| geneid | 401494 |
|---|---|
| ensemblid | ENSG00000188921.14 |
| hgncid | 20920 |
| symbol | HACD4 |
| name | 3-hydroxyacyl-CoA dehydratase 4 |
| refseq_nuc | NM_001010915.5 |
| refseq_prot | NP_001010915.2 |
| ensembl_nuc | ENST00000495827.3 |
| ensembl_prot | ENSP00000419503.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 20999509 |
| end | 21031640 |
| strand | - |
| ver | v1.2 |
| region | chr9:20999509-21031640 |
| region5000 | chr9:20994509-21036640 |
| regionname0 | HACD4_chr9_20999509_21031640 |
| regionname5000 | HACD4_chr9_20994509_21036640 |
| 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 | 232 | 244 | 64 | 46 | 93 | 11 | 28 | 72 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002 | 0/0 | 232 | 186 | 34 | 20 | 117 | 3 | 12 | 97 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0003 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0004 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0005 | 0/0 | 232 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0006 | 0/0 | 232 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 699 | 243 | 63 | 46 | 93 | 11 | 28 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0002 | 0/0 | 699 | 183 | 34 | 20 | 114 | 3 | 12 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0003 | 0/0 | 699 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0004 | 0/0 | 699 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0005 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0006 | 0/0 | 699 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0007 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| c0008 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 7580 | 73 | 3 | 14 | 48 | 3 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0002 | 0/0 | 7580 | 61 | 8 | 8 | 38 | 2 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0003 | 0/0 | 7580 | 57 | 1 | 12 | 39 | 2 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0004 | 0/0 | 7580 | 37 | 9 | 2 | 17 | 2 | 7 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0005 | 0/0 | 7579 | 26 | 0 | 3 | 14 | 3 | 6 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0006 | 0/0 | 7579 | 23 | 5 | 10 | 0 | 0 | 8 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0007 | 0/0 | 7580 | 14 | 0 | 0 | 13 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0008 | 0/0 | 7580 | 14 | 12 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0009 | 0/0 | 7579 | 14 | 0 | 0 | 14 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0010 | 1/0 | 7579 | 13 | 12 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0011 | 0/0 | 7580 | 12 | 12 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0012 | 0/0 | 7580 | 10 | 0 | 0 | 9 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0013 | 0/0 | 7580 | 10 | 6 | 3 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0014 | 0/0 | 7579 | 9 | 5 | 4 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0015 | 0/0 | 7580 | 5 | 5 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0016 | 0/0 | 7580 | 3 | 0 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0017 | 0/0 | 7580 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0018 | 0/0 | 7457 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0019 | 0/0 | 7580 | 3 | 2 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0020 | 0/0 | 7580 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0021 | 0/0 | 7579 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0022 | 0/0 | 7580 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0023 | 0/0 | 7580 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0024 | 0/0 | 7580 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0025 | 0/0 | 7578 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0026 | 0/0 | 7580 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0027 | 0/0 | 7579 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0028 | 0/0 | 7580 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0029 | 0/0 | 7579 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0030 | 0/0 | 7579 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0031 | 0/0 | 7579 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0032 | 0/1 | 7579 | 1 | 0 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0033 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0034 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0035 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0036 | 0/0 | 7580 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0037 | 0/0 | 7580 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0038 | 0/0 | 7580 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0039 | 0/0 | 7580 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0040 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0041 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0042 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0043 | 0/0 | 7580 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0044 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0045 | 0/0 | 7580 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0046 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0047 | 0/0 | 7580 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0048 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0049 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0050 | 0/0 | 7580 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0051 | 0/0 | 7578 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0052 | 0/0 | 7580 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0053 | 0/0 | 7580 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0054 | 0/0 | 7580 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| t0055 | 0/0 | 7579 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| 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 | 25 | 2 | 6 | 16 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0002 | 0/0 | 17 | 0 | 2 | 13 | 1 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0003 | 0/0 | 15 | 1 | 0 | 11 | 0 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0005 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0007 | 0/0 | 9 | 0 | 4 | 0 | 0 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0010 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0014 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0015 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0016 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0019 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0027 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 699 | 243 | 63 | 46 | 93 | 11 | 28 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0005 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002 | 0/0 | 699 | 183 | 34 | 20 | 114 | 3 | 12 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0003 | 0/0 | 699 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0003c0007 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0004c0008 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0005c0006 | 0/0 | 699 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0006c0004 | 0/0 | 699 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8278 | 2 | 0 | 0 | 0 | 2 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0002 | 0/0 | 8278 | 10 | 3 | 4 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0003 | 0/0 | 8278 | 53 | 1 | 10 | 37 | 2 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0004 | 0/0 | 8278 | 32 | 9 | 2 | 12 | 2 | 7 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0005 | 0/0 | 8277 | 26 | 0 | 3 | 14 | 3 | 6 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0006 | 0/0 | 8277 | 23 | 5 | 10 | 0 | 0 | 8 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0007 | 0/0 | 8278 | 14 | 0 | 0 | 13 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0010 | 1/0 | 8277 | 11 | 10 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0011 | 0/0 | 8278 | 9 | 9 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0012 | 0/0 | 8278 | 8 | 0 | 0 | 7 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0013 | 0/0 | 8278 | 10 | 6 | 3 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0014 | 0/0 | 8277 | 8 | 4 | 4 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0016 | 0/0 | 8278 | 3 | 0 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0017 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0018 | 0/0 | 8155 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0019 | 0/0 | 8278 | 3 | 2 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0020 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0021 | 0/0 | 8277 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0024 | 0/0 | 8278 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0025 | 0/0 | 8276 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0027 | 0/0 | 8277 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0028 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0029 | 0/0 | 8277 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0030 | 0/0 | 8277 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0031 | 0/0 | 8277 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0032 | 0/1 | 8277 | 1 | 0 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0034 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0035 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0036 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0037 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0039 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0045 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0051 | 0/0 | 8276 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0052 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0053 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0001t0055 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0001c0005t0010 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0001 | 0/0 | 8278 | 68 | 3 | 14 | 45 | 1 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0002 | 0/0 | 8278 | 50 | 5 | 4 | 34 | 2 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0003 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0004 | 0/0 | 8278 | 5 | 0 | 0 | 5 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0008 | 0/0 | 8278 | 14 | 12 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0009 | 0/0 | 8277 | 14 | 0 | 0 | 14 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0010 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0011 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0012 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0014 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0015 | 0/0 | 8278 | 5 | 5 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0022 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0023 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0026 | 0/0 | 8278 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0033 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0038 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0041 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0042 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0043 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0044 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0046 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0047 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0048 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0049 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0050 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0002t0054 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0003t0001 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0002c0003t0040 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0003c0007t0001 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0004c0008t0002 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0005c0006t0003 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| a0006c0004t0003 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | copy fasta | chr9 | 20994509 | 21036640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0002 | 0/0 | 17 | 0 | 2 | 13 | 1 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0016 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0014 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0019 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0005 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0010 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0007 | 0/0 | 9 | 0 | 4 | 0 | 0 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0010g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0010g0015 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0014g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0014g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0014g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0016g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0016g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0017g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0018g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0019g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0020g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0021g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0024g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0025g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0025g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0027g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0028g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0029g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0031g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0032g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0034g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0035g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0036g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0037g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0039g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0045g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0051g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0052g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0053g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0055g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0005t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0001 | 0/0 | 25 | 2 | 6 | 16 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0003 | 0/0 | 15 | 1 | 0 | 11 | 0 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0027 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0004g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0012g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0022g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0022g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0023g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0023g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0026g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0026g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0033g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0038g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0041g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0042g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0043g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0044g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0046g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0047g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0048g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0049g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0050g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0054g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0003t0040g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0003c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0004c0008t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0005c0006t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0006c0004t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0019 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0019 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0065 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00280 | hp1 | a0001 | c0001 | t0031 | g0078 | EUR | FIN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0184 | EUR | FIN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00408 | hp1 | a0002 | c0003 | t0040 | g0146 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00408 | hp2 | a0001 | c0001 | t0034 | g0127 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0128 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00544 | hp2 | a0002 | c0002 | t0012 | g0049 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00639 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00642 | hp1 | a0001 | c0001 | t0014 | g0110 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00673 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00733 | hp2 | a0005 | c0006 | t0003 | g0161 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00735 | hp1 | a0001 | c0001 | t0013 | g0144 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01069 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01070 | hp1 | a0001 | c0001 | t0024 | g0037 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01071 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01071 | hp2 | a0001 | c0001 | t0024 | g0037 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01074 | hp2 | a0001 | c0001 | t0019 | g0023 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0040 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01099 | hp1 | a0001 | c0001 | t0030 | g0135 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0248 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01167 | hp1 | a0001 | c0001 | t0016 | g0064 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01255 | hp1 | a0006 | c0004 | t0003 | g0118 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0137 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01261 | hp2 | a0002 | c0002 | t0008 | g0236 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01346 | hp2 | a0002 | c0002 | t0043 | g0231 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01358 | hp1 | a0001 | c0001 | t0045 | g0068 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01433 | hp1 | a0001 | c0001 | t0027 | g0066 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01433 | hp2 | a0001 | c0001 | t0016 | g0077 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0010 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0134 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0081 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01884 | hp1 | a0002 | c0002 | t0011 | g0170 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01884 | hp2 | a0002 | c0002 | t0038 | g0221 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0033 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01928 | hp1 | a0001 | c0001 | t0029 | g0121 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0041 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0243 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02071 | hp2 | a0001 | c0001 | t0025 | g0139 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02080 | hp1 | a0002 | c0002 | t0054 | g0206 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02135 | hp2 | a0002 | c0002 | t0022 | g0238 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0190 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02257 | hp2 | a0001 | c0001 | t0036 | g0088 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02258 | hp1 | a0002 | c0002 | t0008 | g0051 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02258 | hp2 | a0001 | c0001 | t0053 | g0152 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0136 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02280 | hp2 | a0001 | c0005 | t0010 | g0092 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02300 | hp1 | a0001 | c0001 | t0016 | g0080 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02451 | hp1 | a0001 | c0001 | t0055 | g0165 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0023 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0087 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0035 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02602 | hp1 | a0002 | c0002 | t0047 | g0209 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0082 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02615 | hp1 | a0002 | c0002 | t0026 | g0233 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02622 | hp2 | a0002 | c0002 | t0010 | g0212 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02630 | hp1 | a0002 | c0002 | t0008 | g0055 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02683 | hp2 | a0001 | c0001 | t0039 | g0122 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0030 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0101 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02723 | hp1 | a0002 | c0002 | t0008 | g0055 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02809 | hp1 | a0002 | c0002 | t0015 | g0154 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02895 | hp1 | a0002 | c0002 | t0008 | g0054 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02896 | hp1 | a0001 | c0001 | t0037 | g0100 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02896 | hp2 | a0002 | c0002 | t0015 | g0050 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02897 | hp1 | a0002 | c0002 | t0015 | g0050 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0091 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0229 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02965 | hp1 | a0002 | c0002 | t0008 | g0051 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0035 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03041 | hp2 | a0002 | c0002 | t0008 | g0189 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03130 | hp1 | a0002 | c0002 | t0008 | g0056 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03130 | hp2 | a0002 | c0002 | t0015 | g0096 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0090 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0085 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03195 | hp2 | a0002 | c0002 | t0011 | g0249 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03209 | hp2 | a0002 | c0002 | t0050 | g0250 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0031 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03225 | hp2 | a0002 | c0002 | t0008 | g0054 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0104 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0023 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0213 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03579 | hp1 | a0002 | c0002 | t0008 | g0191 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03579 | hp2 | a0002 | c0002 | t0026 | g0180 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0024 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0079 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0004 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0084 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0143 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0131 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04199 | hp2 | a0002 | c0002 | t0008 | g0210 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18522 | hp1 | a0002 | c0002 | t0008 | g0056 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18612 | hp1 | a0003 | c0007 | t0001 | g0228 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18747 | hp1 | a0002 | c0002 | t0033 | g0207 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18906 | hp1 | a0001 | c0001 | t0017 | g0102 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18941 | hp2 | a0002 | c0002 | t0004 | g0244 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18942 | hp1 | a0002 | c0002 | t0022 | g0239 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18943 | hp2 | a0001 | c0001 | t0051 | g0138 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18944 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18945 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18945 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0177 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18960 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18961 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18963 | hp1 | a0002 | c0002 | t0042 | g0203 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18963 | hp2 | a0002 | c0002 | t0009 | g0173 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0176 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18967 | hp2 | a0001 | c0001 | t0025 | g0145 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18969 | hp1 | a0001 | c0001 | t0035 | g0155 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18972 | hp2 | a0004 | c0008 | t0002 | g0166 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18973 | hp2 | a0002 | c0002 | t0023 | g0245 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18974 | hp1 | a0001 | c0001 | t0021 | g0072 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18974 | hp2 | a0002 | c0002 | t0023 | g0232 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18977 | hp2 | a0002 | c0002 | t0009 | g0174 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18979 | hp2 | a0002 | c0002 | t0009 | g0175 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18980 | hp1 | a0002 | c0002 | t0041 | g0194 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18986 | hp2 | a0001 | c0001 | t0012 | g0160 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18989 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18992 | hp2 | a0002 | c0002 | t0004 | g0187 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18993 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18997 | hp1 | a0002 | c0002 | t0012 | g0049 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18999 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19002 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19003 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19004 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19043 | hp1 | a0002 | c0002 | t0014 | g0211 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0094 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19054 | hp2 | a0001 | c0001 | t0021 | g0071 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0156 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19066 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19072 | hp1 | a0001 | c0001 | t0007 | g0125 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19072 | hp2 | a0002 | c0002 | t0044 | g0204 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19074 | hp1 | a0002 | c0002 | t0048 | g0205 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19076 | hp2 | a0002 | c0002 | t0009 | g0168 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19078 | hp2 | a0002 | c0002 | t0046 | g0201 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0157 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19084 | hp1 | a0002 | c0002 | t0049 | g0198 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19084 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19090 | hp2 | a0001 | c0001 | t0012 | g0159 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0158 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19240 | hp2 | a0002 | c0002 | t0015 | g0196 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20129 | hp1 | a0001 | c0001 | t0052 | g0105 | AFR | ASW | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | ASW | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0044 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0183 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02109 | hp1 | a0002 | c0002 | t0011 | g0171 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02109 | hp2 | a0002 | c0002 | t0008 | g0220 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02486 | hp2 | a0001 | c0001 | t0020 | g0031 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0033 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0089 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18955 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0032 | g0074 | REF | REF | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0015 | REF | REF | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:21008059
|
G | A | 1 | a0004 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.578C>T | p.Pro193Leu | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/7 | 628/8277 | 578/699 | 193/232 | chr9 | 21008059 | ||
| chr9:21015926
|
C | T | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.355G>A | p.Val119Ile | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 405/8277 | 355/699 | 119/232 | chr9 | 21015926 | ||
| chr9:21015934
|
A | G | 1 | a0003 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.347T>C | p.Val116Ala | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 397/8277 | 347/699 | 116/232 | chr9 | 21015934 | ||
| chr9:21016010
|
G | A | 1 | a0005 | 1 | HG00733.hp2 | missense_variant&splice_region_variant | MODERATE | c.271C>T | p.Leu91Phe | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 321/8277 | 271/699 | 91/232 | chr9 | 21016010 | ||
| chr9:21029331
|
T | C | 3 | a0002a0003a0004 | 188 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(185): Show |
missense_variant | MODERATE | c.106A>G | p.Thr36Ala | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/7 | 156/8277 | 106/699 | 36/232 | chr9 | 21029331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:21015948
|
T | C | 1 | a0001c0005 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.333A>G | p.Lys111Lys | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 383/8277 | 333/699 | 111/232 | chr9 | 21015948 | ||
| chr9:21029383
|
C | T | 1 | a0002c0003 | 3 | HG00408.hp1 NA18960.hp1 NA18964.hp1 |
synonymous_variant | LOW | c.54G>A | p.Ala18Ala | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/7 | 104/8277 | 54/699 | 18/232 | chr9 | 21029383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:20999558
|
A | G | 1 | a0001c0001t0051 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7479T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7479 | chr9 | 20999558 | |||||
| chr9:20999625
|
G | GT | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*7411dupA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7411 | chr9 | 20999625 | |||||
| chr9:20999647
|
G | A | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(33): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*7390C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7390 | chr9 | 20999647 | |||||
| chr9:20999739
|
A | G | 1 | a0002c0003t0040 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7298T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7298 | chr9 | 20999739 | |||||
| chr9:20999771
|
T | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(25): Show | 185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*7266A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7266 | chr9 | 20999771 | |||||
| chr9:20999806
|
ACAAAACG others(116): Show |
A | 1 | a0001c0001t0018 | 3 | HG02572.hp2 HG02970.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7108_*7230del | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7108 | chr9 | 20999806 | |||||
| chr9:20999812
|
C | T | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7225G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7225 | chr9 | 20999812 | |||||
| chr9:20999947
|
A | G | 1 | a0001c0001t0039 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7090T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7090 | chr9 | 20999947 | |||||
| chr9:21000097
|
T | A | 1 | a0002c0002t0041 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6940A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6940 | chr9 | 21000097 | |||||
| chr9:21000326
|
C | T | 1 | a0001c0001t0053 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6711G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6711 | chr9 | 21000326 | |||||
| chr9:21000496
|
G | T | 8 | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(5): Show | 69 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*6541C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6541 | chr9 | 21000496 | |||||
| chr9:21000621
|
C | G | 5 | a0001c0001t0011a0001c0001t0036a0002c0002t0011others(2): Show | 15 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6416G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6416 | chr9 | 21000621 | |||||
| chr9:21000648
|
A | T | 1 | a0002c0002t0023 | 2 | NA18973.hp2 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6389T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6389 | chr9 | 21000648 | |||||
| chr9:21000674
|
C | T | 1 | a0002c0002t0044 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6363G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6363 | chr9 | 21000674 | |||||
| chr9:21000738
|
A | G | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*6299T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6299 | chr9 | 21000738 | |||||
| chr9:21000840
|
C | A | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6197G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6197 | chr9 | 21000840 | |||||
| chr9:21000901
|
A | G | 1 | a0002c0002t0008 | 14 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6136T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6136 | chr9 | 21000901 | |||||
| chr9:21000922
|
C | G | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6115G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6115 | chr9 | 21000922 | |||||
| chr9:21000997
|
C | T | 1 | a0002c0002t0043 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6040G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6040 | chr9 | 21000997 | |||||
| chr9:21001428
|
G | T | 2 | a0001c0001t0037a0001c0001t0052 | 2 | HG02896.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5609C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 5609 | chr9 | 21001428 | |||||
| chr9:21001644
|
A | T | 1 | a0001c0001t0013 | 10 | HG00735.hp1 HG01081.hp2 HG01255.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5393T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 5393 | chr9 | 21001644 | |||||
| chr9:21002226
|
A | C | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(11): Show | 73 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4811T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4811 | chr9 | 21002226 | |||||
| chr9:21002426
|
C | T | 1 | a0001c0001t0021 | 2 | NA18974.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4611G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4611 | chr9 | 21002426 | |||||
| chr9:21002427
|
A | G | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
3_prime_UTR_variant | MODIFIER | c.*4610T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4610 | chr9 | 21002427 | |||||
| chr9:21002458
|
C | T | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 70 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4579G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4579 | chr9 | 21002458 | |||||
| chr9:21002635
|
A | G | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(11): Show | 73 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4402T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4402 | chr9 | 21002635 | |||||
| chr9:21002798
|
T | C | 1 | a0001c0001t0034 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4239A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4239 | chr9 | 21002798 | |||||
| chr9:21002804
|
A | C | 1 | a0002c0002t0042 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4233T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4233 | chr9 | 21002804 | |||||
| chr9:21002869
|
G | A | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4168C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4168 | chr9 | 21002869 | |||||
| chr9:21002869
|
G | C | 1 | a0001c0001t0045 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4168C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4168 | chr9 | 21002869 | |||||
| chr9:21003373
|
G | A | 16 | a0001c0001t0001a0001c0001t0045a0002c0002t0001others(13): Show | 87 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3664C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3664 | chr9 | 21003373 | |||||
| chr9:21003407
|
T | A | 1 | a0001c0001t0030 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3630A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3630 | chr9 | 21003407 | |||||
| chr9:21003524
|
A | G | 1 | a0001c0001t0036 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3513T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3513 | chr9 | 21003524 | |||||
| chr9:21003595
|
T | C | 1 | a0002c0002t0046 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3442A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3442 | chr9 | 21003595 | |||||
| chr9:21003628
|
A | G | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3409T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3409 | chr9 | 21003628 | |||||
| chr9:21003764
|
TCA | T | 2 | a0001c0001t0025a0001c0001t0051 | 3 | HG02071.hp2 NA18943.hp2 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3271_*3272delTG | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3271 | chr9 | 21003764 | |||||
| chr9:21003784
|
C | T | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0016others(6): Show | 59 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3253G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3253 | chr9 | 21003784 | |||||
| chr9:21004245
|
G | A | 10 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(7): Show | 72 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2792C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2792 | chr9 | 21004245 | |||||
| chr9:21004248
|
C | G | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2789G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2789 | chr9 | 21004248 | |||||
| chr9:21004398
|
A | T | 1 | a0001c0001t0035 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2639T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2639 | chr9 | 21004398 | |||||
| chr9:21004556
|
G | A | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2481C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2481 | chr9 | 21004556 | |||||
| chr9:21004675
|
T | C | 1 | a0001c0001t0031 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2362A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2362 | chr9 | 21004675 | |||||
| chr9:21004769
|
C | G | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2268G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2268 | chr9 | 21004769 | |||||
| chr9:21004802
|
T | C | 1 | a0002c0002t0047 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2235 | chr9 | 21004802 | |||||
| chr9:21004883
|
T | C | 1 | a0002c0002t0048 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2154 | chr9 | 21004883 | |||||
| chr9:21004994
|
G | A | 1 | a0002c0002t0049 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2043C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2043 | chr9 | 21004994 | |||||
| chr9:21005306
|
G | C | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1731C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1731 | chr9 | 21005306 | |||||
| chr9:21005366
|
G | A | 1 | a0002c0002t0050 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1671 | chr9 | 21005366 | |||||
| chr9:21005398
|
A | C | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1639T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1639 | chr9 | 21005398 | |||||
| chr9:21005423
|
G | A | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(9): Show | 76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1614C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1614 | chr9 | 21005423 | |||||
| chr9:21005476
|
T | C | 2 | a0001c0001t0005a0001c0001t0021 | 28 | HG00140.hp2 HG00621.hp2 HG00738.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1561A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1561 | chr9 | 21005476 | |||||
| chr9:21005491
|
A | G | 1 | a0001c0001t0055 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1546 | chr9 | 21005491 | |||||
| chr9:21005739
|
G | A | 1 | a0002c0002t0026 | 2 | HG02615.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1298C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1298 | chr9 | 21005739 | |||||
| chr9:21005745
|
C | T | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1292G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1292 | chr9 | 21005745 | |||||
| chr9:21005829
|
G | C | 1 | a0001c0001t0032 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1208 | chr9 | 21005829 | |||||
| chr9:21005896
|
C | A | 1 | a0002c0002t0033 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1141G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1141 | chr9 | 21005896 | |||||
| chr9:21005951
|
A | G | 2 | a0001c0001t0007a0001c0001t0034 | 15 | HG00408.hp2 HG00438.hp1 HG03831.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1086T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1086 | chr9 | 21005951 | |||||
| chr9:21006022
|
C | T | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1015G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1015 | chr9 | 21006022 | |||||
| chr9:21006115
|
T | C | 1 | a0002c0002t0054 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 922 | chr9 | 21006115 | |||||
| chr9:21006400
|
C | T | 1 | a0002c0002t0022 | 2 | HG02135.hp2 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*637G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 637 | chr9 | 21006400 | |||||
| chr9:21006415
|
C | G | 1 | a0002c0002t0033 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 622 | chr9 | 21006415 | |||||
| chr9:21006454
|
C | T | 1 | a0001c0001t0017 | 3 | HG02559.hp1 HG02717.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*583G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 583 | chr9 | 21006454 | |||||
| chr9:21006601
|
C | A | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*436G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 436 | chr9 | 21006601 | |||||
| chr9:21006935
|
A | G | 10 | a0001c0001t0005a0001c0001t0006a0001c0001t0016others(7): Show | 60 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*102T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 102 | chr9 | 21006935 | |||||
| chr9:21006959
|
C | G | 1 | a0001c0001t0027 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 78 | chr9 | 21006959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:21007318
|
T | C | 1 | a0001c0001t0017g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.617-199A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007318 | ||||||
| chr9:21007384
|
C | T | 3 | a0001c0001t0014g0012a0001c0001t0014g0021a0001c0001t0014g0110 | 8 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-265G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007384 | ||||||
| chr9:21007608
|
C | T | 2 | a0002c0002t0008g0220a0002c0002t0038g0221 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.616+413G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007608 | ||||||
| chr9:21007633
|
C | T | 240 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(237): Show | 419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.616+388G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007633 | ||||||
| chr9:21007760
|
A | C | 7 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(4): Show | 9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.616+261T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007760 | ||||||
| chr9:21007762
|
A | G | 2 | a0002c0003t0001g0176a0002c0003t0001g0177 | 2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.616+259T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007762 | ||||||
| chr9:21007766
|
C | A | 5 | a0002c0002t0001g0017a0002c0002t0001g0053a0002c0002t0001g0223others(2): Show | 9 | HG00558.hp2 NA18939.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.616+255G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007766 | ||||||
| chr9:21007936
|
A | G | 201 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0108others(198): Show | 343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.616+85T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007936 | ||||||
| chr9:21007959
|
C | T | 4 | a0002c0002t0001g0017a0002c0002t0001g0223a0002c0002t0001g0237others(1): Show | 7 | HG00558.hp2 NA18939.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.616+62G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007959 | ||||||
| chr9:21008378
|
T | C | 153 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(150): Show | 267 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(264): Show |
intron_variant | MODIFIER | c.491-232A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008378 | ||||||
| chr9:21008391
|
G | T | 1 | a0001c0001t0004g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.491-245C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008391 | ||||||
| chr9:21008415
|
T | C | 1 | a0002c0002t0002g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.491-269A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008415 | ||||||
| chr9:21008417
|
A | G | 35 | a0001c0001t0002g0140a0001c0001t0003g0124a0002c0002t0001g0195others(32): Show | 60 | HG00280.hp2 HG00544.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.491-271T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008417 | ||||||
| chr9:21008535
|
C | T | 1 | a0001c0001t0006g0076 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.491-389G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008535 | ||||||
| chr9:21008580
|
G | A | 2 | a0001c0001t0020g0031a0001c0001t0020g0085 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.491-434C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008580 | ||||||
| chr9:21008581
|
C | A | 1 | a0002c0002t0033g0207 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.491-435G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008581 | ||||||
| chr9:21008713
|
A | C | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.491-567T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008713 | ||||||
| chr9:21008726
|
A | G | 140 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(137): Show | 251 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.491-580T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008726 | ||||||
| chr9:21009192
|
G | A | 107 | a0001c0001t0002g0140a0001c0001t0003g0124a0002c0002t0001g0001others(104): Show | 181 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.491-1046C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009192 | ||||||
| chr9:21009280
|
T | C | 1 | a0001c0001t0005g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.491-1134A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009280 | ||||||
| chr9:21009285
|
A | G | 1 | a0002c0002t0008g0054 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.491-1139T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009285 | ||||||
| chr9:21009404
|
G | A | 2 | a0001c0001t0013g0041a0001c0001t0013g0042 | 4 | HG02055.hp1 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-1258C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009404 | ||||||
| chr9:21009466
|
C | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.491-1320G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009466 | ||||||
| chr9:21009661
|
G | A | 246 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(243): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.491-1515C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009661 | ||||||
| chr9:21009744
|
C | G | 1 | a0002c0002t0015g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.491-1598G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009744 | ||||||
| chr9:21009747
|
G | C | 1 | a0001c0001t0004g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.491-1601C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009747 | ||||||
| chr9:21009803
|
A | C | 234 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(231): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.491-1657T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009803 | ||||||
| chr9:21010038
|
C | A | 7 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(4): Show | 9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+1551G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010038 | ||||||
| chr9:21010114
|
G | A | 234 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(231): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.490+1475C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010114 | ||||||
| chr9:21010170
|
A | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0090a0001c0001t0011g0091 | 4 | HG01891.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1419T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010170 | ||||||
| chr9:21010441
|
C | G | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+1148G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010441 | ||||||
| chr9:21010456
|
A | ACCC | 14 | a0001c0001t0001g0075a0001c0001t0005g0005a0001c0001t0005g0063others(11): Show | 25 | HG00741.hp2 HG01934.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.490+1130_490+1132d others(5): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010456
|
A | ACCCC | 12 | a0001c0001t0001g0073a0001c0001t0005g0028a0001c0001t0005g0067others(9): Show | 21 | HG00099.hp2 HG00621.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.490+1129_490+1132d others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010456
|
A | AT | 15 | a0001c0001t0002g0097a0001c0001t0004g0008a0001c0001t0004g0014others(12): Show | 38 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.490+1132_490+1133i others(3): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010456
|
A | ATC | 17 | a0001c0001t0002g0108a0001c0001t0004g0039a0001c0001t0004g0099others(14): Show | 21 | HG00438.hp1 HG00735.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.490+1132_490+1133i others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010456
|
A | ATCC | 13 | a0001c0001t0002g0109a0001c0001t0004g0086a0001c0001t0004g0093others(10): Show | 13 | HG01243.hp2 HG01255.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+1132_490+1133i others(5): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010456
|
A | ATCCC | 2 | a0001c0001t0018g0035a0001c0001t0055g0165 | 3 | HG02451.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.490+1132_490+1133i others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010456
|
ACC | A | 133 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(130): Show | 245 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.490+1131_490+1132d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | ||||||
| chr9:21010457
|
C | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(4): Show | 9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+1132G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010457 | ||||||
| chr9:21010458
|
C | A | 2 | a0001c0001t0014g0021a0001c0001t0014g0110 | 4 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1131G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010458 | ||||||
| chr9:21010462
|
C | G | 1 | a0002c0002t0008g0054 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.490+1127G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010462 | ||||||
| chr9:21010465
|
C | G | 32 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(29): Show | 68 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.490+1124G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010465 | ||||||
| chr9:21010466
|
C | G | 1 | a0001c0001t0013g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.490+1123G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010466 | ||||||
| chr9:21010467
|
C | G | 109 | a0001c0001t0002g0140a0001c0001t0003g0124a0001c0001t0006g0029others(106): Show | 185 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.490+1122G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010467 | ||||||
| chr9:21010469
|
C | A | 32 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(29): Show | 68 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.490+1120G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010469 | ||||||
| chr9:21010614
|
C | A | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490+975G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010614 | ||||||
| chr9:21010624
|
G | A | 48 | a0001c0001t0002g0097a0001c0001t0002g0108a0001c0001t0002g0109others(45): Show | 76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.490+965C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010624 | ||||||
| chr9:21010877
|
G | A | 1 | a0002c0002t0001g0048 | 2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.490+712C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010877 | ||||||
| chr9:21010905
|
C | T | 1 | a0001c0001t0004g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.490+684G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010905 | ||||||
| chr9:21011017
|
G | A | 9 | a0001c0001t0004g0008a0001c0001t0004g0126a0001c0001t0004g0129others(6): Show | 25 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.490+572C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21011017 | ||||||
| chr9:21011188
|
G | T | 1 | a0001c0001t0053g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490+401C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21011188 | ||||||
| chr9:21011288
|
T | C | 92 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0097others(89): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.490+301A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21011288 | ||||||
| chr9:21011723
|
A | G | 9 | a0001c0001t0011g0094a0001c0001t0012g0024a0001c0001t0012g0156others(6): Show | 11 | HG02451.hp1 HG03669.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-28T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21011723 | ||||||
| chr9:21011834
|
G | C | 32 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(29): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.384-139C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21011834 | ||||||
| chr9:21012028
|
G | A | 3 | a0002c0002t0002g0027a0002c0002t0002g0183a0002c0002t0002g0184 | 5 | HG00280.hp2 HG01256.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-333C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012028 | ||||||
| chr9:21012171
|
G | A | 141 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(138): Show | 252 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.384-476C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012171 | ||||||
| chr9:21012227
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.384-532G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012227 | ||||||
| chr9:21012326
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.384-631T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012326 | ||||||
| chr9:21012448
|
C | A | 26 | a0001c0001t0002g0140a0002c0002t0001g0195a0002c0002t0002g0003others(23): Show | 47 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.384-753G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012448 | ||||||
| chr9:21012746
|
G | A | 141 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(138): Show | 252 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.384-1051C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012746 | ||||||
| chr9:21012788
|
C | T | 47 | a0001c0001t0002g0097a0001c0001t0002g0162a0001c0001t0004g0008others(44): Show | 75 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.384-1093G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012788 | ||||||
| chr9:21012792
|
G | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-1097C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012792 | ||||||
| chr9:21012829
|
G | A | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.384-1134C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012829 | ||||||
| chr9:21012882
|
C | T | 1 | a0002c0002t0002g0061 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.384-1187G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012882 | ||||||
| chr9:21012901
|
C | T | 248 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(245): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.384-1206G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012901 | ||||||
| chr9:21012935
|
C | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(4): Show | 9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.384-1240G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012935 | ||||||
| chr9:21012936
|
G | A | 30 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(27): Show | 64 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.384-1241C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012936 | ||||||
| chr9:21012994
|
G | T | 1 | a0001c0001t0003g0119 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.384-1299C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012994 | ||||||
| chr9:21013066
|
C | CA | 13 | a0001c0001t0004g0131a0001c0001t0013g0040a0001c0001t0013g0041others(10): Show | 17 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.384-1372dupT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013066 | ||||||
| chr9:21013238
|
T | C | 1 | a0001c0001t0011g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.384-1543A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013238 | ||||||
| chr9:21013244
|
G | A | 1 | a0002c0002t0001g0248 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.384-1549C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013244 | ||||||
| chr9:21013246
|
G | T | 2 | a0002c0002t0008g0220a0002c0002t0038g0221 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.384-1551C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013246 | ||||||
| chr9:21013479
|
C | G | 37 | a0001c0001t0002g0162a0001c0001t0004g0008a0001c0001t0004g0014others(34): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.384-1784G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013479 | ||||||
| chr9:21013517
|
G | T | 16 | a0002c0002t0001g0172a0002c0002t0008g0051a0002c0002t0008g0054others(13): Show | 29 | HG01261.hp2 HG02055.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.384-1822C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013517 | ||||||
| chr9:21013593
|
G | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-1898C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013593 | ||||||
| chr9:21013663
|
T | C | 1 | a0001c0001t0013g0042 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.384-1968A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013663 | ||||||
| chr9:21013743
|
A | C | 247 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(244): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.384-2048T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013743 | ||||||
| chr9:21013799
|
T | C | 1 | a0002c0003t0040g0146 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.383+2099A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013799 | ||||||
| chr9:21013903
|
A | G | 2 | a0001c0001t0013g0040a0001c0001t0013g0134 | 3 | HG01081.hp2 HG01516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.383+1995T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013903 | ||||||
| chr9:21013906
|
C | G | 6 | a0001c0001t0004g0086a0001c0001t0004g0106a0001c0001t0018g0035others(3): Show | 7 | HG02572.hp2 HG02896.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+1992G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013906 | ||||||
| chr9:21013969
|
G | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1929C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013969 | ||||||
| chr9:21013978
|
T | C | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1920A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013978 | ||||||
| chr9:21013983
|
C | G | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1915G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013983 | ||||||
| chr9:21013986
|
G | A | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1912C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013986 | ||||||
| chr9:21013987
|
C | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1911G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013987 | ||||||
| chr9:21013988
|
A | G | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1910T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013988 | ||||||
| chr9:21013989
|
A | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1909T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013989 | ||||||
| chr9:21013990
|
G | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1908C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013990 | ||||||
| chr9:21014004
|
G | A | 74 | a0002c0002t0001g0001a0002c0002t0001g0017a0002c0002t0001g0018others(71): Show | 124 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.383+1894C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014004 | ||||||
| chr9:21014062
|
A | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1836T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014062 | ||||||
| chr9:21014077
|
T | C | 8 | a0002c0002t0008g0051a0002c0002t0008g0055a0002c0002t0008g0056others(5): Show | 11 | HG01261.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.383+1821A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014077 | ||||||
| chr9:21014177
|
A | G | 55 | a0002c0002t0001g0001a0002c0002t0001g0017a0002c0002t0001g0018others(52): Show | 92 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.383+1721T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014177 | ||||||
| chr9:21014243
|
T | G | 1 | a0002c0002t0001g0226 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.383+1655A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014243 | ||||||
| chr9:21014253
|
A | G | 4 | a0001c0001t0011g0032a0001c0001t0011g0087a0001c0001t0011g0089others(1): Show | 5 | HG02257.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+1645T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014253 | ||||||
| chr9:21014357
|
C | G | 7 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(4): Show | 9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.383+1541G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014357 | ||||||
| chr9:21014362
|
C | T | 1 | a0002c0002t0001g0199 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.383+1536G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014362 | ||||||
| chr9:21014434
|
A | G | 3 | a0001c0001t0017g0062a0001c0001t0017g0101a0001c0001t0017g0102 | 3 | HG02559.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.383+1464T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014434 | ||||||
| chr9:21014436
|
T | C | 2 | a0001c0001t0020g0031a0001c0001t0020g0085 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.383+1462A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014436 | ||||||
| chr9:21014483
|
C | G | 92 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0097others(89): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.383+1415G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014483 | ||||||
| chr9:21014540
|
T | A | 1 | a0001c0001t0005g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.383+1358A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014540 | ||||||
| chr9:21014571
|
A | C | 2 | a0001c0001t0020g0031a0001c0001t0020g0085 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.383+1327T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014571 | ||||||
| chr9:21014601
|
T | G | 1 | a0001c0001t0027g0066 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.383+1297A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014601 | ||||||
| chr9:21014613
|
A | C | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1285T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014613 | ||||||
| chr9:21014629
|
T | C | 112 | a0001c0001t0002g0140a0001c0001t0003g0124a0001c0001t0006g0150others(109): Show | 189 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.383+1269A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014629 | ||||||
| chr9:21014690
|
G | C | 4 | a0001c0001t0003g0124a0002c0002t0002g0052a0002c0002t0002g0167others(1): Show | 5 | NA18939.hp1 NA18949.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+1208C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014690 | ||||||
| chr9:21014700
|
T | C | 1 | a0001c0001t0012g0158 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.383+1198A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014700 | ||||||
| chr9:21014823
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.383+1075T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014823 | ||||||
| chr9:21014838
|
C | A | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.383+1060G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014838 | ||||||
| chr9:21015113
|
T | C | 1 | a0001c0001t0012g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.383+785A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015113 | ||||||
| chr9:21015198
|
T | C | 1 | a0002c0003t0001g0177 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.383+700A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015198 | ||||||
| chr9:21015430
|
A | G | 1 | a0001c0001t0014g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.383+468T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015430 | ||||||
| chr9:21015624
|
A | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+274T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015624 | ||||||
| chr9:21015652
|
T | G | 79 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(76): Show | 141 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.383+246A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015652 | ||||||
| chr9:21015757
|
A | G | 2 | a0002c0002t0001g0182a0002c0002t0049g0198 | 2 | NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.383+141T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015757 | ||||||
| chr9:21016216
|
T | C | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-206A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016216 | ||||||
| chr9:21016366
|
A | G | 234 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(231): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.271-356T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016366 | ||||||
| chr9:21016367
|
A | G | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-357T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016367 | ||||||
| chr9:21016369
|
A | G | 1 | a0001c0001t0003g0178 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.271-359T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016369 | ||||||
| chr9:21016375
|
G | A | 1 | a0002c0002t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.271-365C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016375 | ||||||
| chr9:21016509
|
A | G | 2 | a0001c0001t0011g0094a0001c0001t0055g0165 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.271-499T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016509 | ||||||
| chr9:21016543
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-533C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016543 | ||||||
| chr9:21016647
|
TG | T | 49 | a0002c0002t0001g0001a0002c0002t0001g0017a0002c0002t0001g0018others(46): Show | 84 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.271-638delC | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016647 | ||||||
| chr9:21016728
|
GT | G | 87 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(84): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.271-719delA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016728 | ||||||
| chr9:21016735
|
A | G | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-725T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016735 | ||||||
| chr9:21016767
|
T | A | 1 | a0001c0001t0004g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-757A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016767 | ||||||
| chr9:21016782
|
C | CT | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.271-773dupA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016782 | ||||||
| chr9:21016793
|
C | T | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-783G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016793 | ||||||
| chr9:21016794
|
T | C | 1 | a0002c0002t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-784A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016794 | ||||||
| chr9:21016930
|
C | G | 124 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(121): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.271-920G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016930 | ||||||
| chr9:21017241
|
A | G | 110 | a0001c0001t0002g0140a0001c0001t0019g0023a0002c0002t0001g0001others(107): Show | 187 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.271-1231T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017241 | ||||||
| chr9:21017335
|
G | T | 1 | a0001c0001t0002g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.271-1325C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017335 | ||||||
| chr9:21017419
|
TTATAA | T | 34 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(31): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.271-1414_271-1410d others(7): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017419 | ||||||
| chr9:21017638
|
C | T | 27 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0019others(24): Show | 53 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.271-1628G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017638 | ||||||
| chr9:21017645
|
A | C | 92 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0097others(89): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.271-1635T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017645 | ||||||
| chr9:21017690
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-1680C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017690 | ||||||
| chr9:21017744
|
C | T | 203 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0097others(200): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.271-1734G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017744 | ||||||
| chr9:21017769
|
C | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-1759G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017769 | ||||||
| chr9:21017829
|
G | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0017a0002c0002t0001g0018others(69): Show | 121 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.271-1819C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017829 | ||||||
| chr9:21017885
|
T | C | 111 | a0001c0001t0002g0140a0001c0001t0019g0023a0001c0001t0020g0031others(108): Show | 188 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(185): Show |
intron_variant | MODIFIER | c.271-1875A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017885 | ||||||
| chr9:21018048
|
A | G | 1 | a0001c0001t0003g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.271-2038T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018048 | ||||||
| chr9:21018061
|
C | A | 1 | a0001c0001t0019g0023 | 3 | HG01074.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-2051G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018061 | ||||||
| chr9:21018178
|
A | C | 1 | a0001c0001t0004g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271-2168T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018178 | ||||||
| chr9:21018472
|
A | C | 88 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(85): Show | 153 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.271-2462T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018472 | ||||||
| chr9:21018529
|
C | T | 1 | a0001c0001t0003g0047 | 2 | NA19004.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.271-2519G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018529 | ||||||
| chr9:21018551
|
G | C | 122 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(119): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.271-2541C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018551 | ||||||
| chr9:21018551
|
G | T | 110 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(107): Show | 186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2541C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018551 | ||||||
| chr9:21018575
|
C | T | 31 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(28): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.271-2565G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018575 | ||||||
| chr9:21018592
|
C | T | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-2582G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018592 | ||||||
| chr9:21018776
|
T | C | 2 | a0001c0001t0002g0095a0001c0001t0053g0152 | 2 | HG01123.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.271-2766A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018776 | ||||||
| chr9:21018812
|
C | A | 110 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(107): Show | 186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2802G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018812 | ||||||
| chr9:21018813
|
ATTTTTAT others(1): Show |
A | 110 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(107): Show | 186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2811_271-2804d others(10): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018813 | ||||||
| chr9:21018823
|
T | C | 110 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(107): Show | 186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2813A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018823 | ||||||
| chr9:21018919
|
G | C | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-2909C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018919 | ||||||
| chr9:21018942
|
C | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-2932G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018942 | ||||||
| chr9:21019058
|
C | T | 1 | a0001c0001t0004g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.271-3048G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019058 | ||||||
| chr9:21019124
|
C | T | 200 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0097others(197): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.271-3114G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019124 | ||||||
| chr9:21019235
|
C | T | 248 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(245): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.271-3225G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019235 | ||||||
| chr9:21019330
|
C | A | 1 | a0002c0002t0008g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.271-3320G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019330 | ||||||
| chr9:21019379
|
T | A | 72 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(69): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.271-3369A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019379 | ||||||
| chr9:21019382
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-3372G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019382 | ||||||
| chr9:21019449
|
C | T | 3 | a0002c0002t0004g0025a0002c0002t0004g0187a0002c0002t0004g0244 | 5 | HG00673.hp2 NA18941.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3439G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019449 | ||||||
| chr9:21019488
|
G | T | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3478C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019488 | ||||||
| chr9:21019546
|
G | C | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3536C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019546 | ||||||
| chr9:21019611
|
T | A | 1 | a0002c0002t0002g0213 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.271-3601A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019611 | ||||||
| chr9:21019645
|
A | G | 1 | a0001c0001t0005g0069 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.271-3635T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019645 | ||||||
| chr9:21019651
|
T | G | 122 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(119): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.271-3641A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019651 | ||||||
| chr9:21019761
|
A | C | 3 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0024g0037 | 4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3751T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019761 | ||||||
| chr9:21019818
|
C | T | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.271-3808G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019818 | ||||||
| chr9:21019869
|
ATTAT | A | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.271-3863_271-3860d others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019869 | ||||||
| chr9:21019896
|
C | T | 12 | a0001c0001t0005g0005a0001c0001t0005g0010a0001c0001t0005g0028others(9): Show | 26 | HG00140.hp2 HG00621.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.271-3886G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019896 | ||||||
| chr9:21019908
|
G | T | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3898C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019908 | ||||||
| chr9:21019938
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3928A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019938 | ||||||
| chr9:21020067
|
A | G | 1 | a0002c0002t0008g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.271-4057T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020067 | ||||||
| chr9:21020096
|
T | A | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.271-4086A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020096 | ||||||
| chr9:21020115
|
T | A | 114 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(111): Show | 190 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(187): Show |
intron_variant | MODIFIER | c.271-4105A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020115 | ||||||
| chr9:21020117
|
A | T | 1 | a0002c0002t0009g0173 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.271-4107T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020117 | ||||||
| chr9:21020128
|
C | T | 248 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(245): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.271-4118G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020128 | ||||||
| chr9:21020169
|
G | A | 33 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(30): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.271-4159C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020169 | ||||||
| chr9:21020175
|
G | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-4165C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020175 | ||||||
| chr9:21020233
|
GAC | G | 116 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0140others(113): Show | 192 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.271-4225_271-4224d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020233 | ||||||
| chr9:21020323
|
G | A | 2 | a0002c0002t0008g0056a0002c0002t0008g0189 | 3 | HG03041.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.271-4313C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020323 | ||||||
| chr9:21020468
|
AAC | A | 10 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(7): Show | 12 | HG02071.hp2 HG03669.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-4460_271-4459d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020468 | ||||||
| chr9:21020503
|
C | G | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.271-4493G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020503 | ||||||
| chr9:21020535
|
T | A | 1 | a0002c0002t0009g0175 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.271-4525A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020535 | ||||||
| chr9:21020620
|
G | A | 1 | a0002c0002t0001g0214 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.271-4610C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020620 | ||||||
| chr9:21020642
|
A | G | 234 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(231): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.271-4632T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020642 | ||||||
| chr9:21020673
|
T | C | 1 | a0001c0001t0028g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.271-4663A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020673 | ||||||
| chr9:21020682
|
T | A | 1 | a0002c0002t0001g0248 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271-4672A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020682 | ||||||
| chr9:21020683
|
C | G | 1 | a0002c0002t0001g0248 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271-4673G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020683 | ||||||
| chr9:21020712
|
G | A | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.271-4702C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020712 | ||||||
| chr9:21020996
|
C | T | 4 | a0001c0001t0002g0097a0001c0001t0017g0062a0001c0001t0017g0101others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4986G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020996 | ||||||
| chr9:21021247
|
T | C | 115 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(112): Show | 192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.271-5237A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021247 | ||||||
| chr9:21021258
|
C | T | 1 | a0002c0002t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-5248G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021258 | ||||||
| chr9:21021259
|
G | C | 1 | a0002c0002t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-5249C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021259 | ||||||
| chr9:21021273
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0004g0093 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271-5263A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021273 | ||||||
| chr9:21021281
|
T | C | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.271-5271A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021281 | ||||||
| chr9:21021386
|
A | G | 115 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(112): Show | 192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+5210T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021386 | ||||||
| chr9:21021480
|
C | G | 2 | a0001c0001t0006g0163a0001c0001t0006g0164 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.270+5116G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021480 | ||||||
| chr9:21021492
|
C | A | 1 | a0002c0002t0002g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.270+5104G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021492 | ||||||
| chr9:21021552
|
C | T | 1 | a0002c0002t0002g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.270+5044G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021552 | ||||||
| chr9:21021553
|
G | A | 1 | a0002c0002t0002g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.270+5043C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021553 | ||||||
| chr9:21021559
|
C | A | 1 | a0002c0002t0002g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.270+5037G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021559 | ||||||
| chr9:21021575
|
T | C | 70 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(67): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.270+5021A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021575 | ||||||
| chr9:21021669
|
A | C | 2 | a0001c0001t0011g0094a0001c0001t0055g0165 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.270+4927T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021669 | ||||||
| chr9:21021705
|
A | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+4891T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021705 | ||||||
| chr9:21021783
|
T | C | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.270+4813A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021783 | ||||||
| chr9:21021903
|
A | G | 1 | a0002c0002t0003g0190 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.270+4693T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021903 | ||||||
| chr9:21021914
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.270+4682T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021914 | ||||||
| chr9:21021943
|
C | T | 1 | a0001c0001t0045g0068 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.270+4653G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021943 | ||||||
| chr9:21021953
|
G | A | 107 | a0001c0001t0002g0140a0002c0002t0001g0001a0002c0002t0001g0017others(104): Show | 181 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.270+4643C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021953 | ||||||
| chr9:21021960
|
C | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+4636G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021960 | ||||||
| chr9:21022000
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+4596G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022000 | ||||||
| chr9:21022085
|
A | G | 1 | a0001c0001t0006g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+4511T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022085 | ||||||
| chr9:21022094
|
A | G | 1 | a0001c0001t0005g0067 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.270+4502T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022094 | ||||||
| chr9:21022158
|
A | G | 1 | a0001c0001t0006g0112 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.270+4438T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022158 | ||||||
| chr9:21022187
|
A | G | 1 | a0001c0001t0004g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.270+4409T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022187 | ||||||
| chr9:21022228
|
C | T | 69 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(66): Show | 131 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.270+4368G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022228 | ||||||
| chr9:21022359
|
A | G | 34 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(31): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.270+4237T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022359 | ||||||
| chr9:21022402
|
G | A | 1 | a0001c0001t0004g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.270+4194C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022402 | ||||||
| chr9:21022501
|
A | C | 115 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(112): Show | 192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+4095T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022501 | ||||||
| chr9:21022570
|
A | G | 10 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(7): Show | 12 | HG02071.hp2 HG03669.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+4026T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022570 | ||||||
| chr9:21022597
|
A | G | 15 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0019others(12): Show | 38 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.270+3999T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022597 | ||||||
| chr9:21022638
|
T | TC | 233 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(230): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.270+3957_270+3958i others(3): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022638 | ||||||
| chr9:21022695
|
A | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(30): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.270+3901T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022695 | ||||||
| chr9:21022815
|
C | G | 5 | a0001c0001t0004g0106a0001c0001t0018g0035a0001c0001t0018g0104others(2): Show | 6 | HG02572.hp2 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+3781G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022815 | ||||||
| chr9:21022870
|
A | C | 115 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(112): Show | 192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+3726T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022870 | ||||||
| chr9:21022901
|
A | G | 8 | a0001c0001t0004g0008a0001c0001t0004g0126a0001c0001t0004g0129others(5): Show | 24 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+3695T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022901 | ||||||
| chr9:21022905
|
A | C | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.270+3691T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022905 | ||||||
| chr9:21023022
|
C | T | 3 | a0001c0001t0011g0094a0001c0001t0055g0165a0002c0002t0008g0189 | 3 | HG02451.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.270+3574G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023022 | ||||||
| chr9:21023052
|
G | C | 2 | a0001c0001t0002g0038a0001c0001t0003g0013 | 6 | HG00544.hp1 HG01993.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+3544C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023052 | ||||||
| chr9:21023090
|
C | G | 1 | a0002c0002t0001g0188 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+3506G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023090 | ||||||
| chr9:21023196
|
T | C | 2 | a0002c0002t0002g0216a0002c0002t0002g0217 | 2 | NA18983.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.270+3400A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023196 | ||||||
| chr9:21023265
|
A | C | 1 | a0002c0002t0004g0187 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.270+3331T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023265 | ||||||
| chr9:21023305
|
C | G | 34 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(31): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.270+3291G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023305 | ||||||
| chr9:21023447
|
C | T | 115 | a0001c0001t0002g0140a0001c0001t0006g0150a0001c0001t0019g0023others(112): Show | 192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+3149G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023447 | ||||||
| chr9:21023574
|
C | CT | 113 | a0001c0001t0002g0140a0001c0001t0003g0036a0001c0001t0003g0114others(110): Show | 191 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.270+3021dupA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023574 | ||||||
| chr9:21023612
|
T | C | 1 | a0002c0002t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.270+2984A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023612 | ||||||
| chr9:21023715
|
C | T | 1 | a0001c0001t0027g0066 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.270+2881G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023715 | ||||||
| chr9:21023737
|
G | C | 2 | a0001c0001t0006g0112a0001c0001t0006g0113 | 2 | HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.270+2859C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023737 | ||||||
| chr9:21023827
|
A | G | 233 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(230): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.270+2769T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023827 | ||||||
| chr9:21023926
|
G | C | 2 | a0002c0002t0001g0185a0002c0002t0001g0186 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.270+2670C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023926 | ||||||
| chr9:21023939
|
A | G | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.270+2657T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023939 | ||||||
| chr9:21024004
|
A | G | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+2592T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024004 | ||||||
| chr9:21024021
|
C | T | 1 | a0002c0002t0023g0232 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.270+2575G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024021 | ||||||
| chr9:21024065
|
C | T | 1 | a0001c0001t0003g0022 | 3 | NA18957.hp2 NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.270+2531G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024065 | ||||||
| chr9:21024104
|
T | C | 231 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(228): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.270+2492A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024104 | ||||||
| chr9:21024119
|
G | A | 2 | a0002c0002t0001g0223a0002c0002t0001g0246 | 2 | NA18950.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.270+2477C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024119 | ||||||
| chr9:21024223
|
A | T | 2 | a0002c0002t0001g0185a0002c0002t0001g0186 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.270+2373T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024223 | ||||||
| chr9:21024236
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.270+2360A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024236 | ||||||
| chr9:21024289
|
A | G | 2 | a0001c0001t0006g0112a0001c0001t0006g0113 | 2 | HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.270+2307T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024289 | ||||||
| chr9:21024295
|
T | C | 231 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(228): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.270+2301A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024295 | ||||||
| chr9:21024385
|
C | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+2211G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024385 | ||||||
| chr9:21024582
|
G | T | 2 | a0002c0002t0002g0183a0002c0002t0002g0184 | 2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.270+2014C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024582 | ||||||
| chr9:21024671
|
G | A | 114 | a0001c0001t0002g0140a0001c0001t0019g0023a0002c0002t0001g0001others(111): Show | 191 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.270+1925C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024671 | ||||||
| chr9:21024724
|
C | A | 38 | a0001c0001t0002g0097a0001c0001t0002g0162a0001c0001t0004g0008others(35): Show | 66 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.270+1872G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024724 | ||||||
| chr9:21024798
|
A | C | 1 | a0001c0001t0019g0023 | 3 | HG01074.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+1798T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024798 | ||||||
| chr9:21024852
|
G | A | 107 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(104): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.270+1744C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024852 | ||||||
| chr9:21024872
|
C | A | 1 | a0002c0002t0001g0044 | 2 | HG03704.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.270+1724G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024872 | ||||||
| chr9:21024881
|
T | A | 1 | a0001c0001t0005g0083 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.270+1715A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024881 | ||||||
| chr9:21024903
|
T | C | 10 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(7): Show | 12 | HG02071.hp2 HG03669.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+1693A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024903 | ||||||
| chr9:21024942
|
A | G | 230 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(227): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.270+1654T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024942 | ||||||
| chr9:21025157
|
A | G | 2 | a0001c0001t0004g0034a0001c0001t0004g0099 | 3 | HG02630.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.270+1439T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025157 | ||||||
| chr9:21025178
|
T | C | 232 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(229): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.270+1418A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025178 | ||||||
| chr9:21025334
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.270+1262T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025334 | ||||||
| chr9:21025409
|
A | ACATT | 115 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(112): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.270+1183_270+1186d others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025409 | ||||||
| chr9:21025703
|
C | G | 1 | a0001c0001t0005g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.270+893G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025703 | ||||||
| chr9:21026317
|
T | C | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.270+279A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026317 | ||||||
| chr9:21026362
|
T | G | 1 | a0002c0002t0002g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.270+234A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026362 | ||||||
| chr9:21026407
|
A | C | 1 | a0001c0001t0052g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+189T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026407 | ||||||
| chr9:21026541
|
G | T | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.270+55C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026541 | ||||||
| chr9:21026801
|
G | A | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.143-78C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026801 | ||||||
| chr9:21026881
|
C | A | 1 | a0001c0001t0012g0158 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.143-158G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026881 | ||||||
| chr9:21026894
|
C | G | 233 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(230): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.143-171G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026894 | ||||||
| chr9:21026948
|
G | A | 1 | a0002c0002t0001g0226 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.143-225C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026948 | ||||||
| chr9:21026982
|
C | G | 2 | a0001c0001t0020g0031a0001c0001t0020g0085 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.143-259G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026982 | ||||||
| chr9:21027003
|
A | G | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.143-280T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027003 | ||||||
| chr9:21027208
|
T | C | 2 | a0001c0001t0012g0157a0001c0001t0012g0158 | 2 | NA19081.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.143-485A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027208 | ||||||
| chr9:21027265
|
C | T | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.143-542G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027265 | ||||||
| chr9:21027299
|
G | C | 4 | a0001c0001t0002g0095a0001c0001t0003g0107a0001c0001t0011g0094others(1): Show | 4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-576C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027299 | ||||||
| chr9:21027321
|
C | A | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.143-598G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027321 | ||||||
| chr9:21027366
|
G | C | 3 | a0001c0001t0014g0012a0001c0001t0014g0021a0001c0001t0014g0110 | 8 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-643C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027366 | ||||||
| chr9:21027434
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.143-711C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027434 | ||||||
| chr9:21027516
|
G | A | 4 | a0001c0001t0003g0011a0001c0001t0003g0047a0001c0001t0003g0178others(1): Show | 9 | NA18964.hp2 NA18973.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-793C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027516 | ||||||
| chr9:21027520
|
G | C | 4 | a0001c0001t0002g0095a0001c0001t0003g0107a0001c0001t0011g0094others(1): Show | 4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-797C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027520 | ||||||
| chr9:21027742
|
A | G | 117 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(114): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.143-1019T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027742 | ||||||
| chr9:21027772
|
T | G | 2 | a0002c0002t0001g0057a0003c0007t0001g0228 | 3 | HG02129.hp1 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.143-1049A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027772 | ||||||
| chr9:21027790
|
T | C | 1 | a0002c0002t0002g0229 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-1067A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027790 | ||||||
| chr9:21027801
|
T | A | 1 | a0002c0002t0001g0230 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.143-1078A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027801 | ||||||
| chr9:21027816
|
G | T | 78 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(75): Show | 142 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.143-1093C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027816 | ||||||
| chr9:21027856
|
C | T | 2 | a0001c0001t0002g0095a0001c0001t0011g0094 | 2 | HG01123.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.143-1133G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027856 | ||||||
| chr9:21027909
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.143-1186G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027909 | ||||||
| chr9:21028003
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.143-1280G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028003 | ||||||
| chr9:21028072
|
T | A | 3 | a0002c0002t0001g0018a0002c0002t0001g0247a0002c0002t0043g0231 | 6 | HG01346.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+1223A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028072 | ||||||
| chr9:21028119
|
G | A | 1 | a0001c0001t0019g0023 | 3 | HG01074.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.142+1176C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028119 | ||||||
| chr9:21028135
|
C | CA | 141 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0095others(138): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.142+1159dupT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028135 | ||||||
| chr9:21028135
|
C | CAA | 8 | a0001c0001t0005g0084a0001c0001t0020g0085a0002c0002t0001g0235others(5): Show | 9 | HG02615.hp1 HG02615.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1158_142+1159d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028135 | ||||||
| chr9:21028162
|
A | G | 1 | a0002c0002t0001g0181 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.142+1133T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028162 | ||||||
| chr9:21028169
|
A | G | 1 | a0002c0002t0001g0048 | 2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.142+1126T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028169 | ||||||
| chr9:21028333
|
A | C | 2 | a0001c0001t0006g0163a0001c0001t0006g0164 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142+962T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028333 | ||||||
| chr9:21028362
|
T | G | 1 | a0002c0002t0008g0236 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.142+933A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028362 | ||||||
| chr9:21028471
|
G | A | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.142+824C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028471 | ||||||
| chr9:21028536
|
C | G | 79 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(76): Show | 143 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.142+759G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028536 | ||||||
| chr9:21028541
|
C | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0156a0001c0001t0012g0157others(4): Show | 9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+754G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028541 | ||||||
| chr9:21028637
|
C | T | 113 | a0002c0002t0001g0001a0002c0002t0001g0017a0002c0002t0001g0018others(110): Show | 188 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.142+658G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028637 | ||||||
| chr9:21028670
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.142+625G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028670 | ||||||
| chr9:21028782
|
C | CTA | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0019g0023 | 5 | HG01074.hp2 HG01243.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+511_142+512dup others(2): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028782 | ||||||
| chr9:21028851
|
G | T | 2 | a0001c0001t0002g0095a0001c0001t0011g0094 | 2 | HG01123.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.142+444C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028851 | ||||||
| chr9:21029067
|
C | G | 1 | a0002c0002t0026g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142+228G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21029067 | ||||||
| chr9:21029239
|
T | A | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.142+56A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21029239 | ||||||
| chr9:21029494
|
G | A | 3 | a0001c0001t0018g0035a0001c0001t0018g0104a0001c0001t0052g0105 | 4 | HG02572.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-96C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029494 | ||||||
| chr9:21029626
|
G | C | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.39-228C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029626 | ||||||
| chr9:21029688
|
A | G | 1 | a0002c0002t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.39-290T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029688 | ||||||
| chr9:21029707
|
C | T | 4 | a0001c0001t0002g0095a0001c0001t0003g0107a0001c0001t0011g0094others(1): Show | 4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-309G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029707 | ||||||
| chr9:21029803
|
G | C | 72 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(69): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.39-405C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029803 | ||||||
| chr9:21029834
|
T | C | 1 | a0002c0002t0001g0237 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.39-436A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029834 | ||||||
| chr9:21029841
|
G | A | 4 | a0001c0001t0002g0095a0001c0001t0003g0107a0001c0001t0011g0094others(1): Show | 4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-443C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029841 | ||||||
| chr9:21029864
|
C | T | 232 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(229): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.39-466G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029864 | ||||||
| chr9:21029877
|
C | T | 65 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(62): Show | 121 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.39-479G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029877 | ||||||
| chr9:21029963
|
T | A | 2 | a0002c0002t0022g0238a0002c0002t0022g0239 | 2 | HG02135.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.39-565A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029963 | ||||||
| chr9:21030093
|
G | T | 6 | a0002c0002t0001g0172a0002c0002t0009g0006a0002c0002t0009g0168others(3): Show | 15 | NA18944.hp2 NA18945.hp1 NA18955.hp2 others(12): Show |
intron_variant | MODIFIER | c.39-695C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030093 | ||||||
| chr9:21030094
|
C | T | 6 | a0002c0002t0001g0172a0002c0002t0009g0006a0002c0002t0009g0168others(3): Show | 15 | NA18944.hp2 NA18945.hp1 NA18955.hp2 others(12): Show |
intron_variant | MODIFIER | c.39-696G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030094 | ||||||
| chr9:21030166
|
C | T | 106 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(103): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.39-768G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030166 | ||||||
| chr9:21030182
|
T | C | 1 | a0001c0001t0055g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.39-784A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030182 | ||||||
| chr9:21030269
|
C | CA | 112 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0003g0011others(109): Show | 195 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.39-872dupT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030269 | ||||||
| chr9:21030269
|
C | CAA | 14 | a0001c0001t0002g0095a0001c0001t0003g0107a0001c0001t0003g0240others(11): Show | 16 | HG00642.hp2 HG01123.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.39-873_39-872dupTT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030269 | ||||||
| chr9:21030269
|
CA | C | 49 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(46): Show | 103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.39-872delT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030269 | ||||||
| chr9:21030284
|
A | C | 1 | a0002c0002t0002g0167 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.39-886T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030284 | ||||||
| chr9:21030387
|
A | T | 2 | a0001c0001t0006g0150a0001c0001t0019g0023 | 4 | HG01074.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.39-989T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030387 | ||||||
| chr9:21030483
|
C | A | 1 | a0002c0002t0001g0248 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.38+1070G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030483 | ||||||
| chr9:21030691
|
C | A | 73 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(70): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.38+862G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030691 | ||||||
| chr9:21030733
|
T | C | 2 | a0002c0002t0011g0249a0002c0002t0050g0250 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.38+820A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030733 | ||||||
| chr9:21030769
|
G | A | 2 | a0001c0001t0006g0150a0001c0001t0019g0023 | 4 | HG01074.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.38+784C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030769 | ||||||
| chr9:21030821
|
C | G | 1 | a0004c0008t0002g0166 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.38+732G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030821 | ||||||
| chr9:21030824
|
A | G | 2 | a0001c0001t0006g0150a0001c0001t0019g0023 | 4 | HG01074.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.38+729T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030824 | ||||||
| chr9:21030852
|
G | A | 120 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0003g0011others(117): Show | 200 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.38+701C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030852 | ||||||
| chr9:21030908
|
G | C | 73 | a0001c0001t0002g0038a0001c0001t0002g0097a0001c0001t0002g0117others(70): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.38+645C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030908 | ||||||
| chr9:21030936
|
T | G | 1 | a0001c0001t0012g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.38+617A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030936 | ||||||
| chr9:21030996
|
T | A | 2 | a0002c0002t0002g0148a0002c0002t0002g0149 | 2 | NA18952.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.38+557A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030996 | ||||||
| chr9:21031116
|
C | T | 29 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0005g0005others(26): Show | 55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.38+437G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031116 | ||||||
| chr9:21031153
|
C | A | 122 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0003g0011others(119): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.38+400G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031153 | ||||||
| chr9:21031154
|
G | C | 191 | a0001c0001t0002g0038a0001c0001t0002g0095a0001c0001t0002g0097others(188): Show | 328 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.38+399C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031154 | ||||||
| chr9:21031264
|
G | C | 1 | a0002c0002t0002g0061 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.38+289C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031264 | ||||||
| chr9:21031353
|
C | A | 3 | a0001c0001t0014g0012a0001c0001t0014g0021a0001c0001t0014g0110 | 8 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.38+200G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031353 | ||||||
| chr9:21031455
|
C | T | 1 | a0001c0001t0017g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.38+98G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031455 | ||||||
| chr9:21031472
|
C | A | 55 | a0001c0001t0002g0038a0001c0001t0002g0117a0001c0001t0002g0123others(52): Show | 105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.38+81G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031472 | ||||||
| chr9:21031480
|
C | T | 118 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0002g0038others(115): Show | 204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.38+73G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031480 |