Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3065 |
|---|---|
| ensemblid | ENSG00000116478.12 |
| hgncid | 4852 |
| symbol | HDAC1 |
| name | histone deacetylase 1 |
| refseq_nuc | NM_004964.3 |
| refseq_prot | NP_004955.2 |
| ensembl_nuc | ENST00000373548.8 |
| ensembl_prot | ENSP00000362649.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 32292083 |
| end | 32333626 |
| strand | + |
| ver | v1.2 |
| region | chr1:32292083-32333626 |
| region5000 | chr1:32287083-32338626 |
| regionname0 | HDAC1_chr1_32292083_32333626 |
| regionname5000 | HDAC1_chr1_32287083_32338626 |
| 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 | 482 | 145 | 65 | 28 | 28 | 6 | 16 | 12 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0002 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| 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 | 1449 | 142 | 63 | 28 | 27 | 6 | 16 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| c0002 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| c0003 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| c0004 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| c0005 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| 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 | 670 | 142 | 63 | 27 | 28 | 6 | 16 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| t0002 | 0/0 | 670 | 4 | 3 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| 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 | 4 | 4 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0002 | 1/0 | 4 | 0 | 2 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0003 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| 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 | 1449 | 142 | 63 | 28 | 27 | 6 | 16 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0002 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0003 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0005 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0002c0004 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2118 | 138 | 60 | 27 | 27 | 6 | 16 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0001t0002 | 0/0 | 2118 | 4 | 3 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0002t0001 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0003t0001 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0001c0005t0001 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| a0002c0004t0001 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | copy fasta | chr1 | 32287083 | 32338626 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0002 | 1/0 | 4 | 0 | 2 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0003 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0001c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| a0002c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0109 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0126 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | YRI | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ASW | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | USA | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0074 | REF | REF | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | HDAC1_chr1_32287083_32338626 | HDAC1 | chr1 | 32287083 | 32338626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32332707
|
C | T | 1 | a0002 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1379C>T | p.Thr460Ile | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 13/14 | 1466/2118 | 1379/1449 | 460/482 | chr1 | 32332707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32292187
|
C | A | 1 | a0001c0002 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.18C>A | p.Gly6Gly | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/14 | 105/2118 | 18/1449 | 6/482 | chr1 | 32292187 | ||
| chr1:32327578
|
T | C | 1 | a0001c0003 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.537T>C | p.His179His | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/14 | 624/2118 | 537/1449 | 179/482 | chr1 | 32327578 | ||
| chr1:32331481
|
A | G | 1 | a0001c0005 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.987A>G | p.Pro329Pro | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 10/14 | 1074/2118 | 987/1449 | 329/482 | chr1 | 32331481 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32333435
|
T | G | 1 | a0001c0001t0002 | 4 | HG01934.hp2 HG06807.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*391T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 14/14 | 391 | chr1 | 32333435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32292445
|
T | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+227T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32292445 | ||||||
| chr1:32292707
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015 | 4 | HG02809.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+489G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32292707 | ||||||
| chr1:32293177
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+959G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32293177 | ||||||
| chr1:32293311
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.49+1093G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32293311 | ||||||
| chr1:32293320
|
T | TA | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG00621.hp1 HG01261.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+1121dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32293320 | |||||
| chr1:32293320
|
T | TAA | 9 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 10 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+1120_49+1121dup others(2): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32293320 | |||||
| chr1:32293320
|
TA | T | 23 | a0001c0001t0001g0015a0001c0001t0001g0110a0001c0001t0001g0111others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.49+1121delA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32293320 | |||||
| chr1:32293552
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.49+1334G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32293552 | ||||||
| chr1:32293798
|
A | C | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+1580A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32293798 | ||||||
| chr1:32293901
|
C | CA | 12 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0110others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+1700dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32293901 | |||||
| chr1:32293901
|
CA | C | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+1700delA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32293901 | |||||
| chr1:32294063
|
G | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0110others(7): Show | 10 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+1845G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294063 | ||||||
| chr1:32294067
|
C | CA | 7 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0037others(4): Show | 7 | HG00642.hp2 HG01261.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+1863dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32294067 | |||||
| chr1:32294067
|
CA | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.49+1863delA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32294067 | |||||
| chr1:32294075
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+1857A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294075 | ||||||
| chr1:32294509
|
C | CT | 12 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 13 | HG00621.hp1 HG01071.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+2311dupT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32294509 | |||||
| chr1:32294550
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+2332C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294550 | ||||||
| chr1:32294680
|
G | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+2462G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294680 | ||||||
| chr1:32294789
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.49+2571C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294789 | ||||||
| chr1:32294804
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49+2586G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294804 | ||||||
| chr1:32294818
|
CT | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0041others(4): Show | 7 | HG00558.hp1 HG00558.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+2617delT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32294818 | |||||
| chr1:32294966
|
G | T | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+2748G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32294966 | ||||||
| chr1:32295100
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01070.hp1 HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.49+2882A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32295100 | ||||||
| chr1:32295151
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.49+2933C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32295151 | ||||||
| chr1:32295658
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49+3440A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32295658 | ||||||
| chr1:32295735
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.49+3517C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32295735 | ||||||
| chr1:32295759
|
T | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+3541T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32295759 | ||||||
| chr1:32295765
|
ATTTG | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0094 | 5 | HG01243.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+3570_49+3573del others(4): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32295765 | |||||
| chr1:32295841
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.49+3623G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32295841 | ||||||
| chr1:32296027
|
C | T | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+3809C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296027 | ||||||
| chr1:32296089
|
G | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+3871G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296089 | ||||||
| chr1:32296223
|
C | T | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+4005C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296223 | ||||||
| chr1:32296594
|
G | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.49+4376G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296594 | ||||||
| chr1:32296659
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.49+4441G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296659 | ||||||
| chr1:32296794
|
T | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.49+4576T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296794 | ||||||
| chr1:32296839
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49+4621T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296839 | ||||||
| chr1:32296935
|
A | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+4717A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32296935 | ||||||
| chr1:32297064
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.49+4846C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297064 | ||||||
| chr1:32297108
|
G | A | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+4890G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297108 | ||||||
| chr1:32297132
|
A | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 6 | HG00140.hp1 HG01255.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4914A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297132 | ||||||
| chr1:32297279
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.49+5061C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297279 | ||||||
| chr1:32297391
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.49+5173A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297391 | ||||||
| chr1:32297408
|
G | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+5190G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297408 | ||||||
| chr1:32297614
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.50-5007T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297614 | ||||||
| chr1:32297657
|
C | T | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-4964C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297657 | ||||||
| chr1:32297707
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0048others(1): Show | 5 | HG02559.hp2 HG02630.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-4914T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297707 | ||||||
| chr1:32297725
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.50-4896C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297725 | ||||||
| chr1:32297777
|
A | AT | 43 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(40): Show | 45 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.50-4814dupT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
A | ATT | 5 | a0001c0001t0001g0035a0001c0001t0001g0085a0001c0001t0001g0107others(2): Show | 5 | HG00639.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-4815_50-4814dup others(2): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0116 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.50-4825_50-4814dup others(12): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
AT | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0108a0001c0001t0001g0123others(5): Show | 8 | HG00738.hp1 HG01934.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-4814delT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
ATT | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG00639.hp1 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-4815_50-4814del others(2): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | NA18983.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.50-4823_50-4814del others(10): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-4825_50-4814del others(12): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297777
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.50-4829_50-4814del others(16): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32297777 | |||||
| chr1:32297991
|
G | A | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-4630G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32297991 | ||||||
| chr1:32298035
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.50-4586C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32298035 | ||||||
| chr1:32298088
|
C | CT | 20 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(17): Show | 21 | HG00140.hp1 HG00621.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.50-4517dupT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 32298088 | |||||
| chr1:32298186
|
T | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.50-4435T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32298186 | ||||||
| chr1:32298245
|
C | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-4376C>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32298245 | ||||||
| chr1:32298414
|
T | C | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-4207T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32298414 | ||||||
| chr1:32298498
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.50-4123G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32298498 | ||||||
| chr1:32298951
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.50-3670A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32298951 | ||||||
| chr1:32299080
|
A | G | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-3541A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299080 | ||||||
| chr1:32299081
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.50-3540T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299081 | ||||||
| chr1:32299192
|
T | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.50-3429T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299192 | ||||||
| chr1:32299214
|
T | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.50-3407T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299214 | ||||||
| chr1:32299345
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-3276G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299345 | ||||||
| chr1:32299486
|
C | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-3135C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299486 | ||||||
| chr1:32299699
|
T | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.50-2922T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299699 | ||||||
| chr1:32299812
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.50-2809T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299812 | ||||||
| chr1:32299832
|
G | A | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-2789G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32299832 | ||||||
| chr1:32300033
|
G | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0108others(5): Show | 8 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-2588G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300033 | ||||||
| chr1:32300092
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.50-2529T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300092 | ||||||
| chr1:32300278
|
T | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0067 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.50-2343T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300278 | ||||||
| chr1:32300362
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.50-2259G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300362 | ||||||
| chr1:32300365
|
A | G | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 27 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-2256A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300365 | ||||||
| chr1:32300518
|
A | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-2103A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300518 | ||||||
| chr1:32300691
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(11): Show | 14 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.50-1930A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300691 | ||||||
| chr1:32300998
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.50-1623G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32300998 | ||||||
| chr1:32301081
|
A | G | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-1540A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301081 | ||||||
| chr1:32301218
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.50-1403G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301218 | ||||||
| chr1:32301314
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-1307C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301314 | ||||||
| chr1:32301418
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.50-1203C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301418 | ||||||
| chr1:32301520
|
G | A | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.50-1101G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301520 | ||||||
| chr1:32301598
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.50-1023C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301598 | ||||||
| chr1:32301757
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.50-864G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301757 | ||||||
| chr1:32301833
|
C | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-788C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32301833 | ||||||
| chr1:32302111
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.50-510G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 1/13 | chr1 | 32302111 | ||||||
| chr1:32303273
|
G | A | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.162+540G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32303273 | ||||||
| chr1:32303280
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.162+547C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32303280 | ||||||
| chr1:32303300
|
A | G | 9 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00642.hp2 HG00738.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.162+567A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32303300 | ||||||
| chr1:32303342
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+609G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32303342 | ||||||
| chr1:32303565
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+832G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32303565 | ||||||
| chr1:32303775
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+1042C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32303775 | ||||||
| chr1:32304275
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0069 | 2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.162+1542G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304275 | ||||||
| chr1:32304299
|
A | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+1566A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304299 | ||||||
| chr1:32304431
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0129 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162+1698C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304431 | ||||||
| chr1:32304441
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01070.hp1 HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.162+1708C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304441 | ||||||
| chr1:32304598
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+1865C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304598 | ||||||
| chr1:32304625
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.162+1892A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304625 | ||||||
| chr1:32304726
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+1993C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304726 | ||||||
| chr1:32304778
|
G | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.162+2045G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304778 | ||||||
| chr1:32304846
|
G | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+2113G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304846 | ||||||
| chr1:32304897
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.162+2164A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32304897 | ||||||
| chr1:32305624
|
T | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+2891T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32305624 | ||||||
| chr1:32305771
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01070.hp1 HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.162+3038C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32305771 | ||||||
| chr1:32305889
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+3156C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32305889 | ||||||
| chr1:32305890
|
G | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+3157G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32305890 | ||||||
| chr1:32305958
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.162+3225A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32305958 | ||||||
| chr1:32306015
|
C | G | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.162+3282C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306015 | ||||||
| chr1:32306119
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.162+3386A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306119 | ||||||
| chr1:32306192
|
CT | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG00639.hp2 HG01109.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+3474delT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32306192 | |||||
| chr1:32306276
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+3543C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306276 | ||||||
| chr1:32306277
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.162+3544G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306277 | ||||||
| chr1:32306318
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0094 | 5 | HG01243.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+3585C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306318 | ||||||
| chr1:32306377
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.162+3644C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306377 | ||||||
| chr1:32306415
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+3682C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306415 | ||||||
| chr1:32306609
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.162+3876C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306609 | ||||||
| chr1:32306682
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.162+3949T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306682 | ||||||
| chr1:32306844
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.162+4111A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306844 | ||||||
| chr1:32306921
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.162+4188G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306921 | ||||||
| chr1:32306967
|
C | T | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.162+4234C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32306967 | ||||||
| chr1:32307017
|
C | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.162+4284C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32307017 | ||||||
| chr1:32307102
|
A | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+4369A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32307102 | ||||||
| chr1:32307125
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.162+4392G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32307125 | ||||||
| chr1:32307217
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.162+4484C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32307217 | ||||||
| chr1:32307241
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.162+4508T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32307241 | ||||||
| chr1:32307749
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.162+5016T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32307749 | ||||||
| chr1:32308036
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.162+5303C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32308036 | ||||||
| chr1:32308314
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+5581C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32308314 | ||||||
| chr1:32308330
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+5597A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32308330 | ||||||
| chr1:32308502
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.162+5769G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32308502 | ||||||
| chr1:32308579
|
C | T | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.162+5846C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32308579 | ||||||
| chr1:32308767
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0127a0001c0001t0002g0011others(2): Show | 5 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+6034C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32308767 | ||||||
| chr1:32309060
|
C | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+6327C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309060 | ||||||
| chr1:32309077
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.162+6344G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309077 | ||||||
| chr1:32309089
|
G | C | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.162+6356G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309089 | ||||||
| chr1:32309301
|
CAG | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6573_162+6574d others(4): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32309301 | |||||
| chr1:32309330
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+6597G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309330 | ||||||
| chr1:32309371
|
TTCTC | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0067 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.162+6650_162+6653d others(6): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32309371 | |||||
| chr1:32309387
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.162+6654T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309387 | ||||||
| chr1:32309666
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162+6933A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309666 | ||||||
| chr1:32309674
|
GAGTCTCA others(18): Show |
G | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01070.hp1 HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.162+6943_163-6965d others(27): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32309674 | |||||
| chr1:32309680
|
C | CA | 27 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0029others(24): Show | 27 | HG00639.hp1 HG01070.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.163-6963dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32309680 | |||||
| chr1:32309894
|
A | G | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-6771A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32309894 | ||||||
| chr1:32310007
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163-6658A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310007 | ||||||
| chr1:32310097
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163-6568A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310097 | ||||||
| chr1:32310450
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-6215C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310450 | ||||||
| chr1:32310451
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-6214G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310451 | ||||||
| chr1:32310588
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-6077G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310588 | ||||||
| chr1:32310606
|
T | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-6059T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310606 | ||||||
| chr1:32310620
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-6045C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310620 | ||||||
| chr1:32310707
|
G | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.163-5958G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310707 | ||||||
| chr1:32310714
|
G | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0120 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.163-5951G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310714 | ||||||
| chr1:32310743
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0078a0001c0001t0001g0097others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-5922G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310743 | ||||||
| chr1:32310772
|
T | C | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-5893T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310772 | ||||||
| chr1:32310854
|
A | AT | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.163-5811_163-5810i others(3): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310854 | ||||||
| chr1:32310855
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.163-5810G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310855 | ||||||
| chr1:32310855
|
G | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-5810G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32310855 | ||||||
| chr1:32310866
|
TAGAG | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-5795_163-5792d others(6): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32310866 | |||||
| chr1:32311065
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0058others(2): Show | 6 | HG00673.hp2 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-5600C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32311065 | ||||||
| chr1:32311334
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163-5331C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32311334 | ||||||
| chr1:32311893
|
T | C | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-4772T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32311893 | ||||||
| chr1:32311931
|
A | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-4734A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32311931 | ||||||
| chr1:32312437
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.163-4228T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32312437 | ||||||
| chr1:32312560
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.163-4105C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32312560 | ||||||
| chr1:32312937
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-3728A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32312937 | ||||||
| chr1:32313044
|
C | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-3621C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313044 | ||||||
| chr1:32313073
|
CTTATT | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.163-3580_163-3576d others(7): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32313073 | |||||
| chr1:32313082
|
T | TTTTA | 7 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0072others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-3555_163-3552d others(6): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32313082 | |||||
| chr1:32313148
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0096 | 2 | HG02040.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163-3517C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313148 | ||||||
| chr1:32313255
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.163-3410C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313255 | ||||||
| chr1:32313291
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-3374C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313291 | ||||||
| chr1:32313310
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-3355G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313310 | ||||||
| chr1:32313476
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0106 | 2 | HG02074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.163-3189A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313476 | ||||||
| chr1:32313618
|
T | C | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-3047T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313618 | ||||||
| chr1:32313754
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0002g0011a0001c0001t0002g0012others(1): Show | 4 | HG01934.hp2 HG06807.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2911C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313754 | ||||||
| chr1:32313889
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2776T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313889 | ||||||
| chr1:32313902
|
T | C | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-2763T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313902 | ||||||
| chr1:32313997
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.163-2668C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32313997 | ||||||
| chr1:32314554
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-2111A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32314554 | ||||||
| chr1:32314670
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0100 | 3 | HG02040.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.163-1995C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32314670 | ||||||
| chr1:32314677
|
T | C | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-1988T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32314677 | ||||||
| chr1:32314825
|
C | CA | 21 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0044others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.163-1822dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32314825 | |||||
| chr1:32314845
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02698.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.163-1820G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32314845 | ||||||
| chr1:32315086
|
G | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-1579G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315086 | ||||||
| chr1:32315331
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-1334C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315331 | ||||||
| chr1:32315385
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.163-1280T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315385 | ||||||
| chr1:32315452
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.163-1213A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315452 | ||||||
| chr1:32315540
|
A | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015 | 4 | HG02809.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-1125A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315540 | ||||||
| chr1:32315678
|
T | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-987T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315678 | ||||||
| chr1:32315890
|
A | G | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-775A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315890 | ||||||
| chr1:32315950
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.163-715G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315950 | ||||||
| chr1:32315981
|
C | CA | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(5): Show | 8 | HG00621.hp1 HG00621.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-675dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32315981 | |||||
| chr1:32315991
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.163-674C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32315991 | ||||||
| chr1:32316200
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.163-465C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32316200 | ||||||
| chr1:32316238
|
T | C | 18 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-427T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32316238 | ||||||
| chr1:32316283
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0103a0001c0001t0001g0127a0001c0001t0002g0011others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-380_163-371dup others(10): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32316283 | |||||
| chr1:32316283
|
C | CAAAAAAA others(11): Show |
6 | a0001c0001t0001g0088a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-371_163-370ins others(18): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32316283 | |||||
| chr1:32316283
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0114 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.163-371_163-370ins others(19): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32316283 | |||||
| chr1:32316283
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.163-371_163-370ins others(20): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32316283 | |||||
| chr1:32316283
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.163-371_163-370ins others(21): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 32316283 | |||||
| chr1:32316341
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.163-324A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32316341 | ||||||
| chr1:32316644
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.163-21T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 2/13 | chr1 | 32316644 | ||||||
| chr1:32316874
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.280+92A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32316874 | ||||||
| chr1:32317377
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.280+595A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32317377 | ||||||
| chr1:32317539
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0103a0001c0001t0001g0127 | 3 | HG00639.hp1 HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.280+757G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32317539 | ||||||
| chr1:32317839
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+1057C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32317839 | ||||||
| chr1:32318287
|
C | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.280+1505C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32318287 | ||||||
| chr1:32318555
|
C | CA | 18 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+1784dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32318555 | |||||
| chr1:32318555
|
C | CAA | 8 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+1783_280+1784d others(4): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32318555 | |||||
| chr1:32318805
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.280+2023A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32318805 | ||||||
| chr1:32319079
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.280+2297A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319079 | ||||||
| chr1:32319106
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.280+2324G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319106 | ||||||
| chr1:32319142
|
T | C | 23 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0088others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+2360T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319142 | ||||||
| chr1:32319247
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280+2465A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319247 | ||||||
| chr1:32319299
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+2517G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319299 | ||||||
| chr1:32319353
|
T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(24): Show | 28 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.280+2571T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319353 | ||||||
| chr1:32319495
|
A | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+2713A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319495 | ||||||
| chr1:32319711
|
G | A | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.280+2929G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319711 | ||||||
| chr1:32319918
|
A | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.280+3136A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319918 | ||||||
| chr1:32319942
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0013 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.280+3160C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32319942 | ||||||
| chr1:32320242
|
A | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.280+3460A>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32320242 | ||||||
| chr1:32320496
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.280+3714T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32320496 | ||||||
| chr1:32320719
|
G | C | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.281-3760G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32320719 | ||||||
| chr1:32320770
|
T | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-3709T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32320770 | ||||||
| chr1:32320899
|
C | CA | 20 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0040others(17): Show | 20 | HG00140.hp2 HG01109.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-3556dupA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32320899 | |||||
| chr1:32320899
|
CA | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 11 | HG01515.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.281-3556delA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32320899 | |||||
| chr1:32320899
|
CAAAAAAA | C | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.281-3562_281-3556d others(9): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32320899 | |||||
| chr1:32320899
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(1): Show | 4 | HG01934.hp2 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-3566_281-3556d others(13): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32320899 | |||||
| chr1:32320899
|
CAAAAAAA others(5): Show |
C | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-3567_281-3556d others(14): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32320899 | |||||
| chr1:32321076
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-3403A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321076 | ||||||
| chr1:32321198
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.281-3281T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321198 | ||||||
| chr1:32321207
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.281-3272G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321207 | ||||||
| chr1:32321212
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.281-3267C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321212 | ||||||
| chr1:32321230
|
CA | C | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0103others(14): Show | 17 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-3236delA | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32321230 | |||||
| chr1:32321241
|
A | T | 10 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0127others(7): Show | 10 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.281-3238A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321241 | ||||||
| chr1:32321243
|
AT | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-3235delT | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321243 | ||||||
| chr1:32321244
|
T | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0016others(20): Show | 24 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.281-3235T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321244 | ||||||
| chr1:32321247
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.281-3232T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321247 | ||||||
| chr1:32321271
|
T | C | 1 | a0001c0001t0002g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-3208T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321271 | ||||||
| chr1:32321482
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.281-2997C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321482 | ||||||
| chr1:32321681
|
A | G | 1 | a0001c0005t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.281-2798A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321681 | ||||||
| chr1:32321963
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-2516G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32321963 | ||||||
| chr1:32322294
|
T | C | 10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.281-2185T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32322294 | ||||||
| chr1:32322329
|
T | C | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.281-2150T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32322329 | ||||||
| chr1:32322345
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02922.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-2134T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32322345 | ||||||
| chr1:32322704
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.281-1775T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32322704 | ||||||
| chr1:32322912
|
G | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0118others(2): Show | 5 | HG00639.hp1 HG01070.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-1567G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32322912 | ||||||
| chr1:32322929
|
AGTT | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.281-1544_281-1542d others(5): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 32322929 | |||||
| chr1:32323447
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.281-1032G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32323447 | ||||||
| chr1:32323639
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.281-840C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32323639 | ||||||
| chr1:32323780
|
G | A | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-699G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32323780 | ||||||
| chr1:32323838
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.281-641G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32323838 | ||||||
| chr1:32323851
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.281-628G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32323851 | ||||||
| chr1:32324048
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281-431C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32324048 | ||||||
| chr1:32324101
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0105 | 3 | HG00642.hp1 HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.281-378A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32324101 | ||||||
| chr1:32324152
|
T | C | 1 | a0002c0004t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-327T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32324152 | ||||||
| chr1:32324170
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-309A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32324170 | ||||||
| chr1:32324445
|
T | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-34T>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 3/13 | chr1 | 32324445 | ||||||
| chr1:32324692
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.355+139T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32324692 | ||||||
| chr1:32324834
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+281G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32324834 | ||||||
| chr1:32325530
|
A | G | 1 | a0001c0001t0002g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+977A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32325530 | ||||||
| chr1:32325805
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG02486.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.356-1134C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32325805 | ||||||
| chr1:32325856
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.356-1083T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32325856 | ||||||
| chr1:32325975
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.356-964C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32325975 | ||||||
| chr1:32326318
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.356-621C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326318 | ||||||
| chr1:32326432
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG02486.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.356-507T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326432 | ||||||
| chr1:32326473
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.356-466G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326473 | ||||||
| chr1:32326650
|
T | TAA | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.356-283_356-282dup others(2): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 32326650 | |||||
| chr1:32326656
|
A | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0127 | 3 | HG00639.hp1 HG01070.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.356-283A>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326656 | ||||||
| chr1:32326658
|
T | A | 16 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0099others(13): Show | 16 | HG01934.hp2 HG02109.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.356-281T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326658 | ||||||
| chr1:32326670
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.356-269T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326670 | ||||||
| chr1:32326670
|
T | TAC | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.356-258_356-257dup others(2): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 32326670 | |||||
| chr1:32326757
|
C | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.356-182C>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 4/13 | chr1 | 32326757 | ||||||
| chr1:32327457
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.495-79C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 5/13 | chr1 | 32327457 | ||||||
| chr1:32327766
|
T | C | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0103others(14): Show | 17 | HG00639.hp1 HG01070.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.636+89T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32327766 | ||||||
| chr1:32327845
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.636+168G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32327845 | ||||||
| chr1:32328116
|
A | G | 1 | a0001c0001t0001g0008 | 2 | HG02135.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.636+439A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32328116 | ||||||
| chr1:32328147
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.636+470C>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32328147 | ||||||
| chr1:32328286
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0090a0001c0001t0001g0092others(1): Show | 4 | HG00738.hp2 HG01109.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+609A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32328286 | ||||||
| chr1:32328316
|
C | CTT | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+653_636+654dup others(2): Show |
HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 32328316 | |||||
| chr1:32328363
|
G | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0045 | 3 | HG00558.hp2 NA18954.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.636+686G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32328363 | ||||||
| chr1:32328846
|
T | C | 9 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0117others(6): Show | 9 | HG00639.hp1 HG01070.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-222T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32328846 | ||||||
| chr1:32328867
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.637-201A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 6/13 | chr1 | 32328867 | ||||||
| chr1:32329447
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.729+287T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32329447 | ||||||
| chr1:32329458
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01934.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.729+298G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32329458 | ||||||
| chr1:32329735
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.729+575C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32329735 | ||||||
| chr1:32329742
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.729+582C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32329742 | ||||||
| chr1:32330031
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0074 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.730-547T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32330031 | ||||||
| chr1:32330147
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.730-431T>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32330147 | ||||||
| chr1:32330362
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.730-216G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 7/13 | chr1 | 32330362 | ||||||
| chr1:32331169
|
T | A | 1 | a0001c0001t0001g0009 | 2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.979+261T>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 9/13 | chr1 | 32331169 | ||||||
| chr1:32331203
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.980-271C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 9/13 | chr1 | 32331203 | ||||||
| chr1:32331329
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.980-145G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 9/13 | chr1 | 32331329 | ||||||
| chr1:32331640
|
G | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-36G>C | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 10/13 | chr1 | 32331640 | ||||||
| chr1:32331982
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1220-108C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 11/13 | chr1 | 32331982 | ||||||
| chr1:32332009
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0044 | 2 | NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1220-81C>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 11/13 | chr1 | 32332009 | ||||||
| chr1:32332013
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1220-77G>T | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 11/13 | chr1 | 32332013 | ||||||
| chr1:32332020
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1220-70A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 11/13 | chr1 | 32332020 | ||||||
| chr1:32332533
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 31 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.1373-168A>G | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 12/13 | chr1 | 32332533 | ||||||
| chr1:32332754
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.1421+5G>A | HDAC1 | ENSG00000116478.12 | transcript | ENST00000373548.8 | protein_coding | 13/13 | chr1 | 32332754 |