
C | T | 130 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(127): Show | 130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.27-27805G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578067 | ||||||
| chr5:148578455
|
G | T | 7 | a0001c0001t0001g0270a0001c0001t0001g0299a0001c0001t0003g0118others(4): Show | 7 | HG00544.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-28193C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578455 | ||||||
| chr5:148578466
|
C | G | 1 | a0001c0001t0002g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.27-28204G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578466 | ||||||
| chr5:148578479
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0002g0036a0001c0001t0002g0063 | 3 | HG02738.hp2 NA18977.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.27-28217G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578479 | ||||||
| chr5:148578500
|
T | G | 1 | a0001c0001t0006g0282 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.27-28238A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578500 | ||||||
| chr5:148578554
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0026g0186 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.27-28292G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578554 | ||||||
| chr5:148578589
|
G | A | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-28327C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578589 | ||||||
| chr5:148578595
|
C | A | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-28333G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578595 | ||||||
| chr5:148578700
|
G | A | 197 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.27-28438C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578700 | ||||||
| chr5:148578976
|
A | C | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27-28714T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578976 | ||||||
| chr5:148579001
|
G | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.27-28739C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579001 | ||||||
| chr5:148579164
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.27-28902G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579164 | ||||||
| chr5:148579219
|
C | A | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-28957G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579219 | ||||||
| chr5:148579221
|
T | C | 2 | a0001c0001t0008g0131a0001c0001t0008g0132 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-28959A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579221 | ||||||
| chr5:148579326
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-29064C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579326 | ||||||
| chr5:148579417
|
T | C | 105 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(102): Show | 105 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.27-29155A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579417 | ||||||
| chr5:148579623
|
T | C | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-29361A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579623 | ||||||
| chr5:148579848
|
C | T | 64 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-29586G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579848 | ||||||
| chr5:148579997
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-29735C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579997 | ||||||
| chr5:148579999
|
G | C | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-29737C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579999 | ||||||
| chr5:148580320
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.27-30058C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580320 | ||||||
| chr5:148580408
|
T | C | 5 | a0001c0001t0003g0107a0001c0001t0011g0108a0001c0001t0011g0110others(2): Show | 5 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-30146A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580408 | ||||||
| chr5:148580448
|
T | C | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0215others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-30186A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580448 | ||||||
| chr5:148580565
|
A | G | 97 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.27-30303T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580565 | ||||||
| chr5:148580609
|
C | T | 2 | a0001c0001t0008g0131a0001c0001t0008g0132 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-30347G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580609 | ||||||
| chr5:148580613
|
A | T | 97 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.27-30351T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580613 | ||||||
| chr5:148580650
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.27-30388C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580650 | ||||||
| chr5:148580784
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0003g0097a0001c0001t0003g0098others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-30522G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580784 | ||||||
| chr5:148580951
|
TC | T | 9 | a0001c0001t0001g0231a0001c0001t0002g0017a0001c0001t0002g0056others(6): Show | 9 | HG02132.hp1 NA18612.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-30690delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580951 | ||||||
| chr5:148581022
|
CT | C | 196 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.27-30761delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581022 | ||||||
| chr5:148581074
|
G | T | 2 | a0001c0001t0002g0049a0001c0001t0003g0127 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.27-30812C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581074 | ||||||
| chr5:148581075
|
T | G | 2 | a0001c0001t0002g0049a0001c0001t0003g0127 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.27-30813A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581075 | ||||||
| chr5:148581245
|
T | A | 1 | a0001c0001t0012g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27-30983A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581245 | ||||||
| chr5:148581394
|
C | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0191a0001c0001t0001g0194others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-31132G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581394 | ||||||
| chr5:148581432
|
A | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-31170T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581432 | ||||||
| chr5:148581433
|
GC | G | 96 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(93): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.27-31172delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581433 | ||||||
| chr5:148581439
|
C | T | 96 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(93): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.27-31177G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581439 | ||||||
| chr5:148581529
|
G | T | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-31267C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581529 | ||||||
| chr5:148581573
|
C | A | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0257others(4): Show | 7 | HG00597.hp1 HG00673.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-31311G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581573 | ||||||
| chr5:148581772
|
G | A | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-31510C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581772 | ||||||
| chr5:148581941
|
C | G | 107 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0174others(104): Show | 107 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.27-31679G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581941 | ||||||
| chr5:148582040
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0002g0036a0001c0001t0002g0063 | 3 | HG02738.hp2 NA18977.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.27-31778G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582040 | ||||||
| chr5:148582069
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.27-31807T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582069 | ||||||
| chr5:148582164
|
G | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-31902C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582164 | ||||||
| chr5:148582314
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-32052T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582314 | ||||||
| chr5:148582396
|
C | T | 97 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.27-32134G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582396 | ||||||
| chr5:148582710
|
G | A | 14 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-32448C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582710 | ||||||
| chr5:148582732
|
C | G | 3 | a0001c0001t0001g0172a0001c0001t0001g0214a0001c0001t0001g0304 | 3 | HG00738.hp2 HG02698.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.27-32470G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582732 | ||||||
| chr5:148582775
|
C | T | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-32513G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582775 | ||||||
| chr5:148582844
|
C | T | 115 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(112): Show | 115 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.27-32582G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582844 | ||||||
| chr5:148582970
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-32708A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582970 | ||||||
| chr5:148583104
|
G | A | 17 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0188others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-32842C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583104 | ||||||
| chr5:148583168
|
C | T | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-32906G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583168 | ||||||
| chr5:148583194
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.27-32932T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583194 | ||||||
| chr5:148583611
|
C | CCAT | 61 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0180others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.27-33352_27-33350d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | ||||||
| chr5:148583611
|
C | CCATCAT | 4 | a0001c0001t0001g0224a0001c0001t0001g0234a0001c0001t0003g0113others(1): Show | 4 | HG01069.hp1 HG01496.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-33355_27-33350d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | ||||||
| chr5:148583611
|
CCAT | C | 34 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0187others(31): Show | 34 | HG00673.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.27-33352_27-33350d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | ||||||
| chr5:148583611
|
CCATCAT | C | 87 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(84): Show | 87 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.27-33355_27-33350d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | ||||||
| chr5:148583651
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27-33389A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583651 | ||||||
| chr5:148583684
|
A | G | 184 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.27-33422T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583684 | ||||||
| chr5:148583860
|
C | G | 118 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(115): Show | 118 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.27-33598G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583860 | ||||||
| chr5:148584110
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.27-33848G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148584110 | ||||||
| chr5:148584821
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-34559A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148584821 | ||||||
| chr5:148585034
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-34772C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148585034 | ||||||
| chr5:148585095
|
C | A | 113 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.27-34833G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148585095 | ||||||
| chr5:148585610
|
A | G | 119 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(116): Show | 119 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.27-35348T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148585610 | ||||||
| chr5:148586107
|
C | CT | 4 | a0001c0001t0001g0187a0001c0001t0001g0292a0001c0001t0003g0097others(1): Show | 4 | HG01167.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-35846dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586107 | ||||||
| chr5:148586330
|
T | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-36068A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586330 | ||||||
| chr5:148586456
|
A | G | 119 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(116): Show | 119 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.27-36194T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586456 | ||||||
| chr5:148586576
|
G | A | 65 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-36314C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586576 | ||||||
| chr5:148586683
|
C | T | 71 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(68): Show | 71 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.27-36421G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586683 | ||||||
| chr5:148586827
|
G | A | 14 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-36565C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586827 | ||||||
| chr5:148587111
|
A | G | 193 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0173others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.27-36849T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587111 | ||||||
| chr5:148587213
|
T | A | 3 | a0001c0001t0003g0084a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG00673.hp1 NA18951.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.27-36951A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587213 | ||||||
| chr5:148587245
|
A | T | 1 | a0001c0001t0002g0047 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.27-36983T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587245 | ||||||
| chr5:148587430
|
A | T | 4 | a0001c0001t0001g0201a0001c0001t0024g0153a0001c0002t0001g0200others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-37168T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587430 | ||||||
| chr5:148587467
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-37205C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587467 | ||||||
| chr5:148587694
|
A | T | 12 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(9): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-37432T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587694 | ||||||
| chr5:148587936
|
A | C | 68 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0230others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.27-37674T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587936 | ||||||
| chr5:148588019
|
C | T | 4 | a0001c0001t0002g0002a0001c0001t0003g0122a0001c0001t0003g0124others(1): Show | 4 | NA18941.hp1 NA18971.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-37757G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588019 | ||||||
| chr5:148588134
|
A | C | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-37872T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588134 | ||||||
| chr5:148588183
|
A | G | 60 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(57): Show | 60 | HG00609.hp2 HG00673.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-37921T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588183 | ||||||
| chr5:148588341
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.27-38079A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588341 | ||||||
| chr5:148588527
|
C | CT | 17 | a0001c0001t0001g0163a0001c0001t0001g0180a0001c0001t0001g0196others(14): Show | 17 | HG02056.hp1 HG02135.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-38266dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | ||||||
| chr5:148588527
|
CT | C | 118 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(115): Show | 118 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.27-38266delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | ||||||
| chr5:148588527
|
CTT | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0078others(4): Show | 7 | HG02145.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-38267_27-38266d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | ||||||
| chr5:148588527
|
CTTTTTTT others(5): Show |
C | 22 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(19): Show | 22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-38277_27-38266d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | ||||||
| chr5:148588528
|
T | C | 3 | a0001c0001t0001g0284a0001c0001t0002g0019a0001c0001t0002g0062 | 3 | HG03654.hp2 NA19067.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.27-38266A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588528 | ||||||
| chr5:148588529
|
T | C | 62 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0230others(59): Show | 62 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.27-38267A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588529 | ||||||
| chr5:148588530
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0003g0096 | 2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.27-38268A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588530 | ||||||
| chr5:148588531
|
T | C | 1 | a0001c0001t0002g0056 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.27-38269A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588531 | ||||||
| chr5:148588603
|
C | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-38341G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588603 | ||||||
| chr5:148588618
|
G | A | 6 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0011g0108others(3): Show | 6 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-38356C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588618 | ||||||
| chr5:148588679
|
T | C | 2 | a0001c0001t0026g0186a0001c0006t0003g0112 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.27-38417A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588679 | ||||||
| chr5:148588772
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.27-38510G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588772 | ||||||
| chr5:148588951
|
G | A | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-38689C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588951 | ||||||
| chr5:148589034
|
C | G | 22 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(19): Show | 22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-38772G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589034 | ||||||
| chr5:148589114
|
T | C | 26 | a0001c0001t0001g0201a0001c0001t0001g0226a0001c0001t0001g0227others(23): Show | 26 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(23): Show |
intron_variant | MODIFIER | c.27-38852A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589114 | ||||||
| chr5:148589147
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.27-38885G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589147 | ||||||
| chr5:148589179
|
T | C | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.27-38917A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589179 | ||||||
| chr5:148589295
|
G | A | 3 | a0001c0004t0003g0115a0001c0005t0005g0141a0001c0005t0005g0146 | 3 | HG02559.hp2 HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.27-39033C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589295 | ||||||
| chr5:148589370
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27-39108G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589370 | ||||||
| chr5:148589378
|
G | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-39116C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589378 | ||||||
| chr5:148589642
|
T | C | 1 | a0001c0001t0003g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.27-39380A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589642 | ||||||
| chr5:148589784
|
C | T | 22 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(19): Show | 22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-39522G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589784 | ||||||
| chr5:148589793
|
A | T | 15 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(12): Show | 15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-39531T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589793 | ||||||
| chr5:148589821
|
C | T | 22 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(19): Show | 22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-39559G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589821 | ||||||
| chr5:148590029
|
A | G | 1 | a0001c0004t0003g0115 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.27-39767T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590029 | ||||||
| chr5:148590287
|
C | CT | 10 | a0001c0001t0001g0184a0001c0001t0001g0276a0001c0001t0001g0291others(7): Show | 10 | HG00438.hp2 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.27-40026dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | ||||||
| chr5:148590287
|
CT | C | 169 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0178others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.27-40026delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | ||||||
| chr5:148590287
|
CTT | C | 32 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0177others(29): Show | 32 | HG01433.hp1 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.27-40027_27-40026d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | ||||||
| chr5:148590287
|
CTTT | C | 7 | a0001c0001t0001g0172a0001c0001t0003g0088a0001c0001t0008g0131others(4): Show | 7 | HG02451.hp2 HG02698.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-40028_27-40026d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | ||||||
| chr5:148590298
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.27-40036A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590298 | ||||||
| chr5:148590320
|
C | CA | 6 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0087others(3): Show | 6 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-40059dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590320 | ||||||
| chr5:148590338
|
G | T | 15 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(12): Show | 15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-40076C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590338 | ||||||
| chr5:148590400
|
G | GT | 60 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(57): Show | 60 | HG00609.hp2 HG00673.hp1 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-40139_27-40138i others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590400 | ||||||
| chr5:148590484
|
C | T | 1 | a0001c0001t0005g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.27-40222G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590484 | ||||||
| chr5:148590538
|
C | G | 2 | a0001c0002t0003g0086a0003c0009t0027g0310 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.27-40276G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590538 | ||||||
| chr5:148590599
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27-40337A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590599 | ||||||
| chr5:148590711
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-40449C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590711 | ||||||
| chr5:148590921
|
C | T | 67 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0230others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.27-40659G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590921 | ||||||
| chr5:148590922
|
G | A | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.27-40660C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590922 | ||||||
| chr5:148591069
|
C | A | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-40807G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591069 | ||||||
| chr5:148591193
|
T | A | 1 | a0001c0001t0005g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27-40931A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591193 | ||||||
| chr5:148591277
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.27-41015C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591277 | ||||||
| chr5:148591308
|
A | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-41046T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591308 | ||||||
| chr5:148591323
|
T | A | 1 | a0001c0001t0001g0256 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.27-41061A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591323 | ||||||
| chr5:148591630
|
A | G | 17 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(14): Show | 17 | HG00609.hp2 HG00673.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-41368T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591630 | ||||||
| chr5:148591873
|
T | C | 22 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0185others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.27-41611A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591873 | ||||||
| chr5:148592105
|
G | A | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-41843C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592105 | ||||||
| chr5:148592113
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-41851G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592113 | ||||||
| chr5:148592135
|
C | CA | 24 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(21): Show | 24 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.27-41874dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592135 | ||||||
| chr5:148592310
|
T | A | 1 | a0001c0001t0008g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27-42048A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592310 | ||||||
| chr5:148592342
|
G | T | 15 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(12): Show | 15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-42080C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592342 | ||||||
| chr5:148592403
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-42141T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592403 | ||||||
| chr5:148592479
|
G | GT | 17 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(14): Show | 17 | HG00609.hp2 HG00673.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-42218dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592479 | ||||||
| chr5:148592543
|
C | T | 43 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(40): Show | 43 | HG01257.hp2 HG01952.hp1 HG02145.hp2 others(40): Show |
intron_variant | MODIFIER | c.27-42281G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592543 | ||||||
| chr5:148592604
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-42342A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592604 | ||||||
| chr5:148592744
|
G | T | 3 | a0001c0001t0001g0185a0001c0001t0026g0186a0001c0006t0003g0112 | 3 | HG01884.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.27-42482C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592744 | ||||||
| chr5:148593056
|
G | A | 9 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0009g0154others(6): Show | 9 | HG02559.hp1 HG02559.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-42794C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593056 | ||||||
| chr5:148593249
|
G | A | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-42987C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593249 | ||||||
| chr5:148593565
|
A | G | 1 | a0001c0001t0002g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.27-43303T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593565 | ||||||
| chr5:148593686
|
C | T | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26+43303G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593686 | ||||||
| chr5:148593694
|
G | C | 3 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0134 | 3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+43295C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593694 | ||||||
| chr5:148593702
|
A | G | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+43287T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593702 | ||||||
| chr5:148593765
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0264a0001c0001t0001g0307 | 3 | HG02615.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.26+43224T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593765 | ||||||
| chr5:148593806
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.26+43183A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593806 | ||||||
| chr5:148593837
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+43152A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593837 | ||||||
| chr5:148593882
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+43107T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593882 | ||||||
| chr5:148594297
|
A | G | 2 | a0001c0001t0001g0305a0001c0001t0012g0208 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.26+42692T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594297 | ||||||
| chr5:148594346
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.26+42643C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594346 | ||||||
| chr5:148594351
|
C | CGT | 33 | a0001c0001t0001g0164a0001c0001t0001g0182a0001c0001t0001g0215others(30): Show | 33 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.26+42636_26+42637d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | ||||||
| chr5:148594351
|
C | CGTGT | 22 | a0001c0001t0001g0201a0001c0001t0001g0226a0001c0001t0001g0227others(19): Show | 22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.26+42634_26+42637d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | ||||||
| chr5:148594351
|
CGT | C | 11 | a0001c0001t0001g0179a0001c0001t0001g0196a0001c0001t0001g0202others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+42636_26+42637d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | ||||||
| chr5:148594351
|
CGTGT | C | 89 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0001t0001g0184others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.26+42634_26+42637d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | ||||||
| chr5:148594387
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.26+42602G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594387 | ||||||
| chr5:148594576
|
A | C | 21 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(18): Show | 21 | HG00423.hp2 HG00544.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+42413T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594576 | ||||||
| chr5:148594690
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26+42299C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594690 | ||||||
| chr5:148594779
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+42210A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594779 | ||||||
| chr5:148594818
|
A | G | 1 | a0001c0001t0005g0137 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.26+42171T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594818 | ||||||
| chr5:148595081
|
G | GT | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+41907dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595081 | ||||||
| chr5:148595082
|
T | G | 15 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(12): Show | 15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.26+41907A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595082 | ||||||
| chr5:148595310
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+41679G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595310 | ||||||
| chr5:148595450
|
C | T | 15 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(12): Show | 15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.26+41539G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595450 | ||||||
| chr5:148595548
|
CA | C | 3 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0134 | 3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+41440delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595548 | ||||||
| chr5:148595670
|
T | C | 2 | a0001c0001t0001g0256a0001c0004t0001g0262 | 2 | HG02300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.26+41319A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595670 | ||||||
| chr5:148595808
|
A | C | 1 | a0001c0001t0003g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.26+41181T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595808 | ||||||
| chr5:148595954
|
A | G | 3 | a0001c0001t0001g0288a0001c0001t0004g0287a0001c0001t0006g0282 | 3 | NA18991.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.26+41035T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595954 | ||||||
| chr5:148596018
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.26+40971A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596018 | ||||||
| chr5:148596401
|
T | C | 1 | a0001c0001t0002g0005 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.26+40588A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596401 | ||||||
| chr5:148596481
|
C | T | 5 | a0001c0001t0001g0201a0001c0001t0010g0083a0001c0001t0024g0153others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+40508G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596481 | ||||||
| chr5:148596638
|
C | A | 1 | a0001c0001t0002g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.26+40351G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596638 | ||||||
| chr5:148596656
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.26+40333T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596656 | ||||||
| chr5:148596783
|
CATCTTTC others(13): Show |
C | 1 | a0001c0001t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.26+40186_26+40205d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596783 | ||||||
| chr5:148596850
|
T | A | 1 | a0001c0001t0002g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.26+40139A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596850 | ||||||
| chr5:148596927
|
A | G | 2 | a0001c0001t0026g0186a0001c0006t0003g0112 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.26+40062T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596927 | ||||||
| chr5:148597221
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26+39768T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597221 | ||||||
| chr5:148597696
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26+39293T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597696 | ||||||
| chr5:148597700
|
C | A | 6 | a0001c0001t0001g0270a0001c0001t0001g0299a0001c0001t0004g0271others(3): Show | 6 | HG00544.hp1 NA18939.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.26+39289G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597700 | ||||||
| chr5:148597860
|
C | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0014others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+39129G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597860 | ||||||
| chr5:148598041
|
T | C | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+38948A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598041 | ||||||
| chr5:148598056
|
G | T | 1 | a0001c0001t0002g0066 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.26+38933C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598056 | ||||||
| chr5:148598057
|
T | C | 21 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(18): Show | 21 | HG00423.hp2 HG00544.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+38932A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598057 | ||||||
| chr5:148598172
|
G | A | 1 | a0001c0001t0011g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26+38817C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598172 | ||||||
| chr5:148598252
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+38737G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598252 | ||||||
| chr5:148598409
|
A | G | 40 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(37): Show | 40 | HG01257.hp2 HG01952.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.26+38580T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598409 | ||||||
| chr5:148598525
|
C | A | 1 | a0001c0001t0001g0276 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.26+38464G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598525 | ||||||
| chr5:148598558
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+38431T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598558 | ||||||
| chr5:148598632
|
C | T | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+38357G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598632 | ||||||
| chr5:148598690
|
A | T | 67 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0230others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.26+38299T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598690 | ||||||
| chr5:148598829
|
G | A | 1 | a0001c0005t0005g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26+38160C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598829 | ||||||
| chr5:148598839
|
T | C | 1 | a0001c0001t0005g0148 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.26+38150A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598839 | ||||||
| chr5:148598895
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26+38094G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598895 | ||||||
| chr5:148599139
|
C | T | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+37850G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599139 | ||||||
| chr5:148599415
|
C | T | 67 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0230others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.26+37574G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599415 | ||||||
| chr5:148599790
|
T | C | 1 | a0001c0001t0004g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.26+37199A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599790 | ||||||
| chr5:148599803
|
A | G | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+37186T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599803 | ||||||
| chr5:148599989
|
C | T | 1 | a0001c0001t0006g0225 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.26+37000G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599989 | ||||||
| chr5:148600091
|
T | C | 16 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(13): Show | 16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36898A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600091 | ||||||
| chr5:148600249
|
A | G | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+36740T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600249 | ||||||
| chr5:148600348
|
TA | T | 14 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0190others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.26+36640delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600348 | ||||||
| chr5:148600349
|
A | T | 11 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0215others(8): Show | 11 | HG01884.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+36640T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600349 | ||||||
| chr5:148600349
|
AT | A | 78 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0185others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.26+36639delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600349 | ||||||
| chr5:148600351
|
T | A | 49 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(46): Show | 49 | HG00609.hp2 HG00673.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.26+36638A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600351 | ||||||
| chr5:148600415
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+36574G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600415 | ||||||
| chr5:148600434
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26+36555A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600434 | ||||||
| chr5:148600474
|
T | C | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+36515A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600474 | ||||||
| chr5:148600493
|
A | C | 1 | a0001c0001t0004g0244 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.26+36496T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600493 | ||||||
| chr5:148600521
|
T | A | 16 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(13): Show | 16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36468A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600521 | ||||||
| chr5:148600739
|
A | T | 1 | a0001c0001t0003g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.26+36250T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600739 | ||||||
| chr5:148600762
|
A | G | 3 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0134 | 3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+36227T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600762 | ||||||
| chr5:148600932
|
C | T | 16 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(13): Show | 16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36057G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600932 | ||||||
| chr5:148600976
|
C | CA | 115 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0178others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.26+36012dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | ||||||
| chr5:148600976
|
C | CAA | 59 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(56): Show | 59 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.26+36011_26+36012d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | ||||||
| chr5:148600976
|
C | CAAA | 10 | a0001c0001t0001g0174a0001c0001t0001g0194a0001c0001t0001g0209others(7): Show | 10 | HG00438.hp1 HG00621.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.26+36010_26+36012d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | ||||||
| chr5:148600976
|
CA | C | 67 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0001g0177others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.26+36012delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | ||||||
| chr5:148600976
|
CAAAAAAA others(2): Show |
C | 16 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(13): Show | 16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36004_26+36012d others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | ||||||
| chr5:148601080
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.26+35909C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601080 | ||||||
| chr5:148601399
|
G | A | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+35590C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601399 | ||||||
| chr5:148601604
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26+35385G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601604 | ||||||
| chr5:148601626
|
C | G | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+35363G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601626 | ||||||
| chr5:148601626
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+35363G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601626 | ||||||
| chr5:148602048
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+34941T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148602048 | ||||||
| chr5:148602110
|
G | C | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+34879C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148602110 | ||||||
| chr5:148602760
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.26+34229A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148602760 | ||||||
| chr5:148603114
|
G | T | 3 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0134 | 3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+33875C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603114 | ||||||
| chr5:148603292
|
C | T | 151 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(148): Show | 151 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.26+33697G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603292 | ||||||
| chr5:148603439
|
G | A | 19 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0305others(16): Show | 19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+33550C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603439 | ||||||
| chr5:148603472
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.26+33517A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603472 | ||||||
| chr5:148603670
|
A | G | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+33319T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603670 | ||||||
| chr5:148603788
|
G | T | 68 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0230others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.26+33201C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603788 | ||||||
| chr5:148603974
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.26+33015A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603974 | ||||||
| chr5:148604034
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.26+32955T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604034 | ||||||
| chr5:148604086
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0192 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.26+32903A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604086 | ||||||
| chr5:148604398
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.26+32591T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604398 | ||||||
| chr5:148604574
|
G | T | 40 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(37): Show | 40 | HG01257.hp2 HG01952.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.26+32415C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604574 | ||||||
| chr5:148604717
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0180 | 3 | NA18994.hp1 NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.26+32272C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604717 | ||||||
| chr5:148605119
|
G | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26+31870C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605119 | ||||||
| chr5:148605252
|
TTTTC | T | 76 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0179others(73): Show | 76 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+31733_26+31736d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605252 | ||||||
| chr5:148605253
|
TTTC | T | 59 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0231others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.26+31733_26+31735d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605253 | ||||||
| chr5:148605254
|
TTC | T | 7 | a0001c0001t0001g0230a0001c0001t0001g0242a0001c0001t0001g0289others(4): Show | 7 | HG00597.hp2 HG02027.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+31733_26+31734d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605254 | ||||||
| chr5:148605256
|
CTTTT | C | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+31729_26+31732d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605256 | ||||||
| chr5:148605298
|
G | A | 4 | a0001c0001t0001g0201a0001c0001t0024g0153a0001c0002t0001g0200others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+31691C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605298 | ||||||
| chr5:148605320
|
G | A | 16 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(13): Show | 16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+31669C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605320 | ||||||
| chr5:148605345
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.26+31644C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605345 | ||||||
| chr5:148605473
|
G | A | 2 | a0001c0005t0005g0141a0001c0005t0005g0146 | 2 | HG02559.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.26+31516C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605473 | ||||||
| chr5:148605652
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26+31337G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605652 | ||||||
| chr5:148605735
|
G | A | 6 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0087others(3): Show | 6 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+31254C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605735 | ||||||
| chr5:148605747
|
TA | T | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0295others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.26+31241delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605747 | ||||||
| chr5:148605925
|
C | T | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+31064G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605925 | ||||||
| chr5:148606062
|
A | C | 98 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0196others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.26+30927T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606062 | ||||||
| chr5:148606406
|
T | C | 1 | a0001c0001t0004g0279 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26+30583A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606406 | ||||||
| chr5:148606454
|
A | G | 9 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.26+30535T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606454 | ||||||
| chr5:148606458
|
A | T | 3 | a0001c0004t0003g0115a0001c0005t0005g0141a0001c0005t0005g0146 | 3 | HG02559.hp2 HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26+30531T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606458 | ||||||
| chr5:148606725
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.26+30264G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606725 | ||||||
| chr5:148606729
|
T | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26+30260A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606729 | ||||||
| chr5:148607252
|
C | T | 1 | a0001c0001t0005g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.26+29737G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607252 | ||||||
| chr5:148607360
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.26+29629A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607360 | ||||||
| chr5:148607439
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0290 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.26+29550G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607439 | ||||||
| chr5:148607539
|
C | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+29450G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607539 | ||||||
| chr5:148607550
|
T | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0202others(2): Show | 5 | HG01361.hp2 HG01433.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+29439A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607550 | ||||||
| chr5:148607615
|
G | C | 69 | a0001c0001t0001g0207a0001c0001t0001g0241a0001c0001t0001g0268others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.26+29374C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607615 | ||||||
| chr5:148607659
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.26+29330A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607659 | ||||||
| chr5:148607741
|
T | C | 8 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.26+29248A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607741 | ||||||
| chr5:148607824
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.26+29165T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607824 | ||||||
| chr5:148607988
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26+29001G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607988 | ||||||
| chr5:148607989
|
G | A | 1 | a0001c0001t0018g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26+29000C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607989 | ||||||
| chr5:148608166
|
C | A | 2 | a0001c0001t0003g0092a0001c0002t0003g0091 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+28823G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608166 | ||||||
| chr5:148608167
|
C | T | 1 | a0001c0001t0006g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.26+28822G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608167 | ||||||
| chr5:148608236
|
T | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(9): Show | 12 | HG00609.hp2 HG01928.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.26+28753A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608236 | ||||||
| chr5:148608303
|
A | G | 21 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(18): Show | 21 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+28686T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608303 | ||||||
| chr5:148608349
|
G | A | 16 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(13): Show | 16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+28640C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608349 | ||||||
| chr5:148608365
|
G | A | 1 | a0001c0001t0007g0038 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.26+28624C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608365 | ||||||
| chr5:148608414
|
C | T | 78 | a0001c0001t0001g0207a0001c0001t0001g0215a0001c0001t0001g0241others(75): Show | 78 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.26+28575G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608414 | ||||||
| chr5:148608420
|
C | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0202others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+28569G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608420 | ||||||
| chr5:148608541
|
A | G | 2 | a0001c0001t0012g0208a0001c0001t0024g0153 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.26+28448T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608541 | ||||||
| chr5:148608588
|
GT | G | 4 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+28400delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608588 | ||||||
| chr5:148608876
|
G | T | 1 | a0001c0001t0002g0032 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.26+28113C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608876 | ||||||
| chr5:148609115
|
G | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(100): Show | 103 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.26+27874C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609115 | ||||||
| chr5:148609247
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26+27742G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609247 | ||||||
| chr5:148609285
|
C | T | 73 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.26+27704G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609285 | ||||||
| chr5:148609581
|
G | GT | 74 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.26+27407dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609581 | ||||||
| chr5:148609581
|
G | GTT | 16 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(13): Show | 16 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.26+27406_26+27407d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609581 | ||||||
| chr5:148609581
|
GT | G | 59 | a0001c0001t0001g0215a0001c0001t0001g0241a0001c0001t0001g0264others(56): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.26+27407delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609581 | ||||||
| chr5:148609602
|
T | C | 68 | a0001c0001t0001g0207a0001c0001t0001g0215a0001c0001t0001g0241others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.26+27387A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609602 | ||||||
| chr5:148609817
|
C | A | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+27172G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609817 | ||||||
| chr5:148609818
|
A | G | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+27171T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609818 | ||||||
| chr5:148609827
|
A | T | 1 | a0001c0001t0003g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.26+27162T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609827 | ||||||
| chr5:148609936
|
AC | A | 75 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.26+27052delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609936 | ||||||
| chr5:148609951
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.26+27038A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609951 | ||||||
| chr5:148609966
|
A | C | 55 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+27023T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609966 | ||||||
| chr5:148609979
|
A | C | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+27010T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609979 | ||||||
| chr5:148610154
|
C | T | 55 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+26835G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610154 | ||||||
| chr5:148610261
|
C | G | 182 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(179): Show | 182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.26+26728G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610261 | ||||||
| chr5:148610290
|
G | T | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+26699C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610290 | ||||||
| chr5:148610315
|
C | T | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+26674G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610315 | ||||||
| chr5:148610316
|
G | A | 2 | a0001c0006t0003g0112a0002c0003t0022g0101 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+26673C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610316 | ||||||
| chr5:148610320
|
C | T | 1 | a0001c0001t0024g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26+26669G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610320 | ||||||
| chr5:148610375
|
C | T | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+26614G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610375 | ||||||
| chr5:148610378
|
C | G | 73 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.26+26611G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610378 | ||||||
| chr5:148610390
|
C | A | 1 | a0001c0006t0003g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26+26599G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610390 | ||||||
| chr5:148610392
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26+26597C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610392 | ||||||
| chr5:148610469
|
G | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26520C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610469 | ||||||
| chr5:148610474
|
C | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26515G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610474 | ||||||
| chr5:148610477
|
C | G | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26512G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610477 | ||||||
| chr5:148610650
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+26339T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610650 | ||||||
| chr5:148610689
|
T | C | 222 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(219): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.26+26300A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610689 | ||||||
| chr5:148610699
|
G | T | 55 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+26290C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610699 | ||||||
| chr5:148610714
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.26+26275G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610714 | ||||||
| chr5:148610751
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.26+26238G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610751 | ||||||
| chr5:148610825
|
T | C | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+26164A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610825 | ||||||
| chr5:148610870
|
T | C | 207 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(204): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.26+26119A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610870 | ||||||
| chr5:148610871
|
G | A | 4 | a0001c0001t0003g0129a0001c0001t0003g0130a0001c0001t0005g0149others(1): Show | 4 | HG01071.hp1 HG01074.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26118C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610871 | ||||||
| chr5:148610902
|
C | T | 9 | a0001c0001t0001g0164a0001c0001t0004g0162a0001c0001t0004g0165others(6): Show | 9 | NA18947.hp2 NA18962.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.26+26087G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610902 | ||||||
| chr5:148610912
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.26+26077C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610912 | ||||||
| chr5:148610921
|
G | C | 2 | a0001c0006t0003g0112a0002c0003t0022g0101 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+26068C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610921 | ||||||
| chr5:148610962
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26+26027T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610962 | ||||||
| chr5:148610998
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.26+25991C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610998 | ||||||
| chr5:148611023
|
T | C | 2 | a0001c0006t0003g0112a0002c0003t0022g0101 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+25966A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611023 | ||||||
| chr5:148611047
|
C | T | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+25942G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611047 | ||||||
| chr5:148611054
|
G | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0003g0097others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+25935C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611054 | ||||||
| chr5:148611132
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.26+25857T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611132 | ||||||
| chr5:148611227
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.26+25762T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611227 | ||||||
| chr5:148611284
|
C | T | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+25705G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611284 | ||||||
| chr5:148611321
|
C | T | 2 | a0001c0001t0010g0083a0001c0001t0024g0153 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26+25668G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611321 | ||||||
| chr5:148611448
|
A | G | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+25541T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611448 | ||||||
| chr5:148611539
|
T | G | 182 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(179): Show | 182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.26+25450A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611539 | ||||||
| chr5:148611594
|
C | T | 76 | a0001c0001t0001g0207a0001c0001t0001g0215a0001c0001t0001g0241others(73): Show | 76 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+25395G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611594 | ||||||
| chr5:148611635
|
C | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+25354G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611635 | ||||||
| chr5:148611677
|
C | A | 1 | a0001c0001t0007g0038 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.26+25312G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611677 | ||||||
| chr5:148611722
|
C | T | 67 | a0001c0001t0001g0207a0001c0001t0001g0241a0001c0001t0001g0268others(64): Show | 67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.26+25267G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611722 | ||||||
| chr5:148611740
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26+25249C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611740 | ||||||
| chr5:148611766
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18612.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.26+25223G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611766 | ||||||
| chr5:148611943
|
A | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+25046T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611943 | ||||||
| chr5:148612020
|
T | C | 19 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(16): Show | 19 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+24969A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612020 | ||||||
| chr5:148612326
|
G | A | 2 | a0001c0001t0003g0092a0001c0002t0003g0091 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+24663C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612326 | ||||||
| chr5:148612437
|
A | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0006g0203 | 3 | HG01361.hp2 HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.26+24552T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612437 | ||||||
| chr5:148612442
|
G | A | 3 | a0001c0001t0005g0147a0001c0006t0003g0112a0002c0003t0022g0101 | 3 | HG02148.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+24547C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612442 | ||||||
| chr5:148612454
|
G | A | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26+24535C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612454 | ||||||
| chr5:148612481
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0280a0001c0001t0006g0272 | 3 | NA18955.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.26+24508T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612481 | ||||||
| chr5:148612516
|
C | T | 19 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(16): Show | 19 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+24473G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612516 | ||||||
| chr5:148612621
|
A | G | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+24368T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612621 | ||||||
| chr5:148612698
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | NA18945.hp1 NA18952.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.26+24291A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612698 | ||||||
| chr5:148612857
|
G | A | 1 | a0001c0001t0006g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.26+24132C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612857 | ||||||
| chr5:148612907
|
C | T | 1 | a0001c0001t0002g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.26+24082G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612907 | ||||||
| chr5:148612963
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.26+24026A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612963 | ||||||
| chr5:148612984
|
A | C | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+24005T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612984 | ||||||
| chr5:148613184
|
G | A | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+23805C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613184 | ||||||
| chr5:148613210
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+23779C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613210 | ||||||
| chr5:148613257
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26+23732A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613257 | ||||||
| chr5:148613264
|
T | C | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+23725A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613264 | ||||||
| chr5:148613289
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.26+23700G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613289 | ||||||
| chr5:148613299
|
A | G | 190 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(187): Show | 190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.26+23690T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613299 | ||||||
| chr5:148613379
|
C | T | 74 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.26+23610G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613379 | ||||||
| chr5:148613421
|
G | C | 2 | a0001c0001t0003g0092a0001c0002t0003g0091 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+23568C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613421 | ||||||
| chr5:148613478
|
C | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02055.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+23511G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613478 | ||||||
| chr5:148613482
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0062 | 2 | NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.26+23507G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613482 | ||||||
| chr5:148613558
|
A | C | 1 | a0001c0001t0002g0017 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.26+23431T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613558 | ||||||
| chr5:148613575
|
T | C | 8 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.26+23414A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613575 | ||||||
| chr5:148613579
|
G | A | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+23410C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613579 | ||||||
| chr5:148613630
|
T | A | 18 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(15): Show | 18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+23359A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613630 | ||||||
| chr5:148613667
|
G | C | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+23322C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613667 | ||||||
| chr5:148613721
|
G | C | 26 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(23): Show | 26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+23268C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613721 | ||||||
| chr5:148613764
|
T | C | 69 | a0001c0001t0001g0207a0001c0001t0001g0241a0001c0001t0001g0268others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.26+23225A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613764 | ||||||
| chr5:148613775
|
G | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+23214C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613775 | ||||||
| chr5:148613786
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0280a0001c0001t0006g0272 | 3 | NA18955.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.26+23203A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613786 | ||||||
| chr5:148613787
|
G | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0280a0001c0001t0006g0272 | 3 | NA18955.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.26+23202C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613787 | ||||||
| chr5:148614010
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0003g0116a0001c0001t0005g0139others(1): Show | 4 | HG01192.hp2 HG01978.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+22979G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614010 | ||||||
| chr5:148614011
|
G | A | 20 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(17): Show | 20 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.26+22978C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614011 | ||||||
| chr5:148614200
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.26+22789G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614200 | ||||||
| chr5:148614307
|
C | G | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22682G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614307 | ||||||
| chr5:148614322
|
A | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0198others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+22667T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614322 | ||||||
| chr5:148614379
|
A | T | 1 | a0001c0001t0001g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.26+22610T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614379 | ||||||
| chr5:148614386
|
C | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22603G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614386 | ||||||
| chr5:148614422
|
G | C | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.26+22567C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614422 | ||||||
| chr5:148614655
|
G | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22334C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614655 | ||||||
| chr5:148614658
|
A | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22331T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614658 | ||||||
| chr5:148614743
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.26+22246G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614743 | ||||||
| chr5:148614770
|
A | G | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+22219T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614770 | ||||||
| chr5:148615122
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.26+21867G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615122 | ||||||
| chr5:148615261
|
C | T | 3 | a0001c0001t0001g0288a0001c0001t0004g0287a0001c0001t0006g0282 | 3 | NA18991.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.26+21728G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615261 | ||||||
| chr5:148615351
|
T | TA | 5 | a0001c0001t0001g0160a0001c0001t0017g0082a0001c0002t0001g0159others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+21637dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615351 | ||||||
| chr5:148615402
|
T | A | 26 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(23): Show | 26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+21587A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615402 | ||||||
| chr5:148615424
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+21565T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615424 | ||||||
| chr5:148615542
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0290 | 2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.26+21447T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615542 | ||||||
| chr5:148615563
|
GAGATATA others(4): Show |
G | 7 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0003g0107others(4): Show | 7 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+21415_26+21425d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615563 | ||||||
| chr5:148615681
|
A | G | 18 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(15): Show | 18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+21308T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615681 | ||||||
| chr5:148615692
|
TAAAG | T | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21293_26+21296d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615692 | ||||||
| chr5:148615696
|
G | T | 22 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(19): Show | 22 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.26+21293C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615696 | ||||||
| chr5:148615700
|
G | T | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21289C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615700 | ||||||
| chr5:148615704
|
G | T | 5 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0003g0086others(2): Show | 5 | HG02647.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+21285C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615704 | ||||||
| chr5:148615707
|
A | AT | 12 | a0001c0001t0001g0164a0001c0001t0001g0177a0001c0001t0001g0214others(9): Show | 12 | HG03017.hp2 HG03710.hp2 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.26+21281_26+21282i others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | ||||||
| chr5:148615707
|
A | ATAAAAT | 7 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0181others(4): Show | 7 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21281_26+21282i others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | ||||||
| chr5:148615707
|
A | ATAAATAA others(3): Show |
2 | a0001c0002t0008g0133a0001c0002t0008g0134 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.26+21281_26+21282i others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | ||||||
| chr5:148615707
|
A | ATAAATAA others(8): Show |
1 | a0001c0001t0008g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26+21281_26+21282i others(17): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | ||||||
| chr5:148615708
|
G | A | 23 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(20): Show | 23 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.26+21281C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | ||||||
| chr5:148615708
|
G | GAAATA | 66 | a0001c0001t0001g0204a0001c0001t0001g0227a0001c0001t0001g0230others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.26+21276_26+21280d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | ||||||
| chr5:148615708
|
G | GAAATAAA others(3): Show |
20 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(17): Show | 20 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.26+21271_26+21280d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | ||||||
| chr5:148615708
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0248 | 2 | NA18967.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.26+21281C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | ||||||
| chr5:148615713
|
A | T | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+21276T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615713 | ||||||
| chr5:148615813
|
C | T | 3 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015 | 3 | HG00099.hp2 HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.26+21176G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615813 | ||||||
| chr5:148615851
|
C | G | 13 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.26+21138G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615851 | ||||||
| chr5:148615861
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+21128T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615861 | ||||||
| chr5:148615898
|
C | T | 3 | a0001c0001t0003g0092a0001c0001t0003g0103a0001c0002t0003g0091 | 3 | HG02630.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+21091G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615898 | ||||||
| chr5:148616042
|
T | C | 73 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.26+20947A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616042 | ||||||
| chr5:148616127
|
A | T | 18 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(15): Show | 18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+20862T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616127 | ||||||
| chr5:148616524
|
T | C | 236 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(233): Show | 236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.26+20465A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616524 | ||||||
| chr5:148616557
|
T | C | 1 | a0001c0001t0006g0225 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.26+20432A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616557 | ||||||
| chr5:148616566
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.26+20423G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616566 | ||||||
| chr5:148616584
|
A | C | 2 | a0001c0001t0001g0256a0001c0004t0001g0262 | 2 | HG02300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.26+20405T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616584 | ||||||
| chr5:148616767
|
AT | A | 54 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.26+20221delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616767 | ||||||
| chr5:148616842
|
A | C | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.26+20147T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616842 | ||||||
| chr5:148617092
|
G | A | 5 | a0001c0001t0002g0016a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00408.hp2 HG00438.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+19897C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617092 | ||||||
| chr5:148617141
|
T | C | 18 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(15): Show | 18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+19848A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617141 | ||||||
| chr5:148617196
|
G | A | 1 | a0001c0001t0004g0171 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.26+19793C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617196 | ||||||
| chr5:148617295
|
G | T | 1 | a0001c0001t0002g0017 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.26+19694C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617295 | ||||||
| chr5:148617325
|
C | T | 72 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.26+19664G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617325 | ||||||
| chr5:148617360
|
T | G | 18 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(15): Show | 18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+19629A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617360 | ||||||
| chr5:148617366
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.26+19623A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617366 | ||||||
| chr5:148617469
|
TTTTTTTT others(2): Show |
T | 54 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.26+19511_26+19519d others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617469 | ||||||
| chr5:148617477
|
T | TTG | 26 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(23): Show | 26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+19511_26+19512i others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617477 | ||||||
| chr5:148617478
|
G | GT | 21 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(18): Show | 21 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+19510dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617478 | ||||||
| chr5:148617478
|
G | T | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+19511C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617478 | ||||||
| chr5:148617530
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26+19459C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617530 | ||||||
| chr5:148617592
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.26+19397G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617592 | ||||||
| chr5:148617629
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.26+19360G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617629 | ||||||
| chr5:148617714
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.26+19275C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617714 | ||||||
| chr5:148617816
|
G | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0263 | 3 | HG01069.hp2 HG01071.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.26+19173C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617816 | ||||||
| chr5:148617883
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.26+19106C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617883 | ||||||
| chr5:148617922
|
T | C | 6 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0195others(3): Show | 6 | HG01243.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+19067A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617922 | ||||||
| chr5:148618015
|
G | A | 11 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0001t0001g0214others(8): Show | 11 | HG02056.hp2 NA18947.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+18974C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618015 | ||||||
| chr5:148618034
|
C | G | 32 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0008others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+18955G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618034 | ||||||
| chr5:148618036
|
T | A | 32 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0008others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+18953A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618036 | ||||||
| chr5:148618038
|
AG | A | 32 | a0001c0001t0001g0207a0001c0001t0002g0005a0001c0001t0002g0008others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+18950delC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618038 | ||||||
| chr5:148618069
|
A | T | 1 | a0001c0001t0026g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+18920T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618069 | ||||||
| chr5:148618213
|
G | A | 1 | a0001c0001t0006g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.26+18776C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618213 | ||||||
| chr5:148618250
|
A | G | 1 | a0001c0001t0005g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.26+18739T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618250 | ||||||
| chr5:148618503
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.26+18486G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618503 | ||||||
| chr5:148618556
|
G | A | 71 | a0001c0001t0001g0207a0001c0001t0001g0215a0001c0001t0001g0241others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.26+18433C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618556 | ||||||
| chr5:148618581
|
G | C | 1 | a0001c0001t0006g0240 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.26+18408C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618581 | ||||||
| chr5:148618644
|
TC | T | 77 | a0001c0001t0001g0207a0001c0001t0001g0215a0001c0001t0001g0241others(74): Show | 77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.26+18344delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618644 | ||||||
| chr5:148618668
|
C | T | 1 | a0001c0001t0004g0279 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26+18321G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618668 | ||||||
| chr5:148618813
|
A | T | 54 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.26+18176T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618813 | ||||||
| chr5:148618928
|
A | G | 205 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(202): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.26+18061T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618928 | ||||||
| chr5:148619016
|
G | T | 236 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(233): Show | 236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.26+17973C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619016 | ||||||
| chr5:148619147
|
A | G | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+17842T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619147 | ||||||
| chr5:148619293
|
A | G | 1 | a0001c0001t0005g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.26+17696T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619293 | ||||||
| chr5:148619340
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | NA18945.hp1 NA18952.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.26+17649C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619340 | ||||||
| chr5:148619452
|
TAAGTTA | T | 27 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(24): Show | 27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+17531_26+17536d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619452 | ||||||
| chr5:148619508
|
CT | C | 3 | a0001c0001t0001g0201a0001c0001t0001g0226a0001c0002t0001g0200 | 3 | HG02257.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.26+17480delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619508 | ||||||
| chr5:148619769
|
A | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.26+17220T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619769 | ||||||
| chr5:148620187
|
G | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+16802C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620187 | ||||||
| chr5:148620340
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG02486.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.26+16649A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620340 | ||||||
| chr5:148620361
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0263 | 3 | HG01069.hp2 HG01071.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.26+16628C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620361 | ||||||
| chr5:148620466
|
G | A | 18 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(15): Show | 18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+16523C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620466 | ||||||
| chr5:148620754
|
A | G | 5 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+16235T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620754 | ||||||
| chr5:148620981
|
G | A | 309 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.26+16008C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620981 | ||||||
| chr5:148621170
|
A | G | 1 | a0001c0001t0015g0012 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26+15819T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621170 | ||||||
| chr5:148621782
|
ATTTCCT | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0007g0031others(1): Show | 4 | HG00408.hp2 HG00438.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+15201_26+15206d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621782 | ||||||
| chr5:148621879
|
G | C | 1 | a0001c0001t0004g0279 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26+15110C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621879 | ||||||
| chr5:148621898
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.26+15091T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621898 | ||||||
| chr5:148621907
|
T | C | 55 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+15082A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621907 | ||||||
| chr5:148622049
|
G | C | 13 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.26+14940C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622049 | ||||||
| chr5:148622762
|
G | A | 26 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(23): Show | 26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+14227C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622762 | ||||||
| chr5:148622771
|
T | A | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+14218A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622771 | ||||||
| chr5:148622891
|
T | A | 26 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(23): Show | 26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+14098A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622891 | ||||||
| chr5:148623117
|
A | C | 1 | a0001c0001t0006g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.26+13872T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623117 | ||||||
| chr5:148623291
|
A | G | 5 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0003g0086others(2): Show | 5 | HG02647.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+13698T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623291 | ||||||
| chr5:148623779
|
C | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0226a0001c0002t0001g0200 | 3 | HG02257.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.26+13210G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623779 | ||||||
| chr5:148623917
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+13072C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623917 | ||||||
| chr5:148624236
|
G | C | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26+12753C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624236 | ||||||
| chr5:148624400
|
A | C | 1 | a0001c0002t0003g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+12589T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624400 | ||||||
| chr5:148624669
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+12320G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624669 | ||||||
| chr5:148624680
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.26+12309G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624680 | ||||||
| chr5:148624872
|
T | C | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.26+12117A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624872 | ||||||
| chr5:148625155
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.26+11834C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625155 | ||||||
| chr5:148625190
|
A | T | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+11799T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625190 | ||||||
| chr5:148625684
|
G | A | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+11305C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625684 | ||||||
| chr5:148625886
|
C | CT | 12 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0198others(9): Show | 12 | HG01192.hp2 HG01978.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.26+11102dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625886 | ||||||
| chr5:148626511
|
T | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+10478A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626511 | ||||||
| chr5:148626687
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.26+10302G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626687 | ||||||
| chr5:148626699
|
A | T | 53 | a0001c0001t0001g0215a0001c0001t0001g0241a0001c0001t0001g0264others(50): Show | 53 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.26+10290T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626699 | ||||||
| chr5:148626709
|
G | A | 7 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0003g0107others(4): Show | 7 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+10280C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626709 | ||||||
| chr5:148627018
|
C | A | 2 | a0001c0001t0001g0288a0001c0001t0004g0287 | 2 | NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.26+9971G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627018 | ||||||
| chr5:148627041
|
A | T | 1 | a0001c0001t0006g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.26+9948T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627041 | ||||||
| chr5:148627188
|
T | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26+9801A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627188 | ||||||
| chr5:148627309
|
A | T | 17 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(14): Show | 17 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.26+9680T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627309 | ||||||
| chr5:148627338
|
G | A | 76 | a0001c0001t0001g0207a0001c0001t0001g0230a0001c0001t0001g0231others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+9651C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627338 | ||||||
| chr5:148627342
|
AT | A | 76 | a0001c0001t0001g0207a0001c0001t0001g0230a0001c0001t0001g0231others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+9646delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627342 | ||||||
| chr5:148627344
|
T | C | 76 | a0001c0001t0001g0207a0001c0001t0001g0230a0001c0001t0001g0231others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+9645A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627344 | ||||||
| chr5:148627367
|
T | G | 1 | a0001c0004t0001g0262 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.26+9622A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627367 | ||||||
| chr5:148627383
|
C | A | 84 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(81): Show | 84 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.26+9606G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627383 | ||||||
| chr5:148627390
|
C | T | 84 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(81): Show | 84 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.26+9599G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627390 | ||||||
| chr5:148627450
|
G | A | 183 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(180): Show | 183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.26+9539C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627450 | ||||||
| chr5:148627589
|
T | C | 1 | a0001c0001t0003g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.26+9400A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627589 | ||||||
| chr5:148627680
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0289 | 2 | NA19000.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.26+9309A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627680 | ||||||
| chr5:148627690
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.26+9299T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627690 | ||||||
| chr5:148627826
|
C | T | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.26+9163G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627826 | ||||||
| chr5:148628102
|
T | A | 1 | a0001c0001t0024g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26+8887A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628102 | ||||||
| chr5:148628149
|
T | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0013others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.26+8840A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628149 | ||||||
| chr5:148628261
|
G | T | 1 | a0001c0001t0002g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.26+8728C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628261 | ||||||
| chr5:148628297
|
C | A | 183 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(180): Show | 183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.26+8692G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628297 | ||||||
| chr5:148628502
|
T | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0006g0203 | 3 | HG01361.hp2 HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.26+8487A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628502 | ||||||
| chr5:148628757
|
T | A | 1 | a0001c0001t0024g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26+8232A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628757 | ||||||
| chr5:148628858
|
T | G | 24 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(21): Show | 24 | HG01071.hp1 HG01074.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.26+8131A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628858 | ||||||
| chr5:148629028
|
C | T | 24 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(21): Show | 24 | HG01071.hp1 HG01074.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.26+7961G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629028 | ||||||
| chr5:148629044
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.26+7945G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629044 | ||||||
| chr5:148629538
|
G | A | 47 | a0001c0001t0001g0215a0001c0001t0001g0241a0001c0001t0001g0264others(44): Show | 47 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.26+7451C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629538 | ||||||
| chr5:148629567
|
G | C | 2 | a0001c0001t0002g0033a0001c0001t0002g0065 | 2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.26+7422C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629567 | ||||||
| chr5:148629831
|
C | T | 11 | a0001c0001t0002g0005a0001c0001t0003g0092a0001c0001t0003g0096others(8): Show | 11 | HG00438.hp1 HG00558.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+7158G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629831 | ||||||
| chr5:148629851
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.26+7138A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629851 | ||||||
| chr5:148629918
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26+7071C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629918 | ||||||
| chr5:148629961
|
A | G | 13 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(10): Show | 13 | HG00609.hp2 HG01928.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.26+7028T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629961 | ||||||
| chr5:148630485
|
C | A | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+6504G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630485 | ||||||
| chr5:148630506
|
G | A | 188 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(185): Show | 188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.26+6483C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630506 | ||||||
| chr5:148630566
|
C | T | 4 | a0001c0001t0003g0129a0001c0001t0003g0130a0001c0001t0005g0149others(1): Show | 4 | HG01071.hp1 HG01074.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+6423G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630566 | ||||||
| chr5:148630573
|
T | C | 1 | a0001c0001t0009g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26+6416A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630573 | ||||||
| chr5:148630630
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+6359T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630630 | ||||||
| chr5:148631219
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+5770A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631219 | ||||||
| chr5:148631350
|
G | A | 78 | a0001c0001t0001g0207a0001c0001t0001g0230a0001c0001t0001g0231others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.26+5639C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631350 | ||||||
| chr5:148631549
|
C | T | 1 | a0001c0001t0003g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.26+5440G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631549 | ||||||
| chr5:148631608
|
G | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+5381C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631608 | ||||||
| chr5:148631644
|
A | T | 1 | a0001c0001t0002g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26+5345T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631644 | ||||||
| chr5:148631771
|
G | C | 3 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0290 | 3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.26+5218C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631771 | ||||||
| chr5:148631792
|
C | T | 1 | a0001c0001t0006g0282 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.26+5197G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631792 | ||||||
| chr5:148632009
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26+4980C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632009 | ||||||
| chr5:148632167
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.26+4822G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632167 | ||||||
| chr5:148632172
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.26+4817G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632172 | ||||||
| chr5:148632176
|
T | C | 238 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0172others(235): Show | 238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.26+4813A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632176 | ||||||
| chr5:148632299
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.26+4690G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632299 | ||||||
| chr5:148632393
|
C | T | 161 | a0001c0001t0001g0173a0001c0001t0001g0185a0001c0001t0001g0187others(158): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.26+4596G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632393 | ||||||
| chr5:148632411
|
C | G | 1 | a0001c0001t0002g0025 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.26+4578G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632411 | ||||||
| chr5:148632483
|
A | G | 1 | a0001c0001t0006g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.26+4506T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632483 | ||||||
| chr5:148632496
|
G | A | 2 | a0001c0001t0001g0195a0003c0009t0027g0310 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.26+4493C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632496 | ||||||
| chr5:148632664
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+4325A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632664 | ||||||
| chr5:148632742
|
G | A | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+4247C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632742 | ||||||
| chr5:148632746
|
G | GA | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+4242dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632746 | ||||||
| chr5:148632849
|
A | C | 1 | a0001c0001t0005g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.26+4140T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632849 | ||||||
| chr5:148632851
|
A | G | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+4138T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632851 | ||||||
| chr5:148632860
|
T | C | 1 | a0001c0001t0003g0124 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.26+4129A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632860 | ||||||
| chr5:148632990
|
A | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+3999T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632990 | ||||||
| chr5:148633126
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.26+3863C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633126 | ||||||
| chr5:148633164
|
A | T | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+3825T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633164 | ||||||
| chr5:148633353
|
C | T | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG01891.hp1 HG02698.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+3636G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633353 | ||||||
| chr5:148633382
|
C | CT | 128 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.26+3606dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633382 | ||||||
| chr5:148633486
|
A | G | 152 | a0001c0001t0001g0173a0001c0001t0001g0185a0001c0001t0001g0187others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.26+3503T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633486 | ||||||
| chr5:148633528
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.26+3461G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633528 | ||||||
| chr5:148633539
|
C | T | 2 | a0001c0006t0003g0112a0002c0003t0022g0101 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+3450G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633539 | ||||||
| chr5:148633612
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+3377C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633612 | ||||||
| chr5:148633625
|
C | T | 13 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.26+3364G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633625 | ||||||
| chr5:148633890
|
G | C | 17 | a0001c0001t0001g0173a0001c0001t0002g0020a0001c0001t0002g0021others(14): Show | 17 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.26+3099C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633890 | ||||||
| chr5:148634166
|
C | A | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.26+2823G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634166 | ||||||
| chr5:148634179
|
G | C | 142 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.26+2810C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634179 | ||||||
| chr5:148634215
|
T | C | 1 | a0001c0001t0003g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.26+2774A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634215 | ||||||
| chr5:148634335
|
G | A | 2 | a0001c0002t0001g0161a0001c0002t0003g0085 | 2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.26+2654C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634335 | ||||||
| chr5:148634424
|
T | C | 3 | a0001c0001t0002g0017a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | NA18965.hp1 NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.26+2565A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634424 | ||||||
| chr5:148634553
|
T | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0006g0203 | 3 | HG01361.hp2 HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.26+2436A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634553 | ||||||
| chr5:148634704
|
T | C | 2 | a0001c0001t0001g0201a0001c0002t0001g0200 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.26+2285A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634704 | ||||||
| chr5:148635022
|
C | T | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+1967G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635022 | ||||||
| chr5:148635050
|
C | A | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+1939G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635050 | ||||||
| chr5:148635344
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+1645A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635344 | ||||||
| chr5:148635463
|
A | G | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.26+1526T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635463 | ||||||
| chr5:148635554
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26+1435A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635554 | ||||||
| chr5:148635678
|
A | G | 2 | a0001c0001t0004g0157a0001c0001t0004g0247 | 2 | NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.26+1311T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635678 | ||||||
| chr5:148635922
|
A | T | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+1067T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635922 | ||||||
| chr5:148635941
|
A | G | 3 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156 | 3 | HG02559.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.26+1048T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635941 | ||||||
| chr5:148636206
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+783A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636206 | ||||||
| chr5:148636240
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0006g0203 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.26+749T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636240 | ||||||
| chr5:148636355
|
A | C | 3 | a0001c0001t0010g0080a0001c0001t0010g0081a0001c0001t0017g0082 | 3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.26+634T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636355 | ||||||
| chr5:148636430
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.26+559A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636430 | ||||||
| chr5:148636501
|
G | A | 14 | a0001c0001t0002g0002a0001c0001t0003g0117a0001c0001t0003g0118others(11): Show | 14 | HG00140.hp2 HG01071.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.26+488C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636501 | ||||||
| chr5:148636556
|
C | A | 1 | a0001c0001t0003g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.26+433G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636556 | ||||||
| chr5:148636632
|
C | T | 5 | a0001c0001t0002g0005a0001c0001t0003g0093a0001c0001t0003g0094others(2): Show | 5 | NA18951.hp2 NA18975.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+357G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636632 | ||||||
| chr5:148636801
|
C | T | 2 | a0001c0006t0003g0112a0002c0003t0022g0101 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+188G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636801 | ||||||
| chr5:148636868
|
T | C | 2 | a0001c0002t0008g0133a0001c0002t0008g0134 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.26+121A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636868 | ||||||
| chr5:148636974
|
A | G | 14 | a0001c0001t0002g0002a0001c0001t0003g0117a0001c0001t0003g0118others(11): Show | 14 | HG00140.hp2 HG01071.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.26+15T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636974 | ||||||
| chr5:148637073
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-47-12C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637073 | ||||||
| chr5:148637184
|
A | G | 1 | a0001c0001t0006g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-123T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637184 | ||||||
| chr5:148637200
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-47-139G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637200 | ||||||
| chr5:148637222
|
C | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-161G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637222 | ||||||
| chr5:148637291
|
T | C | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-230A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637291 | ||||||
| chr5:148637294
|
G | T | 163 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-47-233C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637294 | ||||||
| chr5:148637362
|
G | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-301C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637362 | ||||||
| chr5:148637377
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-316A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637377 | ||||||
| chr5:148637421
|
TTGCCCAA others(2): Show |
T | 24 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(21): Show | 24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-369_-47-361del others(9): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637421 | ||||||
| chr5:148637432
|
G | C | 1 | a0001c0001t0005g0147 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-47-371C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637432 | ||||||
| chr5:148637446
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-385A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637446 | ||||||
| chr5:148637457
|
T | TA | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-397dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637457 | ||||||
| chr5:148637861
|
C | T | 5 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0010g0080others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-800G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637861 | ||||||
| chr5:148637874
|
T | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-813A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637874 | ||||||
| chr5:148638041
|
T | A | 2 | a0001c0001t0001g0246a0001c0001t0006g0265 | 2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-47-980A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638041 | ||||||
| chr5:148638044
|
G | GT | 171 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-984dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638044 | ||||||
| chr5:148638096
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1035C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638096 | ||||||
| chr5:148638561
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0252 | 2 | NA18942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-47-1500G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638561 | ||||||
| chr5:148638626
|
G | GAC | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1567_-47-1566d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638626 | ||||||
| chr5:148638638
|
T | G | 167 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-47-1577A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638638 | ||||||
| chr5:148638647
|
C | G | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1586G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638647 | ||||||
| chr5:148638760
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1699C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638760 | ||||||
| chr5:148638786
|
A | G | 171 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-1725T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638786 | ||||||
| chr5:148638809
|
C | T | 1 | a0002c0003t0019g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-47-1748G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638809 | ||||||
| chr5:148638829
|
T | C | 171 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-1768A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638829 | ||||||
| chr5:148638830
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0065 | 2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-47-1769C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638830 | ||||||
| chr5:148638835
|
G | A | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1774C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638835 | ||||||
| chr5:148638891
|
C | T | 24 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(21): Show | 24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-1830G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638891 | ||||||
| chr5:148638919
|
TG | T | 24 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(21): Show | 24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-1859delC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638919 | ||||||
| chr5:148639122
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-47-2061A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639122 | ||||||
| chr5:148639264
|
A | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2203T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639264 | ||||||
| chr5:148639275
|
C | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2214G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639275 | ||||||
| chr5:148639410
|
C | T | 1 | a0001c0001t0003g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-47-2349G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639410 | ||||||
| chr5:148639553
|
C | A | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-2492G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639553 | ||||||
| chr5:148639617
|
G | GTA | 23 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0201others(20): Show | 23 | HG00544.hp1 HG00673.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-2558_-47-2557d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATA | 28 | a0001c0001t0001g0250a0001c0001t0001g0295a0001c0001t0001g0296others(25): Show | 28 | HG00738.hp1 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-47-2560_-47-2557d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATA | 64 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-47-2562_-47-2557d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(1): Show |
33 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0022others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.-47-2564_-47-2557d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(3): Show |
11 | a0001c0001t0002g0005a0001c0001t0002g0072a0001c0001t0002g0075others(8): Show | 11 | HG00558.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47-2566_-47-2557d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0003g0092 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-47-2568_-47-2557d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(9): Show |
15 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0177others(12): Show | 15 | HG02886.hp1 HG02895.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-2572_-47-2557d others(18): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(11): Show |
10 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0178others(7): Show | 10 | HG01361.hp2 HG01433.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-2574_-47-2557d others(20): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0175 | 2 | NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-47-2576_-47-2557d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(15): Show |
4 | a0001c0001t0001g0174a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG02056.hp2 HG02818.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2578_-47-2557d others(24): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0003g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-2580_-47-2557d others(26): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639617
|
GTA | G | 8 | a0001c0001t0001g0195a0001c0001t0001g0202a0001c0001t0001g0216others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-2558_-47-2557d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | ||||||
| chr5:148639985
|
C | T | 138 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-47-2924G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639985 | ||||||
| chr5:148639987
|
C | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | NA18955.hp2 NA18970.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-2926G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639987 | ||||||
| chr5:148640004
|
C | A | 2 | a0001c0001t0001g0201a0001c0002t0001g0200 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-47-2943G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640004 | ||||||
| chr5:148640024
|
C | T | 138 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-47-2963G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640024 | ||||||
| chr5:148640066
|
T | C | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-3005A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640066 | ||||||
| chr5:148640168
|
T | G | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3107A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640168 | ||||||
| chr5:148640210
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-47-3149C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640210 | ||||||
| chr5:148640477
|
A | G | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-3416T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640477 | ||||||
| chr5:148640573
|
G | A | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-3512C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640573 | ||||||
| chr5:148640591
|
T | G | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-47-3530A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640591 | ||||||
| chr5:148640696
|
G | C | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3635C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640696 | ||||||
| chr5:148641023
|
C | T | 6 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(3): Show | 6 | HG01928.hp2 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-3962G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641023 | ||||||
| chr5:148641260
|
T | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0180 | 2 | NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-47-4199A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641260 | ||||||
| chr5:148641276
|
A | C | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-47-4215T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641276 | ||||||
| chr5:148641387
|
T | G | 166 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-47-4326A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641387 | ||||||
| chr5:148641444
|
C | A | 1 | a0001c0001t0003g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-47-4383G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641444 | ||||||
| chr5:148641448
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-4387C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641448 | ||||||
| chr5:148641449
|
C | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-4388G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641449 | ||||||
| chr5:148641450
|
A | C | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-4389T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641450 | ||||||
| chr5:148641471
|
C | T | 1 | a0001c0001t0009g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-47-4410G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641471 | ||||||
| chr5:148641479
|
T | C | 171 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-4418A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641479 | ||||||
| chr5:148641768
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0182 | 3 | HG01361.hp2 HG01433.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-47-4707C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641768 | ||||||
| chr5:148641806
|
G | A | 1 | a0001c0001t0003g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-47-4745C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641806 | ||||||
| chr5:148641949
|
G | A | 6 | a0001c0001t0001g0270a0001c0001t0001g0299a0001c0001t0004g0271others(3): Show | 6 | HG00544.hp1 NA18939.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-4888C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641949 | ||||||
| chr5:148641951
|
T | C | 5 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-4890A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641951 | ||||||
| chr5:148642322
|
T | C | 13 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47-5261A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642322 | ||||||
| chr5:148642397
|
A | G | 13 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47-5336T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642397 | ||||||
| chr5:148642459
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-47-5398T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642459 | ||||||
| chr5:148642485
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-5424G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642485 | ||||||
| chr5:148642607
|
A | G | 143 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-47-5546T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642607 | ||||||
| chr5:148642621
|
G | A | 24 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(21): Show | 24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-5560C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642621 | ||||||
| chr5:148643185
|
A | T | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-6124T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643185 | ||||||
| chr5:148643188
|
AG | A | 3 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156 | 3 | HG02559.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47-6128delC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643188 | ||||||
| chr5:148643402
|
C | G | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-47-6341G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643402 | ||||||
| chr5:148643514
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-47-6453A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643514 | ||||||
| chr5:148643535
|
G | C | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-6474C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643535 | ||||||
| chr5:148643563
|
C | G | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-6502G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643563 | ||||||
| chr5:148643715
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-47-6654A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643715 | ||||||
| chr5:148643789
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-47-6728T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643789 | ||||||
| chr5:148643823
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-47-6762G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643823 | ||||||
| chr5:148643990
|
T | C | 1 | a0001c0001t0005g0148 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-47-6929A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643990 | ||||||
| chr5:148644009
|
T | C | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-6948A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644009 | ||||||
| chr5:148644024
|
C | T | 5 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-6963G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644024 | ||||||
| chr5:148644070
|
G | T | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-7009C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644070 | ||||||
| chr5:148644206
|
C | T | 1 | a0001c0001t0005g0137 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-47-7145G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644206 | ||||||
| chr5:148644364
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47-7303G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644364 | ||||||
| chr5:148644421
|
AGTTTTTT others(3): Show |
A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-7370_-47-7361d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644421 | ||||||
| chr5:148644422
|
G | GT | 49 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.-47-7362dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
G | GTT | 36 | a0001c0001t0001g0185a0001c0001t0001g0205a0001c0001t0001g0216others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-7363_-47-7362d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
G | GTTT | 14 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0209others(11): Show | 14 | HG02055.hp1 HG02074.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-7364_-47-7362d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0024g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-47-7373_-47-7362d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
GT | G | 24 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0001g0194others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-7362delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
GTT | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0013others(47): Show | 50 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.-47-7363_-47-7362d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
GTTT | G | 39 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(36): Show | 39 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47-7364_-47-7362d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
GTTTTTTT others(3): Show |
G | 21 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(18): Show | 21 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.-47-7371_-47-7362d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644422
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-7372_-47-7362d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | ||||||
| chr5:148644614
|
A | C | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-7553T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644614 | ||||||
| chr5:148644719
|
G | A | 1 | a0001c0001t0003g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-47-7658C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644719 | ||||||
| chr5:148644719
|
G | C | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-7658C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644719 | ||||||
| chr5:148644829
|
C | G | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-47-7768G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644829 | ||||||
| chr5:148644895
|
G | T | 19 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(16): Show | 19 | HG02056.hp2 HG02451.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.-47-7834C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644895 | ||||||
| chr5:148645084
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47-8023A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645084 | ||||||
| chr5:148645124
|
A | G | 1 | a0001c0001t0012g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-8063T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645124 | ||||||
| chr5:148645138
|
A | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0092others(44): Show | 47 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-47-8077T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645138 | ||||||
| chr5:148645259
|
C | A | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-8198G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645259 | ||||||
| chr5:148645369
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47-8308G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645369 | ||||||
| chr5:148645389
|
G | A | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-8328C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645389 | ||||||
| chr5:148645507
|
T | C | 129 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-47-8446A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645507 | ||||||
| chr5:148645595
|
C | T | 274 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(271): Show | 274 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.-48+8467G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645595 | ||||||
| chr5:148645621
|
A | G | 8 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(5): Show | 8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+8441T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645621 | ||||||
| chr5:148645656
|
T | C | 47 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0092others(44): Show | 47 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-48+8406A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645656 | ||||||
| chr5:148645812
|
A | C | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-48+8250T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645812 | ||||||
| chr5:148645857
|
G | T | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+8205C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645857 | ||||||
| chr5:148645904
|
A | G | 134 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-48+8158T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645904 | ||||||
| chr5:148645993
|
G | T | 169 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-48+8069C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645993 | ||||||
| chr5:148646041
|
C | T | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+8021G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646041 | ||||||
| chr5:148646115
|
ACATTCAA others(16): Show |
A | 1 | a0001c0001t0014g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48+7924_-48+7946d others(25): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646115 | ||||||
| chr5:148646215
|
G | C | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+7847C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646215 | ||||||
| chr5:148646403
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-48+7659G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646403 | ||||||
| chr5:148646456
|
A | G | 1 | a0001c0001t0002g0078 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-48+7606T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646456 | ||||||
| chr5:148646702
|
A | G | 8 | a0001c0001t0003g0084a0001c0001t0003g0087a0001c0001t0003g0088others(5): Show | 8 | HG00673.hp1 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+7360T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646702 | ||||||
| chr5:148646736
|
C | T | 79 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(76): Show | 79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.-48+7326G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646736 | ||||||
| chr5:148646737
|
T | C | 3 | a0001c0001t0010g0080a0001c0001t0010g0081a0001c0001t0017g0082 | 3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-48+7325A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646737 | ||||||
| chr5:148646747
|
C | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | NA18945.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-48+7315G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646747 | ||||||
| chr5:148646776
|
C | T | 3 | a0001c0001t0010g0080a0001c0001t0010g0081a0001c0001t0017g0082 | 3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-48+7286G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646776 | ||||||
| chr5:148646814
|
A | G | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+7248T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646814 | ||||||
| chr5:148646822
|
A | G | 169 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-48+7240T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646822 | ||||||
| chr5:148646855
|
A | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+7207T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646855 | ||||||
| chr5:148646970
|
A | G | 2 | a0001c0001t0001g0201a0001c0002t0001g0200 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+7092T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646970 | ||||||
| chr5:148647023
|
C | T | 7 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+7039G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647023 | ||||||
| chr5:148647154
|
C | T | 133 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(130): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-48+6908G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647154 | ||||||
| chr5:148647323
|
T | C | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+6739A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647323 | ||||||
| chr5:148647376
|
G | C | 1 | a0001c0001t0010g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+6686C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647376 | ||||||
| chr5:148647412
|
T | A | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG00738.hp2 HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-48+6650A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647412 | ||||||
| chr5:148647526
|
CA | C | 5 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+6535delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647526 | ||||||
| chr5:148647618
|
A | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0084others(58): Show | 61 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-48+6444T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647618 | ||||||
| chr5:148647636
|
C | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0084others(58): Show | 61 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-48+6426G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647636 | ||||||
| chr5:148647639
|
G | A | 15 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(12): Show | 15 | HG00673.hp1 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+6423C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647639 | ||||||
| chr5:148647650
|
A | G | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+6412T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647650 | ||||||
| chr5:148647674
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0084others(56): Show | 59 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-48+6388A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647674 | ||||||
| chr5:148647705
|
T | C | 54 | a0001c0001t0002g0002a0001c0001t0003g0084a0001c0001t0003g0087others(51): Show | 54 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-48+6357A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647705 | ||||||
| chr5:148647834
|
G | A | 1 | a0001c0001t0006g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+6228C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647834 | ||||||
| chr5:148647945
|
T | A | 61 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0084others(58): Show | 61 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-48+6117A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647945 | ||||||
| chr5:148648287
|
C | G | 6 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0013others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+5775G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648287 | ||||||
| chr5:148648301
|
G | A | 3 | a0001c0001t0010g0080a0001c0001t0010g0081a0001c0001t0017g0082 | 3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-48+5761C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648301 | ||||||
| chr5:148648317
|
TAG | T | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+5743_-48+5744d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648317 | ||||||
| chr5:148648376
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18967.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-48+5686T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648376 | ||||||
| chr5:148648549
|
C | T | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+5513G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648549 | ||||||
| chr5:148648573
|
C | A | 74 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-48+5489G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648573 | ||||||
| chr5:148648640
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-48+5422A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648640 | ||||||
| chr5:148648645
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-48+5417C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648645 | ||||||
| chr5:148648698
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48+5364C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648698 | ||||||
| chr5:148648816
|
G | A | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+5246C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648816 | ||||||
| chr5:148648910
|
A | G | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+5152T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648910 | ||||||
| chr5:148648946
|
G | GT | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+5115dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648946 | ||||||
| chr5:148649056
|
G | T | 4 | a0001c0001t0003g0116a0001c0001t0003g0129a0001c0001t0003g0130others(1): Show | 4 | HG01192.hp2 HG02257.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+5006C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649056 | ||||||
| chr5:148649077
|
C | T | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4985G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649077 | ||||||
| chr5:148649200
|
T | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4862A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649200 | ||||||
| chr5:148649234
|
C | T | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4828G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649234 | ||||||
| chr5:148649260
|
A | T | 4 | a0001c0001t0003g0116a0001c0001t0003g0129a0001c0001t0003g0130others(1): Show | 4 | HG01192.hp2 HG02257.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+4802T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649260 | ||||||
| chr5:148649273
|
GAA | G | 74 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-48+4787_-48+4788d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649273 | ||||||
| chr5:148649424
|
T | C | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+4638A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649424 | ||||||
| chr5:148649534
|
A | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4528T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649534 | ||||||
| chr5:148649683
|
A | G | 2 | a0001c0001t0003g0092a0001c0002t0003g0091 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+4379T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649683 | ||||||
| chr5:148649734
|
G | GA | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4327dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649734 | ||||||
| chr5:148649776
|
G | T | 1 | a0001c0001t0001g0306 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-48+4286C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649776 | ||||||
| chr5:148649879
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+4183C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649879 | ||||||
| chr5:148650025
|
T | TG | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+4036dupC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650025 | ||||||
| chr5:148650026
|
G | GT | 130 | a0001c0001t0001g0195a0001c0001t0002g0002a0001c0001t0002g0004others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-48+4035dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650026 | ||||||
| chr5:148650036
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-48+4026A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650036 | ||||||
| chr5:148650128
|
A | G | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3934T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650128 | ||||||
| chr5:148650338
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-48+3724G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650338 | ||||||
| chr5:148650375
|
A | G | 45 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0092others(42): Show | 45 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-48+3687T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650375 | ||||||
| chr5:148650501
|
C | T | 184 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(181): Show | 184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-48+3561G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650501 | ||||||
| chr5:148650557
|
T | C | 1 | a0003c0009t0027g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-48+3505A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650557 | ||||||
| chr5:148650576
|
A | T | 86 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(83): Show | 86 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-48+3486T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650576 | ||||||
| chr5:148650587
|
T | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3475A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650587 | ||||||
| chr5:148650614
|
T | G | 1 | a0001c0001t0003g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-48+3448A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650614 | ||||||
| chr5:148650723
|
A | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3339T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650723 | ||||||
| chr5:148650785
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0003g0130 | 2 | HG02257.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-48+3277C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650785 | ||||||
| chr5:148650846
|
A | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3216T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650846 | ||||||
| chr5:148650852
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-48+3210G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650852 | ||||||
| chr5:148650946
|
G | C | 17 | a0001c0001t0002g0002a0001c0001t0003g0116a0001c0001t0003g0117others(14): Show | 17 | HG00140.hp2 HG01192.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+3116C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650946 | ||||||
| chr5:148651031
|
A | G | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3031T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651031 | ||||||
| chr5:148651064
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-48+2998A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651064 | ||||||
| chr5:148651073
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-48+2989G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651073 | ||||||
| chr5:148651086
|
TGAGAGTA others(3): Show |
T | 1 | a0001c0001t0002g0007 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-48+2966_-48+2975d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651086 | ||||||
| chr5:148651092
|
T | A | 75 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0008others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-48+2970A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651092 | ||||||
| chr5:148651199
|
G | T | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2863C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651199 | ||||||
| chr5:148651226
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+2836A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651226 | ||||||
| chr5:148651298
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+2764C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651298 | ||||||
| chr5:148651357
|
G | A | 2 | a0001c0001t0005g0149a0001c0001t0005g0150 | 2 | HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-48+2705C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651357 | ||||||
| chr5:148651398
|
C | A | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2664G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651398 | ||||||
| chr5:148651488
|
C | T | 74 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-48+2574G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651488 | ||||||
| chr5:148651511
|
T | G | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2551A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651511 | ||||||
| chr5:148651512
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-48+2550C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651512 | ||||||
| chr5:148651569
|
C | T | 3 | a0001c0001t0001g0160a0001c0002t0001g0159a0001c0002t0001g0161 | 3 | HG02451.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-48+2493G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651569 | ||||||
| chr5:148651618
|
A | G | 1 | a0001c0001t0002g0006 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-48+2444T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651618 | ||||||
| chr5:148651627
|
T | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2435A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651627 | ||||||
| chr5:148651707
|
TTATTGAA others(32): Show |
T | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+2316_-48+2354d others(41): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651707 | ||||||
| chr5:148651880
|
C | T | 4 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+2182G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651880 | ||||||
| chr5:148651907
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48+2155T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651907 | ||||||
| chr5:148651949
|
C | T | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2113G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651949 | ||||||
| chr5:148652104
|
A | G | 77 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-48+1958T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652104 | ||||||
| chr5:148652377
|
G | A | 4 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1685C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652377 | ||||||
| chr5:148652393
|
A | G | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+1669T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652393 | ||||||
| chr5:148652395
|
C | T | 76 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+1667G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652395 | ||||||
| chr5:148652405
|
T | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0092others(42): Show | 45 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-48+1657A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652405 | ||||||
| chr5:148652433
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-48+1629A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652433 | ||||||
| chr5:148652521
|
C | T | 2 | a0001c0002t0003g0085a0001c0002t0003g0086 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-48+1541G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652521 | ||||||
| chr5:148652591
|
A | G | 54 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0084others(51): Show | 54 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-48+1471T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652591 | ||||||
| chr5:148652651
|
T | G | 1 | a0001c0001t0004g0308 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-48+1411A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652651 | ||||||
| chr5:148652669
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-48+1393G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652669 | ||||||
| chr5:148652728
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0008g0132a0001c0002t0008g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1334C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652728 | ||||||
| chr5:148653165
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-48+897T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653165 | ||||||
| chr5:148653219
|
G | T | 24 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(21): Show | 24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-48+843C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653219 | ||||||
| chr5:148653306
|
C | G | 1 | a0001c0008t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-48+756G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653306 | ||||||
| chr5:148653368
|
C | T | 77 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-48+694G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653368 | ||||||
| chr5:148653608
|
AAC | A | 58 | a0001c0001t0001g0309a0001c0001t0002g0002a0001c0001t0003g0084others(55): Show | 58 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-48+452_-48+453del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653608 | ||||||
| chr5:148653608
|
AACAC | A | 77 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-48+450_-48+453del others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653608 | ||||||
| chr5:148653910
|
C | A | 75 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-48+152G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653910 | ||||||
| chr5:148653975
|
C | T | 1 | a0001c0001t0004g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-48+87G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653975 |