| geneid | 57531 |
|---|---|
| ensemblid | ENSG00000085382.12 |
| hgncid | 21033 |
| symbol | HACE1 |
| name | HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 |
| refseq_nuc | NM_020771.4 |
| refseq_prot | NP_065822.2 |
| ensembl_nuc | ENST00000262903.9 |
| ensembl_prot | ENSP00000262903.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 104728094 |
| end | 104859919 |
| strand | - |
| ver | v1.2 |
| region | chr6:104728094-104859919 |
| region5000 | chr6:104723094-104864919 |
| regionname0 | HACE1_chr6_104728094_104859919 |
| regionname5000 | HACE1_chr6_104723094_104864919 |
| 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 | 909 | 346 | 82 | 60 | 152 | 14 | 36 | 112 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2730 | 281 | 45 | 48 | 150 | 8 | 29 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| c0002 | 0/1 | 2730 | 60 | 33 | 12 | 1 | 6 | 7 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| c0003 | 0/0 | 2730 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| c0004 | 0/0 | 2730 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| c0005 | 0/0 | 2730 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| 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 | 1846 | 269 | 70 | 49 | 107 | 11 | 30 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0002 | 0/0 | 1846 | 71 | 11 | 11 | 43 | 2 | 4 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0003 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0004 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0005 | 0/0 | 1846 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0006 | 0/0 | 1846 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0007 | 0/0 | 1846 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| t0008 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2730 | 281 | 45 | 48 | 150 | 8 | 29 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0002 | 0/1 | 2730 | 60 | 33 | 12 | 1 | 6 | 7 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0003 | 0/0 | 2730 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0004 | 0/0 | 2730 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0005 | 0/0 | 2730 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4575 | 205 | 34 | 37 | 105 | 5 | 23 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0001t0002 | 0/0 | 4575 | 71 | 11 | 11 | 43 | 2 | 4 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0001t0003 | 0/0 | 4575 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0001t0004 | 0/0 | 4575 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0001t0005 | 0/0 | 4575 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0001t0006 | 0/0 | 4575 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0001t0007 | 0/0 | 4575 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0002t0001 | 0/1 | 4575 | 59 | 32 | 12 | 1 | 6 | 7 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0002t0008 | 0/0 | 4575 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0003t0001 | 0/0 | 4575 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0004t0001 | 0/0 | 4575 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| a0001c0005t0001 | 0/0 | 4575 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | copy fasta | chr6 | 104723094 | 104864919 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0002t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| a0001c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0269 | EUR | GBR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | FIN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0129 | EUR | FIN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0100 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0342 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0131 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0343 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0132 | EUR | IBS | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0073 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0143 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0147 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0229 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0341 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | ESN | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0105 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18954 | hp2 | a0001 | c0005 | t0001 | g0318 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ASW | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ASW | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0133 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0134 | EUR | TSI | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02109 | hp2 | a0001 | c0002 | t0008 | g0344 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | USA | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0228 | AFR | USA | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0124 | REF | REF | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0120 | REF | REF | HACE1_chr6_104723094_104864919 | HACE1 | chr6 | 104723094 | 104864919 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104750392
|
A | G | 1 | a0001c0002 | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
synonymous_variant | LOW | c.2292T>C | p.Phe764Phe | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/24 | 2569/4575 | 2292/2730 | 764/909 | chr6 | 104750392 | ||
| chr6:104750449
|
A | T | 1 | a0001c0003 | 2 | HG03195.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.2235T>A | p.Thr745Thr | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/24 | 2512/4575 | 2235/2730 | 745/909 | chr6 | 104750449 | ||
| chr6:104796938
|
T | C | 1 | a0001c0004 | 2 | HG03130.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.705A>G | p.Leu235Leu | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 8/24 | 982/4575 | 705/2730 | 235/909 | chr6 | 104796938 | ||
| chr6:104833054
|
G | A | 1 | a0001c0005 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.522C>T | p.Asn174Asn | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/24 | 799/4575 | 522/2730 | 174/909 | chr6 | 104833054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104728121
|
C | T | 1 | a0001c0001t0005 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1541 | chr6 | 104728121 | |||||
| chr6:104728134
|
C | T | 1 | a0001c0001t0004 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1528G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1528 | chr6 | 104728134 | |||||
| chr6:104728525
|
A | C | 1 | a0001c0001t0004 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1137T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1137 | chr6 | 104728525 | |||||
| chr6:104728653
|
G | A | 3 | a0001c0001t0002a0001c0001t0004a0001c0001t0005 | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1009C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 1009 | chr6 | 104728653 | |||||
| chr6:104728787
|
T | A | 1 | a0001c0001t0006 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 875 | chr6 | 104728787 | |||||
| chr6:104728900
|
T | C | 1 | a0001c0001t0007 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*762A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 762 | chr6 | 104728900 | |||||
| chr6:104729579
|
C | T | 1 | a0001c0001t0003 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 24/24 | 83 | chr6 | 104729579 | |||||
| chr6:104859687
|
G | C | 1 | a0001c0002t0008 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-45C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/24 | 45 | chr6 | 104859687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104729841
|
C | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2628-77G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 23/23 | chr6 | 104729841 | ||||||
| chr6:104730521
|
A | C | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2514-105T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730521 | ||||||
| chr6:104730664
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2514-248G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730664 | ||||||
| chr6:104730773
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2514-357G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730773 | ||||||
| chr6:104730804
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2514-388T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730804 | ||||||
| chr6:104730825
|
T | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2514-409A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104730825 | ||||||
| chr6:104731198
|
CA | C | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2514-783delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731198 | ||||||
| chr6:104731348
|
G | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2514-932C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731348 | ||||||
| chr6:104731371
|
T | C | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2514-955A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731371 | ||||||
| chr6:104731446
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2514-1030G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731446 | ||||||
| chr6:104731471
|
T | A | 1 | a0001c0003t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2514-1055A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731471 | ||||||
| chr6:104731654
|
G | C | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2514-1238C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731654 | ||||||
| chr6:104731742
|
C | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(154): Show | 158 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2514-1326G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731742 | ||||||
| chr6:104731751
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2514-1335T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731751 | ||||||
| chr6:104731794
|
A | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-1378T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731794 | ||||||
| chr6:104731869
|
G | GA | 19 | a0001c0001t0001g0281a0001c0002t0001g0076a0001c0002t0001g0077others(16): Show | 19 | HG01516.hp1 HG01517.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2514-1454dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | ||||||
| chr6:104731869
|
G | GAA | 40 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(37): Show | 40 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.2514-1455_2514-145 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | ||||||
| chr6:104731869
|
G | GGA | 3 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219 | 4 | HG02572.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2514-1454_2514-145 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | ||||||
| chr6:104731869
|
GA | G | 95 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2514-1454delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731869 | ||||||
| chr6:104731883
|
T | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514-1467A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731883 | ||||||
| chr6:104731888
|
A | G | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514-1472T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731888 | ||||||
| chr6:104731973
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2514-1557T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731973 | ||||||
| chr6:104731975
|
A | G | 94 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(91): Show | 94 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2514-1559T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104731975 | ||||||
| chr6:104732269
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2514-1853G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732269 | ||||||
| chr6:104732280
|
A | G | 8 | a0001c0001t0002g0008a0001c0001t0002g0036a0001c0001t0002g0040others(5): Show | 8 | HG00099.hp1 HG01928.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2514-1864T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732280 | ||||||
| chr6:104732546
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2514-2130C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732546 | ||||||
| chr6:104732706
|
T | TAC | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2514-2292_2514-229 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732706 | ||||||
| chr6:104732763
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2514-2347C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732763 | ||||||
| chr6:104732768
|
G | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2514-2352C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732768 | ||||||
| chr6:104732771
|
T | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2514-2355A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732771 | ||||||
| chr6:104732910
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(151): Show | 155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2514-2494G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732910 | ||||||
| chr6:104732945
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2514-2529G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732945 | ||||||
| chr6:104732965
|
A | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-2549T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104732965 | ||||||
| chr6:104733018
|
G | A | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2514-2602C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733018 | ||||||
| chr6:104733134
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2514-2718C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733134 | ||||||
| chr6:104733215
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2514-2799G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733215 | ||||||
| chr6:104733245
|
T | G | 1 | a0001c0001t0001g0289 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2514-2829A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733245 | ||||||
| chr6:104733308
|
TAAC | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2514-2895_2514-289 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733308 | ||||||
| chr6:104733581
|
G | A | 3 | a0001c0001t0001g0322a0001c0003t0001g0228a0001c0003t0001g0229 | 3 | HG03195.hp2 NA18962.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2514-3165C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733581 | ||||||
| chr6:104733712
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2514-3296T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733712 | ||||||
| chr6:104733732
|
T | C | 2 | a0001c0002t0001g0085a0001c0002t0001g0086 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2514-3316A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733732 | ||||||
| chr6:104733800
|
C | T | 9 | a0001c0002t0001g0094a0001c0002t0001g0096a0001c0002t0001g0099others(6): Show | 9 | HG01515.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514-3384G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733800 | ||||||
| chr6:104733827
|
A | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2514-3411T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733827 | ||||||
| chr6:104733838
|
C | CAA | 150 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(147): Show | 151 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.2514-3424_2514-342 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104733838 | ||||||
| chr6:104734012
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2514-3596G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734012 | ||||||
| chr6:104734113
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2514-3697T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734113 | ||||||
| chr6:104734142
|
C | CA | 220 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.2514-3727dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734142 | ||||||
| chr6:104734142
|
C | CAA | 12 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0149others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2514-3728_2514-372 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734142 | ||||||
| chr6:104734315
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2514-3899T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734315 | ||||||
| chr6:104734338
|
ATTATACT others(8): Show |
A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2514-3937_2514-392 others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734338 | ||||||
| chr6:104734613
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2514-4197C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734613 | ||||||
| chr6:104734769
|
G | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2514-4353C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734769 | ||||||
| chr6:104734800
|
C | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2514-4384G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734800 | ||||||
| chr6:104734842
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2514-4426G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734842 | ||||||
| chr6:104734964
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2514-4548A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734964 | ||||||
| chr6:104734973
|
G | C | 6 | a0001c0001t0001g0267a0001c0001t0001g0314a0001c0001t0001g0316others(3): Show | 6 | HG00408.hp2 HG02155.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2514-4557C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104734973 | ||||||
| chr6:104735014
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(47): Show | 51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2514-4598T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735014 | ||||||
| chr6:104735015
|
T | C | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-4599A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735015 | ||||||
| chr6:104735100
|
C | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-4684G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735100 | ||||||
| chr6:104735116
|
G | C | 1 | a0001c0001t0002g0007 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2514-4700C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735116 | ||||||
| chr6:104735290
|
G | A | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2514-4874C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735290 | ||||||
| chr6:104735367
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2514-4951C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735367 | ||||||
| chr6:104735377
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2514-4961T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735377 | ||||||
| chr6:104735398
|
C | T | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-4982G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735398 | ||||||
| chr6:104735461
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(162): Show | 166 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.2514-5045G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735461 | ||||||
| chr6:104735499
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2514-5083G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735499 | ||||||
| chr6:104735563
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2514-5147C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735563 | ||||||
| chr6:104735608
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2514-5192T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735608 | ||||||
| chr6:104735638
|
A | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2514-5222T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735638 | ||||||
| chr6:104735689
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2514-5273G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735689 | ||||||
| chr6:104735734
|
A | G | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-5318T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735734 | ||||||
| chr6:104735883
|
G | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2514-5467C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104735883 | ||||||
| chr6:104736084
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2514-5668A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736084 | ||||||
| chr6:104736377
|
C | A | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2514-5961G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736377 | ||||||
| chr6:104736472
|
C | G | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2514-6056G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736472 | ||||||
| chr6:104736492
|
G | A | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2514-6076C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736492 | ||||||
| chr6:104736600
|
C | G | 1 | a0001c0001t0001g0249 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2514-6184G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736600 | ||||||
| chr6:104736765
|
T | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(151): Show | 155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2514-6349A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736765 | ||||||
| chr6:104736766
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2514-6350A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104736766 | ||||||
| chr6:104737041
|
T | C | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2514-6625A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737041 | ||||||
| chr6:104737063
|
C | T | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2514-6647G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737063 | ||||||
| chr6:104737121
|
TA | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(150): Show | 154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2514-6706delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737121 | ||||||
| chr6:104737219
|
G | C | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2514-6803C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737219 | ||||||
| chr6:104737237
|
C | T | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2514-6821G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737237 | ||||||
| chr6:104737275
|
T | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0293a0001c0001t0001g0302 | 3 | HG02698.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2514-6859A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737275 | ||||||
| chr6:104737280
|
C | CAA | 3 | a0001c0001t0001g0141a0001c0003t0001g0228a0001c0003t0001g0229 | 3 | HG03139.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2514-6865_2514-686 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737280 | ||||||
| chr6:104737280
|
C | CAAAAA | 3 | a0001c0001t0001g0149a0001c0004t0001g0143a0001c0004t0001g0147 | 3 | HG03130.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2514-6865_2514-686 others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737280 | ||||||
| chr6:104737281
|
T | A | 9 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(6): Show | 9 | HG02055.hp1 HG02965.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514-6865A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737281 | ||||||
| chr6:104737282
|
C | A | 9 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(6): Show | 9 | HG02055.hp1 HG02965.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514-6866G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737282
|
C | CA | 27 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0238others(24): Show | 27 | HG00438.hp1 HG00597.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.2514-6867dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737282
|
C | CAA | 48 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2514-6868_2514-686 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737282
|
C | CAAA | 21 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0012others(18): Show | 21 | HG00597.hp2 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2514-6869_2514-686 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737282
|
CA | C | 80 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(77): Show | 80 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.2514-6867delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737282
|
CAA | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0176a0001c0001t0001g0181others(4): Show | 7 | HG01516.hp2 HG02056.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2514-6868_2514-686 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737282
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2513+6863_2514-686 others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737282 | ||||||
| chr6:104737297
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2513+6863T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737297 | ||||||
| chr6:104737305
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2513+6855T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737305 | ||||||
| chr6:104737353
|
G | A | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+6807C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737353 | ||||||
| chr6:104737409
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2513+6751A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737409 | ||||||
| chr6:104737476
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2513+6684C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737476 | ||||||
| chr6:104737546
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2513+6614A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737546 | ||||||
| chr6:104737601
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2513+6559C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737601 | ||||||
| chr6:104737618
|
G | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2513+6542C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737618 | ||||||
| chr6:104737667
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2513+6493G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737667 | ||||||
| chr6:104737675
|
C | G | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2513+6485G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737675 | ||||||
| chr6:104737679
|
C | CG | 3 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0057 | 3 | HG02809.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2513+6480_2513+648 others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737679 | ||||||
| chr6:104737693
|
G | A | 70 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(67): Show | 70 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2513+6467C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737693 | ||||||
| chr6:104737710
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2513+6450G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737710 | ||||||
| chr6:104737716
|
G | A | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2513+6444C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737716 | ||||||
| chr6:104737734
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2513+6426T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737734 | ||||||
| chr6:104737740
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+6420C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737740 | ||||||
| chr6:104737745
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2513+6415A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737745 | ||||||
| chr6:104737797
|
G | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2513+6363C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737797 | ||||||
| chr6:104737805
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2513+6355G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737805 | ||||||
| chr6:104737806
|
C | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2513+6354G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737806 | ||||||
| chr6:104737817
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2513+6343C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737817 | ||||||
| chr6:104737932
|
C | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(152): Show | 156 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.2513+6228G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737932 | ||||||
| chr6:104737976
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2513+6184C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737976 | ||||||
| chr6:104737981
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2513+6179C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737981 | ||||||
| chr6:104737996
|
G | GCCT | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0170 | 3 | HG00609.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2513+6161_2513+616 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104737996 | ||||||
| chr6:104738080
|
T | C | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2513+6080A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738080 | ||||||
| chr6:104738092
|
C | A | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2513+6068G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738092 | ||||||
| chr6:104738153
|
CA | C | 6 | a0001c0002t0001g0094a0001c0002t0001g0108a0001c0002t0001g0109others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2513+6006delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738153 | ||||||
| chr6:104738194
|
T | C | 2 | a0001c0001t0002g0048a0001c0001t0004g0032 | 2 | NA18941.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2513+5966A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738194 | ||||||
| chr6:104738213
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2513+5947C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738213 | ||||||
| chr6:104738215
|
G | T | 1 | a0001c0001t0001g0338 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2513+5945C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738215 | ||||||
| chr6:104738238
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2513+5922C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738238 | ||||||
| chr6:104738258
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2513+5902A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738258 | ||||||
| chr6:104738330
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2513+5830A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738330 | ||||||
| chr6:104738355
|
C | T | 4 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0081others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2513+5805G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738355 | ||||||
| chr6:104738512
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2513+5648C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738512 | ||||||
| chr6:104738551
|
A | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(151): Show | 155 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.2513+5609T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738551 | ||||||
| chr6:104738569
|
C | T | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+5591G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738569 | ||||||
| chr6:104738610
|
T | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+5550A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738610 | ||||||
| chr6:104738637
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2513+5523C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738637 | ||||||
| chr6:104738713
|
G | C | 1 | a0001c0001t0001g0281 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2513+5447C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738713 | ||||||
| chr6:104738773
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2513+5387C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738773 | ||||||
| chr6:104738860
|
T | C | 1 | a0001c0001t0001g0309 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2513+5300A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738860 | ||||||
| chr6:104738963
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2513+5197C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738963 | ||||||
| chr6:104738995
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(229): Show | 233 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2513+5165T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738995 | ||||||
| chr6:104738999
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2513+5161C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104738999 | ||||||
| chr6:104739168
|
G | A | 7 | a0001c0001t0001g0257a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG03669.hp2 NA18943.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.2513+4992C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739168 | ||||||
| chr6:104739190
|
T | C | 4 | a0001c0001t0001g0214a0001c0001t0001g0276a0001c0001t0001g0288others(1): Show | 4 | HG00099.hp2 HG00735.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513+4970A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739190 | ||||||
| chr6:104739262
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2513+4898G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739262 | ||||||
| chr6:104739289
|
C | G | 1 | a0001c0001t0005g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2513+4871G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739289 | ||||||
| chr6:104739429
|
G | A | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2513+4731C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739429 | ||||||
| chr6:104739450
|
C | T | 1 | a0001c0001t0002g0005 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2513+4710G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739450 | ||||||
| chr6:104739474
|
C | T | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2513+4686G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739474 | ||||||
| chr6:104739531
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+4629T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739531 | ||||||
| chr6:104739563
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0249 | 2 | HG02027.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2513+4597T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739563 | ||||||
| chr6:104739586
|
A | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0317 | 2 | HG01106.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2513+4574T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739586 | ||||||
| chr6:104739644
|
C | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513+4516G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739644 | ||||||
| chr6:104739741
|
A | C | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2513+4419T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739741 | ||||||
| chr6:104739771
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2513+4389G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739771 | ||||||
| chr6:104739804
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2513+4356C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739804 | ||||||
| chr6:104739997
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2513+4163G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104739997 | ||||||
| chr6:104740118
|
A | G | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2513+4042T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740118 | ||||||
| chr6:104740119
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+4041A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740119 | ||||||
| chr6:104740155
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+4005A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740155 | ||||||
| chr6:104740185
|
T | TATAGCAC | 7 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2513+3968_2513+397 others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740185 | ||||||
| chr6:104740255
|
G | T | 1 | a0001c0001t0001g0205 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2513+3905C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740255 | ||||||
| chr6:104740380
|
G | C | 50 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(47): Show | 50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2513+3780C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740380 | ||||||
| chr6:104740383
|
G | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2513+3777C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740383 | ||||||
| chr6:104740416
|
G | A | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+3744C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740416 | ||||||
| chr6:104740607
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2513+3553A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740607 | ||||||
| chr6:104740628
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2513+3532T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740628 | ||||||
| chr6:104740678
|
A | T | 24 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0153others(21): Show | 24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.2513+3482T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740678 | ||||||
| chr6:104740714
|
C | T | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+3446G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740714 | ||||||
| chr6:104740855
|
A | C | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+3305T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740855 | ||||||
| chr6:104740928
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2513+3232G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104740928 | ||||||
| chr6:104741009
|
C | T | 24 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0153others(21): Show | 24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.2513+3151G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741009 | ||||||
| chr6:104741016
|
C | A | 24 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0153others(21): Show | 24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.2513+3144G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741016 | ||||||
| chr6:104741110
|
A | AC | 230 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2513+3049dupG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741110 | ||||||
| chr6:104741129
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2513+3031G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741129 | ||||||
| chr6:104741222
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2513+2938A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741222 | ||||||
| chr6:104741245
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2513+2915C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741245 | ||||||
| chr6:104741260
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2513+2900G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741260 | ||||||
| chr6:104741263
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+2897G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741263 | ||||||
| chr6:104741316
|
T | C | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2513+2844A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741316 | ||||||
| chr6:104741484
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2513+2676C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741484 | ||||||
| chr6:104741519
|
GACAA | G | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+2637_2513+264 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741519 | ||||||
| chr6:104741588
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2513+2572C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741588 | ||||||
| chr6:104741695
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2513+2465A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741695 | ||||||
| chr6:104741780
|
T | C | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+2380A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741780 | ||||||
| chr6:104741807
|
CTACTT | C | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+2348_2513+235 others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741807 | ||||||
| chr6:104741860
|
T | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(335): Show | 340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.2513+2300A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741860 | ||||||
| chr6:104741895
|
A | T | 2 | a0001c0001t0001g0342a0001c0001t0001g0343 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2513+2265T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741895 | ||||||
| chr6:104741913
|
C | T | 1 | a0001c0003t0001g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2513+2247G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741913 | ||||||
| chr6:104741914
|
G | T | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2513+2246C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104741914 | ||||||
| chr6:104742002
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0304a0001c0001t0001g0334 | 3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2513+2158G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742002 | ||||||
| chr6:104742008
|
G | A | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2513+2152C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742008 | ||||||
| chr6:104742035
|
A | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513+2125T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742035 | ||||||
| chr6:104742111
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2513+2049A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742111 | ||||||
| chr6:104742130
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2513+2030G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742130 | ||||||
| chr6:104742131
|
T | C | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+2029A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742131 | ||||||
| chr6:104742161
|
C | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(92): Show | 96 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.2513+1999G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742161 | ||||||
| chr6:104742207
|
A | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(152): Show | 156 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.2513+1953T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742207 | ||||||
| chr6:104742380
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2513+1780G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742380 | ||||||
| chr6:104742421
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0249 | 2 | HG02027.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2513+1739C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742421 | ||||||
| chr6:104742441
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2513+1719C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742441 | ||||||
| chr6:104742460
|
T | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(150): Show | 154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2513+1700A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742460 | ||||||
| chr6:104742617
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(152): Show | 156 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.2513+1543C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742617 | ||||||
| chr6:104742638
|
C | T | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2513+1522G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742638 | ||||||
| chr6:104742655
|
G | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2513+1505C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742655 | ||||||
| chr6:104742689
|
C | T | 3 | a0001c0001t0001g0174a0001c0003t0001g0228a0001c0003t0001g0229 | 3 | HG02738.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2513+1471G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742689 | ||||||
| chr6:104742711
|
G | C | 2 | a0001c0003t0001g0228a0001c0003t0001g0229 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2513+1449C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742711 | ||||||
| chr6:104742740
|
G | T | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+1420C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742740 | ||||||
| chr6:104742872
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+1288A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742872 | ||||||
| chr6:104742980
|
C | A | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2513+1180G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104742980 | ||||||
| chr6:104743009
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2513+1151C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743009 | ||||||
| chr6:104743035
|
C | G | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2513+1125G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743035 | ||||||
| chr6:104743052
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2513+1108A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743052 | ||||||
| chr6:104743056
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2513+1104C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743056 | ||||||
| chr6:104743098
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+1062A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743098 | ||||||
| chr6:104743176
|
G | C | 17 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0155others(14): Show | 17 | HG00621.hp2 HG02055.hp1 HG02965.hp2 others(14): Show |
intron_variant | MODIFIER | c.2513+984C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743176 | ||||||
| chr6:104743184
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+976C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743184 | ||||||
| chr6:104743191
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513+969A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743191 | ||||||
| chr6:104743197
|
G | T | 7 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2513+963C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743197 | ||||||
| chr6:104743306
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2513+854C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743306 | ||||||
| chr6:104743315
|
T | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2513+845A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743315 | ||||||
| chr6:104743315
|
TA | T | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2513+844delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743315 | ||||||
| chr6:104743402
|
A | G | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2513+758T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743402 | ||||||
| chr6:104743512
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2513+648G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743512 | ||||||
| chr6:104743629
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0334 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2513+531T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743629 | ||||||
| chr6:104743652
|
C | T | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+508G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743652 | ||||||
| chr6:104743822
|
CAAATATT others(1): Show |
C | 62 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(59): Show | 63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.2513+330_2513+337d others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743822 | ||||||
| chr6:104743830
|
A | AAAATAAT others(4): Show |
1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2513+329_2513+330i others(13): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743830 | ||||||
| chr6:104743836
|
TTAAAA | T | 92 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(89): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2513+319_2513+323d others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743836 | ||||||
| chr6:104743939
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(152): Show | 156 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.2513+221G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104743939 | ||||||
| chr6:104744134
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2513+26G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104744134 | ||||||
| chr6:104744140
|
A | T | 1 | a0001c0003t0001g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2513+20T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 22/23 | chr6 | 104744140 | ||||||
| chr6:104744232
|
TAAC | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
splice_region_variant&intron_variant | LOW | c.2443-5_2443-3delGT others(1): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 21/23 | chr6 | 104744232 | ||||||
| chr6:104744260
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2443-30A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 21/23 | chr6 | 104744260 | ||||||
| chr6:104744365
|
G | C | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2443-135C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 21/23 | chr6 | 104744365 | ||||||
| chr6:104744815
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2344-205T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104744815 | ||||||
| chr6:104744942
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2344-332A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104744942 | ||||||
| chr6:104745103
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2344-493G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745103 | ||||||
| chr6:104745104
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2344-494C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745104 | ||||||
| chr6:104745138
|
C | A | 2 | a0001c0002t0001g0084a0001c0002t0001g0117 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2344-528G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745138 | ||||||
| chr6:104745433
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2344-823A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745433 | ||||||
| chr6:104745455
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0195 | 2 | HG02015.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2344-846_2344-845i others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | ||||||
| chr6:104745455
|
C | CTTTTTTT others(4): Show |
104 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(101): Show | 105 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.2344-846_2344-845i others(13): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | ||||||
| chr6:104745455
|
C | CTTTTTTT others(5): Show |
109 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0001g0149others(106): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2344-846_2344-845i others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | ||||||
| chr6:104745455
|
C | CTTTTTTT others(6): Show |
14 | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0062others(11): Show | 14 | HG01515.hp1 HG01952.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2344-846_2344-845i others(15): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745455 | ||||||
| chr6:104745541
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2344-931G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745541 | ||||||
| chr6:104745768
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2344-1158C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745768 | ||||||
| chr6:104745966
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2344-1356T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104745966 | ||||||
| chr6:104746014
|
T | C | 1 | a0001c0002t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2344-1404A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746014 | ||||||
| chr6:104746078
|
A | G | 6 | a0001c0002t0001g0094a0001c0002t0001g0108a0001c0002t0001g0109others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2344-1468T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746078 | ||||||
| chr6:104746158
|
T | C | 1 | a0001c0002t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2344-1548A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746158 | ||||||
| chr6:104746196
|
G | A | 11 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(8): Show | 11 | HG01515.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2344-1586C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746196 | ||||||
| chr6:104746303
|
G | T | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2344-1693C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746303 | ||||||
| chr6:104746638
|
A | C | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2344-2028T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746638 | ||||||
| chr6:104746776
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(150): Show | 154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2344-2166T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746776 | ||||||
| chr6:104746905
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(45): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.2344-2295A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746905 | ||||||
| chr6:104746911
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2344-2301T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104746911 | ||||||
| chr6:104747130
|
T | C | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2344-2520A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747130 | ||||||
| chr6:104747369
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2344-2759G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747369 | ||||||
| chr6:104747396
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2344-2786G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747396 | ||||||
| chr6:104747516
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | NA18962.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2343+2825C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747516 | ||||||
| chr6:104747528
|
G | A | 42 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(39): Show | 42 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.2343+2813C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747528 | ||||||
| chr6:104747662
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2343+2679G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747662 | ||||||
| chr6:104747700
|
T | C | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2343+2641A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747700 | ||||||
| chr6:104747716
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2343+2625T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747716 | ||||||
| chr6:104747732
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2343+2609A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747732 | ||||||
| chr6:104747792
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2343+2549G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747792 | ||||||
| chr6:104747838
|
G | C | 1 | a0001c0001t0007g0269 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2343+2503C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104747838 | ||||||
| chr6:104748248
|
G | GA | 153 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(150): Show | 154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2343+2092dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748248 | ||||||
| chr6:104748284
|
T | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2343+2057A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748284 | ||||||
| chr6:104748482
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2343+1859C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748482 | ||||||
| chr6:104748761
|
T | C | 1 | a0001c0002t0001g0126 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2343+1580A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748761 | ||||||
| chr6:104748908
|
C | G | 91 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(88): Show | 91 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2343+1433G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104748908 | ||||||
| chr6:104749096
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2343+1245T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749096 | ||||||
| chr6:104749119
|
T | C | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2343+1222A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749119 | ||||||
| chr6:104749126
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2343+1215G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749126 | ||||||
| chr6:104749216
|
G | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(150): Show | 154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2343+1125C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749216 | ||||||
| chr6:104749349
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2343+992G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749349 | ||||||
| chr6:104749410
|
A | G | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2343+931T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749410 | ||||||
| chr6:104749430
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2343+911T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749430 | ||||||
| chr6:104749549
|
C | T | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2343+792G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749549 | ||||||
| chr6:104749866
|
T | C | 1 | a0001c0001t0001g0324 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2343+475A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749866 | ||||||
| chr6:104749991
|
C | T | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0242others(3): Show | 6 | HG00609.hp1 HG02027.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.2343+350G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749991 | ||||||
| chr6:104749999
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(150): Show | 154 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2343+342T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104749999 | ||||||
| chr6:104750084
|
G | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2343+257C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750084 | ||||||
| chr6:104750195
|
C | T | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2343+146G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750195 | ||||||
| chr6:104750220
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2343+121G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750220 | ||||||
| chr6:104750238
|
AC | A | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2343+102delG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750238 | ||||||
| chr6:104750249
|
T | G | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2343+92A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750249 | ||||||
| chr6:104750290
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+51A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750290 | ||||||
| chr6:104750291
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+50T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750291 | ||||||
| chr6:104750292
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+49C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750292 | ||||||
| chr6:104750303
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+38A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750303 | ||||||
| chr6:104750304
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+37C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750304 | ||||||
| chr6:104750305
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+36A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750305 | ||||||
| chr6:104750308
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+33A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750308 | ||||||
| chr6:104750309
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2343+32C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750309 | ||||||
| chr6:104750316
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2343+25G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 20/23 | chr6 | 104750316 | ||||||
| chr6:104750535
|
T | G | 1 | a0001c0001t0002g0024 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2212-63A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750535 | ||||||
| chr6:104750721
|
T | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-249A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750721 | ||||||
| chr6:104750733
|
C | T | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2212-261G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750733 | ||||||
| chr6:104750819
|
T | G | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2212-347A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750819 | ||||||
| chr6:104750838
|
C | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0216 | 2 | NA18987.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2212-366G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750838 | ||||||
| chr6:104750879
|
T | C | 3 | a0001c0001t0001g0276a0001c0001t0001g0288a0001c0001t0007g0269 | 3 | HG00099.hp2 HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2212-407A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750879 | ||||||
| chr6:104750943
|
G | A | 60 | a0001c0001t0001g0295a0001c0002t0001g0076a0001c0002t0001g0077others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.2212-471C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750943 | ||||||
| chr6:104750943
|
G | C | 1 | a0001c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2212-471C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750943 | ||||||
| chr6:104750963
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG00621.hp1 HG02015.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.2212-491G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104750963 | ||||||
| chr6:104751031
|
A | G | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2212-559T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751031 | ||||||
| chr6:104751076
|
C | A | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2212-604G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751076 | ||||||
| chr6:104751198
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2212-726G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751198 | ||||||
| chr6:104751520
|
T | C | 6 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG00544.hp1 HG02165.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.2212-1048A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751520 | ||||||
| chr6:104751640
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2212-1168T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751640 | ||||||
| chr6:104751743
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-1271A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751743 | ||||||
| chr6:104751809
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2212-1337A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751809 | ||||||
| chr6:104751896
|
TC | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-1425delG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751896 | ||||||
| chr6:104751897
|
C | T | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2212-1425G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751897 | ||||||
| chr6:104751916
|
G | C | 53 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0001g0163others(50): Show | 53 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.2212-1444C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751916 | ||||||
| chr6:104751955
|
C | CA | 74 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(71): Show | 74 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2212-1484dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751955 | ||||||
| chr6:104751955
|
C | CAAA | 77 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0142others(74): Show | 77 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.2212-1486_2212-148 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751955 | ||||||
| chr6:104751955
|
C | CAAAA | 14 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0148others(11): Show | 15 | HG02896.hp2 HG02897.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.2212-1487_2212-148 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104751955 | ||||||
| chr6:104752131
|
G | A | 1 | a0001c0001t0003g0140 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2212-1659C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752131 | ||||||
| chr6:104752241
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2212-1769G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752241 | ||||||
| chr6:104752248
|
T | C | 1 | a0001c0001t0005g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2212-1776A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752248 | ||||||
| chr6:104752272
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2212-1800A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752272 | ||||||
| chr6:104752325
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-1853C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752325 | ||||||
| chr6:104752425
|
T | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-1953A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752425 | ||||||
| chr6:104752732
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-2260T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752732 | ||||||
| chr6:104752785
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-2313G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752785 | ||||||
| chr6:104752821
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150 | 3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2212-2349A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104752821 | ||||||
| chr6:104753226
|
C | T | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2212-2754G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753226 | ||||||
| chr6:104753256
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-2784C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753256 | ||||||
| chr6:104753278
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2212-2806C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753278 | ||||||
| chr6:104753372
|
G | A | 75 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2212-2900C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753372 | ||||||
| chr6:104753414
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2212-2942G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753414 | ||||||
| chr6:104753479
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2212-3007C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753479 | ||||||
| chr6:104753512
|
C | G | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2212-3040G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753512 | ||||||
| chr6:104753594
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2212-3122A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753594 | ||||||
| chr6:104753694
|
C | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(163): Show | 167 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2212-3222G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753694 | ||||||
| chr6:104753892
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2212-3420C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104753892 | ||||||
| chr6:104754153
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2212-3681G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754153 | ||||||
| chr6:104754168
|
A | ACTAT | 62 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(59): Show | 62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.2212-3697_2212-369 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754168 | ||||||
| chr6:104754316
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2212-3844A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754316 | ||||||
| chr6:104754338
|
T | C | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0319 | 3 | HG02132.hp2 HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2212-3866A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754338 | ||||||
| chr6:104754392
|
A | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-3920T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754392 | ||||||
| chr6:104754851
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2212-4379T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754851 | ||||||
| chr6:104754994
|
A | G | 42 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(39): Show | 42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.2212-4522T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104754994 | ||||||
| chr6:104755067
|
G | T | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2212-4595C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755067 | ||||||
| chr6:104755258
|
T | C | 62 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(59): Show | 62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.2212-4786A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755258 | ||||||
| chr6:104755290
|
G | C | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2212-4818C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755290 | ||||||
| chr6:104755312
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2212-4840G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755312 | ||||||
| chr6:104755899
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-5427T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104755899 | ||||||
| chr6:104756140
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-5668G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756140 | ||||||
| chr6:104756150
|
T | C | 8 | a0001c0002t0001g0124a0001c0002t0001g0127a0001c0002t0001g0128others(5): Show | 8 | HG01167.hp2 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5678A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756150 | ||||||
| chr6:104756237
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-5765C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756237 | ||||||
| chr6:104756246
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2212-5774T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756246 | ||||||
| chr6:104756384
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2212-5912G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756384 | ||||||
| chr6:104756397
|
G | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-5925C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756397 | ||||||
| chr6:104756398
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2212-5926G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756398 | ||||||
| chr6:104756404
|
T | G | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2212-5932A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756404 | ||||||
| chr6:104756411
|
C | CA | 44 | a0001c0001t0001g0188a0001c0001t0001g0199a0001c0001t0001g0313others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.2212-5940dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756411 | ||||||
| chr6:104756411
|
CA | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(38): Show | 42 | HG00621.hp2 HG02055.hp1 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.2212-5940delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756411 | ||||||
| chr6:104756421
|
AAAAAAAT | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0043others(6): Show | 9 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.2212-5956_2212-595 others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756421 | ||||||
| chr6:104756422
|
AAAAAATA others(1): Show |
A | 8 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0010others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5958_2212-595 others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756422 | ||||||
| chr6:104756423
|
AAAAATAT | A | 36 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(33): Show | 36 | HG00735.hp2 HG01106.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.2212-5958_2212-595 others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756423 | ||||||
| chr6:104756424
|
AAAATATA others(1): Show |
A | 19 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0008others(16): Show | 19 | HG00099.hp1 HG00597.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2212-5960_2212-595 others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756424 | ||||||
| chr6:104756426
|
A | AT | 8 | a0001c0001t0001g0268a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2212-5955_2212-595 others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756426 | ||||||
| chr6:104756426
|
A | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(18): Show | 22 | HG01168.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.2212-5954T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756426 | ||||||
| chr6:104756427
|
AT | A | 51 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0142others(48): Show | 51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.2212-5956delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756427 | ||||||
| chr6:104756428
|
T | A | 48 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0273others(45): Show | 48 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2212-5956A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756428 | ||||||
| chr6:104756430
|
T | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0178a0001c0001t0001g0182others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5958A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756430 | ||||||
| chr6:104756446
|
T | C | 60 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0002t0001g0076others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2212-5974A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756446 | ||||||
| chr6:104756448
|
C | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2212-5976G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756448 | ||||||
| chr6:104756564
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-6092G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756564 | ||||||
| chr6:104756588
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2212-6116C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756588 | ||||||
| chr6:104756623
|
G | C | 3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030 | 3 | HG00735.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2212-6151C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756623 | ||||||
| chr6:104756746
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2212-6274A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756746 | ||||||
| chr6:104756897
|
G | A | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-6425C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756897 | ||||||
| chr6:104756998
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2212-6526C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104756998 | ||||||
| chr6:104757188
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-6716G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757188 | ||||||
| chr6:104757312
|
G | A | 46 | a0001c0001t0001g0141a0001c0002t0001g0083a0001c0002t0001g0085others(43): Show | 46 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.2212-6840C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757312 | ||||||
| chr6:104757637
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0304a0001c0001t0001g0334 | 3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2212-7165T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757637 | ||||||
| chr6:104757687
|
A | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2212-7215T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757687 | ||||||
| chr6:104757804
|
G | C | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2212-7332C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757804 | ||||||
| chr6:104757951
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(212): Show | 216 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.2212-7479G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104757951 | ||||||
| chr6:104758049
|
G | A | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2212-7577C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758049 | ||||||
| chr6:104758200
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2212-7728G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758200 | ||||||
| chr6:104758289
|
C | A | 1 | a0001c0001t0001g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2212-7817G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758289 | ||||||
| chr6:104758293
|
CAGAG | C | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2212-7825_2212-782 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758293 | ||||||
| chr6:104758314
|
C | T | 42 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(39): Show | 42 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.2212-7842G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758314 | ||||||
| chr6:104758445
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-7973T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758445 | ||||||
| chr6:104758454
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0011 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2212-7982A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758454 | ||||||
| chr6:104758500
|
G | A | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2212-8028C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758500 | ||||||
| chr6:104758544
|
A | AG | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2212-8073dupC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758544 | ||||||
| chr6:104758574
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0011 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2212-8102C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758574 | ||||||
| chr6:104758619
|
C | T | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2212-8147G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758619 | ||||||
| chr6:104758645
|
T | C | 62 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(59): Show | 62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.2212-8173A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104758645 | ||||||
| chr6:104759109
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0205 | 2 | HG02027.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2212-8637T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759109 | ||||||
| chr6:104759252
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0145others(5): Show | 9 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2212-8780G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759252 | ||||||
| chr6:104759263
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2212-8791T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759263 | ||||||
| chr6:104759433
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-8961C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759433 | ||||||
| chr6:104759568
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2212-9096A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759568 | ||||||
| chr6:104759633
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2212-9161C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759633 | ||||||
| chr6:104759640
|
C | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0101others(1): Show | 4 | HG01257.hp1 HG01433.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212-9168G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759640 | ||||||
| chr6:104759704
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2212-9232G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759704 | ||||||
| chr6:104759710
|
T | A | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2212-9238A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759710 | ||||||
| chr6:104759798
|
A | G | 62 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(59): Show | 62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.2212-9326T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759798 | ||||||
| chr6:104759818
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2212-9346T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759818 | ||||||
| chr6:104759827
|
GAGA | G | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2212-9358_2212-935 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759827 | ||||||
| chr6:104759874
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2212-9402G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759874 | ||||||
| chr6:104759919
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2212-9447T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759919 | ||||||
| chr6:104759956
|
G | A | 12 | a0001c0001t0001g0231a0001c0001t0001g0245a0001c0001t0001g0250others(9): Show | 12 | HG00438.hp1 HG00558.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.2212-9484C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759956 | ||||||
| chr6:104759973
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2212-9501G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104759973 | ||||||
| chr6:104760074
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(164): Show | 168 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2212-9602T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760074 | ||||||
| chr6:104760084
|
G | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2212-9612C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760084 | ||||||
| chr6:104760101
|
C | T | 50 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(47): Show | 50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2212-9629G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760101 | ||||||
| chr6:104760130
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-9658G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760130 | ||||||
| chr6:104760142
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2212-9670G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760142 | ||||||
| chr6:104760206
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212-9734T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760206 | ||||||
| chr6:104760264
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2212-9792T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760264 | ||||||
| chr6:104760275
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2212-9803A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760275 | ||||||
| chr6:104760309
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-9837C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760309 | ||||||
| chr6:104760360
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2212-9888C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760360 | ||||||
| chr6:104760370
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2212-9898G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760370 | ||||||
| chr6:104760504
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2212-10032G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760504 | ||||||
| chr6:104760524
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2212-10052T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760524 | ||||||
| chr6:104760574
|
C | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2212-10102G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760574 | ||||||
| chr6:104760608
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212-10136G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760608 | ||||||
| chr6:104760613
|
A | G | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2212-10141T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760613 | ||||||
| chr6:104760705
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2212-10233C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760705 | ||||||
| chr6:104760828
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2212-10356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760828 | ||||||
| chr6:104760866
|
A | T | 1 | a0001c0002t0001g0100 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2211+10327T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760866 | ||||||
| chr6:104760938
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+10255T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760938 | ||||||
| chr6:104760939
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+10254T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104760939 | ||||||
| chr6:104761055
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2211+10138C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761055 | ||||||
| chr6:104761204
|
T | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+9989A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761204 | ||||||
| chr6:104761290
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2211+9903A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761290 | ||||||
| chr6:104761553
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0222 | 2 | HG00544.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2211+9640G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761553 | ||||||
| chr6:104761760
|
C | T | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2211+9433G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761760 | ||||||
| chr6:104761828
|
C | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | NA18962.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2211+9365G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761828 | ||||||
| chr6:104761837
|
TAAAC | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+9352_2211+935 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104761837 | ||||||
| chr6:104762003
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+9190A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762003 | ||||||
| chr6:104762004
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+9189C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762004 | ||||||
| chr6:104762151
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2211+9042T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762151 | ||||||
| chr6:104762226
|
G | A | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2211+8967C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762226 | ||||||
| chr6:104762388
|
T | C | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2211+8805A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762388 | ||||||
| chr6:104762491
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2211+8702A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762491 | ||||||
| chr6:104762510
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2211+8683A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762510 | ||||||
| chr6:104762567
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2211+8626C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762567 | ||||||
| chr6:104762584
|
G | A | 75 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2211+8609C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762584 | ||||||
| chr6:104762620
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+8573T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762620 | ||||||
| chr6:104762637
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0283a0001c0001t0001g0335 | 3 | HG00733.hp2 HG01175.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2211+8556C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762637 | ||||||
| chr6:104762729
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+8464T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762729 | ||||||
| chr6:104762807
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+8386T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762807 | ||||||
| chr6:104762888
|
G | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0141a0001c0001t0001g0145others(5): Show | 9 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2211+8305C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762888 | ||||||
| chr6:104762906
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+8287A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762906 | ||||||
| chr6:104762989
|
C | CA | 19 | a0001c0001t0001g0152a0001c0001t0001g0175a0001c0001t0001g0276others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2211+8203dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762989 | ||||||
| chr6:104762989
|
CA | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0246a0001c0001t0001g0248others(5): Show | 8 | HG01255.hp1 HG01934.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.2211+8203delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104762989 | ||||||
| chr6:104763183
|
C | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+8010G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763183 | ||||||
| chr6:104763278
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2211+7915A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763278 | ||||||
| chr6:104763286
|
A | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0326 | 2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2211+7907T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763286 | ||||||
| chr6:104763485
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2211+7708C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763485 | ||||||
| chr6:104763706
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+7487G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763706 | ||||||
| chr6:104763725
|
T | C | 62 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(59): Show | 62 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.2211+7468A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763725 | ||||||
| chr6:104763836
|
G | A | 3 | a0001c0001t0001g0276a0001c0001t0001g0288a0001c0001t0007g0269 | 3 | HG00099.hp2 HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2211+7357C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763836 | ||||||
| chr6:104763856
|
C | T | 2 | a0001c0002t0001g0106a0001c0002t0001g0119 | 2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2211+7337G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104763856 | ||||||
| chr6:104764062
|
A | C | 9 | a0001c0001t0001g0233a0001c0001t0001g0253a0001c0001t0001g0309others(6): Show | 9 | NA18969.hp1 NA19000.hp1 NA19056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2211+7131T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764062 | ||||||
| chr6:104764250
|
G | A | 50 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(47): Show | 50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2211+6943C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764250 | ||||||
| chr6:104764607
|
ACTT | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(164): Show | 168 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2211+6583_2211+658 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764607 | ||||||
| chr6:104764706
|
T | C | 1 | a0001c0001t0002g0005 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2211+6487A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764706 | ||||||
| chr6:104764941
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2211+6252C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104764941 | ||||||
| chr6:104765048
|
A | G | 7 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0180others(4): Show | 7 | HG00621.hp2 NA18947.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.2211+6145T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765048 | ||||||
| chr6:104765053
|
T | A | 1 | a0001c0002t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2211+6140A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765053 | ||||||
| chr6:104765389
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2211+5804G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765389 | ||||||
| chr6:104765428
|
C | G | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2211+5765G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765428 | ||||||
| chr6:104765450
|
T | G | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0215 | 3 | NA18957.hp1 NA18973.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2211+5743A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765450 | ||||||
| chr6:104765736
|
A | C | 64 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0145others(61): Show | 64 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.2211+5457T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765736 | ||||||
| chr6:104765802
|
T | C | 1 | a0001c0005t0001g0318 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2211+5391A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765802 | ||||||
| chr6:104765893
|
T | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0338 | 2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2211+5300A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765893 | ||||||
| chr6:104765973
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+5220G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104765973 | ||||||
| chr6:104766176
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2211+5017G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766176 | ||||||
| chr6:104766253
|
G | A | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2211+4940C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766253 | ||||||
| chr6:104766408
|
G | A | 2 | a0001c0001t0001g0148a0001c0002t0008g0344 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2211+4785C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766408 | ||||||
| chr6:104766703
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0338 | 2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2211+4490C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766703 | ||||||
| chr6:104766910
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2211+4283T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104766910 | ||||||
| chr6:104767084
|
A | T | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2211+4109T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767084 | ||||||
| chr6:104767148
|
G | A | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2211+4045C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767148 | ||||||
| chr6:104767216
|
G | T | 13 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG00621.hp2 NA18947.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.2211+3977C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767216 | ||||||
| chr6:104767268
|
C | T | 6 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0043others(3): Show | 6 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+3925G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767268 | ||||||
| chr6:104767351
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2211+3842G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767351 | ||||||
| chr6:104767414
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2211+3779A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767414 | ||||||
| chr6:104767478
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2211+3715C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767478 | ||||||
| chr6:104767481
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2211+3712G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767481 | ||||||
| chr6:104767490
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2211+3703G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767490 | ||||||
| chr6:104767540
|
A | T | 2 | a0001c0002t0001g0106a0001c0002t0001g0119 | 2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2211+3653T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104767540 | ||||||
| chr6:104768143
|
G | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+3050C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768143 | ||||||
| chr6:104768271
|
T | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+2922A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768271 | ||||||
| chr6:104768273
|
A | G | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2211+2920T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768273 | ||||||
| chr6:104768359
|
G | C | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2211+2834C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768359 | ||||||
| chr6:104768530
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+2663A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768530 | ||||||
| chr6:104768576
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2211+2617G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768576 | ||||||
| chr6:104768625
|
G | GA | 169 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(166): Show | 170 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.2211+2567dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768625 | ||||||
| chr6:104768820
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2211+2373A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768820 | ||||||
| chr6:104768890
|
T | A | 1 | a0001c0001t0001g0271 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2211+2303A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768890 | ||||||
| chr6:104768895
|
T | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2211+2298A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104768895 | ||||||
| chr6:104769016
|
T | C | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2211+2177A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769016 | ||||||
| chr6:104769054
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+2139A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769054 | ||||||
| chr6:104769075
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2211+2118G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769075 | ||||||
| chr6:104769094
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2211+2099T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769094 | ||||||
| chr6:104769240
|
G | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+1953C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769240 | ||||||
| chr6:104769313
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+1880A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769313 | ||||||
| chr6:104769319
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2211+1874A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769319 | ||||||
| chr6:104769334
|
T | C | 1 | a0001c0002t0001g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2211+1859A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769334 | ||||||
| chr6:104769341
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2211+1852A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769341 | ||||||
| chr6:104769766
|
G | A | 50 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(47): Show | 50 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2211+1427C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769766 | ||||||
| chr6:104769813
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2211+1380T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769813 | ||||||
| chr6:104769895
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2211+1298C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769895 | ||||||
| chr6:104769989
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+1204G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104769989 | ||||||
| chr6:104770017
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2211+1176T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770017 | ||||||
| chr6:104770043
|
C | T | 2 | a0001c0002t0001g0101a0001c0002t0001g0103 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2211+1150G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770043 | ||||||
| chr6:104770051
|
C | G | 2 | a0001c0001t0001g0327a0001c0001t0001g0336 | 2 | NA19000.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2211+1142G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770051 | ||||||
| chr6:104770156
|
T | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150 | 3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2211+1037A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770156 | ||||||
| chr6:104770214
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2211+979C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770214 | ||||||
| chr6:104770556
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2211+637A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770556 | ||||||
| chr6:104770750
|
C | T | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2211+443G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770750 | ||||||
| chr6:104770845
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2211+348G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770845 | ||||||
| chr6:104770856
|
C | T | 31 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(28): Show | 31 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2211+337G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770856 | ||||||
| chr6:104770970
|
C | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211+223G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104770970 | ||||||
| chr6:104771085
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2211+108G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104771085 | ||||||
| chr6:104771107
|
A | G | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2211+86T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 19/23 | chr6 | 104771107 | ||||||
| chr6:104771662
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2014+263G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771662 | ||||||
| chr6:104771697
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2014+228G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771697 | ||||||
| chr6:104771698
|
A | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2014+227T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771698 | ||||||
| chr6:104771705
|
G | GA | 88 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0142others(85): Show | 88 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.2014+219dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771705 | ||||||
| chr6:104771845
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2014+80G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771845 | ||||||
| chr6:104771873
|
G | GA | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2014+51dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771873 | ||||||
| chr6:104771898
|
T | C | 45 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(42): Show | 45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.2014+27A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 18/23 | chr6 | 104771898 | ||||||
| chr6:104772198
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-124G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104772198 | ||||||
| chr6:104772383
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1865-309C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104772383 | ||||||
| chr6:104773044
|
C | CA | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0183others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865-971dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773044 | ||||||
| chr6:104773245
|
T | G | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1865-1171A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773245 | ||||||
| chr6:104773359
|
C | T | 2 | a0001c0002t0001g0084a0001c0002t0001g0117 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1865-1285G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773359 | ||||||
| chr6:104773550
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1865-1476C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773550 | ||||||
| chr6:104773580
|
C | G | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1865-1506G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773580 | ||||||
| chr6:104773647
|
A | G | 7 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1865-1573T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773647 | ||||||
| chr6:104773765
|
CT | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0221a0001c0001t0002g0046others(1): Show | 4 | HG01943.hp2 HG02040.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1865-1692delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773765 | ||||||
| chr6:104773770
|
T | TA | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0191 | 3 | HG02895.hp1 HG02897.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1865-1697_1865-169 others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773770 | ||||||
| chr6:104773771
|
T | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(165): Show | 169 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1865-1697A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773771 | ||||||
| chr6:104773771
|
T | TA | 53 | a0001c0001t0001g0234a0001c0001t0001g0331a0001c0001t0001g0334others(50): Show | 53 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1865-1698dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104773771 | ||||||
| chr6:104774024
|
C | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0292 | 2 | HG00323.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1865-1950G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774024 | ||||||
| chr6:104774076
|
TTCTCTTT others(306): Show |
T | 52 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(49): Show | 52 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1865-2315_1865-200 others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774076 | ||||||
| chr6:104774080
|
C | CT | 17 | a0001c0001t0001g0232a0001c0001t0001g0239a0001c0001t0001g0243others(14): Show | 17 | HG00423.hp2 HG00741.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1865-2007dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | ||||||
| chr6:104774080
|
CTTT | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0167a0001c0001t0001g0180others(7): Show | 10 | HG01109.hp1 HG02027.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-2009_1865-200 others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | ||||||
| chr6:104774080
|
CTTTT | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(83): Show | 87 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1865-2010_1865-200 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | ||||||
| chr6:104774080
|
CTTTTT | C | 68 | a0001c0001t0001g0169a0001c0001t0001g0213a0001c0001t0002g0003others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1865-2011_1865-200 others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | ||||||
| chr6:104774080
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1865-2021_1865-200 others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774080 | ||||||
| chr6:104774081
|
TTTTTTTT others(305): Show |
T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-2319_1865-200 others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774081 | ||||||
| chr6:104774113
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1865-2039C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774113 | ||||||
| chr6:104774122
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1865-2048G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774122 | ||||||
| chr6:104774151
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1865-2077C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774151 | ||||||
| chr6:104774217
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1865-2143C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774217 | ||||||
| chr6:104774381
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1865-2307G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774381 | ||||||
| chr6:104774382
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1865-2308C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774382 | ||||||
| chr6:104774388
|
CCTCT | C | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.1865-2318_1865-231 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774388 | ||||||
| chr6:104774446
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1864+2295T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774446 | ||||||
| chr6:104774663
|
C | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0292 | 2 | HG00323.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1864+2078G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774663 | ||||||
| chr6:104774673
|
C | T | 2 | a0001c0002t0001g0106a0001c0002t0001g0119 | 2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1864+2068G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774673 | ||||||
| chr6:104774715
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0325 | 2 | NA18747.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1864+2026C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774715 | ||||||
| chr6:104774740
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1864+2001G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774740 | ||||||
| chr6:104774852
|
A | C | 1 | a0001c0001t0001g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1864+1889T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774852 | ||||||
| chr6:104774874
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1864+1867A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104774874 | ||||||
| chr6:104775049
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1864+1692A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775049 | ||||||
| chr6:104775068
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1864+1673C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775068 | ||||||
| chr6:104775112
|
C | A | 6 | a0001c0002t0001g0094a0001c0002t0001g0108a0001c0002t0001g0109others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1864+1629G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775112 | ||||||
| chr6:104775353
|
T | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(328): Show | 333 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.1864+1388A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775353 | ||||||
| chr6:104775380
|
T | C | 42 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(39): Show | 42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1864+1361A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775380 | ||||||
| chr6:104775413
|
G | A | 51 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(48): Show | 51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1864+1328C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775413 | ||||||
| chr6:104775601
|
T | A | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1140A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775601 | ||||||
| chr6:104775602
|
T | C | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1139A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775602 | ||||||
| chr6:104775605
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1136T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775605 | ||||||
| chr6:104775606
|
C | A | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1135G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775606 | ||||||
| chr6:104775609
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1132T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775609 | ||||||
| chr6:104775610
|
T | C | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1131A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775610 | ||||||
| chr6:104775612
|
A | T | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1129T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775612 | ||||||
| chr6:104775613
|
C | G | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1864+1128G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775613 | ||||||
| chr6:104775788
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1864+953A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775788 | ||||||
| chr6:104775916
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1864+825C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775916 | ||||||
| chr6:104775989
|
G | A | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 5 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1864+752C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104775989 | ||||||
| chr6:104776249
|
G | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0180others(3): Show | 6 | NA18947.hp2 NA18984.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864+492C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104776249 | ||||||
| chr6:104776361
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1864+380G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104776361 | ||||||
| chr6:104776512
|
C | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864+229G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 17/23 | chr6 | 104776512 | ||||||
| chr6:104777337
|
T | C | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567-20A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777337 | ||||||
| chr6:104777372
|
T | G | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1567-55A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777372 | ||||||
| chr6:104777406
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-89T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777406 | ||||||
| chr6:104777525
|
T | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1567-208A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777525 | ||||||
| chr6:104777537
|
A | T | 12 | a0001c0001t0001g0286a0001c0001t0001g0310a0001c0001t0001g0314others(9): Show | 12 | HG00408.hp2 HG01943.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1567-220T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777537 | ||||||
| chr6:104777628
|
A | AT | 230 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1567-312dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777628 | ||||||
| chr6:104777907
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1567-590C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777907 | ||||||
| chr6:104777979
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1567-662C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104777979 | ||||||
| chr6:104778116
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1567-799G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778116 | ||||||
| chr6:104778375
|
A | AAT | 14 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(11): Show | 14 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1567-1060_1567-105 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778375 | ||||||
| chr6:104778375
|
A | AATAT | 12 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0014others(9): Show | 12 | HG00597.hp2 HG02135.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.1567-1062_1567-105 others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778375 | ||||||
| chr6:104778375
|
A | T | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1567-1058T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778375 | ||||||
| chr6:104778601
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1567-1284G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778601 | ||||||
| chr6:104778630
|
C | CA | 75 | a0001c0001t0001g0259a0001c0001t0001g0272a0001c0001t0001g0275others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1567-1314dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778630 | ||||||
| chr6:104778647
|
T | A | 85 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(82): Show | 85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-1330A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778647 | ||||||
| chr6:104778719
|
T | G | 85 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(82): Show | 85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-1402A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778719 | ||||||
| chr6:104778794
|
C | G | 85 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(82): Show | 85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-1477G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778794 | ||||||
| chr6:104778844
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1567-1527A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104778844 | ||||||
| chr6:104779068
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1567-1751C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779068 | ||||||
| chr6:104779441
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1567-2124T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779441 | ||||||
| chr6:104779546
|
A | G | 85 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(82): Show | 85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-2229T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779546 | ||||||
| chr6:104779734
|
C | G | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1567-2417G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779734 | ||||||
| chr6:104779857
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567-2540A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779857 | ||||||
| chr6:104779874
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567-2557T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779874 | ||||||
| chr6:104779911
|
A | G | 75 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1567-2594T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104779911 | ||||||
| chr6:104780098
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1567-2781G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780098 | ||||||
| chr6:104780135
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1567-2818C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780135 | ||||||
| chr6:104780216
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1567-2899G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780216 | ||||||
| chr6:104780608
|
C | G | 85 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(82): Show | 85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1567-3291G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780608 | ||||||
| chr6:104780673
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-3356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780673 | ||||||
| chr6:104780776
|
C | T | 30 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(27): Show | 30 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1566+3310G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780776 | ||||||
| chr6:104780804
|
C | A | 1 | a0001c0001t0001g0329 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1566+3282G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780804 | ||||||
| chr6:104780887
|
A | G | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566+3199T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104780887 | ||||||
| chr6:104781233
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1566+2853G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781233 | ||||||
| chr6:104781258
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1566+2828T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781258 | ||||||
| chr6:104781302
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1566+2784G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781302 | ||||||
| chr6:104781330
|
CT | C | 4 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0001g0164others(1): Show | 4 | HG00741.hp2 HG01516.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566+2755delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781330 | ||||||
| chr6:104781431
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1566+2655A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781431 | ||||||
| chr6:104781635
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1566+2451G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781635 | ||||||
| chr6:104781646
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1566+2440A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781646 | ||||||
| chr6:104781733
|
A | G | 1 | a0001c0001t0001g0281 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1566+2353T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781733 | ||||||
| chr6:104781734
|
T | C | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1566+2352A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781734 | ||||||
| chr6:104781771
|
C | G | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1566+2315G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781771 | ||||||
| chr6:104781932
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(229): Show | 233 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1566+2154A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781932 | ||||||
| chr6:104781953
|
G | C | 1 | a0001c0004t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1566+2133C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104781953 | ||||||
| chr6:104782013
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1566+2073A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782013 | ||||||
| chr6:104782209
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1566+1877G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782209 | ||||||
| chr6:104782299
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1566+1787C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782299 | ||||||
| chr6:104782437
|
C | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(225): Show | 229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1566+1649G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782437 | ||||||
| chr6:104782457
|
C | A | 3 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02132.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1566+1629G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782457 | ||||||
| chr6:104782482
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1566+1604G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782482 | ||||||
| chr6:104782487
|
A | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1566+1599T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782487 | ||||||
| chr6:104782761
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1566+1325G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782761 | ||||||
| chr6:104782805
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1566+1281A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782805 | ||||||
| chr6:104782854
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(225): Show | 229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1566+1232G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782854 | ||||||
| chr6:104782937
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1566+1149G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782937 | ||||||
| chr6:104782965
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1566+1121C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104782965 | ||||||
| chr6:104783135
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1566+951G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783135 | ||||||
| chr6:104783349
|
C | A | 1 | a0001c0001t0001g0287 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1566+737G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783349 | ||||||
| chr6:104783380
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(162): Show | 166 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1566+706T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783380 | ||||||
| chr6:104783382
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(225): Show | 229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1566+704C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783382 | ||||||
| chr6:104783656
|
G | A | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1566+430C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783656 | ||||||
| chr6:104783855
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1566+231G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104783855 | ||||||
| chr6:104784055
|
A | C | 51 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(48): Show | 51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1566+31T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 14/23 | chr6 | 104784055 | ||||||
| chr6:104784329
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(225): Show | 229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1478+88G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 13/23 | chr6 | 104784329 | ||||||
| chr6:104784330
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1478+87C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 13/23 | chr6 | 104784330 | ||||||
| chr6:104784358
|
A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(142): Show | 146 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1478+59T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 13/23 | chr6 | 104784358 | ||||||
| chr6:104784562
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410-77G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784562 | ||||||
| chr6:104784585
|
C | CA | 145 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(142): Show | 146 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1410-101dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784585 | ||||||
| chr6:104784710
|
A | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410-225T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784710 | ||||||
| chr6:104784952
|
GA | G | 12 | a0001c0001t0002g0008a0001c0001t0002g0031a0001c0001t0002g0036others(9): Show | 12 | HG00099.hp1 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409+32delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 12/23 | chr6 | 104784952 | ||||||
| chr6:104785369
|
T | TA | 6 | a0001c0001t0001g0197a0001c0001t0001g0259a0001c0001t0001g0310others(3): Show | 6 | HG02004.hp2 HG02056.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-51dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785369 | ||||||
| chr6:104785369
|
TA | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-51delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785369 | ||||||
| chr6:104785382
|
AC | A | 10 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087others(7): Show | 10 | HG01168.hp2 HG01256.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-64delG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785382 | ||||||
| chr6:104785383
|
C | A | 42 | a0001c0001t0001g0221a0001c0002t0001g0083a0001c0002t0001g0088others(39): Show | 42 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1075-64G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785383 | ||||||
| chr6:104785610
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1075-291A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785610 | ||||||
| chr6:104785626
|
A | C | 1 | a0001c0002t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1075-307T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785626 | ||||||
| chr6:104785822
|
T | C | 5 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0011others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-503A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785822 | ||||||
| chr6:104785955
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1075-636A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104785955 | ||||||
| chr6:104786294
|
T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0319 | 2 | HG02155.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1075-975A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786294 | ||||||
| chr6:104786340
|
C | CA | 24 | a0001c0001t0001g0159a0001c0001t0001g0176a0001c0001t0001g0261others(21): Show | 24 | HG01515.hp1 HG02040.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1075-1022dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786340 | ||||||
| chr6:104786407
|
T | TA | 270 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0122others(267): Show | 271 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1075-1089dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786407 | ||||||
| chr6:104786407
|
T | TAA | 10 | a0001c0001t0001g0282a0001c0001t0001g0287a0001c0001t0001g0309others(7): Show | 10 | HG01433.hp1 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075-1090_1075-108 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786407 | ||||||
| chr6:104786468
|
C | G | 63 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(60): Show | 63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-1149G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786468 | ||||||
| chr6:104786530
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-1211C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786530 | ||||||
| chr6:104786566
|
T | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1075-1247A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786566 | ||||||
| chr6:104786600
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1075-1281A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786600 | ||||||
| chr6:104786604
|
C | CA | 19 | a0001c0001t0001g0174a0001c0001t0001g0197a0001c0001t0001g0205others(16): Show | 19 | HG00735.hp1 HG01433.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1075-1286dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786604 | ||||||
| chr6:104786613
|
A | C | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1075-1294T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786613 | ||||||
| chr6:104786617
|
A | C | 88 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(85): Show | 88 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1075-1298T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786617 | ||||||
| chr6:104786621
|
C | A | 7 | a0001c0002t0001g0089a0001c0002t0001g0100a0001c0002t0001g0115others(4): Show | 7 | HG01515.hp1 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-1302G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786621 | ||||||
| chr6:104786625
|
C | A | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1075-1306G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786625 | ||||||
| chr6:104786633
|
C | CA | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0326others(4): Show | 7 | HG02055.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-1315dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786633 | ||||||
| chr6:104786633
|
C | CAA | 7 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-1316_1075-131 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786633 | ||||||
| chr6:104786637
|
A | C | 55 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0235others(52): Show | 55 | HG00099.hp2 HG00323.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1075-1318T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786637 | ||||||
| chr6:104786922
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1075-1603G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786922 | ||||||
| chr6:104786930
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1075-1611A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786930 | ||||||
| chr6:104786962
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1075-1643C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104786962 | ||||||
| chr6:104787699
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1075-2380C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787699 | ||||||
| chr6:104787715
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-2396A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787715 | ||||||
| chr6:104787882
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(142): Show | 146 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1075-2563T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787882 | ||||||
| chr6:104787946
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-2627A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104787946 | ||||||
| chr6:104788022
|
T | C | 1 | a0001c0002t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1075-2703A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788022 | ||||||
| chr6:104788027
|
A | G | 51 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(48): Show | 51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-2708T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788027 | ||||||
| chr6:104788100
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(164): Show | 168 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1075-2781T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788100 | ||||||
| chr6:104788112
|
C | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-2793G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788112 | ||||||
| chr6:104788295
|
T | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-2976A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788295 | ||||||
| chr6:104788413
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+3091T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788413 | ||||||
| chr6:104788427
|
T | G | 75 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+3077A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788427 | ||||||
| chr6:104788577
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074+2927T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788577 | ||||||
| chr6:104788597
|
T | C | 75 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+2907A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788597 | ||||||
| chr6:104788730
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1074+2774C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788730 | ||||||
| chr6:104788844
|
A | G | 13 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG00621.hp2 NA18947.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074+2660T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104788844 | ||||||
| chr6:104789214
|
C | T | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1074+2290G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789214 | ||||||
| chr6:104789270
|
A | T | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1074+2234T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789270 | ||||||
| chr6:104789281
|
T | C | 3 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0057 | 3 | HG02809.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1074+2223A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789281 | ||||||
| chr6:104789452
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+2052T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789452 | ||||||
| chr6:104789826
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1074+1678C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104789826 | ||||||
| chr6:104790068
|
G | GA | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1074+1435dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790068 | ||||||
| chr6:104790216
|
C | T | 1 | a0001c0001t0002g0005 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1074+1288G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790216 | ||||||
| chr6:104790352
|
A | T | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1074+1152T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790352 | ||||||
| chr6:104790359
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+1145G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790359 | ||||||
| chr6:104790577
|
G | A | 63 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(60): Show | 63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.1074+927C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790577 | ||||||
| chr6:104790750
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074+754C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790750 | ||||||
| chr6:104790900
|
A | AATTTAAC others(2): Show |
53 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(50): Show | 53 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1074+595_1074+603d others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104790900 | ||||||
| chr6:104791172
|
A | G | 75 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+332T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104791172 | ||||||
| chr6:104791477
|
C | T | 27 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(24): Show | 27 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+27G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 11/23 | chr6 | 104791477 | ||||||
| chr6:104792165
|
T | C | 5 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116others(2): Show | 5 | HG02809.hp2 HG02895.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.924-511A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792165 | ||||||
| chr6:104792229
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.924-575G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792229 | ||||||
| chr6:104792435
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-781G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792435 | ||||||
| chr6:104792525
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.924-871T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792525 | ||||||
| chr6:104792554
|
G | A | 4 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0081others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-900C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792554 | ||||||
| chr6:104792653
|
A | AC | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.924-1000dupG | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792653 | ||||||
| chr6:104792706
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-1052G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792706 | ||||||
| chr6:104792717
|
A | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(89): Show | 93 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.924-1063T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792717 | ||||||
| chr6:104792846
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.924-1192G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792846 | ||||||
| chr6:104792960
|
G | C | 11 | a0001c0001t0002g0050a0001c0002t0001g0076a0001c0002t0001g0077others(8): Show | 11 | HG01928.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.924-1306C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104792960 | ||||||
| chr6:104793192
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0051a0001c0001t0002g0053 | 3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.924-1538C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793192 | ||||||
| chr6:104793222
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.924-1568C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793222 | ||||||
| chr6:104793232
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.924-1578T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793232 | ||||||
| chr6:104793233
|
C | CGAACCCC others(16): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.924-1580_924-1579i others(25): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793233 | ||||||
| chr6:104793254
|
G | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078 | 3 | HG02257.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.924-1600C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793254 | ||||||
| chr6:104793262
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-1608T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793262 | ||||||
| chr6:104793266
|
C | CA | 129 | a0001c0001t0001g0139a0001c0001t0001g0166a0001c0001t0001g0173others(126): Show | 129 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.924-1613dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793266 | ||||||
| chr6:104793266
|
C | CAA | 13 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0006others(10): Show | 13 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.924-1614_924-1613d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793266 | ||||||
| chr6:104793449
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.924-1795C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793449 | ||||||
| chr6:104793477
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-1823C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793477 | ||||||
| chr6:104793522
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.924-1868T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793522 | ||||||
| chr6:104793933
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.923+1646T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104793933 | ||||||
| chr6:104794064
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.923+1515G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794064 | ||||||
| chr6:104794286
|
A | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.923+1293T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794286 | ||||||
| chr6:104794309
|
A | G | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.923+1270T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794309 | ||||||
| chr6:104794638
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.923+941C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794638 | ||||||
| chr6:104794670
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(89): Show | 93 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.923+909C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794670 | ||||||
| chr6:104794716
|
C | A | 1 | a0001c0001t0002g0017 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.923+863G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794716 | ||||||
| chr6:104794870
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.923+709C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794870 | ||||||
| chr6:104794910
|
A | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0326 | 2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.923+669T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794910 | ||||||
| chr6:104794926
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.923+653C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104794926 | ||||||
| chr6:104795070
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.923+509A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795070 | ||||||
| chr6:104795158
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.923+421A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795158 | ||||||
| chr6:104795346
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.923+233G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795346 | ||||||
| chr6:104795531
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.923+48G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 10/23 | chr6 | 104795531 | ||||||
| chr6:104795962
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-277C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104795962 | ||||||
| chr6:104796068
|
C | A | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.817-383G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104796068 | ||||||
| chr6:104796263
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.816+392T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104796263 | ||||||
| chr6:104796651
|
A | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(225): Show | 229 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
splice_region_variant&intron_variant | LOW | c.816+4T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 9/23 | chr6 | 104796651 | ||||||
| chr6:104797174
|
C | CT | 227 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(224): Show | 228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.618-150dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797174 | ||||||
| chr6:104797193
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.618-168A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797193 | ||||||
| chr6:104797489
|
T | TA | 10 | a0001c0001t0001g0292a0001c0002t0001g0076a0001c0002t0001g0077others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-465dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797489 | ||||||
| chr6:104797489
|
TA | T | 6 | a0001c0001t0001g0144a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG02040.hp1 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-465delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797489 | ||||||
| chr6:104797496
|
A | AG | 53 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(50): Show | 53 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.618-472_618-471ins others(1): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797496 | ||||||
| chr6:104797546
|
T | C | 53 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(50): Show | 53 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.618-521A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797546 | ||||||
| chr6:104797724
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.618-699C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797724 | ||||||
| chr6:104797763
|
A | G | 63 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(60): Show | 63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.618-738T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104797763 | ||||||
| chr6:104798064
|
G | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0014others(8): Show | 11 | HG00597.hp2 HG02135.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-1039C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798064 | ||||||
| chr6:104798069
|
GA | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(224): Show | 228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.618-1045delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798069 | ||||||
| chr6:104798103
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-1078C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798103 | ||||||
| chr6:104798245
|
C | T | 24 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0153others(21): Show | 24 | HG00621.hp2 HG02055.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.618-1220G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798245 | ||||||
| chr6:104798248
|
A | G | 7 | a0001c0002t0001g0094a0001c0002t0001g0096a0001c0002t0001g0108others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-1223T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798248 | ||||||
| chr6:104798286
|
A | T | 1 | a0001c0002t0001g0135 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.618-1261T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798286 | ||||||
| chr6:104798346
|
A | G | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.618-1321T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798346 | ||||||
| chr6:104798399
|
T | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-1374A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798399 | ||||||
| chr6:104798414
|
A | G | 46 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(43): Show | 46 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.618-1389T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798414 | ||||||
| chr6:104798479
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.618-1454C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798479 | ||||||
| chr6:104798559
|
A | G | 1 | a0001c0002t0001g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-1534T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104798559 | ||||||
| chr6:104799064
|
C | T | 51 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(48): Show | 51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.618-2039G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799064 | ||||||
| chr6:104799166
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-2141G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799166 | ||||||
| chr6:104799167
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-2142C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799167 | ||||||
| chr6:104799172
|
C | A | 1 | a0001c0001t0001g0320 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.618-2147G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799172 | ||||||
| chr6:104799249
|
T | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0315 | 2 | NA18969.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.618-2224A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799249 | ||||||
| chr6:104799404
|
C | A | 27 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(24): Show | 27 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.618-2379G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799404 | ||||||
| chr6:104799405
|
A | G | 27 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(24): Show | 27 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.618-2380T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799405 | ||||||
| chr6:104799432
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618-2407A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799432 | ||||||
| chr6:104799484
|
A | G | 53 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(50): Show | 53 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.618-2459T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799484 | ||||||
| chr6:104799559
|
T | G | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.618-2534A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799559 | ||||||
| chr6:104799616
|
T | C | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.618-2591A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799616 | ||||||
| chr6:104799824
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.618-2799G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799824 | ||||||
| chr6:104799909
|
G | GCCAAAGT others(12): Show |
229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.618-2885_618-2884i others(21): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104799909 | ||||||
| chr6:104800146
|
C | A | 1 | a0001c0001t0001g0190 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.618-3121G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800146 | ||||||
| chr6:104800177
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.618-3152T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800177 | ||||||
| chr6:104800178
|
C | A | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.618-3153G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800178 | ||||||
| chr6:104800221
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.618-3196A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800221 | ||||||
| chr6:104800309
|
G | C | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.618-3284C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800309 | ||||||
| chr6:104800324
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.618-3299G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800324 | ||||||
| chr6:104800699
|
C | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 8 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.618-3674G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800699 | ||||||
| chr6:104800981
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618-3956G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800981 | ||||||
| chr6:104800981
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-3956G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104800981 | ||||||
| chr6:104801071
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.618-4046G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801071 | ||||||
| chr6:104801072
|
A | G | 3 | a0001c0001t0002g0007a0001c0001t0002g0051a0001c0001t0002g0053 | 3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.618-4047T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801072 | ||||||
| chr6:104801111
|
A | C | 3 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0057 | 3 | HG02809.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.618-4086T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801111 | ||||||
| chr6:104801275
|
C | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-4250G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801275 | ||||||
| chr6:104801297
|
G | T | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.618-4272C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801297 | ||||||
| chr6:104801366
|
A | G | 74 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(71): Show | 74 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.618-4341T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801366 | ||||||
| chr6:104801558
|
T | C | 2 | a0001c0002t0001g0085a0001c0002t0001g0086 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.618-4533A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801558 | ||||||
| chr6:104801561
|
T | C | 25 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(22): Show | 25 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.618-4536A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801561 | ||||||
| chr6:104801632
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.618-4607C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801632 | ||||||
| chr6:104801667
|
G | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0180others(4): Show | 7 | HG00621.hp2 NA18947.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-4642C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801667 | ||||||
| chr6:104801934
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.618-4909G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104801934 | ||||||
| chr6:104802033
|
C | CA | 8 | a0001c0001t0001g0152a0001c0001t0001g0217a0001c0001t0001g0241others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.618-5009dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | ||||||
| chr6:104802033
|
C | CAA | 47 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0020others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.618-5010_618-5009d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | ||||||
| chr6:104802033
|
C | CAAA | 26 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0002g0003others(23): Show | 26 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.618-5011_618-5009d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | ||||||
| chr6:104802033
|
CAA | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-5010_618-5009d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802033 | ||||||
| chr6:104802095
|
G | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.618-5070C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802095 | ||||||
| chr6:104802187
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-5162G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802187 | ||||||
| chr6:104802254
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.618-5229T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802254 | ||||||
| chr6:104802327
|
G | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.618-5302C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802327 | ||||||
| chr6:104802463
|
C | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-5438G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802463 | ||||||
| chr6:104802649
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618-5624T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802649 | ||||||
| chr6:104802699
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-5674C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802699 | ||||||
| chr6:104802734
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.618-5709A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802734 | ||||||
| chr6:104802776
|
C | T | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.618-5751G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802776 | ||||||
| chr6:104802915
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.618-5890C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104802915 | ||||||
| chr6:104803034
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.618-6009G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803034 | ||||||
| chr6:104803080
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.618-6055T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803080 | ||||||
| chr6:104803159
|
G | A | 54 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0001g0163others(51): Show | 54 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.618-6134C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803159 | ||||||
| chr6:104803166
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.618-6141G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803166 | ||||||
| chr6:104803194
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.618-6169A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803194 | ||||||
| chr6:104803233
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.618-6208T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803233 | ||||||
| chr6:104803235
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618-6210C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803235 | ||||||
| chr6:104803381
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.618-6356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803381 | ||||||
| chr6:104803448
|
T | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6423A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803448 | ||||||
| chr6:104803514
|
C | A | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.618-6489G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803514 | ||||||
| chr6:104803554
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6529G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803554 | ||||||
| chr6:104803635
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6610C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803635 | ||||||
| chr6:104803649
|
C | T | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.618-6624G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803649 | ||||||
| chr6:104803653
|
A | G | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.618-6628T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803653 | ||||||
| chr6:104803766
|
T | G | 1 | a0001c0001t0002g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.618-6741A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803766 | ||||||
| chr6:104803799
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.618-6774G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803799 | ||||||
| chr6:104803831
|
T | C | 1 | a0001c0002t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.618-6806A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803831 | ||||||
| chr6:104803875
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.618-6850G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803875 | ||||||
| chr6:104803977
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.618-6952G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803977 | ||||||
| chr6:104803980
|
A | C | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618-6955T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104803980 | ||||||
| chr6:104804005
|
C | T | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.618-6980G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804005 | ||||||
| chr6:104804039
|
C | CA | 15 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0044others(12): Show | 15 | HG02080.hp1 NA18939.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.618-7015dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804039 | ||||||
| chr6:104804290
|
C | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.617+7021G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804290 | ||||||
| chr6:104804436
|
G | T | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+6875C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804436 | ||||||
| chr6:104804447
|
C | G | 1 | a0001c0001t0002g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.617+6864G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804447 | ||||||
| chr6:104804631
|
G | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02055.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.617+6680C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804631 | ||||||
| chr6:104804784
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.617+6527T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804784 | ||||||
| chr6:104804877
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.617+6434C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804877 | ||||||
| chr6:104804883
|
C | T | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.617+6428G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104804883 | ||||||
| chr6:104805278
|
A | T | 14 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(11): Show | 14 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.617+6033T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805278 | ||||||
| chr6:104805279
|
T | C | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.617+6032A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805279 | ||||||
| chr6:104805372
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.617+5939T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805372 | ||||||
| chr6:104805414
|
T | C | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.617+5897A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805414 | ||||||
| chr6:104805466
|
C | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+5845G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805466 | ||||||
| chr6:104805623
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.617+5688T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805623 | ||||||
| chr6:104805866
|
C | CA | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+5444dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104805866 | ||||||
| chr6:104806125
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(224): Show | 228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.617+5186G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104806125 | ||||||
| chr6:104806951
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.617+4360A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104806951 | ||||||
| chr6:104806958
|
G | A | 45 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(42): Show | 45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.617+4353C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104806958 | ||||||
| chr6:104807052
|
C | T | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.617+4259G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807052 | ||||||
| chr6:104807168
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.617+4143G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807168 | ||||||
| chr6:104807231
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0304a0001c0001t0001g0334 | 3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.617+4080G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807231 | ||||||
| chr6:104807236
|
A | T | 3 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02132.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.617+4075T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807236 | ||||||
| chr6:104807304
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.617+4007C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807304 | ||||||
| chr6:104807880
|
CACT | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+3428_617+3430d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807880 | ||||||
| chr6:104807914
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.617+3397G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807914 | ||||||
| chr6:104807977
|
G | A | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.617+3334C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104807977 | ||||||
| chr6:104808175
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.617+3136C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808175 | ||||||
| chr6:104808227
|
A | G | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.617+3084T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808227 | ||||||
| chr6:104808319
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.617+2992C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808319 | ||||||
| chr6:104808362
|
T | A | 1 | a0001c0001t0002g0045 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.617+2949A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808362 | ||||||
| chr6:104808382
|
T | C | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.617+2929A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808382 | ||||||
| chr6:104808443
|
C | T | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.617+2868G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808443 | ||||||
| chr6:104808577
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.617+2734T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808577 | ||||||
| chr6:104808615
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.617+2696T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808615 | ||||||
| chr6:104808618
|
T | C | 88 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(85): Show | 88 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.617+2693A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808618 | ||||||
| chr6:104808669
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.617+2642G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808669 | ||||||
| chr6:104808679
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.617+2632C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104808679 | ||||||
| chr6:104809109
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+2202A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809109 | ||||||
| chr6:104809122
|
T | G | 1 | a0001c0001t0001g0293 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.617+2189A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809122 | ||||||
| chr6:104809135
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 8 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+2176T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809135 | ||||||
| chr6:104809655
|
C | CT | 118 | a0001c0001t0001g0121a0001c0001t0001g0177a0001c0001t0001g0190others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.617+1655dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809655 | ||||||
| chr6:104809655
|
C | CTT | 11 | a0001c0001t0004g0032a0001c0002t0001g0076a0001c0002t0001g0077others(8): Show | 11 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+1654_617+1655d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809655 | ||||||
| chr6:104809655
|
CT | C | 9 | a0001c0001t0001g0204a0001c0001t0001g0210a0001c0001t0001g0216others(6): Show | 9 | HG00609.hp1 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+1655delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809655 | ||||||
| chr6:104809700
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.617+1611C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809700 | ||||||
| chr6:104809756
|
C | A | 30 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(27): Show | 30 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.617+1555G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809756 | ||||||
| chr6:104809815
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(224): Show | 228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.617+1496C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809815 | ||||||
| chr6:104809886
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.617+1425T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104809886 | ||||||
| chr6:104810072
|
A | T | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.617+1239T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810072 | ||||||
| chr6:104810250
|
C | A | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.617+1061G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810250 | ||||||
| chr6:104810302
|
T | G | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.617+1009A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810302 | ||||||
| chr6:104810461
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+850G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810461 | ||||||
| chr6:104810694
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.617+617G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810694 | ||||||
| chr6:104810862
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.617+449T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810862 | ||||||
| chr6:104810911
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.617+400G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104810911 | ||||||
| chr6:104811019
|
A | T | 1 | a0001c0001t0001g0288 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.617+292T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811019 | ||||||
| chr6:104811112
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+199T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811112 | ||||||
| chr6:104811207
|
AT | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+103delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811207 | ||||||
| chr6:104811238
|
T | TTATACAT others(1): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0003t0001g0229 | 3 | HG03195.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.617+72_617+73insTA others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(3): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0148others(4): Show | 8 | HG02055.hp1 HG02165.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(5): Show |
9 | a0001c0001t0001g0146a0001c0001t0001g0152a0001c0001t0001g0155others(6): Show | 9 | HG00738.hp1 HG01361.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(7): Show |
13 | a0001c0001t0001g0139a0001c0001t0001g0156a0001c0001t0001g0163others(10): Show | 13 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(9): Show |
12 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0001g0154others(9): Show | 12 | HG01993.hp2 HG02027.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(11): Show |
11 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0162others(8): Show | 11 | HG00621.hp1 HG01516.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(16): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(13): Show |
13 | a0001c0001t0001g0142a0001c0001t0001g0159a0001c0001t0001g0160others(10): Show | 13 | HG00733.hp1 HG00741.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(15): Show |
5 | a0001c0001t0001g0171a0001c0001t0001g0198a0001c0001t0001g0217others(2): Show | 5 | HG00408.hp1 HG02004.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(20): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(17): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0180a0001c0001t0001g0204others(1): Show | 4 | HG01167.hp1 NA19010.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+72_617+73insTA others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811238
|
T | TTATACAT others(19): Show |
1 | a0001c0001t0001g0167 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.617+72_617+73insTA others(24): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811238 | ||||||
| chr6:104811240
|
ATT | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0002g0065 | 3 | NA18972.hp1 NA18972.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.617+69_617+70delAA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811240 | ||||||
| chr6:104811241
|
T | TAC | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | NA18961.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.617+69_617+70insGT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811241 | ||||||
| chr6:104811242
|
T | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(88): Show | 92 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.617+69A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811242 | ||||||
| chr6:104811243
|
T | C | 7 | a0001c0001t0001g0153a0001c0001t0001g0165a0001c0001t0001g0174others(4): Show | 7 | HG00609.hp2 HG01109.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+68A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811243 | ||||||
| chr6:104811245
|
T | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0002g0065 | 3 | NA18972.hp1 NA18972.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.617+66A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811245 | ||||||
| chr6:104811247
|
C | CAT | 16 | a0001c0001t0001g0238a0001c0001t0001g0246a0001c0001t0001g0248others(13): Show | 16 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.617+62_617+63dupAT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATAT | 5 | a0001c0001t0001g0284a0001c0001t0001g0286a0001c0001t0001g0292others(2): Show | 5 | HG00323.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+60_617+63dupAT others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATATAT | 5 | a0001c0001t0002g0009a0001c0001t0002g0014a0001c0001t0002g0068others(2): Show | 5 | HG02647.hp2 HG03540.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+58_617+63dupAT others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATATATA others(1): Show |
10 | a0001c0001t0001g0283a0001c0001t0002g0003a0001c0001t0002g0006others(7): Show | 10 | HG00733.hp2 HG01175.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+56_617+63dupAT others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATATATA others(3): Show |
11 | a0001c0001t0001g0252a0001c0001t0002g0004a0001c0001t0002g0005others(8): Show | 11 | HG00597.hp2 HG02572.hp2 HG03688.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+54_617+63dupAT others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATATATA others(5): Show |
1 | a0001c0001t0002g0023 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.617+52_617+63dupAT others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATATATA others(7): Show |
1 | a0001c0001t0002g0024 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.617+50_617+63dupAT others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0335 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.617+48_617+63dupAT others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.617+64G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
CAT | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0255a0001c0001t0001g0256others(9): Show | 13 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.617+62_617+63delAT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
CATAT | C | 43 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.617+60_617+63delAT others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811247
|
CATATAT | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+58_617+63delAT others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811247 | ||||||
| chr6:104811277
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(224): Show | 228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.617+34G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 7/23 | chr6 | 104811277 | ||||||
| chr6:104811513
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-120A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811513 | ||||||
| chr6:104811573
|
G | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-180C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811573 | ||||||
| chr6:104811588
|
C | T | 10 | a0001c0002t0001g0124a0001c0002t0001g0127a0001c0002t0001g0128others(7): Show | 10 | HG01167.hp2 HG01168.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-195G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811588 | ||||||
| chr6:104811793
|
A | T | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535-400T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811793 | ||||||
| chr6:104811977
|
T | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0026 | 2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.535-584A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104811977 | ||||||
| chr6:104812065
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.535-672G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812065 | ||||||
| chr6:104812092
|
G | A | 2 | a0001c0003t0001g0228a0001c0003t0001g0229 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.535-699C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812092 | ||||||
| chr6:104812100
|
A | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.535-707T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812100 | ||||||
| chr6:104812120
|
TA | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(214): Show | 218 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.535-728delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812120 | ||||||
| chr6:104812229
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.535-836C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812229 | ||||||
| chr6:104812375
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.535-982C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812375 | ||||||
| chr6:104812476
|
C | A | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.535-1083G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812476 | ||||||
| chr6:104812830
|
G | C | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.535-1437C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812830 | ||||||
| chr6:104812837
|
T | C | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1444A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812837 | ||||||
| chr6:104812908
|
T | C | 2 | a0001c0002t0001g0106a0001c0002t0001g0119 | 2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.535-1515A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812908 | ||||||
| chr6:104812951
|
TGCACAAA others(2924): Show |
T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.535-4489_535-1559d others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104812951 | ||||||
| chr6:104813017
|
G | A | 4 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1624C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813017 | ||||||
| chr6:104813048
|
C | T | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.535-1655G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813048 | ||||||
| chr6:104813060
|
A | G | 4 | a0001c0001t0001g0254a0001c0001t0001g0272a0001c0001t0001g0275others(1): Show | 4 | NA18747.hp2 NA18984.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1667T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813060 | ||||||
| chr6:104813207
|
T | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0122others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.535-1814A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813207 | ||||||
| chr6:104813304
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.535-1911A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813304 | ||||||
| chr6:104813465
|
C | T | 41 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.535-2072G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813465 | ||||||
| chr6:104813785
|
G | A | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.535-2392C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813785 | ||||||
| chr6:104813835
|
A | G | 30 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(27): Show | 30 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.535-2442T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104813835 | ||||||
| chr6:104814121
|
A | C | 3 | a0001c0001t0002g0007a0001c0001t0002g0051a0001c0001t0002g0053 | 3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.535-2728T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814121 | ||||||
| chr6:104814249
|
C | T | 61 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(58): Show | 61 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.535-2856G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814249 | ||||||
| chr6:104814306
|
G | A | 133 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(130): Show | 133 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.535-2913C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814306 | ||||||
| chr6:104814668
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-3275A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814668 | ||||||
| chr6:104814735
|
T | A | 1 | a0001c0001t0001g0320 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.535-3342A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814735 | ||||||
| chr6:104814790
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.535-3397G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104814790 | ||||||
| chr6:104815008
|
A | G | 134 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(131): Show | 134 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.535-3615T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815008 | ||||||
| chr6:104815404
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.535-4011C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815404 | ||||||
| chr6:104815528
|
A | G | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.535-4135T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815528 | ||||||
| chr6:104815586
|
G | A | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.535-4193C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815586 | ||||||
| chr6:104815704
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.535-4311A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815704 | ||||||
| chr6:104815869
|
T | C | 134 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0003others(131): Show | 134 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.535-4476A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815869 | ||||||
| chr6:104815918
|
T | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.535-4525A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104815918 | ||||||
| chr6:104816005
|
G | A | 1 | a0001c0001t0005g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.535-4612C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816005 | ||||||
| chr6:104816027
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.535-4634G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816027 | ||||||
| chr6:104816050
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-4657C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816050 | ||||||
| chr6:104816073
|
CA | C | 63 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0179others(60): Show | 63 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.535-4681delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816073 | ||||||
| chr6:104816203
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.535-4810C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816203 | ||||||
| chr6:104816328
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-4935G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816328 | ||||||
| chr6:104816331
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.535-4938T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816331 | ||||||
| chr6:104816410
|
A | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-5017T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816410 | ||||||
| chr6:104816592
|
G | T | 4 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0081others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-5199C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816592 | ||||||
| chr6:104816593
|
AG | A | 45 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(42): Show | 45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.535-5201delC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816593 | ||||||
| chr6:104816666
|
C | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.535-5273G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816666 | ||||||
| chr6:104816765
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.535-5372C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816765 | ||||||
| chr6:104816773
|
T | C | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-5380A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816773 | ||||||
| chr6:104816887
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.535-5494C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816887 | ||||||
| chr6:104816966
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-5573G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104816966 | ||||||
| chr6:104817172
|
T | C | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.535-5779A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104817172 | ||||||
| chr6:104817187
|
C | T | 1 | a0001c0001t0002g0019 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.535-5794G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104817187 | ||||||
| chr6:104818118
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0206 | 2 | HG01167.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.535-6725A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818118 | ||||||
| chr6:104818171
|
T | C | 1 | a0001c0003t0001g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.535-6778A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818171 | ||||||
| chr6:104818243
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122others(224): Show | 228 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.535-6850T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818243 | ||||||
| chr6:104818274
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-6881C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818274 | ||||||
| chr6:104818314
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.535-6921T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818314 | ||||||
| chr6:104818322
|
C | T | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.535-6929G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818322 | ||||||
| chr6:104818363
|
G | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0011others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-6970C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818363 | ||||||
| chr6:104818455
|
A | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0082 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.535-7062T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818455 | ||||||
| chr6:104818494
|
T | C | 8 | a0001c0001t0001g0233a0001c0001t0001g0309a0001c0001t0001g0311others(5): Show | 8 | NA18969.hp1 NA19000.hp1 NA19056.hp1 others(5): Show |
intron_variant | MODIFIER | c.535-7101A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818494 | ||||||
| chr6:104818565
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.535-7172A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818565 | ||||||
| chr6:104818754
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.535-7361C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818754 | ||||||
| chr6:104818829
|
A | G | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0055 | 3 | NA18947.hp1 NA18970.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.535-7436T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818829 | ||||||
| chr6:104818939
|
A | G | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.535-7546T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104818939 | ||||||
| chr6:104819070
|
C | T | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0013others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-7677G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819070 | ||||||
| chr6:104819087
|
A | T | 1 | a0001c0001t0002g0023 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.535-7694T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819087 | ||||||
| chr6:104819314
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.535-7921C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819314 | ||||||
| chr6:104819337
|
G | A | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.535-7944C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819337 | ||||||
| chr6:104819513
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.535-8120C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819513 | ||||||
| chr6:104819581
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-8188G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819581 | ||||||
| chr6:104819883
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-8490T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819883 | ||||||
| chr6:104819934
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.535-8541G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819934 | ||||||
| chr6:104819965
|
T | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.535-8572A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104819965 | ||||||
| chr6:104820126
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.535-8733A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820126 | ||||||
| chr6:104820181
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.535-8788A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820181 | ||||||
| chr6:104820187
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0170 | 3 | HG00609.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.535-8794A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820187 | ||||||
| chr6:104820194
|
C | CA | 15 | a0001c0001t0001g0165a0001c0001t0001g0238a0001c0001t0001g0247others(12): Show | 15 | HG00609.hp2 HG01981.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-8802dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820194 | ||||||
| chr6:104820194
|
CA | C | 11 | a0001c0001t0001g0146a0001c0001t0001g0162a0001c0001t0001g0204others(8): Show | 11 | HG01167.hp1 HG01516.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.535-8802delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820194 | ||||||
| chr6:104820326
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-8933A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820326 | ||||||
| chr6:104820371
|
T | C | 2 | a0001c0001t0001g0292a0001c0002t0001g0099 | 2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.535-8978A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820371 | ||||||
| chr6:104820705
|
T | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-9312A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820705 | ||||||
| chr6:104820742
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.535-9349C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820742 | ||||||
| chr6:104820982
|
T | C | 1 | a0001c0001t0003g0140 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.535-9589A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104820982 | ||||||
| chr6:104821005
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.535-9612C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821005 | ||||||
| chr6:104821006
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535-9613G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821006 | ||||||
| chr6:104821296
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.535-9903G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821296 | ||||||
| chr6:104821336
|
T | C | 1 | a0001c0005t0001g0318 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.535-9943A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821336 | ||||||
| chr6:104821392
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01978.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.535-9999T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821392 | ||||||
| chr6:104821532
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.535-10139G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821532 | ||||||
| chr6:104821561
|
G | C | 1 | a0001c0001t0003g0140 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.535-10168C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821561 | ||||||
| chr6:104821610
|
G | T | 51 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0083others(48): Show | 51 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.535-10217C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104821610 | ||||||
| chr6:104822060
|
A | AT | 7 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.535-10668dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822060 | ||||||
| chr6:104822071
|
A | T | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535-10678T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822071 | ||||||
| chr6:104822084
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.535-10691C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822084 | ||||||
| chr6:104822143
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.535-10750A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822143 | ||||||
| chr6:104822203
|
T | TA | 135 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(132): Show | 136 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.535-10811dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822203 | ||||||
| chr6:104822203
|
T | TAA | 16 | a0001c0001t0001g0141a0001c0001t0001g0165a0001c0001t0001g0197others(13): Show | 16 | HG00609.hp2 HG02056.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.535-10812_535-1081 others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822203 | ||||||
| chr6:104822203
|
TA | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(108): Show | 112 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.535-10811delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822203 | ||||||
| chr6:104822264
|
T | C | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.534+10778A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822264 | ||||||
| chr6:104822314
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534+10728G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822314 | ||||||
| chr6:104822333
|
C | A | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.534+10709G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822333 | ||||||
| chr6:104822384
|
G | GA | 14 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 15 | HG01175.hp2 HG02027.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.534+10657dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822384 | ||||||
| chr6:104822384
|
GA | G | 6 | a0001c0001t0001g0198a0001c0001t0001g0213a0001c0001t0001g0221others(3): Show | 6 | HG00323.hp1 HG01167.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+10657delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822384 | ||||||
| chr6:104822402
|
A | T | 1 | a0001c0001t0001g0320 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.534+10640T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822402 | ||||||
| chr6:104822420
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.534+10622C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822420 | ||||||
| chr6:104822518
|
G | A | 1 | a0001c0001t0002g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.534+10524C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822518 | ||||||
| chr6:104822578
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.534+10464G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822578 | ||||||
| chr6:104822718
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.534+10324C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822718 | ||||||
| chr6:104822726
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.534+10316T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822726 | ||||||
| chr6:104822751
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.534+10291C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822751 | ||||||
| chr6:104822938
|
A | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.534+10104T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822938 | ||||||
| chr6:104822983
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+10059C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104822983 | ||||||
| chr6:104823015
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(268): Show | 273 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.534+10027T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823015 | ||||||
| chr6:104823231
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.534+9811G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823231 | ||||||
| chr6:104823254
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.534+9788A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823254 | ||||||
| chr6:104823295
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.534+9747T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823295 | ||||||
| chr6:104823398
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.534+9644G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823398 | ||||||
| chr6:104823431
|
CA | C | 6 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0198others(3): Show | 6 | HG01993.hp1 HG03490.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+9610delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823431 | ||||||
| chr6:104823504
|
A | AT | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.534+9537dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823504 | ||||||
| chr6:104823511
|
T | A | 6 | a0001c0002t0001g0094a0001c0002t0001g0108a0001c0002t0001g0109others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+9531A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823511 | ||||||
| chr6:104823512
|
A | T | 7 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+9530T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823512 | ||||||
| chr6:104823558
|
A | AGAAACAT others(6102): Show |
1 | a0001c0001t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.534+9483_534+9484i others(6111): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823558 | ||||||
| chr6:104823636
|
A | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.534+9406T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823636 | ||||||
| chr6:104823758
|
TA | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(4): Show | 7 | HG01978.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+9283delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823758 | ||||||
| chr6:104823914
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534+9128C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104823914 | ||||||
| chr6:104824158
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.534+8884A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824158 | ||||||
| chr6:104824197
|
G | A | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.534+8845C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824197 | ||||||
| chr6:104824298
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.534+8744G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824298 | ||||||
| chr6:104824397
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.534+8645C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824397 | ||||||
| chr6:104824795
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.534+8247G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824795 | ||||||
| chr6:104824909
|
T | TA | 17 | a0001c0001t0001g0001a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 18 | HG01081.hp1 HG02257.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.534+8132dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824909 | ||||||
| chr6:104824945
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.534+8097A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104824945 | ||||||
| chr6:104825076
|
CG | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.534+7965delC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825076 | ||||||
| chr6:104825081
|
C | CA | 77 | a0001c0001t0001g0167a0001c0001t0002g0003a0001c0001t0002g0004others(74): Show | 77 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.534+7960dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825081 | ||||||
| chr6:104825081
|
C | CAA | 13 | a0001c0001t0002g0014a0001c0001t0002g0045a0001c0002t0001g0076others(10): Show | 13 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.534+7959_534+7960d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825081 | ||||||
| chr6:104825130
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 8 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+7912T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825130 | ||||||
| chr6:104825283
|
G | A | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+7759C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825283 | ||||||
| chr6:104825310
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0246a0001c0001t0001g0248 | 3 | HG01934.hp1 HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.534+7732C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825310 | ||||||
| chr6:104825325
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.534+7717A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825325 | ||||||
| chr6:104825327
|
G | A | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+7715C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825327 | ||||||
| chr6:104825341
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG00621.hp1 HG02015.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.534+7701A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825341 | ||||||
| chr6:104825483
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.534+7559A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825483 | ||||||
| chr6:104825496
|
G | A | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+7546C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825496 | ||||||
| chr6:104825529
|
T | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | NA18994.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.534+7513A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825529 | ||||||
| chr6:104825667
|
C | A | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+7375G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825667 | ||||||
| chr6:104825790
|
T | C | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.534+7252A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825790 | ||||||
| chr6:104825849
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.534+7193G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104825849 | ||||||
| chr6:104826063
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150 | 3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.534+6979T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826063 | ||||||
| chr6:104826176
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.534+6866A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826176 | ||||||
| chr6:104826222
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+6820G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826222 | ||||||
| chr6:104826316
|
G | A | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.534+6726C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826316 | ||||||
| chr6:104826464
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.534+6578A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826464 | ||||||
| chr6:104826471
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.534+6571G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826471 | ||||||
| chr6:104826543
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.534+6499A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826543 | ||||||
| chr6:104826641
|
T | C | 3 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078 | 3 | HG02257.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.534+6401A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826641 | ||||||
| chr6:104826671
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+6371A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826671 | ||||||
| chr6:104826696
|
T | C | 59 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(56): Show | 59 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.534+6346A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826696 | ||||||
| chr6:104826986
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.534+6056G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104826986 | ||||||
| chr6:104827399
|
C | G | 25 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(22): Show | 25 | HG00597.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.534+5643G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827399 | ||||||
| chr6:104827723
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.534+5319G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827723 | ||||||
| chr6:104827795
|
T | C | 15 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0044others(12): Show | 15 | HG02080.hp1 NA18939.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.534+5247A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827795 | ||||||
| chr6:104827866
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.534+5176C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104827866 | ||||||
| chr6:104828044
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.534+4998G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828044 | ||||||
| chr6:104828069
|
A | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.534+4973T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828069 | ||||||
| chr6:104828517
|
A | C | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.534+4525T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828517 | ||||||
| chr6:104828517
|
A | G | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.534+4525T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828517 | ||||||
| chr6:104828549
|
A | G | 1 | a0001c0001t0007g0269 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.534+4493T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828549 | ||||||
| chr6:104828609
|
T | C | 41 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.534+4433A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828609 | ||||||
| chr6:104828971
|
G | A | 42 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(39): Show | 42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.534+4071C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104828971 | ||||||
| chr6:104829059
|
T | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0304a0001c0001t0001g0334 | 3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.534+3983A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829059 | ||||||
| chr6:104829076
|
AATAT | A | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+3962_534+3965d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829076 | ||||||
| chr6:104829260
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.534+3782A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829260 | ||||||
| chr6:104829423
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.534+3619G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829423 | ||||||
| chr6:104829574
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.534+3468C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829574 | ||||||
| chr6:104829627
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0001g0183others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+3415G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829627 | ||||||
| chr6:104829720
|
A | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+3322T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829720 | ||||||
| chr6:104829899
|
A | T | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.534+3143T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829899 | ||||||
| chr6:104829918
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.534+3124A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104829918 | ||||||
| chr6:104830134
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+2908A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830134 | ||||||
| chr6:104830321
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.534+2721A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830321 | ||||||
| chr6:104830551
|
C | T | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.534+2491G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830551 | ||||||
| chr6:104830758
|
C | CT | 157 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(154): Show | 157 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.534+2283dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | ||||||
| chr6:104830758
|
C | CTT | 11 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(8): Show | 12 | HG01934.hp2 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.534+2282_534+2283d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | ||||||
| chr6:104830758
|
C | CTTT | 53 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0076others(50): Show | 53 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.534+2281_534+2283d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | ||||||
| chr6:104830758
|
C | CTTTT | 7 | a0001c0002t0001g0084a0001c0002t0001g0089a0001c0002t0001g0095others(4): Show | 7 | HG02809.hp2 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+2280_534+2283d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | ||||||
| chr6:104830758
|
CT | C | 7 | a0001c0001t0001g0236a0001c0001t0001g0239a0001c0001t0001g0261others(4): Show | 7 | HG00558.hp2 HG01074.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+2283delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830758 | ||||||
| chr6:104830913
|
C | A | 1 | a0001c0001t0002g0070 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.534+2129G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104830913 | ||||||
| chr6:104831049
|
G | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.534+1993C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831049 | ||||||
| chr6:104831312
|
C | T | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.534+1730G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831312 | ||||||
| chr6:104831465
|
A | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0196 | 2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.534+1577T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831465 | ||||||
| chr6:104831484
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.534+1558G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831484 | ||||||
| chr6:104831496
|
G | A | 46 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(43): Show | 46 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.534+1546C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831496 | ||||||
| chr6:104831584
|
C | CA | 9 | a0001c0001t0001g0244a0001c0001t0001g0311a0001c0002t0001g0076others(6): Show | 9 | HG00609.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1457dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831584 | ||||||
| chr6:104831591
|
A | AG | 3 | a0001c0002t0001g0084a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02965.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+1450_534+1451i others(3): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831591 | ||||||
| chr6:104831591
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.534+1451T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831591 | ||||||
| chr6:104831622
|
G | A | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.534+1420C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831622 | ||||||
| chr6:104831635
|
T | C | 6 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG00621.hp2 NA18947.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+1407A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831635 | ||||||
| chr6:104831708
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.534+1334C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831708 | ||||||
| chr6:104831750
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.534+1292C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831750 | ||||||
| chr6:104831754
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.534+1288C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831754 | ||||||
| chr6:104831918
|
A | AAGAAG | 43 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(40): Show | 43 | HG00408.hp1 HG00597.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.534+1119_534+1123d others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(3): Show |
46 | a0001c0001t0001g0142a0001c0001t0001g0151a0001c0001t0001g0154others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.534+1114_534+1123d others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(8): Show |
53 | a0001c0001t0001g0235a0001c0001t0001g0239a0001c0001t0001g0242others(50): Show | 53 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.534+1109_534+1123d others(17): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(13): Show |
41 | a0001c0001t0001g0161a0001c0001t0001g0182a0001c0001t0001g0231others(38): Show | 41 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.534+1104_534+1123d others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(18): Show |
23 | a0001c0001t0001g0002a0001c0001t0001g0164a0001c0001t0001g0230others(20): Show | 24 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.534+1099_534+1123d others(27): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(23): Show |
9 | a0001c0001t0001g0246a0001c0001t0001g0267a0001c0001t0001g0296others(6): Show | 9 | HG00323.hp2 HG01255.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1094_534+1123d others(32): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(28): Show |
3 | a0001c0002t0001g0098a0001c0002t0001g0113a0001c0002t0001g0126 | 3 | HG01243.hp1 HG01256.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.534+1089_534+1123d others(37): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(33): Show |
5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG04115.hp1 NA18965.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+1084_534+1123d others(42): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(38): Show |
1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.534+1079_534+1123d others(47): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
A | AAGAAGAG others(43): Show |
2 | a0001c0001t0001g0237a0001c0001t0001g0277 | 2 | HG00738.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.534+1074_534+1123d others(52): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
AAGAAG | A | 34 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0144others(31): Show | 34 | HG00738.hp1 HG01256.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.534+1119_534+1123d others(7): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
AAGAAGAG others(3): Show |
A | 21 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0167others(18): Show | 21 | HG00621.hp2 HG00733.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.534+1114_534+1123d others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
AAGAAGAG others(8): Show |
A | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.534+1109_534+1123d others(17): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831918
|
AAGAAGAG others(23): Show |
A | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534+1094_534+1123d others(32): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831918 | ||||||
| chr6:104831945
|
GAAGAGAA others(32): Show |
G | 1 | a0001c0002t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.534+1058_534+1096d others(41): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831945 | ||||||
| chr6:104831946
|
AAGAGAAG others(10): Show |
A | 2 | a0001c0002t0001g0079a0001c0002t0001g0082 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534+1079_534+1095d others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831946 | ||||||
| chr6:104831946
|
AAGAGAAG others(15): Show |
A | 2 | a0001c0002t0001g0078a0001c0002t0001g0081 | 2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.534+1074_534+1095d others(24): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831946 | ||||||
| chr6:104831946
|
AAGAGAAG others(20): Show |
A | 4 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0080others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1069_534+1095d others(29): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831946 | ||||||
| chr6:104831947
|
A | G | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+1095T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831947 | ||||||
| chr6:104831949
|
AGAAGAGA others(24): Show |
A | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.534+1062_534+1092d others(33): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831949 | ||||||
| chr6:104831950
|
GAAGAGAA others(31): Show |
G | 3 | a0001c0001t0001g0001a0001c0001t0001g0219a0001c0003t0001g0228 | 4 | HG02970.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1054_534+1091d others(40): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831950 | ||||||
| chr6:104831950
|
GAAGAGAA others(35): Show |
G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0003t0001g0229 | 3 | HG02055.hp1 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.534+1050_534+1091d others(44): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831950 | ||||||
| chr6:104831950
|
GAAGAGAA others(39): Show |
G | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.534+1046_534+1091d others(48): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831950 | ||||||
| chr6:104831960
|
GAAGAGAA others(21): Show |
G | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.534+1054_534+1081d others(30): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831960 | ||||||
| chr6:104831960
|
GAAGAGAA others(29): Show |
G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534+1046_534+1081d others(38): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831960 | ||||||
| chr6:104831962
|
A | G | 1 | a0001c0002t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.534+1080T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831962 | ||||||
| chr6:104831964
|
A | G | 2 | a0001c0002t0001g0079a0001c0002t0001g0082 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534+1078T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831964 | ||||||
| chr6:104831965
|
GAAGAGAA others(16): Show |
G | 1 | a0001c0001t0001g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.534+1054_534+1076d others(25): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831965 | ||||||
| chr6:104831965
|
GAAGAGAA others(28): Show |
G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.534+1042_534+1076d others(37): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831965 | ||||||
| chr6:104831968
|
G | GAGAAGAG others(13): Show |
1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.534+1073_534+1074i others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831968 | ||||||
| chr6:104831969
|
A | G | 2 | a0001c0002t0001g0078a0001c0002t0001g0081 | 2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.534+1073T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831969 | ||||||
| chr6:104831971
|
A | G | 1 | a0001c0002t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.534+1071T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831971 | ||||||
| chr6:104831973
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.534+1069C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831973 | ||||||
| chr6:104831973
|
GA | G | 4 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0002t0001g0081others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+1068delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831973 | ||||||
| chr6:104831974
|
A | G | 5 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0080others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+1068T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831974 | ||||||
| chr6:104831977
|
A | AGAGAGGA others(3): Show |
1 | a0001c0001t0001g0241 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.534+1064_534+1065i others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831977 | ||||||
| chr6:104831979
|
A | AGAAGAGA others(9): Show |
1 | a0001c0001t0001g0276 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.534+1062_534+1063i others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831979 | ||||||
| chr6:104831979
|
A | G | 9 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1063T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831979 | ||||||
| chr6:104831980
|
G | A | 9 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1062C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
G | GAAGAGAA others(12): Show |
1 | a0001c0001t0002g0054 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.534+1061_534+1062i others(21): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
G | GAGGA | 37 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0284others(34): Show | 37 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.534+1058_534+1061d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
G | GAGGAAGG others(1): Show |
10 | a0001c0001t0001g0285a0001c0001t0001g0302a0001c0001t0002g0027others(7): Show | 10 | HG00423.hp1 HG01257.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+1054_534+1061d others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
G | GAGGAAGG others(5): Show |
3 | a0001c0001t0001g0289a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG01074.hp1 NA18994.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.534+1050_534+1061d others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
G | GAGGAAGG others(13): Show |
1 | a0001c0002t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.534+1042_534+1061d others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
GAGGA | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0158a0001c0001t0001g0159others(92): Show | 96 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.534+1058_534+1061d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
GAGGAAGG others(1): Show |
G | 69 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0154others(66): Show | 69 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.534+1054_534+1061d others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
GAGGAAGG others(5): Show |
G | 27 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0001g0150others(24): Show | 27 | HG00099.hp1 HG00621.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.534+1050_534+1061d others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
GAGGAAGG others(9): Show |
G | 1 | a0001c0001t0001g0180 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.534+1046_534+1061d others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831980
|
GAGGAAGG others(13): Show |
G | 3 | a0001c0001t0001g0328a0001c0004t0001g0143a0001c0004t0001g0147 | 3 | HG03130.hp1 HG03139.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.534+1042_534+1061d others(22): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831980 | ||||||
| chr6:104831981
|
A | AAGAGAAG others(10): Show |
1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+1060_534+1061i others(19): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831981 | ||||||
| chr6:104831982
|
G | A | 5 | a0001c0001t0001g0288a0001c0001t0001g0319a0001c0001t0001g0331others(2): Show | 5 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+1060C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831982 | ||||||
| chr6:104831984
|
A | AGAAGAGA others(9): Show |
1 | a0001c0001t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.534+1057_534+1058i others(18): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831984 | ||||||
| chr6:104831984
|
A | AGAAGAGA others(5): Show |
1 | a0001c0001t0007g0269 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.534+1057_534+1058i others(14): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831984 | ||||||
| chr6:104831991
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+1051C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831991 | ||||||
| chr6:104831992
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+1050T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104831992 | ||||||
| chr6:104832168
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.534+874A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832168 | ||||||
| chr6:104832357
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.534+685A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832357 | ||||||
| chr6:104832381
|
TTTG | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.534+658_534+660del others(3): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832381 | ||||||
| chr6:104832384
|
G | T | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.534+658C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832384 | ||||||
| chr6:104832387
|
G | T | 14 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(11): Show | 14 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.534+655C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832387 | ||||||
| chr6:104832474
|
A | C | 7 | a0001c0002t0001g0094a0001c0002t0001g0096a0001c0002t0001g0108others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+568T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832474 | ||||||
| chr6:104832517
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.534+525G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832517 | ||||||
| chr6:104832760
|
G | A | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.534+282C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832760 | ||||||
| chr6:104832844
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.534+198T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832844 | ||||||
| chr6:104832870
|
G | C | 2 | a0001c0001t0001g0224a0001c0001t0003g0140 | 2 | HG00408.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.534+172C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 6/23 | chr6 | 104832870 | ||||||
| chr6:104833193
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.403-20G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833193 | ||||||
| chr6:104833233
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150 | 3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.403-60T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833233 | ||||||
| chr6:104833259
|
C | T | 7 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | HG00544.hp1 HG02165.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-86G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833259 | ||||||
| chr6:104833337
|
C | T | 20 | a0001c0001t0001g0230a0001c0001t0001g0235a0001c0001t0001g0236others(17): Show | 20 | HG00609.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.403-164G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833337 | ||||||
| chr6:104833448
|
T | A | 1 | a0001c0001t0001g0293 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-275A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833448 | ||||||
| chr6:104833616
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-443T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833616 | ||||||
| chr6:104833622
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403-449A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833622 | ||||||
| chr6:104833624
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-451C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833624 | ||||||
| chr6:104833854
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.403-681C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104833854 | ||||||
| chr6:104834147
|
C | CA | 9 | a0001c0001t0001g0161a0001c0001t0001g0174a0001c0001t0001g0281others(6): Show | 9 | HG01109.hp2 HG02738.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-975dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834147 | ||||||
| chr6:104834303
|
G | A | 82 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0142others(79): Show | 82 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.403-1130C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834303 | ||||||
| chr6:104834388
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.403-1215G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834388 | ||||||
| chr6:104834437
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.403-1264G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834437 | ||||||
| chr6:104834588
|
G | A | 2 | a0001c0002t0001g0106a0001c0002t0001g0119 | 2 | HG02109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.403-1415C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834588 | ||||||
| chr6:104834679
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-1506A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834679 | ||||||
| chr6:104834839
|
T | A | 1 | a0001c0002t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.403-1666A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834839 | ||||||
| chr6:104834933
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.403-1760G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834933 | ||||||
| chr6:104834971
|
T | A | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.403-1798A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104834971 | ||||||
| chr6:104835152
|
T | C | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.403-1979A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835152 | ||||||
| chr6:104835278
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.403-2105C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835278 | ||||||
| chr6:104835410
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.403-2237A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835410 | ||||||
| chr6:104835542
|
GAAAAGAA others(8): Show |
G | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.403-2384_403-2370d others(17): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835542 | ||||||
| chr6:104835661
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.403-2488C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104835661 | ||||||
| chr6:104836126
|
G | C | 49 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(46): Show | 49 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.403-2953C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836126 | ||||||
| chr6:104836243
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.403-3070C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836243 | ||||||
| chr6:104836397
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-3224G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836397 | ||||||
| chr6:104836432
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.403-3259C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836432 | ||||||
| chr6:104836439
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.403-3266C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836439 | ||||||
| chr6:104836487
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.403-3314A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836487 | ||||||
| chr6:104836496
|
G | A | 78 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0152others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.403-3323C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836496 | ||||||
| chr6:104836700
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403-3527C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836700 | ||||||
| chr6:104836911
|
A | G | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-3738T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836911 | ||||||
| chr6:104836956
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.403-3783G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836956 | ||||||
| chr6:104836986
|
T | A | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-3813A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104836986 | ||||||
| chr6:104837066
|
A | G | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-3893T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837066 | ||||||
| chr6:104837263
|
T | A | 1 | a0001c0002t0001g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.403-4090A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837263 | ||||||
| chr6:104837356
|
T | G | 1 | a0001c0001t0001g0324 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.403-4183A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837356 | ||||||
| chr6:104837433
|
T | C | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-4260A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837433 | ||||||
| chr6:104837677
|
C | G | 1 | a0001c0001t0001g0340 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.403-4504G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837677 | ||||||
| chr6:104837740
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.403-4567C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837740 | ||||||
| chr6:104837875
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(123): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.403-4702A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837875 | ||||||
| chr6:104837884
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.403-4711G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104837884 | ||||||
| chr6:104838020
|
C | G | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-4847G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838020 | ||||||
| chr6:104838022
|
A | G | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.403-4849T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838022 | ||||||
| chr6:104838128
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403-4955G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838128 | ||||||
| chr6:104838238
|
T | C | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+4985A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838238 | ||||||
| chr6:104838249
|
A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.402+4974T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838249 | ||||||
| chr6:104838352
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.402+4871T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838352 | ||||||
| chr6:104838671
|
C | T | 1 | a0001c0001t0001g0320 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.402+4552G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838671 | ||||||
| chr6:104838890
|
T | TA | 91 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0230others(88): Show | 92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.402+4332dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838890
|
T | TAA | 19 | a0001c0001t0001g0252a0001c0001t0001g0282a0001c0001t0001g0283others(16): Show | 19 | HG00323.hp1 HG00733.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.402+4331_402+4332d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838890
|
TA | T | 82 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0144others(79): Show | 82 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.402+4332delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838890
|
TAA | T | 31 | a0001c0001t0001g0188a0001c0001t0001g0204a0001c0001t0002g0004others(28): Show | 31 | HG00597.hp2 HG00735.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.402+4331_402+4332d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838890
|
TAAA | T | 43 | a0001c0001t0001g0121a0001c0001t0002g0007a0001c0001t0002g0008others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.402+4330_402+4332d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838890
|
TAAAAAAA others(2): Show |
T | 43 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(40): Show | 43 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.402+4324_402+4332d others(11): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838890
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0002t0001g0135 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.402+4323_402+4332d others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838890 | ||||||
| chr6:104838916
|
A | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0002g0034 | 3 | HG01256.hp2 HG01258.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.402+4307T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104838916 | ||||||
| chr6:104839145
|
G | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+4078C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839145 | ||||||
| chr6:104839263
|
A | G | 11 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+3960T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839263 | ||||||
| chr6:104839292
|
C | T | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.402+3931G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839292 | ||||||
| chr6:104839699
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0304a0001c0001t0001g0334 | 3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.402+3524G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839699 | ||||||
| chr6:104839748
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3475C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839748 | ||||||
| chr6:104839776
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0004t0001g0143others(1): Show | 4 | HG03130.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+3447G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104839776 | ||||||
| chr6:104840250
|
A | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.402+2973T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840250 | ||||||
| chr6:104840301
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.402+2922C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840301 | ||||||
| chr6:104840551
|
C | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0001g0164others(1): Show | 4 | HG00741.hp2 HG01516.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+2672G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840551 | ||||||
| chr6:104840600
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.402+2623C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840600 | ||||||
| chr6:104840711
|
C | T | 44 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(41): Show | 44 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.402+2512G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840711 | ||||||
| chr6:104840722
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.402+2501C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840722 | ||||||
| chr6:104840792
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.402+2431G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840792 | ||||||
| chr6:104840824
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.402+2399C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840824 | ||||||
| chr6:104840926
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.402+2297C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840926 | ||||||
| chr6:104840955
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.402+2268G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104840955 | ||||||
| chr6:104841052
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(108): Show | 112 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.402+2171A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841052 | ||||||
| chr6:104841053
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.402+2170C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841053 | ||||||
| chr6:104841118
|
C | CA | 10 | a0001c0001t0001g0170a0001c0001t0001g0310a0001c0001t0001g0327others(7): Show | 10 | HG01952.hp1 HG02004.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+2104dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841118 | ||||||
| chr6:104841476
|
C | T | 1 | a0001c0002t0001g0135 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.402+1747G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841476 | ||||||
| chr6:104841744
|
T | C | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.402+1479A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841744 | ||||||
| chr6:104841797
|
G | T | 1 | a0001c0001t0001g0260 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.402+1426C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841797 | ||||||
| chr6:104841886
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402+1337C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104841886 | ||||||
| chr6:104842008
|
TATATAAA | T | 11 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(8): Show | 11 | HG01515.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+1208_402+1214d others(9): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842008 | ||||||
| chr6:104842139
|
T | C | 53 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0001g0163others(50): Show | 53 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.402+1084A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842139 | ||||||
| chr6:104842316
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.402+907C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842316 | ||||||
| chr6:104842348
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.402+875C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842348 | ||||||
| chr6:104842356
|
A | T | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.402+867T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842356 | ||||||
| chr6:104842374
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.402+849G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842374 | ||||||
| chr6:104842499
|
C | T | 1 | a0001c0002t0001g0124 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.402+724G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842499 | ||||||
| chr6:104842500
|
AG | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150 | 3 | HG02145.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.402+722delC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842500 | ||||||
| chr6:104842551
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.402+672A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842551 | ||||||
| chr6:104842686
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402+537C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842686 | ||||||
| chr6:104842878
|
G | C | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.402+345C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 5/23 | chr6 | 104842878 | ||||||
| chr6:104843537
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.327-239T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104843537 | ||||||
| chr6:104844002
|
G | A | 80 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0148others(77): Show | 80 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.327-704C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844002 | ||||||
| chr6:104844034
|
G | GT | 28 | a0001c0001t0001g0145a0001c0001t0001g0179a0001c0001t0001g0182others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-737dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844034 | ||||||
| chr6:104844049
|
T | C | 28 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(25): Show | 28 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-751A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844049 | ||||||
| chr6:104844104
|
GCTCA | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.327-810_327-807del others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844104 | ||||||
| chr6:104844212
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.327-914A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844212 | ||||||
| chr6:104844310
|
C | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-1012G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844310 | ||||||
| chr6:104844314
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.327-1016G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844314 | ||||||
| chr6:104844344
|
A | AT | 7 | a0001c0001t0001g0174a0001c0001t0001g0224a0001c0001t0001g0248others(4): Show | 7 | HG00408.hp1 HG01934.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-1047dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844344 | ||||||
| chr6:104844344
|
ATTT | A | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.327-1049_327-1047d others(5): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844344 | ||||||
| chr6:104844365
|
G | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.327-1067C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844365 | ||||||
| chr6:104844469
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-1171C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844469 | ||||||
| chr6:104844504
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.327-1206T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844504 | ||||||
| chr6:104844567
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.327-1269T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844567 | ||||||
| chr6:104844599
|
C | A | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.327-1301G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844599 | ||||||
| chr6:104844662
|
C | CT | 18 | a0001c0001t0001g0165a0001c0001t0001g0205a0001c0001t0002g0010others(15): Show | 18 | HG00609.hp2 HG01175.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.327-1365dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844662 | ||||||
| chr6:104844672
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.327-1374A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844672 | ||||||
| chr6:104844821
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.327-1523G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844821 | ||||||
| chr6:104844856
|
G | T | 1 | a0001c0001t0001g0340 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.327-1558C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844856 | ||||||
| chr6:104844925
|
A | C | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-1627T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844925 | ||||||
| chr6:104844934
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327-1636C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104844934 | ||||||
| chr6:104845227
|
T | G | 1 | a0001c0001t0001g0172 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.327-1929A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845227 | ||||||
| chr6:104845273
|
T | C | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.327-1975A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845273 | ||||||
| chr6:104845476
|
C | CT | 176 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0142others(173): Show | 177 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.327-2179dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845476 | ||||||
| chr6:104845476
|
C | CTT | 15 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0180others(12): Show | 15 | HG00408.hp1 HG01981.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.327-2180_327-2179d others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845476 | ||||||
| chr6:104845546
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.327-2248G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845546 | ||||||
| chr6:104845654
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.327-2356A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845654 | ||||||
| chr6:104845707
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0006g0341 | 2 | HG02145.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.327-2409T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845707 | ||||||
| chr6:104845728
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.327-2430G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845728 | ||||||
| chr6:104845759
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.327-2461T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104845759 | ||||||
| chr6:104846269
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+2873T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846269 | ||||||
| chr6:104846296
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.326+2846A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846296 | ||||||
| chr6:104846304
|
T | G | 5 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(2): Show | 5 | NA18962.hp2 NA18993.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+2838A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846304 | ||||||
| chr6:104846625
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.326+2517G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846625 | ||||||
| chr6:104846955
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0249 | 2 | HG02027.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.326+2187A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846955 | ||||||
| chr6:104846981
|
T | C | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.326+2161A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104846981 | ||||||
| chr6:104847087
|
CTTTA | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG01257.hp2 HG01258.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+2051_326+2054d others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847087 | ||||||
| chr6:104847433
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.326+1709A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847433 | ||||||
| chr6:104847660
|
C | G | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.326+1482G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847660 | ||||||
| chr6:104847755
|
TA | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+1386delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847755 | ||||||
| chr6:104847772
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.326+1370G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847772 | ||||||
| chr6:104847810
|
G | GT | 6 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0243others(3): Show | 6 | HG03942.hp2 HG04199.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+1331dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104847810 | ||||||
| chr6:104848059
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.326+1083A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848059 | ||||||
| chr6:104848094
|
C | T | 6 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0011others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+1048G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848094 | ||||||
| chr6:104848098
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.326+1044G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848098 | ||||||
| chr6:104848191
|
C | T | 47 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.326+951G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848191 | ||||||
| chr6:104848275
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.326+867C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848275 | ||||||
| chr6:104848387
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.326+755A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848387 | ||||||
| chr6:104848400
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.326+742C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848400 | ||||||
| chr6:104848411
|
G | A | 3 | a0001c0002t0001g0089a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02809.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.326+731C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848411 | ||||||
| chr6:104848515
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | NA18943.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.326+627T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848515 | ||||||
| chr6:104848553
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG02055.hp1 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+589C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848553 | ||||||
| chr6:104848977
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.326+165T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104848977 | ||||||
| chr6:104849007
|
A | G | 1 | a0001c0004t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.326+135T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104849007 | ||||||
| chr6:104849021
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.326+121G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 4/23 | chr6 | 104849021 | ||||||
| chr6:104849504
|
A | AT | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.222-259dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849504 | ||||||
| chr6:104849504
|
A | ATT | 7 | a0001c0001t0001g0152a0001c0001t0001g0177a0001c0001t0001g0178others(4): Show | 7 | HG00735.hp2 HG02135.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-260_222-259dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849504 | ||||||
| chr6:104849604
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-358T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849604 | ||||||
| chr6:104849641
|
C | T | 2 | a0001c0004t0001g0143a0001c0004t0001g0147 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.222-395G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849641 | ||||||
| chr6:104849651
|
A | ATT | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0121others(329): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.222-407_222-406dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849651 | ||||||
| chr6:104849767
|
G | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.222-521C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849767 | ||||||
| chr6:104849773
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.222-527G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849773 | ||||||
| chr6:104849852
|
A | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-606T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849852 | ||||||
| chr6:104849893
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222-647C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849893 | ||||||
| chr6:104849908
|
C | T | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.222-662G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849908 | ||||||
| chr6:104849942
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.222-696C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849942 | ||||||
| chr6:104849949
|
C | CT | 13 | a0001c0001t0001g0144a0001c0001t0001g0164a0001c0001t0002g0027others(10): Show | 13 | HG00423.hp1 HG00741.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.222-704dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849949 | ||||||
| chr6:104849949
|
CT | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0174a0001c0001t0001g0175others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.222-704delA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104849949 | ||||||
| chr6:104850014
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.222-768T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850014 | ||||||
| chr6:104850123
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221+784A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850123 | ||||||
| chr6:104850568
|
C | A | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+339G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850568 | ||||||
| chr6:104850599
|
A | C | 1 | a0001c0001t0002g0014 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.221+308T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850599 | ||||||
| chr6:104850697
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.221+210T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850697 | ||||||
| chr6:104850852
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | NA18943.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.221+55C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 3/23 | chr6 | 104850852 | ||||||
| chr6:104851056
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.132-60A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851056 | ||||||
| chr6:104851471
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.132-475A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851471 | ||||||
| chr6:104851508
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.132-512C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851508 | ||||||
| chr6:104851649
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.132-653C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851649 | ||||||
| chr6:104851719
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219 | 4 | HG02572.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+598C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851719 | ||||||
| chr6:104851730
|
CA | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.131+586delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851730 | ||||||
| chr6:104851741
|
A | T | 14 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0250others(11): Show | 14 | HG02080.hp2 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.131+576T>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851741 | ||||||
| chr6:104851960
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131+357G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104851960 | ||||||
| chr6:104852055
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.131+262C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852055 | ||||||
| chr6:104852086
|
T | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.131+231A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852086 | ||||||
| chr6:104852195
|
C | CTG | 61 | a0001c0001t0001g0002a0001c0001t0001g0231a0001c0001t0001g0233others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.131+120_131+121dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | ||||||
| chr6:104852195
|
C | CTGTG | 17 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0243others(14): Show | 17 | HG00609.hp1 HG01175.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.131+121_131+122ins others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | ||||||
| chr6:104852195
|
C | CTGTGTG | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01981.hp1 HG03130.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+121_131+122ins others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | ||||||
| chr6:104852195
|
CTGTCTG | C | 3 | a0001c0001t0001g0234a0001c0001t0001g0304a0001c0001t0001g0334 | 3 | HG01891.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.131+116_131+121del others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852195 | ||||||
| chr6:104852199
|
C | CTG | 19 | a0001c0001t0001g0139a0001c0001t0001g0151a0001c0001t0002g0003others(16): Show | 19 | HG00597.hp2 HG01175.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.131+116_131+117dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852199
|
C | CTGTG | 9 | a0001c0001t0001g0138a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.131+114_131+117dup others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852199
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0002g0009 | 3 | HG02055.hp1 HG02965.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.131+110_131+117dup others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852199
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0001g0141a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02572.hp1 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+108_131+117dup others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852199
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0121a0001c0001t0001g0122 | 4 | HG02895.hp1 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+106_131+117dup others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852199
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.131+118G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852199
|
CTG | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0027others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.131+116_131+117del others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852199 | ||||||
| chr6:104852209
|
G | GTT | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 5 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+107_131+108ins others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852209 | ||||||
| chr6:104852210
|
T | TGC | 4 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 4 | NA18965.hp1 NA18967.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+106_131+107ins others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852210 | ||||||
| chr6:104852228
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.131+89A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGC | 12 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(9): Show | 12 | HG01167.hp1 HG02896.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.131+87_131+88dupGC | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGC | 48 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(45): Show | 48 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGCGC | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGTGC | 47 | a0001c0001t0001g0142a0001c0001t0001g0163a0001c0001t0001g0164others(44): Show | 47 | HG00323.hp2 HG00609.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(4): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGTGTG others(1): Show |
17 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(14): Show | 17 | HG01515.hp1 HG01516.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(6): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGTGTG others(3): Show |
7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0001g0077others(4): Show | 7 | HG02280.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.131+88_131+89insGC others(8): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGTGTG others(5): Show |
2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131+88_131+89insGC others(10): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852228
|
T | TGTGTGTG others(7): Show |
2 | a0001c0002t0001g0076a0001c0003t0001g0229 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.131+88_131+89insGC others(12): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852228 | ||||||
| chr6:104852230
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0144a0001c0001t0001g0230others(147): Show | 151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.131+87G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852230 | ||||||
| chr6:104852232
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.131+85G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852232 | ||||||
| chr6:104852234
|
C | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0094a0001c0002t0001g0115others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+83G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852234 | ||||||
| chr6:104852246
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.131+71G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 2/23 | chr6 | 104852246 | ||||||
| chr6:104852375
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
splice_region_variant&intron_variant | LOW | c.77-4T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852375 | ||||||
| chr6:104852387
|
C | CAG | 177 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0122others(174): Show | 178 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.77-17_77-16insCT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852387 | ||||||
| chr6:104852445
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.77-74T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852445 | ||||||
| chr6:104852531
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.77-160G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852531 | ||||||
| chr6:104852695
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.77-324G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852695 | ||||||
| chr6:104852723
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.77-352C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852723 | ||||||
| chr6:104852733
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.77-362A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852733 | ||||||
| chr6:104852854
|
T | A | 1 | a0001c0001t0001g0337 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.77-483A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104852854 | ||||||
| chr6:104853302
|
T | C | 1 | a0001c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.77-931A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853302 | ||||||
| chr6:104853375
|
A | C | 4 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-1004T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853375 | ||||||
| chr6:104853609
|
C | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.77-1238G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853609 | ||||||
| chr6:104853708
|
G | T | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-1337C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853708 | ||||||
| chr6:104853723
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.77-1352T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853723 | ||||||
| chr6:104853780
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.77-1409A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853780 | ||||||
| chr6:104853803
|
C | T | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-1432G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853803 | ||||||
| chr6:104853837
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.77-1466C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853837 | ||||||
| chr6:104853902
|
A | G | 3 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0087 | 3 | HG03471.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.77-1531T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104853902 | ||||||
| chr6:104854075
|
G | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(90): Show | 94 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.77-1704C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854075 | ||||||
| chr6:104854206
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.77-1835C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854206 | ||||||
| chr6:104854347
|
T | C | 45 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(42): Show | 45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.77-1976A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854347 | ||||||
| chr6:104854575
|
A | AT | 45 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(42): Show | 45 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.77-2205dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854575 | ||||||
| chr6:104854595
|
T | C | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-2224A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854595 | ||||||
| chr6:104854785
|
C | A | 1 | a0001c0003t0001g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77-2414G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854785 | ||||||
| chr6:104854856
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.77-2485C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854856 | ||||||
| chr6:104854888
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.77-2517G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104854888 | ||||||
| chr6:104855009
|
T | C | 1 | a0001c0002t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.77-2638A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855009 | ||||||
| chr6:104855057
|
T | A | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.77-2686A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855057 | ||||||
| chr6:104855254
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.77-2883G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855254 | ||||||
| chr6:104855429
|
C | G | 1 | a0001c0002t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77-3058G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855429 | ||||||
| chr6:104855430
|
G | A | 1 | a0001c0002t0001g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.77-3059C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855430 | ||||||
| chr6:104855749
|
C | T | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77-3378G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855749 | ||||||
| chr6:104855777
|
T | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.77-3406A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855777 | ||||||
| chr6:104855868
|
G | A | 48 | a0001c0001t0001g0334a0001c0002t0001g0083a0001c0002t0001g0085others(45): Show | 48 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.77-3497C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104855868 | ||||||
| chr6:104856245
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.76+3322T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856245 | ||||||
| chr6:104856362
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.76+3205A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856362 | ||||||
| chr6:104856441
|
G | GT | 20 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0002t0001g0076others(17): Show | 20 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.76+3125dupA | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856441 | ||||||
| chr6:104856441
|
G | GTT | 42 | a0001c0002t0001g0083a0001c0002t0001g0090a0001c0002t0001g0091others(39): Show | 42 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.76+3124_76+3125dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856441 | ||||||
| chr6:104856494
|
G | C | 2 | a0001c0003t0001g0228a0001c0003t0001g0229 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.76+3073C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856494 | ||||||
| chr6:104856532
|
T | G | 72 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.76+3035A>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856532 | ||||||
| chr6:104856803
|
C | T | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.76+2764G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104856803 | ||||||
| chr6:104857164
|
T | C | 2 | a0001c0002t0001g0089a0001c0002t0001g0116 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.76+2403A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857164 | ||||||
| chr6:104857169
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.76+2398T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857169 | ||||||
| chr6:104857178
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.76+2389G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857178 | ||||||
| chr6:104857202
|
C | CAT | 8 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+2363_76+2364dup others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857202 | ||||||
| chr6:104857202
|
CAT | C | 41 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(38): Show | 41 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.76+2363_76+2364del others(2): Show |
HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857202 | ||||||
| chr6:104857275
|
A | G | 60 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(57): Show | 60 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.76+2292T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857275 | ||||||
| chr6:104857343
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.76+2224A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857343 | ||||||
| chr6:104857627
|
G | C | 1 | a0001c0002t0008g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76+1940C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857627 | ||||||
| chr6:104857653
|
C | CA | 8 | a0001c0001t0001g0001a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 9 | HG02074.hp1 HG02074.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.76+1913dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857653 | ||||||
| chr6:104857747
|
G | C | 1 | a0001c0002t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.76+1820C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857747 | ||||||
| chr6:104857774
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.76+1793C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857774 | ||||||
| chr6:104857774
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.76+1793C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857774 | ||||||
| chr6:104857874
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.76+1693C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857874 | ||||||
| chr6:104857956
|
C | CA | 10 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(7): Show | 10 | HG00733.hp1 HG01943.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.76+1610dupT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857956 | ||||||
| chr6:104857956
|
CA | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0122others(169): Show | 173 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.76+1610delT | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104857956 | ||||||
| chr6:104858027
|
G | T | 1 | a0001c0001t0002g0004 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.76+1540C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858027 | ||||||
| chr6:104858091
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.76+1476A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858091 | ||||||
| chr6:104858269
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.76+1298G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858269 | ||||||
| chr6:104858384
|
G | A | 2 | a0001c0001t0001g0340a0001c0001t0006g0341 | 2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.76+1183C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858384 | ||||||
| chr6:104858460
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01978.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.76+1107C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858460 | ||||||
| chr6:104858460
|
G | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0342others(1): Show | 4 | HG01515.hp2 HG01517.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+1107C>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858460 | ||||||
| chr6:104858460
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76+1107C>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858460 | ||||||
| chr6:104858527
|
T | A | 15 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(12): Show | 15 | HG00323.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.76+1040A>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858527 | ||||||
| chr6:104858531
|
C | T | 1 | a0001c0001t0003g0140 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.76+1036G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858531 | ||||||
| chr6:104858547
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.76+1020T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858547 | ||||||
| chr6:104858659
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.76+908T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858659 | ||||||
| chr6:104858983
|
T | C | 1 | a0001c0001t0002g0075 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.76+584A>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104858983 | ||||||
| chr6:104859039
|
A | C | 73 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.76+528T>G | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859039 | ||||||
| chr6:104859311
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.76+256T>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859311 | ||||||
| chr6:104859349
|
C | A | 2 | a0001c0003t0001g0228a0001c0003t0001g0229 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.76+218G>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859349 | ||||||
| chr6:104859486
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.76+81G>C | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859486 | ||||||
| chr6:104859486
|
C | T | 1 | a0001c0001t0002g0003 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.76+81G>A | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859486 | ||||||
| chr6:104859503
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.76+64C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859503 | ||||||
| chr6:104859560
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0230a0001c0001t0001g0231others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
splice_region_variant&intron_variant | LOW | c.76+7C>T | HACE1 | ENSG00000085382.12 | transcript | ENST00000262903.9 | protein_coding | 1/23 | chr6 | 104859560 |