Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2180 |
|---|---|
| ensemblid | ENSG00000151726.16 |
| hgncid | 3569 |
| symbol | ACSL1 |
| name | acyl-CoA synthetase long chain family member 1 |
| refseq_nuc | NM_001995.5 |
| refseq_prot | NP_001986.2 |
| ensembl_nuc | ENST00000281455.7 |
| ensembl_prot | ENSP00000281455.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 184755595 |
| end | 184825968 |
| strand | - |
| ver | v1.2 |
| region | chr4:184755595-184825968 |
| region5000 | chr4:184750595-184830968 |
| regionname0 | ACSL1_chr4_184755595_184825968 |
| regionname5000 | ACSL1_chr4_184750595_184830968 |
| 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 | 698 | 390 | 95 | 71 | 166 | 14 | 42 | 130 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0002 | 0/0 | 698 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0003 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| 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 | 0/0 | 2097 | 241 | 68 | 36 | 106 | 10 | 21 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0002 | 0/1 | 2097 | 73 | 18 | 10 | 34 | 2 | 8 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0003 | 0/0 | 2097 | 42 | 3 | 13 | 14 | 2 | 10 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0004 | 0/0 | 2097 | 12 | 0 | 7 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0005 | 1/0 | 2097 | 9 | 4 | 0 | 2 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0006 | 0/0 | 2097 | 5 | 0 | 0 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0007 | 0/0 | 2097 | 3 | 2 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0008 | 0/0 | 2097 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0009 | 0/0 | 2097 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0010 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0011 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| c0012 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| 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 | 1616 | 166 | 30 | 20 | 98 | 5 | 13 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0002 | 0/1 | 1616 | 143 | 55 | 22 | 49 | 4 | 12 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0003 | 0/0 | 1616 | 45 | 4 | 13 | 16 | 3 | 9 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0004 | 0/0 | 1616 | 26 | 2 | 15 | 0 | 2 | 7 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0005 | 0/0 | 1616 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0006 | 1/0 | 1616 | 2 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0007 | 0/0 | 1616 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0008 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0009 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0010 | 0/0 | 1616 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0011 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0012 | 0/0 | 1616 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0013 | 0/0 | 1616 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| t0014 | 0/0 | 1616 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| 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 | 0/0 | 2097 | 241 | 68 | 36 | 106 | 10 | 21 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0002 | 0/1 | 2097 | 73 | 18 | 10 | 34 | 2 | 8 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0003 | 0/0 | 2097 | 42 | 3 | 13 | 14 | 2 | 10 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0004 | 0/0 | 2097 | 12 | 0 | 7 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005 | 1/0 | 2097 | 9 | 4 | 0 | 2 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0006 | 0/0 | 2097 | 5 | 0 | 0 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0007 | 0/0 | 2097 | 3 | 2 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0008 | 0/0 | 2097 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0009 | 0/0 | 2097 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0010 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0002c0011 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0003c0012 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3712 | 151 | 30 | 12 | 93 | 5 | 11 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0002 | 0/0 | 3712 | 60 | 35 | 10 | 10 | 2 | 3 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0003 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0004 | 0/0 | 3712 | 23 | 2 | 12 | 0 | 2 | 7 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0005 | 0/0 | 3712 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0008 | 0/0 | 3712 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0009 | 0/0 | 3712 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0010 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0001t0011 | 0/0 | 3712 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0002t0002 | 0/1 | 3712 | 71 | 17 | 9 | 34 | 2 | 8 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0002t0004 | 0/0 | 3712 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0002t0007 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0003t0003 | 0/0 | 3712 | 41 | 3 | 13 | 14 | 2 | 9 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0003t0013 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0004t0001 | 0/0 | 3712 | 12 | 0 | 7 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005t0001 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005t0002 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005t0003 | 0/0 | 3712 | 3 | 1 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005t0006 | 1/0 | 3712 | 2 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005t0012 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0005t0014 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0006t0002 | 0/0 | 3712 | 5 | 0 | 0 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0007t0002 | 0/0 | 3712 | 3 | 2 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0008t0004 | 0/0 | 3712 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0009t0002 | 0/0 | 3712 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0001c0010t0001 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0002c0011t0001 | 0/0 | 3712 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| a0003c0012t0002 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | copy fasta | chr4 | 184750595 | 184830968 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0009g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0007g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0013g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0006g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0007t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0007t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0007t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0008t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0008t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0009t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0009t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0010t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0002c0011t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0003c0012t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0204 | EUR | GBR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0074 | EUR | GBR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0267 | EUR | FIN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0099 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0273 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00639 | hp1 | a0001 | c0009 | t0002 | g0142 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00639 | hp2 | a0001 | c0008 | t0004 | g0304 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0260 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0055 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0059 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00733 | hp1 | a0001 | c0008 | t0004 | g0313 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00738 | hp1 | a0002 | c0011 | t0001 | g0337 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00738 | hp2 | a0001 | c0009 | t0002 | g0090 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0318 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0366 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0331 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0319 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0297 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0330 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0321 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01081 | hp2 | a0001 | c0007 | t0002 | g0156 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0203 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0281 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0217 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0365 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0317 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0364 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0143 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01257 | hp1 | a0001 | c0003 | t0003 | g0284 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0144 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0283 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0271 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0363 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0320 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0347 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0032 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0240 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0352 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01891 | hp1 | a0001 | c0005 | t0003 | g0223 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0355 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0106 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0272 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0291 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0250 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02015 | hp2 | a0001 | c0005 | t0003 | g0266 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0275 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02040 | hp2 | a0001 | c0005 | t0003 | g0046 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02055 | hp1 | a0001 | c0003 | t0003 | g0182 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0274 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0282 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02258 | hp2 | a0003 | c0012 | t0002 | g0152 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02451 | hp1 | a0001 | c0007 | t0002 | g0155 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0362 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02602 | hp1 | a0001 | c0005 | t0002 | g0295 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0357 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0373 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0008 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0206 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02723 | hp2 | a0001 | c0005 | t0006 | g0231 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0335 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0374 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0361 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0244 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03017 | hp2 | a0001 | c0010 | t0001 | g0311 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0375 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0372 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03209 | hp1 | a0001 | c0005 | t0014 | g0153 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0268 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0310 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03516 | hp1 | a0001 | c0002 | t0007 | g0356 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0245 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0344 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0008 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03831 | hp1 | a0001 | c0003 | t0013 | g0269 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03831 | hp2 | a0001 | c0003 | t0003 | g0285 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03834 | hp1 | a0001 | c0003 | t0003 | g0270 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0052 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0338 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0314 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0296 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0302 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0343 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0148 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0353 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0349 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18950 | hp2 | a0001 | c0003 | t0003 | g0236 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18965 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18966 | hp2 | a0001 | c0003 | t0003 | g0308 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18973 | hp2 | a0001 | c0006 | t0002 | g0033 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18979 | hp1 | a0001 | c0006 | t0002 | g0205 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18984 | hp1 | a0001 | c0001 | t0009 | g0350 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0306 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0022 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0237 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19005 | hp1 | a0001 | c0006 | t0002 | g0086 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19010 | hp1 | a0001 | c0003 | t0003 | g0096 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19030 | hp2 | a0001 | c0007 | t0002 | g0154 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0025 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19056 | hp1 | a0001 | c0006 | t0002 | g0253 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0062 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19068 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19075 | hp1 | a0001 | c0003 | t0003 | g0307 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19076 | hp2 | a0001 | c0006 | t0002 | g0298 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ASW | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0329 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0145 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0041 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0346 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0323 | SAS | GIH | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0360 | SAS | GIH | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0312 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03471 | hp1 | a0001 | c0005 | t0012 | g0151 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0371 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20300 | hp2 | a0001 | c0003 | t0003 | g0358 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0243 | REF | REF | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0006 | g0215 | REF | REF | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184773859
|
T | A | 1 | a0002 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.773A>T | p.Asn258Ile | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 8/21 | 858/3712 | 773/2097 | 258/698 | chr4 | 184773859 | ||
| chr4:184776913
|
T | C | 1 | a0003 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.548A>G | p.Asn183Ser | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 6/21 | 633/3712 | 548/2097 | 183/698 | chr4 | 184776913 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184757686
|
G | A | 1 | a0001c0006 | 5 | NA18973.hp2 NA18979.hp1 NA19005.hp1 others(2): Show |
synonymous_variant | LOW | c.1905C>T | p.Leu635Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/21 | 1990/3712 | 1905/2097 | 635/698 | chr4 | 184757686 | ||
| chr4:184760360
|
C | A | 1 | a0001c0008 | 2 | HG00639.hp2 HG00733.hp1 |
synonymous_variant | LOW | c.1779G>T | p.Leu593Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/21 | 1864/3712 | 1779/2097 | 593/698 | chr4 | 184760360 | ||
| chr4:184762473
|
C | T | 1 | a0001c0007 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1572G>A | p.Ala524Ala | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/21 | 1657/3712 | 1572/2097 | 524/698 | chr4 | 184762473 | ||
| chr4:184764878
|
C | T | 10 | a0001c0001a0001c0002a0001c0004others(7): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(338): Show |
synonymous_variant | LOW | c.1407G>A | p.Leu469Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/21 | 1492/3712 | 1407/2097 | 469/698 | chr4 | 184764878 | ||
| chr4:184764911
|
G | A | 1 | a0001c0009 | 2 | HG00639.hp1 HG00738.hp2 |
synonymous_variant | LOW | c.1374C>T | p.Tyr458Tyr | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/21 | 1459/3712 | 1374/2097 | 458/698 | chr4 | 184764911 | ||
| chr4:184765975
|
G | A | 2 | a0001c0004a0002c0011 | 13 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(10): Show |
synonymous_variant | LOW | c.1275C>T | p.Gly425Gly | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/21 | 1360/3712 | 1275/2097 | 425/698 | chr4 | 184765975 | ||
| chr4:184766709
|
A | G | 5 | a0001c0002a0001c0006a0001c0008others(2): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(80): Show |
synonymous_variant | LOW | c.1176T>C | p.Phe392Phe | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/21 | 1261/3712 | 1176/2097 | 392/698 | chr4 | 184766709 | ||
| chr4:184766717
|
A | G | 1 | a0001c0010 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1168T>C | p.Leu390Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/21 | 1253/3712 | 1168/2097 | 390/698 | chr4 | 184766717 | ||
| chr4:184780395
|
G | T | 1 | a0001c0003 | 42 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
synonymous_variant | LOW | c.414C>A | p.Ile138Ile | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/21 | 499/3712 | 414/2097 | 138/698 | chr4 | 184780395 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184755898
|
G | T | 1 | a0001c0001t0010 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1227C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 1227 | chr4 | 184755898 | |||||
| chr4:184755983
|
A | G | 1 | a0001c0001t0009 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 1142 | chr4 | 184755983 | |||||
| chr4:184756209
|
T | C | 3 | a0001c0001t0004a0001c0002t0004a0001c0008t0004 | 26 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*916A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 916 | chr4 | 184756209 | |||||
| chr4:184756267
|
C | T | 4 | a0001c0001t0003a0001c0003t0003a0001c0003t0013others(1): Show | 46 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*858G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 858 | chr4 | 184756267 | |||||
| chr4:184756431
|
C | T | 1 | a0001c0001t0008 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 694 | chr4 | 184756431 | |||||
| chr4:184756434
|
G | A | 1 | a0001c0003t0013 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 691 | chr4 | 184756434 | |||||
| chr4:184756710
|
T | G | 1 | a0001c0001t0005 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*415A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 415 | chr4 | 184756710 | |||||
| chr4:184756798
|
G | A | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
3_prime_UTR_variant | MODIFIER | c.*327C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 327 | chr4 | 184756798 | |||||
| chr4:184756927
|
T | C | 1 | a0001c0001t0011 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 198 | chr4 | 184756927 | |||||
| chr4:184756956
|
A | G | 10 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(7): Show | 172 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 169 | chr4 | 184756956 | |||||
| chr4:184756964
|
C | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 161 | chr4 | 184756964 | |||||
| chr4:184757007
|
T | C | 1 | a0001c0005t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*118A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 118 | chr4 | 184757007 | |||||
| chr4:184757029
|
C | T | 1 | a0001c0002t0007 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 96 | chr4 | 184757029 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184757336
|
T | C | 4 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 5 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1957-71A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/20 | chr4 | 184757336 | ||||||
| chr4:184757402
|
A | C | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1957-137T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/20 | chr4 | 184757402 | ||||||
| chr4:184757439
|
G | T | 1 | a0001c0003t0003g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1957-174C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/20 | chr4 | 184757439 | ||||||
| chr4:184757937
|
T | C | 12 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(9): Show | 12 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1783-17A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184757937 | ||||||
| chr4:184758022
|
A | G | 1 | a0001c0001t0001g0327 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1783-102T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758022 | ||||||
| chr4:184758053
|
A | AC | 11 | a0001c0001t0001g0039a0001c0001t0001g0110a0001c0001t0001g0124others(8): Show | 11 | NA18747.hp1 NA18940.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.1783-134dupG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758053 | ||||||
| chr4:184758185
|
C | T | 150 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0354others(147): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1783-265G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758185 | ||||||
| chr4:184758263
|
A | T | 1 | a0001c0001t0011g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1783-343T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758263 | ||||||
| chr4:184758314
|
G | T | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1783-394C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758314 | ||||||
| chr4:184758352
|
C | T | 2 | a0001c0005t0012g0151a0001c0005t0014g0153 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1783-432G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758352 | ||||||
| chr4:184758353
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1783-433C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758353 | ||||||
| chr4:184758469
|
C | T | 54 | a0001c0001t0001g0015a0001c0001t0001g0173a0001c0001t0001g0214others(51): Show | 58 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1783-549G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758469 | ||||||
| chr4:184758509
|
C | CT | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1783-590dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758509 | ||||||
| chr4:184758522
|
C | G | 14 | a0001c0001t0004g0044a0001c0001t0004g0140a0001c0001t0004g0141others(11): Show | 14 | HG00735.hp1 HG01106.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1783-602G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758522 | ||||||
| chr4:184758661
|
G | A | 25 | a0001c0001t0004g0044a0001c0001t0004g0140a0001c0001t0004g0141others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1783-741C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758661 | ||||||
| chr4:184758684
|
T | C | 4 | a0001c0002t0002g0032a0001c0002t0002g0130a0001c0009t0002g0090others(1): Show | 4 | HG00639.hp1 HG00738.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783-764A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758684 | ||||||
| chr4:184758757
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1783-837T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758757 | ||||||
| chr4:184758775
|
T | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(150): Show | 162 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.1783-855A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758775 | ||||||
| chr4:184758819
|
G | T | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1783-899C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758819 | ||||||
| chr4:184758836
|
G | C | 43 | a0001c0001t0003g0352a0001c0003t0003g0003a0001c0003t0003g0008others(40): Show | 45 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1783-916C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758836 | ||||||
| chr4:184759003
|
G | GT | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1783-1084dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759003 | ||||||
| chr4:184759012
|
C | G | 1 | a0001c0001t0002g0226 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1783-1092G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759012 | ||||||
| chr4:184759036
|
A | G | 4 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0322others(1): Show | 4 | HG01081.hp1 HG01243.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1783-1116T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759036 | ||||||
| chr4:184759193
|
G | C | 5 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0045others(2): Show | 5 | HG00741.hp1 HG02027.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1782+1164C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759193 | ||||||
| chr4:184759397
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1782+960C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759397 | ||||||
| chr4:184759409
|
A | G | 25 | a0001c0001t0004g0044a0001c0001t0004g0140a0001c0001t0004g0141others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1782+948T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759409 | ||||||
| chr4:184759412
|
G | A | 51 | a0001c0001t0001g0354a0001c0001t0002g0011a0001c0001t0002g0016others(48): Show | 54 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1782+945C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759412 | ||||||
| chr4:184759711
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 62 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1782+646A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759711 | ||||||
| chr4:184760279
|
A | G | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1782+78T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184760279 | ||||||
| chr4:184760296
|
C | T | 7 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0160others(4): Show | 7 | HG01975.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1782+61G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184760296 | ||||||
| chr4:184760321
|
G | C | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1782+36C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184760321 | ||||||
| chr4:184760599
|
T | C | 11 | a0001c0001t0004g0344a0001c0001t0004g0346a0001c0001t0004g0347others(8): Show | 11 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639-99A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184760599 | ||||||
| chr4:184760966
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0124a0001c0001t0001g0288 | 3 | NA18940.hp2 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1639-466C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184760966 | ||||||
| chr4:184761029
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1639-529T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761029 | ||||||
| chr4:184761099
|
C | T | 7 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0160others(4): Show | 7 | HG01975.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-599G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761099 | ||||||
| chr4:184761119
|
A | C | 1 | a0001c0001t0001g0238 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1639-619T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761119 | ||||||
| chr4:184761166
|
C | T | 5 | a0001c0002t0002g0018a0001c0002t0002g0049a0001c0002t0002g0050others(2): Show | 5 | HG00438.hp2 HG00558.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1639-666G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761166 | ||||||
| chr4:184761240
|
A | T | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1639-740T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761240 | ||||||
| chr4:184761413
|
A | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(248): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1639-913T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761413 | ||||||
| chr4:184761461
|
A | C | 46 | a0001c0001t0003g0352a0001c0003t0003g0003a0001c0003t0003g0008others(43): Show | 48 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1638+946T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761461 | ||||||
| chr4:184761480
|
A | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1638+927T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761480 | ||||||
| chr4:184761540
|
A | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(263): Show | 278 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.1638+867T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761540 | ||||||
| chr4:184761672
|
C | A | 1 | a0001c0004t0001g0275 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1638+735G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761672 | ||||||
| chr4:184761783
|
T | C | 4 | a0001c0002t0002g0063a0001c0002t0002g0064a0001c0002t0002g0068others(1): Show | 4 | NA18612.hp2 NA18962.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638+624A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761783 | ||||||
| chr4:184761820
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638+587T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761820 | ||||||
| chr4:184761956
|
G | A | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1638+451C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761956 | ||||||
| chr4:184762083
|
C | T | 3 | a0001c0001t0002g0160a0001c0001t0002g0373a0001c0001t0002g0374 | 3 | HG02486.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1638+324G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762083 | ||||||
| chr4:184762084
|
G | A | 14 | a0001c0001t0004g0044a0001c0001t0004g0140a0001c0001t0004g0141others(11): Show | 14 | HG00735.hp1 HG01106.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638+323C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762084 | ||||||
| chr4:184762126
|
C | T | 12 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(9): Show | 12 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638+281G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762126 | ||||||
| chr4:184762131
|
C | CA | 25 | a0001c0001t0001g0078a0001c0001t0001g0279a0001c0001t0001g0327others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1638+275dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762131 | ||||||
| chr4:184762131
|
C | CAA | 7 | a0001c0001t0001g0354a0001c0001t0002g0011a0001c0001t0002g0016others(4): Show | 8 | HG00733.hp2 HG01358.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638+274_1638+275d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762131 | ||||||
| chr4:184762236
|
ACCCTGTC | A | 5 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 6 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638+164_1638+170d others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762236 | ||||||
| chr4:184762238
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638+169G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762238 | ||||||
| chr4:184762596
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1522-73A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762596 | ||||||
| chr4:184762686
|
A | G | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(370): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.1522-163T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762686 | ||||||
| chr4:184762790
|
C | G | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1522-267G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762790 | ||||||
| chr4:184762791
|
G | A | 44 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0017others(41): Show | 45 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1522-268C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762791 | ||||||
| chr4:184762856
|
G | A | 1 | a0001c0001t0004g0146 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1521+311C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762856 | ||||||
| chr4:184762974
|
G | T | 1 | a0001c0010t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1521+193C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762974 | ||||||
| chr4:184763093
|
T | C | 25 | a0001c0001t0004g0044a0001c0001t0004g0140a0001c0001t0004g0141others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1521+74A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184763093 | ||||||
| chr4:184763123
|
C | A | 1 | a0001c0007t0002g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1521+44G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184763123 | ||||||
| chr4:184763840
|
A | G | 2 | a0001c0005t0012g0151a0001c0005t0014g0153 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1433-585T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184763840 | ||||||
| chr4:184763946
|
CTG | C | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-693_1433-692d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184763946 | ||||||
| chr4:184763989
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1433-734T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184763989 | ||||||
| chr4:184764091
|
T | G | 1 | a0003c0012t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432+762A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764091 | ||||||
| chr4:184764109
|
C | T | 1 | a0001c0006t0002g0033 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1432+744G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764109 | ||||||
| chr4:184764203
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1432+650G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764203 | ||||||
| chr4:184764226
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1432+627A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764226 | ||||||
| chr4:184764453
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(155): Show | 168 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.1432+400T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764453 | ||||||
| chr4:184764568
|
T | C | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432+285A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764568 | ||||||
| chr4:184764651
|
C | T | 2 | a0001c0001t0005g0330a0001c0001t0005g0331 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1432+202G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764651 | ||||||
| chr4:184765498
|
G | A | 94 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0002g0004others(91): Show | 97 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1359+393C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765498 | ||||||
| chr4:184765513
|
G | A | 6 | a0001c0003t0003g0143a0001c0003t0003g0144a0001c0003t0003g0319others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1359+378C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765513 | ||||||
| chr4:184765634
|
T | C | 5 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 6 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1359+257A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765634 | ||||||
| chr4:184765653
|
C | T | 1 | a0001c0002t0002g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1359+238G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765653 | ||||||
| chr4:184765702
|
C | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(324): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1359+189G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765702 | ||||||
| chr4:184765735
|
T | C | 15 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0160others(12): Show | 15 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1359+156A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765735 | ||||||
| chr4:184765794
|
A | AAC | 9 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0017others(6): Show | 10 | HG00735.hp1 HG01358.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1359+95_1359+96dup others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765794 | ||||||
| chr4:184766079
|
C | T | 79 | a0001c0001t0002g0004a0001c0001t0002g0030a0001c0001t0002g0093others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1264-93G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766079 | ||||||
| chr4:184766201
|
A | G | 15 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0160others(12): Show | 15 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-215T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766201 | ||||||
| chr4:184766219
|
A | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(173): Show | 186 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.1264-233T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766219 | ||||||
| chr4:184766366
|
C | T | 12 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0354others(9): Show | 14 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1263+256G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766366 | ||||||
| chr4:184766430
|
A | G | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1263+192T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766430 | ||||||
| chr4:184766533
|
A | C | 83 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0016others(80): Show | 87 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1263+89T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766533 | ||||||
| chr4:184766590
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1263+32G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766590 | ||||||
| chr4:184766764
|
G | A | 1 | a0001c0003t0003g0268 | 1 | HG03239.hp2 | splice_region_variant&intron_variant | LOW | c.1129-8C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766764 | ||||||
| chr4:184766898
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1129-142C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766898 | ||||||
| chr4:184766938
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1129-182C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766938 | ||||||
| chr4:184766994
|
T | C | 5 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 6 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-238A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766994 | ||||||
| chr4:184767118
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1129-362G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767118 | ||||||
| chr4:184767139
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1129-383C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767139 | ||||||
| chr4:184767283
|
C | CA | 80 | a0001c0001t0001g0229a0001c0001t0002g0004a0001c0001t0002g0016others(77): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1129-528dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767283 | ||||||
| chr4:184767283
|
CA | C | 30 | a0001c0001t0001g0168a0001c0001t0001g0251a0001c0001t0002g0092others(27): Show | 30 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1129-528delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767283 | ||||||
| chr4:184767447
|
A | C | 1 | a0001c0002t0002g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1129-691T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767447 | ||||||
| chr4:184767494
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1129-738C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767494 | ||||||
| chr4:184767497
|
G | A | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1129-741C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767497 | ||||||
| chr4:184767600
|
C | T | 42 | a0001c0003t0003g0003a0001c0003t0003g0008a0001c0003t0003g0022others(39): Show | 44 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1128+716G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767600 | ||||||
| chr4:184767825
|
G | A | 1 | a0001c0001t0004g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1128+491C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767825 | ||||||
| chr4:184768013
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 178 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.1128+303C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768013 | ||||||
| chr4:184768065
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0157a0001c0001t0002g0218 | 4 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+251C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768065 | ||||||
| chr4:184768195
|
C | T | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+121G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768195 | ||||||
| chr4:184768221
|
G | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0336 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1128+95C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768221 | ||||||
| chr4:184768678
|
C | A | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.994-228G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768678 | ||||||
| chr4:184768711
|
G | A | 4 | a0001c0004t0001g0043a0001c0004t0001g0273a0001c0004t0001g0274others(1): Show | 4 | HG00609.hp2 HG02040.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.994-261C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768711 | ||||||
| chr4:184768730
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.994-280C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768730 | ||||||
| chr4:184768737
|
A | G | 1 | a0001c0003t0003g0338 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.994-287T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768737 | ||||||
| chr4:184768798
|
G | A | 26 | a0001c0001t0003g0352a0001c0001t0004g0044a0001c0001t0004g0140others(23): Show | 26 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.994-348C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768798 | ||||||
| chr4:184768833
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 178 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.994-383C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768833 | ||||||
| chr4:184769070
|
A | AAT | 21 | a0001c0001t0001g0329a0001c0001t0002g0160a0001c0001t0002g0161others(18): Show | 22 | HG00733.hp2 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.994-622_994-621dup others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATAT | 48 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0017others(45): Show | 50 | HG00099.hp1 HG00558.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.994-624_994-621dup others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATATAT | 14 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0045others(11): Show | 14 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.994-626_994-621dup others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATATATA others(1): Show |
11 | a0001c0002t0002g0032a0001c0002t0002g0053a0001c0002t0002g0060others(8): Show | 11 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.994-628_994-621dup others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATATATA others(3): Show |
2 | a0001c0002t0002g0054a0001c0002t0002g0056 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.994-630_994-621dup others(10): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATATATA others(7): Show |
1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.994-634_994-621dup others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATATATA others(19): Show |
1 | a0001c0001t0002g0218 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.994-621_994-620ins others(26): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
A | AATATATA others(21): Show |
1 | a0001c0001t0002g0011 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.994-621_994-620ins others(28): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
AAT | A | 17 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0169others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.994-622_994-621del others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
AATAT | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(199): Show | 212 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(209): Show |
intron_variant | MODIFIER | c.994-624_994-621del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769070
|
AATATAT | A | 49 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0354others(46): Show | 52 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.994-626_994-621del others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | ||||||
| chr4:184769112
|
A | G | 6 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0085others(3): Show | 6 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-662T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769112 | ||||||
| chr4:184769177
|
C | T | 31 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(28): Show | 31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.994-727G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769177 | ||||||
| chr4:184769249
|
G | A | 1 | a0001c0006t0002g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.994-799C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769249 | ||||||
| chr4:184769285
|
A | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 15 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.994-835T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769285 | ||||||
| chr4:184769438
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.993+961C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769438 | ||||||
| chr4:184769447
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 178 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.993+952T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769447 | ||||||
| chr4:184769859
|
A | G | 6 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0085others(3): Show | 6 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+540T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769859 | ||||||
| chr4:184770002
|
G | A | 1 | a0001c0005t0012g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.993+397C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770002 | ||||||
| chr4:184770051
|
T | C | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.993+348A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770051 | ||||||
| chr4:184770260
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.993+139T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770260 | ||||||
| chr4:184770361
|
T | C | 27 | a0001c0001t0001g0329a0001c0001t0002g0088a0001c0001t0002g0150others(24): Show | 27 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.993+38A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770361 | ||||||
| chr4:184770541
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0299a0001c0001t0001g0300 | 4 | NA18943.hp1 NA18964.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-65G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770541 | ||||||
| chr4:184770654
|
T | C | 1 | a0001c0003t0003g0260 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.916-178A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770654 | ||||||
| chr4:184770719
|
A | T | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.916-243T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770719 | ||||||
| chr4:184770729
|
G | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-253C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770729 | ||||||
| chr4:184770734
|
C | T | 42 | a0001c0003t0003g0003a0001c0003t0003g0008a0001c0003t0003g0022others(39): Show | 44 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.916-258G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770734 | ||||||
| chr4:184770809
|
C | A | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.916-333G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770809 | ||||||
| chr4:184770824
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.916-348T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770824 | ||||||
| chr4:184771007
|
C | G | 1 | a0001c0002t0002g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.916-531G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771007 | ||||||
| chr4:184771279
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.916-803G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771279 | ||||||
| chr4:184771300
|
C | A | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.916-824G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771300 | ||||||
| chr4:184771352
|
A | G | 5 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-876T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771352 | ||||||
| chr4:184771600
|
G | C | 1 | a0001c0003t0003g0338 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.916-1124C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771600 | ||||||
| chr4:184771665
|
A | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0218 | 3 | HG01358.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.916-1189T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771665 | ||||||
| chr4:184771700
|
T | C | 1 | a0001c0002t0007g0356 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-1224A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771700 | ||||||
| chr4:184771838
|
GC | G | 31 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(28): Show | 31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.915+1242delG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771838 | ||||||
| chr4:184771931
|
T | C | 2 | a0001c0002t0002g0158a0001c0002t0002g0224 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.915+1150A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771931 | ||||||
| chr4:184772200
|
T | A | 2 | a0001c0002t0002g0049a0001c0002t0002g0051 | 2 | HG00558.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.915+881A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772200 | ||||||
| chr4:184772303
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0157a0001c0001t0002g0218 | 4 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+778G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772303 | ||||||
| chr4:184772401
|
T | C | 20 | a0001c0001t0001g0329a0001c0001t0002g0161a0001c0001t0002g0162others(17): Show | 20 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+680A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772401 | ||||||
| chr4:184772479
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.915+602G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772479 | ||||||
| chr4:184772482
|
T | A | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.915+599A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772482 | ||||||
| chr4:184772563
|
C | T | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.915+518G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772563 | ||||||
| chr4:184772800
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(163): Show | 176 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.915+281C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772800 | ||||||
| chr4:184772896
|
C | T | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.915+185G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772896 | ||||||
| chr4:184772911
|
T | A | 6 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0085others(3): Show | 6 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+170A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772911 | ||||||
| chr4:184772962
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+119A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772962 | ||||||
| chr4:184773263
|
G | A | 1 | a0001c0002t0002g0221 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.842-109C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773263 | ||||||
| chr4:184773399
|
T | G | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.842-245A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773399 | ||||||
| chr4:184773535
|
C | G | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.841+128G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773535 | ||||||
| chr4:184773543
|
G | A | 42 | a0001c0003t0003g0003a0001c0003t0003g0008a0001c0003t0003g0022others(39): Show | 44 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.841+120C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773543 | ||||||
| chr4:184773622
|
A | G | 26 | a0001c0001t0003g0352a0001c0001t0004g0044a0001c0001t0004g0140others(23): Show | 26 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.841+41T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773622 | ||||||
| chr4:184773623
|
T | C | 4 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0189others(1): Show | 4 | HG01975.hp2 HG02572.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+40A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773623 | ||||||
| chr4:184773636
|
T | C | 1 | a0001c0002t0002g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.841+27A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773636 | ||||||
| chr4:184773723
|
T | TA | 33 | a0001c0001t0001g0329a0001c0001t0002g0036a0001c0001t0002g0071others(30): Show | 33 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.790-10dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 8/20 | chr4 | 184773723 | ||||||
| chr4:184773981
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.757-106G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184773981 | ||||||
| chr4:184774109
|
T | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0027others(79): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.757-234A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774109 | ||||||
| chr4:184774170
|
G | A | 43 | a0001c0003t0003g0003a0001c0003t0003g0008a0001c0003t0003g0022others(40): Show | 45 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.757-295C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774170 | ||||||
| chr4:184774264
|
T | C | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.757-389A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774264 | ||||||
| chr4:184774407
|
A | C | 12 | a0001c0001t0001g0329a0001c0001t0002g0161a0001c0001t0002g0162others(9): Show | 12 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.757-532T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774407 | ||||||
| chr4:184774487
|
T | C | 3 | a0001c0002t0002g0276a0001c0002t0002g0277a0001c0002t0002g0351 | 3 | NA18939.hp1 NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.757-612A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774487 | ||||||
| chr4:184774583
|
C | T | 4 | a0001c0001t0004g0044a0001c0001t0004g0140a0001c0001t0004g0141others(1): Show | 4 | HG00735.hp1 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-708G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774583 | ||||||
| chr4:184774623
|
A | G | 2 | a0001c0001t0001g0334a0001c0001t0001g0336 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.757-748T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774623 | ||||||
| chr4:184774740
|
C | T | 2 | a0001c0001t0005g0330a0001c0001t0005g0331 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.757-865G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774740 | ||||||
| chr4:184774791
|
ACATT | A | 84 | a0001c0001t0001g0342a0001c0001t0002g0004a0001c0001t0002g0016others(81): Show | 87 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.757-920_757-917del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774791 | ||||||
| chr4:184775094
|
G | A | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.757-1219C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775094 | ||||||
| chr4:184775143
|
A | T | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.757-1268T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775143 | ||||||
| chr4:184775471
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0305 | 3 | HG01361.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.756+1013T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775471 | ||||||
| chr4:184775537
|
C | T | 31 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(28): Show | 31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.756+947G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775537 | ||||||
| chr4:184775551
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756+933G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775551 | ||||||
| chr4:184775579
|
G | A | 34 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(31): Show | 34 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.756+905C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775579 | ||||||
| chr4:184775585
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.756+899A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775585 | ||||||
| chr4:184775702
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.756+782G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775702 | ||||||
| chr4:184775843
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01099.hp1 HG01167.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.756+641G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775843 | ||||||
| chr4:184775894
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0089others(2): Show | 5 | HG00597.hp1 HG02523.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.756+590C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775894 | ||||||
| chr4:184776035
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756+449G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776035 | ||||||
| chr4:184776067
|
C | T | 1 | a0001c0004t0001g0275 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.756+417G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776067 | ||||||
| chr4:184776132
|
T | C | 1 | a0001c0004t0001g0274 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.756+352A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776132 | ||||||
| chr4:184776222
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.756+262C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776222 | ||||||
| chr4:184776260
|
T | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | NA18955.hp2 NA19063.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+224A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776260 | ||||||
| chr4:184776287
|
G | T | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(370): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.756+197C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776287 | ||||||
| chr4:184776327
|
C | A | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.756+157G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776327 | ||||||
| chr4:184776364
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.756+120G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776364 | ||||||
| chr4:184776370
|
C | A | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756+114G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776370 | ||||||
| chr4:184776376
|
GCC | G | 4 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0045others(1): Show | 4 | HG00741.hp1 HG02027.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+106_756+107del others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776376 | ||||||
| chr4:184776387
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.756+97C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776387 | ||||||
| chr4:184776422
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.756+62G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776422 | ||||||
| chr4:184776812
|
G | A | 3 | a0001c0003t0003g0283a0001c0003t0003g0284a0001c0003t0003g0318 | 3 | HG00741.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.577+72C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 6/20 | chr4 | 184776812 | ||||||
| chr4:184776853
|
C | T | 2 | a0001c0002t0002g0220a0001c0002t0002g0221 | 2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.577+31G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 6/20 | chr4 | 184776853 | ||||||
| chr4:184777029
|
T | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0157a0001c0001t0002g0218 | 4 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-46A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777029 | ||||||
| chr4:184777186
|
G | T | 2 | a0001c0001t0004g0044a0001c0001t0004g0210 | 2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.478-203C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777186 | ||||||
| chr4:184777291
|
A | G | 15 | a0001c0001t0003g0352a0001c0001t0004g0044a0001c0001t0004g0140others(12): Show | 15 | HG00735.hp1 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.478-308T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777291 | ||||||
| chr4:184777497
|
G | A | 1 | a0001c0002t0002g0323 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.478-514C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777497 | ||||||
| chr4:184777557
|
G | C | 27 | a0001c0001t0001g0329a0001c0001t0002g0088a0001c0001t0002g0150others(24): Show | 27 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.478-574C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777557 | ||||||
| chr4:184777577
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.478-594T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777577 | ||||||
| chr4:184777781
|
A | AAG | 25 | a0001c0001t0003g0352a0001c0001t0004g0044a0001c0001t0004g0140others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.478-800_478-799dup others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777781 | ||||||
| chr4:184777903
|
C | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.478-920G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777903 | ||||||
| chr4:184778020
|
CAA | C | 82 | a0001c0001t0002g0004a0001c0001t0002g0016a0001c0001t0002g0017others(79): Show | 85 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.478-1039_478-1038d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778020 | ||||||
| chr4:184778134
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.478-1151A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778134 | ||||||
| chr4:184778225
|
T | C | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.478-1242A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778225 | ||||||
| chr4:184778246
|
T | A | 5 | a0001c0006t0002g0033a0001c0006t0002g0086a0001c0006t0002g0205others(2): Show | 5 | NA18973.hp2 NA18979.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1263A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778246 | ||||||
| chr4:184778478
|
C | T | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(325): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.478-1495G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778478 | ||||||
| chr4:184778479
|
G | A | 31 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(28): Show | 31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.478-1496C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778479 | ||||||
| chr4:184778744
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(169): Show | 182 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.477+1588A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778744 | ||||||
| chr4:184778764
|
T | C | 11 | a0001c0001t0004g0344a0001c0001t0004g0346a0001c0001t0004g0347others(8): Show | 11 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.477+1568A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778764 | ||||||
| chr4:184778873
|
G | T | 3 | a0001c0003t0003g0003a0001c0003t0003g0022a0001c0003t0003g0099 | 4 | HG00544.hp1 NA18965.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+1459C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778873 | ||||||
| chr4:184778884
|
G | A | 15 | a0001c0003t0003g0003a0001c0003t0003g0022a0001c0003t0003g0025others(12): Show | 16 | HG00544.hp1 HG02015.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.477+1448C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778884 | ||||||
| chr4:184778943
|
T | TA | 44 | a0001c0001t0001g0216a0001c0002t0002g0323a0001c0003t0003g0003others(41): Show | 46 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.477+1388dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778943 | ||||||
| chr4:184779050
|
T | C | 1 | a0001c0003t0003g0008 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.477+1282A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779050 | ||||||
| chr4:184779073
|
T | G | 1 | a0001c0001t0001g0368 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.477+1259A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779073 | ||||||
| chr4:184779075
|
T | C | 1 | a0001c0001t0002g0185 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.477+1257A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779075 | ||||||
| chr4:184779110
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.477+1222A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779110 | ||||||
| chr4:184779122
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.477+1210G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779122 | ||||||
| chr4:184779175
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.477+1157C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779175 | ||||||
| chr4:184779223
|
A | G | 2 | a0001c0001t0004g0364a0001c0001t0004g0365 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.477+1109T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779223 | ||||||
| chr4:184779323
|
G | T | 6 | a0001c0001t0005g0330a0001c0001t0005g0331a0001c0002t0002g0201others(3): Show | 6 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+1009C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779323 | ||||||
| chr4:184779327
|
T | C | 6 | a0001c0001t0005g0330a0001c0001t0005g0331a0001c0002t0002g0201others(3): Show | 6 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+1005A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779327 | ||||||
| chr4:184779355
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.477+977C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779355 | ||||||
| chr4:184779386
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0089others(4): Show | 7 | HG00597.hp1 HG02523.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+946G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779386 | ||||||
| chr4:184779400
|
A | G | 1 | a0001c0001t0001g0370 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.477+932T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779400 | ||||||
| chr4:184779615
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.477+717C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779615 | ||||||
| chr4:184779622
|
T | G | 153 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0121others(150): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.477+710A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779622 | ||||||
| chr4:184779812
|
A | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(147): Show | 159 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.477+520T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779812 | ||||||
| chr4:184779842
|
C | T | 2 | a0001c0001t0002g0071a0001c0001t0002g0085 | 2 | NA18944.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.477+490G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779842 | ||||||
| chr4:184779866
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.477+466A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779866 | ||||||
| chr4:184779874
|
C | CT | 15 | a0001c0001t0001g0216a0001c0001t0004g0344a0001c0001t0004g0346others(12): Show | 15 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.477+457dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779874 | ||||||
| chr4:184779874
|
CT | C | 7 | a0001c0001t0001g0228a0001c0001t0002g0036a0001c0001t0002g0071others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+457delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779874 | ||||||
| chr4:184780181
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.477+151C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184780181 | ||||||
| chr4:184780289
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.477+43C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184780289 | ||||||
| chr4:184780466
|
T | C | 43 | a0001c0003t0003g0003a0001c0003t0003g0008a0001c0003t0003g0022others(40): Show | 45 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.376-33A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780466 | ||||||
| chr4:184780478
|
T | A | 3 | a0001c0002t0002g0067a0001c0002t0002g0109a0001c0002t0002g0112 | 3 | HG02109.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.376-45A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780478 | ||||||
| chr4:184780659
|
A | C | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(370): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.376-226T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780659 | ||||||
| chr4:184780868
|
T | TAG | 10 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0081others(7): Show | 10 | HG02071.hp2 NA18949.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-436_376-435ins others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780868 | ||||||
| chr4:184780912
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.376-479C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780912 | ||||||
| chr4:184780976
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0294 | 3 | HG00280.hp2 HG00438.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.376-543G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780976 | ||||||
| chr4:184781016
|
A | T | 96 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0219others(93): Show | 100 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.376-583T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781016 | ||||||
| chr4:184781018
|
CACTT | C | 96 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0219others(93): Show | 100 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.376-589_376-586del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781018 | ||||||
| chr4:184781229
|
CAA | C | 7 | a0001c0002t0002g0053a0001c0002t0002g0076a0001c0002t0002g0222others(4): Show | 7 | HG02027.hp2 HG03516.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-798_376-797del others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | ||||||
| chr4:184781229
|
CAAA | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0047others(137): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.376-799_376-797del others(3): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | ||||||
| chr4:184781229
|
CAAAA | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 223 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-800_376-797del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | ||||||
| chr4:184781229
|
CAAAAA | C | 9 | a0001c0001t0001g0048a0001c0001t0001g0264a0001c0001t0001g0279others(6): Show | 10 | HG01257.hp2 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-801_376-797del others(5): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | ||||||
| chr4:184781229
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.376-807_376-797del others(11): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | ||||||
| chr4:184781460
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376-1027A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781460 | ||||||
| chr4:184781481
|
T | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1048A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781481 | ||||||
| chr4:184781536
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.376-1103T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781536 | ||||||
| chr4:184781554
|
A | T | 1 | a0001c0001t0001g0249 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.376-1121T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781554 | ||||||
| chr4:184781797
|
G | A | 1 | a0001c0003t0003g0317 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.376-1364C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781797 | ||||||
| chr4:184781921
|
T | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1488A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781921 | ||||||
| chr4:184781950
|
A | C | 1 | a0001c0001t0002g0226 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.376-1517T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781950 | ||||||
| chr4:184781953
|
A | G | 1 | a0001c0002t0002g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.376-1520T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781953 | ||||||
| chr4:184781979
|
A | G | 366 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(363): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.376-1546T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781979 | ||||||
| chr4:184782160
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.376-1727T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782160 | ||||||
| chr4:184782201
|
C | T | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(370): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.375+1726G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782201 | ||||||
| chr4:184782264
|
T | TA | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(187): Show | 202 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.375+1662dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782264 | ||||||
| chr4:184782264
|
T | TAAA | 94 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0219others(91): Show | 98 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.375+1660_375+1662d others(5): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782264 | ||||||
| chr4:184782446
|
A | AT | 5 | a0001c0003t0003g0025a0001c0003t0003g0236a0001c0003t0003g0282others(2): Show | 5 | HG02083.hp2 HG03831.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+1480dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782446 | ||||||
| chr4:184782493
|
T | C | 1 | a0001c0004t0001g0271 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.375+1434A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782493 | ||||||
| chr4:184782513
|
A | T | 2 | a0001c0001t0003g0352a0001c0001t0004g0207 | 2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.375+1414T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782513 | ||||||
| chr4:184782591
|
C | G | 2 | a0001c0002t0002g0220a0001c0002t0002g0221 | 2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.375+1336G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782591 | ||||||
| chr4:184782628
|
T | C | 1 | a0001c0002t0002g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.375+1299A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782628 | ||||||
| chr4:184782998
|
T | C | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+929A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782998 | ||||||
| chr4:184783022
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(202): Show | 217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.375+905C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783022 | ||||||
| chr4:184783045
|
G | A | 27 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(24): Show | 27 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.375+882C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783045 | ||||||
| chr4:184783111
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.375+816G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783111 | ||||||
| chr4:184783258
|
T | C | 141 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0219others(138): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.375+669A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783258 | ||||||
| chr4:184783280
|
G | A | 10 | a0001c0001t0001g0114a0001c0002t0002g0035a0001c0002t0002g0111others(7): Show | 10 | HG00099.hp1 HG01099.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.375+647C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783280 | ||||||
| chr4:184783294
|
T | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.375+633A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783294 | ||||||
| chr4:184783436
|
T | C | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(370): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.375+491A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783436 | ||||||
| chr4:184783546
|
C | T | 96 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0219others(93): Show | 100 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.375+381G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783546 | ||||||
| chr4:184783652
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 161 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.375+275C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783652 | ||||||
| chr4:184783804
|
G | A | 1 | a0001c0003t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.375+123C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783804 | ||||||
| chr4:184783851
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.375+76G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783851 | ||||||
| chr4:184783852
|
G | A | 96 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0219others(93): Show | 100 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.375+75C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783852 | ||||||
| chr4:184784027
|
G | A | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.311-36C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784027 | ||||||
| chr4:184784052
|
T | A | 1 | a0001c0002t0002g0221 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.311-61A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784052 | ||||||
| chr4:184784240
|
T | C | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-249A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784240 | ||||||
| chr4:184784267
|
G | C | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.311-276C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784267 | ||||||
| chr4:184784271
|
CCTCTTT | C | 5 | a0001c0003t0003g0003a0001c0003t0003g0022a0001c0003t0003g0080others(2): Show | 6 | HG00544.hp1 NA18947.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-286_311-281del others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784271 | ||||||
| chr4:184784287
|
C | T | 5 | a0001c0003t0003g0003a0001c0003t0003g0022a0001c0003t0003g0080others(2): Show | 6 | HG00544.hp1 NA18947.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-296G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784287 | ||||||
| chr4:184784497
|
G | A | 25 | a0001c0001t0001g0042a0001c0001t0004g0044a0001c0001t0004g0140others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.311-506C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784497 | ||||||
| chr4:184784812
|
G | T | 1 | a0001c0002t0002g0221 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.311-821C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784812 | ||||||
| chr4:184784953
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.311-962A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784953 | ||||||
| chr4:184784997
|
T | C | 99 | a0001c0001t0001g0114a0001c0001t0001g0136a0001c0001t0001g0139others(96): Show | 103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.311-1006A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784997 | ||||||
| chr4:184784999
|
C | T | 96 | a0001c0001t0001g0114a0001c0001t0001g0136a0001c0001t0001g0139others(93): Show | 99 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.311-1008G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784999 | ||||||
| chr4:184785343
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0324 | 2 | NA18949.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.311-1352T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785343 | ||||||
| chr4:184785360
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-1369G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785360 | ||||||
| chr4:184785596
|
TGGGCGG | T | 8 | a0001c0001t0001g0104a0001c0001t0001g0359a0001c0002t0002g0112others(5): Show | 8 | HG01261.hp2 HG02622.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.311-1611_311-1606d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785596 | ||||||
| chr4:184785600
|
C | CCGGG | 5 | a0001c0001t0002g0374a0001c0003t0003g0284a0001c0003t0003g0314others(2): Show | 5 | HG01168.hp2 HG01257.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
C | CCGGGG | 10 | a0001c0001t0002g0160a0001c0003t0003g0003a0001c0003t0003g0008others(7): Show | 12 | HG01070.hp2 HG02486.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
C | CCGGGGG | 13 | a0001c0001t0002g0373a0001c0003t0003g0096a0001c0003t0003g0143others(10): Show | 13 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
C | CCGGGGGG | 11 | a0001c0003t0003g0025a0001c0003t0003g0099a0001c0003t0003g0144others(8): Show | 11 | HG00544.hp1 HG00741.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
C | CCGGGGGG others(4): Show |
1 | a0001c0003t0003g0320 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.311-1610_311-1609i others(13): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
CGGGGGCG | C | 33 | a0001c0001t0001g0027a0001c0001t0001g0108a0001c0001t0001g0136others(30): Show | 34 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.311-1616_311-1610d others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
CGGGGGCG others(1): Show |
C | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(141): Show | 151 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.311-1617_311-1610d others(10): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
CGGGGGCG others(2): Show |
C | 53 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0075others(50): Show | 56 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.311-1618_311-1610d others(11): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
CGGGGGCG others(3): Show |
C | 6 | a0001c0001t0001g0139a0001c0001t0002g0226a0001c0002t0002g0049others(3): Show | 6 | HG00558.hp2 HG01081.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-1619_311-1610d others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
CGGGGGCG others(5): Show |
C | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.311-1621_311-1610d others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785600
|
CGGGGGCG others(6): Show |
C | 21 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(18): Show | 22 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.311-1622_311-1610d others(15): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | ||||||
| chr4:184785605
|
GC | G | 3 | a0001c0001t0001g0171a0001c0001t0002g0036a0001c0001t0002g0101 | 3 | HG02602.hp2 HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.311-1615delG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785605 | ||||||
| chr4:184785606
|
C | G | 75 | a0001c0001t0001g0042a0001c0001t0002g0160a0001c0001t0002g0161others(72): Show | 77 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.311-1615G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785606 | ||||||
| chr4:184785607
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0002g0057 | 2 | NA18952.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.311-1616C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785607 | ||||||
| chr4:184785609
|
G | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0168others(2): Show | 7 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-1618C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785609 | ||||||
| chr4:184785613
|
G | T | 1 | a0001c0002t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311-1622C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785613 | ||||||
| chr4:184785614
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0004g0210 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.311-1624_311-1623i others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785614 | ||||||
| chr4:184785614
|
G | T | 1 | a0001c0002t0002g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.311-1623C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785614 | ||||||
| chr4:184785615
|
G | A | 49 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0085others(46): Show | 51 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.311-1624C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785615 | ||||||
| chr4:184785615
|
G | GGGGGGGG others(3): Show |
2 | a0001c0001t0004g0146a0001c0001t0004g0363 | 2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.311-1625_311-1624i others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785615 | ||||||
| chr4:184785615
|
G | GGGGGGGG others(8): Show |
1 | a0001c0001t0004g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.311-1625_311-1624i others(17): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785615 | ||||||
| chr4:184785616
|
G | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0134others(2): Show | 5 | HG01891.hp2 HG03516.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1625C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785616 | ||||||
| chr4:184785617
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.311-1626C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785617 | ||||||
| chr4:184785622
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.311-1631T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785622 | ||||||
| chr4:184785683
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.311-1692C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785683 | ||||||
| chr4:184785713
|
T | A | 2 | a0001c0002t0002g0158a0001c0002t0002g0224 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.311-1722A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785713 | ||||||
| chr4:184786005
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.311-2014C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786005 | ||||||
| chr4:184786119
|
C | T | 1 | a0001c0001t0011g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.311-2128G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786119 | ||||||
| chr4:184786191
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.311-2200C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786191 | ||||||
| chr4:184786305
|
G | T | 23 | a0001c0002t0002g0007a0001c0002t0002g0032a0001c0002t0002g0034others(20): Show | 24 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.310+2312C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786305 | ||||||
| chr4:184786349
|
A | G | 1 | a0001c0002t0002g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.310+2268T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786349 | ||||||
| chr4:184786418
|
G | GCA | 3 | a0001c0001t0001g0010a0001c0001t0001g0190a0001c0005t0012g0151 | 4 | HG01074.hp1 HG01109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+2197_310+2198d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
G | GCACGCAC others(9): Show |
2 | a0001c0002t0002g0158a0001c0002t0002g0224 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.310+2198_310+2199i others(18): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
GCA | G | 36 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0114others(33): Show | 36 | HG00558.hp1 HG00735.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.310+2197_310+2198d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
GCACA | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.310+2195_310+2198d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
GCACACA | G | 11 | a0001c0001t0004g0344a0001c0001t0004g0346a0001c0001t0004g0347others(8): Show | 11 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.310+2193_310+2198d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
GCACACAC others(3): Show |
G | 15 | a0001c0001t0001g0042a0001c0001t0004g0044a0001c0001t0004g0140others(12): Show | 15 | HG00642.hp2 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.310+2189_310+2198d others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
GCACACAC others(5): Show |
G | 5 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0085others(2): Show | 5 | HG02602.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+2187_310+2198d others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786418
|
GCACACAC others(11): Show |
G | 1 | a0001c0002t0002g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.310+2181_310+2198d others(20): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | ||||||
| chr4:184786420
|
A | ACG | 14 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.310+2196_310+2197i others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786420 | ||||||
| chr4:184786422
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0168others(51): Show | 58 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.310+2195T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786422 | ||||||
| chr4:184786424
|
A | G | 26 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0114others(23): Show | 26 | HG00558.hp1 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.310+2193T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786424 | ||||||
| chr4:184786425
|
C | T | 3 | a0001c0001t0001g0280a0001c0001t0001g0368a0001c0001t0001g0369 | 3 | HG00597.hp2 HG02165.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.310+2192G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786425 | ||||||
| chr4:184786426
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.310+2191T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786426 | ||||||
| chr4:184786427
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0168others(3): Show | 8 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.310+2190G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786427 | ||||||
| chr4:184786428
|
A | G | 15 | a0001c0001t0002g0011a0001c0001t0002g0218a0001c0001t0004g0344others(12): Show | 16 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.310+2189T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786428 | ||||||
| chr4:184786430
|
A | G | 4 | a0001c0001t0001g0256a0001c0002t0002g0116a0001c0002t0002g0117others(1): Show | 4 | HG00438.hp1 NA18960.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2187T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786430 | ||||||
| chr4:184786432
|
A | G | 15 | a0001c0001t0001g0042a0001c0001t0004g0044a0001c0001t0004g0140others(12): Show | 15 | HG00642.hp2 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.310+2185T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786432 | ||||||
| chr4:184786434
|
A | G | 5 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0085others(2): Show | 5 | HG02602.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+2183T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786434 | ||||||
| chr4:184786440
|
A | G | 1 | a0001c0002t0002g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.310+2177T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786440 | ||||||
| chr4:184786456
|
ACACT | A | 40 | a0001c0001t0003g0352a0001c0001t0004g0207a0001c0003t0003g0003others(37): Show | 42 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.310+2157_310+2160d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786456 | ||||||
| chr4:184786458
|
ACT | A | 4 | a0001c0001t0002g0160a0001c0001t0002g0373a0001c0001t0002g0374others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2157_310+2158d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786458 | ||||||
| chr4:184786460
|
T | A | 1 | a0001c0003t0003g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.310+2157A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786460 | ||||||
| chr4:184786553
|
T | C | 1 | a0001c0001t0001g0327 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.310+2064A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786553 | ||||||
| chr4:184786596
|
A | G | 6 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0229others(3): Show | 7 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+2021T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786596 | ||||||
| chr4:184786692
|
C | CTT | 44 | a0001c0001t0002g0160a0001c0001t0002g0373a0001c0001t0002g0374others(41): Show | 46 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.310+1923_310+1924d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786692 | ||||||
| chr4:184786692
|
CT | C | 14 | a0001c0001t0001g0039a0001c0001t0001g0135a0001c0001t0001g0264others(11): Show | 14 | HG01069.hp1 HG01257.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.310+1924delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786692 | ||||||
| chr4:184786692
|
CTT | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.310+1923_310+1924d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786692 | ||||||
| chr4:184786716
|
C | T | 2 | a0001c0008t0004g0304a0001c0008t0004g0313 | 2 | HG00639.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.310+1901G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786716 | ||||||
| chr4:184786725
|
G | A | 22 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(19): Show | 23 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.310+1892C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786725 | ||||||
| chr4:184787025
|
C | T | 35 | a0001c0001t0001g0136a0001c0001t0002g0004a0001c0001t0002g0030others(32): Show | 36 | HG00438.hp2 HG00558.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.310+1592G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787025 | ||||||
| chr4:184787026
|
C | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(288): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.310+1591G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787026 | ||||||
| chr4:184787265
|
G | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+1352C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787265 | ||||||
| chr4:184787274
|
G | A | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+1343C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787274 | ||||||
| chr4:184787319
|
C | T | 6 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0229others(3): Show | 7 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1298G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787319 | ||||||
| chr4:184787330
|
A | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0168others(3): Show | 8 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.310+1287T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787330 | ||||||
| chr4:184787441
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(289): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.310+1176T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787441 | ||||||
| chr4:184787482
|
G | A | 73 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0038others(70): Show | 74 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.310+1135C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787482 | ||||||
| chr4:184787596
|
A | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.310+1021T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787596 | ||||||
| chr4:184787601
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.310+1016G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787601 | ||||||
| chr4:184787613
|
C | T | 21 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(18): Show | 22 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.310+1004G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787613 | ||||||
| chr4:184787653
|
T | C | 38 | a0001c0001t0001g0042a0001c0001t0002g0036a0001c0001t0002g0071others(35): Show | 38 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.310+964A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787653 | ||||||
| chr4:184787724
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.310+893G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787724 | ||||||
| chr4:184787757
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.310+860T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787757 | ||||||
| chr4:184787867
|
G | GA | 293 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.310+749dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787867 | ||||||
| chr4:184787904
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0001g0131 | 4 | HG02683.hp1 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+713T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787904 | ||||||
| chr4:184788043
|
G | C | 1 | a0001c0001t0001g0300 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.310+574C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788043 | ||||||
| chr4:184788203
|
T | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+414A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788203 | ||||||
| chr4:184788219
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.310+398T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788219 | ||||||
| chr4:184788394
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.310+223C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788394 | ||||||
| chr4:184788502
|
G | A | 1 | a0001c0002t0002g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.310+115C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788502 | ||||||
| chr4:184788524
|
G | A | 2 | a0001c0002t0002g0158a0001c0002t0002g0224 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.310+93C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788524 | ||||||
| chr4:184788737
|
A | G | 8 | a0001c0001t0004g0346a0001c0001t0004g0347a0001c0001t0004g0360others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.196-6T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184788737 | ||||||
| chr4:184788875
|
T | C | 2 | a0001c0001t0003g0352a0001c0001t0004g0207 | 2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.196-144A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184788875 | ||||||
| chr4:184789546
|
T | C | 1 | a0001c0001t0004g0310 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.196-815A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789546 | ||||||
| chr4:184789651
|
T | C | 8 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | HG02615.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-920A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789651 | ||||||
| chr4:184789684
|
T | C | 39 | a0001c0003t0003g0003a0001c0003t0003g0008a0001c0003t0003g0022others(36): Show | 41 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.196-953A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789684 | ||||||
| chr4:184789705
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.196-974C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789705 | ||||||
| chr4:184789883
|
CT | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.196-1153delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789883 | ||||||
| chr4:184789883
|
CTT | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0138others(24): Show | 29 | HG00609.hp1 HG01123.hp2 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-1154_196-1153d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789883 | ||||||
| chr4:184789944
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.196-1213A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789944 | ||||||
| chr4:184789959
|
G | A | 1 | a0001c0006t0002g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.196-1228C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789959 | ||||||
| chr4:184790063
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196-1332T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790063 | ||||||
| chr4:184790068
|
T | C | 45 | a0001c0001t0002g0160a0001c0001t0002g0373a0001c0001t0002g0374others(42): Show | 47 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.196-1337A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790068 | ||||||
| chr4:184790081
|
T | A | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-1350A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790081 | ||||||
| chr4:184790113
|
G | A | 2 | a0001c0001t0002g0199a0001c0002t0002g0107 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.196-1382C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790113 | ||||||
| chr4:184790398
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.196-1667A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790398 | ||||||
| chr4:184790520
|
G | A | 2 | a0001c0001t0002g0373a0001c0001t0002g0374 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.196-1789C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790520 | ||||||
| chr4:184790848
|
T | TAGC | 26 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(23): Show | 26 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-2120_196-2118d others(5): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790848 | ||||||
| chr4:184790942
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.196-2211C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790942 | ||||||
| chr4:184790980
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0168others(48): Show | 54 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.196-2249C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790980 | ||||||
| chr4:184791000
|
T | A | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.196-2269A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791000 | ||||||
| chr4:184791061
|
T | C | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196-2330A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791061 | ||||||
| chr4:184791142
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.196-2411A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791142 | ||||||
| chr4:184791173
|
T | C | 44 | a0001c0001t0002g0160a0001c0001t0002g0373a0001c0001t0002g0374others(41): Show | 46 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.196-2442A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791173 | ||||||
| chr4:184791443
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.196-2712G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791443 | ||||||
| chr4:184791454
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.196-2723C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791454 | ||||||
| chr4:184791455
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.196-2724G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791455 | ||||||
| chr4:184791525
|
G | C | 38 | a0001c0002t0002g0281a0001c0003t0003g0003a0001c0003t0003g0008others(35): Show | 40 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.196-2794C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791525 | ||||||
| chr4:184791616
|
A | G | 3 | a0001c0001t0001g0301a0001c0001t0001g0322a0001c0001t0001g0345 | 3 | HG00735.hp2 HG01081.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.196-2885T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791616 | ||||||
| chr4:184791701
|
G | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0216a0001c0001t0001g0219others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2970C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791701 | ||||||
| chr4:184792163
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(17): Show | 22 | HG02280.hp2 HG02602.hp1 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-3432A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792163 | ||||||
| chr4:184792185
|
A | G | 1 | a0001c0005t0012g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196-3454T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792185 | ||||||
| chr4:184792195
|
T | C | 45 | a0001c0001t0001g0234a0001c0001t0001g0239a0001c0001t0001g0303others(42): Show | 47 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.196-3464A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792195 | ||||||
| chr4:184792255
|
C | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(16): Show | 21 | HG02280.hp2 HG02602.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-3524G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792255 | ||||||
| chr4:184792414
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(171): Show | 185 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(182): Show |
intron_variant | MODIFIER | c.196-3683T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792414 | ||||||
| chr4:184792441
|
A | AT | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-3711dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792441 | ||||||
| chr4:184792454
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-3723C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792454 | ||||||
| chr4:184792484
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(199): Show | 215 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(212): Show |
intron_variant | MODIFIER | c.196-3753T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792484 | ||||||
| chr4:184792524
|
C | T | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196-3793G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792524 | ||||||
| chr4:184792525
|
G | A | 1 | a0001c0002t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196-3794C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792525 | ||||||
| chr4:184792586
|
G | A | 1 | a0001c0001t0004g0363 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.196-3855C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792586 | ||||||
| chr4:184792761
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 107 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.196-4030C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792761 | ||||||
| chr4:184792769
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(36): Show | 42 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.196-4038T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792769 | ||||||
| chr4:184792878
|
G | A | 3 | a0001c0002t0002g0054a0001c0002t0002g0056a0001c0002t0004g0055 | 3 | HG00642.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.196-4147C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792878 | ||||||
| chr4:184792947
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-4216T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792947 | ||||||
| chr4:184792976
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196-4245T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792976 | ||||||
| chr4:184793135
|
G | T | 42 | a0001c0001t0001g0042a0001c0001t0001g0174a0001c0001t0001g0175others(39): Show | 42 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.196-4404C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793135 | ||||||
| chr4:184793165
|
C | CTTTAATG | 2 | a0001c0001t0001g0015a0001c0001t0001g0305 | 3 | HG01361.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.196-4441_196-4435d others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793165 | ||||||
| chr4:184793194
|
TA | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 187 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.196-4464delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793194 | ||||||
| chr4:184793194
|
TAA | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0081a0001c0001t0001g0186others(6): Show | 10 | HG01256.hp1 HG01361.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-4465_196-4464d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793194 | ||||||
| chr4:184793244
|
G | A | 12 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(9): Show | 12 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-4513C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793244 | ||||||
| chr4:184793247
|
G | A | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196-4516C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793247 | ||||||
| chr4:184793425
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(9): Show | 14 | HG02280.hp2 HG02602.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-4694G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793425 | ||||||
| chr4:184793540
|
G | A | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.196-4809C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793540 | ||||||
| chr4:184793541
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.196-4810T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793541 | ||||||
| chr4:184793649
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.196-4918C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793649 | ||||||
| chr4:184793751
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196-5020G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793751 | ||||||
| chr4:184793802
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 156 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(153): Show |
intron_variant | MODIFIER | c.196-5071G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793802 | ||||||
| chr4:184793819
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 8 | HG02280.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-5088G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793819 | ||||||
| chr4:184794013
|
A | G | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-5282T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794013 | ||||||
| chr4:184794111
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5380G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794111 | ||||||
| chr4:184794130
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.196-5399C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794130 | ||||||
| chr4:184794132
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5401C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794132 | ||||||
| chr4:184794170
|
T | C | 44 | a0001c0001t0001g0042a0001c0001t0001g0174a0001c0001t0001g0175others(41): Show | 44 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.196-5439A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794170 | ||||||
| chr4:184794203
|
A | AAC | 45 | a0001c0001t0001g0042a0001c0001t0001g0174a0001c0001t0001g0175others(42): Show | 45 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.196-5473_196-5472i others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794203 | ||||||
| chr4:184794297
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196-5566G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794297 | ||||||
| chr4:184794342
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196-5611T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794342 | ||||||
| chr4:184794376
|
A | T | 1 | a0001c0008t0004g0304 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.196-5645T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794376 | ||||||
| chr4:184794397
|
A | G | 1 | a0001c0004t0001g0058 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.196-5666T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794397 | ||||||
| chr4:184794451
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.196-5720G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794451 | ||||||
| chr4:184794452
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5721C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794452 | ||||||
| chr4:184794531
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5800A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794531 | ||||||
| chr4:184794532
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5801C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794532 | ||||||
| chr4:184794535
|
A | G | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5804T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794535 | ||||||
| chr4:184794584
|
C | G | 1 | a0001c0001t0002g0375 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-5853G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794584 | ||||||
| chr4:184794698
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5967C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794698 | ||||||
| chr4:184794747
|
A | G | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6016T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794747 | ||||||
| chr4:184794903
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6172A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794903 | ||||||
| chr4:184794915
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.196-6184G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794915 | ||||||
| chr4:184794922
|
C | CCAAT | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 156 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(153): Show |
intron_variant | MODIFIER | c.196-6192_196-6191i others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794922 | ||||||
| chr4:184794936
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6205C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794936 | ||||||
| chr4:184794946
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6215C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794946 | ||||||
| chr4:184795078
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6347A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795078 | ||||||
| chr4:184795108
|
G | A | 1 | a0001c0003t0003g0008 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.196-6377C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795108 | ||||||
| chr4:184795114
|
A | AT | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6384dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795114 | ||||||
| chr4:184795138
|
T | C | 2 | a0001c0001t0004g0364a0001c0001t0004g0365 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.196-6407A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795138 | ||||||
| chr4:184795335
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6604G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795335 | ||||||
| chr4:184795347
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-6616C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795347 | ||||||
| chr4:184795452
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6721G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795452 | ||||||
| chr4:184795463
|
T | G | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6732A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795463 | ||||||
| chr4:184795499
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6768G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795499 | ||||||
| chr4:184795783
|
T | C | 23 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(20): Show | 23 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.196-7052A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795783 | ||||||
| chr4:184795875
|
G | C | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7144C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795875 | ||||||
| chr4:184795930
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-7199A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795930 | ||||||
| chr4:184796091
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+7229C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796091 | ||||||
| chr4:184796148
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+7172A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796148 | ||||||
| chr4:184796195
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.195+7125C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796195 | ||||||
| chr4:184796243
|
G | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0279others(1): Show | 4 | HG00609.hp1 HG01074.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+7077C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796243 | ||||||
| chr4:184796323
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6997A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796323 | ||||||
| chr4:184796469
|
C | G | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6851G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796469 | ||||||
| chr4:184796474
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6846G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796474 | ||||||
| chr4:184796568
|
T | C | 47 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(44): Show | 49 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.195+6752A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796568 | ||||||
| chr4:184796590
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6730G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796590 | ||||||
| chr4:184796605
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6715A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796605 | ||||||
| chr4:184796649
|
T | G | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6671A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796649 | ||||||
| chr4:184796955
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6365A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796955 | ||||||
| chr4:184796978
|
A | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 157 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(154): Show |
intron_variant | MODIFIER | c.195+6342T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796978 | ||||||
| chr4:184797067
|
C | T | 34 | a0001c0001t0001g0042a0001c0001t0002g0161a0001c0001t0002g0162others(31): Show | 34 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.195+6253G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797067 | ||||||
| chr4:184797077
|
A | G | 1 | a0001c0001t0002g0353 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195+6243T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797077 | ||||||
| chr4:184797146
|
A | C | 39 | a0001c0001t0001g0042a0001c0001t0001g0173a0001c0001t0001g0214others(36): Show | 40 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+6174T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797146 | ||||||
| chr4:184797160
|
CCGCTCA | C | 39 | a0001c0001t0001g0042a0001c0001t0001g0173a0001c0001t0001g0214others(36): Show | 40 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+6154_195+6159d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797160 | ||||||
| chr4:184797167
|
C | G | 39 | a0001c0001t0001g0042a0001c0001t0001g0173a0001c0001t0001g0214others(36): Show | 40 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+6153G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797167 | ||||||
| chr4:184797303
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+6017G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797303 | ||||||
| chr4:184797332
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5988A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797332 | ||||||
| chr4:184797339
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5981A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797339 | ||||||
| chr4:184797365
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5955C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797365 | ||||||
| chr4:184797378
|
G | A | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+5942C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797378 | ||||||
| chr4:184797429
|
C | G | 1 | a0001c0003t0003g0318 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195+5891G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797429 | ||||||
| chr4:184797452
|
C | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5868G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797452 | ||||||
| chr4:184797504
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.195+5816G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797504 | ||||||
| chr4:184797573
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 165 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(162): Show |
intron_variant | MODIFIER | c.195+5747C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797573 | ||||||
| chr4:184797599
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.195+5721C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797599 | ||||||
| chr4:184797622
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5698A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797622 | ||||||
| chr4:184797764
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0089 | 3 | HG00597.hp1 HG02523.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.195+5556G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797764 | ||||||
| chr4:184797816
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.195+5504A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797816 | ||||||
| chr4:184797915
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.195+5405G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797915 | ||||||
| chr4:184797918
|
C | T | 1 | a0001c0002t0002g0109 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.195+5402G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797918 | ||||||
| chr4:184797970
|
G | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5350C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797970 | ||||||
| chr4:184797972
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5348G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797972 | ||||||
| chr4:184797997
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5323A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797997 | ||||||
| chr4:184798021
|
A | T | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+5299T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798021 | ||||||
| chr4:184798037
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.195+5283C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798037 | ||||||
| chr4:184798085
|
G | T | 1 | a0001c0002t0002g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.195+5235C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798085 | ||||||
| chr4:184798103
|
G | A | 10 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+5217C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798103 | ||||||
| chr4:184798166
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0299others(2): Show | 6 | NA18941.hp1 NA18943.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+5154T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798166 | ||||||
| chr4:184798306
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.195+5014G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798306 | ||||||
| chr4:184798453
|
C | T | 2 | a0001c0002t0002g0281a0001c0003t0003g0267 | 2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.195+4867G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798453 | ||||||
| chr4:184798545
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.195+4775C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798545 | ||||||
| chr4:184799061
|
TC | T | 10 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+4258delG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799061 | ||||||
| chr4:184799085
|
C | A | 1 | a0001c0002t0002g0031 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.195+4235G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799085 | ||||||
| chr4:184799086
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 130 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(127): Show |
intron_variant | MODIFIER | c.195+4234G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799086 | ||||||
| chr4:184799102
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(157): Show | 171 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(168): Show |
intron_variant | MODIFIER | c.195+4218A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799102 | ||||||
| chr4:184799116
|
C | CT | 25 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(22): Show | 25 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.195+4203dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799116 | ||||||
| chr4:184799116
|
CT | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(97): Show | 108 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.195+4203delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799116 | ||||||
| chr4:184799116
|
CTT | C | 17 | a0001c0001t0001g0121a0001c0001t0001g0133a0001c0001t0001g0173others(14): Show | 18 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+4202_195+4203d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799116 | ||||||
| chr4:184799150
|
G | T | 12 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(9): Show | 12 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+4170C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799150 | ||||||
| chr4:184799155
|
G | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 112 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.195+4165C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799155 | ||||||
| chr4:184799168
|
G | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+4152C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799168 | ||||||
| chr4:184799274
|
G | A | 10 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+4046C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799274 | ||||||
| chr4:184799305
|
C | T | 5 | a0001c0001t0001g0238a0001c0003t0003g0237a0001c0003t0003g0306others(2): Show | 5 | NA18966.hp2 NA18994.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+4015G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799305 | ||||||
| chr4:184799318
|
T | C | 9 | a0001c0001t0004g0346a0001c0001t0004g0347a0001c0001t0004g0360others(6): Show | 9 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+4002A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799318 | ||||||
| chr4:184799489
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.195+3831G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799489 | ||||||
| chr4:184799689
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.195+3631T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799689 | ||||||
| chr4:184800138
|
T | C | 1 | a0001c0001t0001g0369 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.195+3182A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800138 | ||||||
| chr4:184800144
|
T | C | 4 | a0001c0001t0001g0038a0001c0003t0003g0319a0001c0003t0003g0320others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+3176A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800144 | ||||||
| chr4:184800198
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 102 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+3122C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800198 | ||||||
| chr4:184800216
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 165 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(162): Show |
intron_variant | MODIFIER | c.195+3104C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800216 | ||||||
| chr4:184800579
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 102 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+2741A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800579 | ||||||
| chr4:184800646
|
C | T | 1 | a0001c0001t0004g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.195+2674G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800646 | ||||||
| chr4:184800721
|
A | G | 1 | a0001c0003t0003g0317 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.195+2599T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800721 | ||||||
| chr4:184801107
|
C | T | 5 | a0001c0001t0001g0208a0001c0001t0001g0252a0001c0001t0001g0257others(2): Show | 5 | NA18747.hp1 NA18949.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2213G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801107 | ||||||
| chr4:184801133
|
G | GT | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 102 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+2186_195+2187i others(3): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801133 | ||||||
| chr4:184801293
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+2027A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801293 | ||||||
| chr4:184801342
|
T | C | 1 | a0001c0001t0002g0293 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.195+1978A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801342 | ||||||
| chr4:184801474
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0102others(4): Show | 7 | HG02071.hp2 NA18962.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+1846A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801474 | ||||||
| chr4:184801565
|
G | C | 1 | a0001c0002t0002g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.195+1755C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801565 | ||||||
| chr4:184801572
|
T | C | 6 | a0001c0001t0001g0280a0001c0002t0002g0063a0001c0002t0002g0064others(3): Show | 6 | NA18612.hp2 NA18962.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+1748A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801572 | ||||||
| chr4:184801688
|
A | G | 9 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0102others(6): Show | 9 | HG02071.hp2 NA18950.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+1632T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801688 | ||||||
| chr4:184801692
|
C | G | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1628G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801692 | ||||||
| chr4:184801737
|
C | G | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.195+1583G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801737 | ||||||
| chr4:184801766
|
C | T | 10 | a0001c0001t0001g0136a0001c0001t0002g0004a0001c0001t0002g0030others(7): Show | 11 | NA18939.hp1 NA18951.hp1 NA18969.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+1554G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801766 | ||||||
| chr4:184801844
|
C | G | 5 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(2): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1476G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801844 | ||||||
| chr4:184802052
|
GA | G | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.195+1267delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802052 | ||||||
| chr4:184802556
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.195+764C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802556 | ||||||
| chr4:184802557
|
C | T | 41 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0001g0239others(38): Show | 42 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.195+763G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802557 | ||||||
| chr4:184802618
|
C | A | 7 | a0001c0001t0002g0226a0001c0001t0002g0235a0001c0002t0002g0012others(4): Show | 8 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.195+702G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802618 | ||||||
| chr4:184802657
|
C | T | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+663G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802657 | ||||||
| chr4:184802688
|
G | A | 1 | a0001c0004t0001g0058 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.195+632C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802688 | ||||||
| chr4:184802688
|
G | T | 9 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(6): Show | 9 | HG02615.hp1 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+632C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802688 | ||||||
| chr4:184802767
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0202 | 2 | HG02071.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.195+553G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802767 | ||||||
| chr4:184802778
|
G | A | 3 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149 | 3 | HG01123.hp2 HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.195+542C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802778 | ||||||
| chr4:184802855
|
C | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(7): Show | 12 | HG02280.hp2 HG02602.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.195+465G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802855 | ||||||
| chr4:184802927
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.195+393C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802927 | ||||||
| chr4:184802936
|
C | A | 1 | a0001c0001t0002g0341 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.195+384G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802936 | ||||||
| chr4:184802945
|
A | G | 17 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(14): Show | 18 | HG01081.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+375T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802945 | ||||||
| chr4:184803060
|
G | A | 1 | a0001c0002t0002g0123 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.195+260C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184803060 | ||||||
| chr4:184803101
|
C | T | 1 | a0001c0003t0003g0318 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195+219G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184803101 | ||||||
| chr4:184803303
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0305 | 3 | HG01361.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.195+17G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184803303 | ||||||
| chr4:184803594
|
C | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0211a0001c0002t0002g0107others(7): Show | 10 | HG01928.hp2 NA18953.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-48G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803594 | ||||||
| chr4:184803607
|
C | A | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-61G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803607 | ||||||
| chr4:184803944
|
C | G | 1 | a0001c0003t0003g0317 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-32-398G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803944 | ||||||
| chr4:184803994
|
C | T | 10 | a0001c0001t0001g0136a0001c0001t0002g0004a0001c0001t0002g0030others(7): Show | 11 | NA18939.hp1 NA18951.hp1 NA18969.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-448G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803994 | ||||||
| chr4:184804000
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32-454C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804000 | ||||||
| chr4:184804255
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32-709A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804255 | ||||||
| chr4:184804262
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(201): Show | 217 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.-32-716T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804262 | ||||||
| chr4:184804342
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 178 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(175): Show |
intron_variant | MODIFIER | c.-32-796T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804342 | ||||||
| chr4:184804366
|
G | A | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-820C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804366 | ||||||
| chr4:184804530
|
G | A | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-984C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804530 | ||||||
| chr4:184804587
|
GA | G | 11 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0002g0009others(8): Show | 12 | HG01891.hp1 HG01993.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32-1042delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804587 | ||||||
| chr4:184804587
|
GAA | G | 11 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(8): Show | 11 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-1043_-32-1042d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804587 | ||||||
| chr4:184804674
|
C | A | 1 | a0001c0006t0002g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-32-1128G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804674 | ||||||
| chr4:184804709
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-32-1163T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804709 | ||||||
| chr4:184804790
|
C | A | 2 | a0001c0001t0002g0195a0001c0001t0002g0198 | 2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-32-1244G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804790 | ||||||
| chr4:184804968
|
G | A | 1 | a0001c0001t0004g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-32-1422C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804968 | ||||||
| chr4:184805070
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-32-1524G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805070 | ||||||
| chr4:184805113
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0336 | 2 | HG02027.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-32-1567A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805113 | ||||||
| chr4:184805267
|
T | A | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-1721A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805267 | ||||||
| chr4:184805380
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0129 | 3 | NA18978.hp1 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-32-1834A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805380 | ||||||
| chr4:184805394
|
C | T | 163 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0037others(160): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-32-1848G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805394 | ||||||
| chr4:184805395
|
TCACA | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0024others(9): Show | 15 | HG00544.hp2 NA18612.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32-1853_-32-1850d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805395 | ||||||
| chr4:184805507
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-32-1961G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805507 | ||||||
| chr4:184805524
|
C | T | 1 | a0001c0002t0002g0221 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-32-1978G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805524 | ||||||
| chr4:184805760
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-2214A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805760 | ||||||
| chr4:184805847
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 8 | HG02280.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-2301C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805847 | ||||||
| chr4:184805956
|
C | G | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-2410G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805956 | ||||||
| chr4:184805987
|
C | G | 1 | a0001c0001t0002g0339 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-32-2441G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805987 | ||||||
| chr4:184806593
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-32-3047C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184806593 | ||||||
| chr4:184806685
|
T | A | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-3139A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184806685 | ||||||
| chr4:184807570
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32-4024G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807570 | ||||||
| chr4:184807657
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 136 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(133): Show |
intron_variant | MODIFIER | c.-32-4111T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807657 | ||||||
| chr4:184807685
|
T | C | 67 | a0001c0001t0001g0037a0001c0001t0001g0136a0001c0001t0001g0211others(64): Show | 69 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-32-4139A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807685 | ||||||
| chr4:184807767
|
AAAAGC | A | 11 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-4226_-32-4222d others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807767 | ||||||
| chr4:184807836
|
A | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(10): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-4290T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807836 | ||||||
| chr4:184807869
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32-4323G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807869 | ||||||
| chr4:184808084
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-32-4538C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808084 | ||||||
| chr4:184808202
|
A | G | 1 | a0001c0002t0002g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-32-4656T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808202 | ||||||
| chr4:184808240
|
T | TAC | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 110 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.-32-4696_-32-4695d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808240 | ||||||
| chr4:184808733
|
C | A | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-5187G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808733 | ||||||
| chr4:184808894
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32-5348C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808894 | ||||||
| chr4:184808920
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32-5374G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808920 | ||||||
| chr4:184808980
|
T | C | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-5434A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808980 | ||||||
| chr4:184809038
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-32-5492G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809038 | ||||||
| chr4:184809145
|
G | A | 38 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0001g0239others(35): Show | 39 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-32-5599C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809145 | ||||||
| chr4:184809485
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(5): Show | 10 | HG02280.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-5939A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809485 | ||||||
| chr4:184809531
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-32-5985T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809531 | ||||||
| chr4:184809596
|
T | C | 22 | a0001c0001t0001g0042a0001c0001t0003g0352a0001c0001t0004g0044others(19): Show | 22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-6050A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809596 | ||||||
| chr4:184809636
|
C | CA | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 108 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(105): Show |
intron_variant | MODIFIER | c.-32-6091dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809636 | ||||||
| chr4:184809775
|
G | A | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-6229C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809775 | ||||||
| chr4:184809800
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 202 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.-32-6254T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809800 | ||||||
| chr4:184809946
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-32-6400A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809946 | ||||||
| chr4:184810049
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-32-6503A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810049 | ||||||
| chr4:184810157
|
C | T | 6 | a0001c0001t0002g0093a0001c0004t0001g0013a0001c0004t0001g0250others(3): Show | 7 | HG00738.hp1 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-6611G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810157 | ||||||
| chr4:184810275
|
G | A | 1 | a0001c0001t0001g0327 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-32-6729C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810275 | ||||||
| chr4:184810288
|
G | A | 36 | a0001c0001t0001g0083a0001c0001t0001g0234a0001c0001t0001g0238others(33): Show | 37 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-32-6742C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810288 | ||||||
| chr4:184810311
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-32-6765G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810311 | ||||||
| chr4:184810429
|
C | T | 38 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0001g0239others(35): Show | 39 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-32-6883G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810429 | ||||||
| chr4:184810669
|
C | T | 1 | a0001c0002t0002g0323 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-32-7123G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810669 | ||||||
| chr4:184810708
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0001g0131 | 4 | HG02683.hp1 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-7162C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810708 | ||||||
| chr4:184810721
|
C | CGGATA | 10 | a0001c0001t0001g0329a0001c0001t0002g0161a0001c0001t0002g0162others(7): Show | 10 | HG02615.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-7180_-32-7176d others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810721 | ||||||
| chr4:184810786
|
G | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0138others(71): Show | 78 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-32-7240C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810786 | ||||||
| chr4:184810934
|
G | C | 12 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0216others(9): Show | 13 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-7388C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810934 | ||||||
| chr4:184810976
|
G | C | 12 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(9): Show | 12 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-7430C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810976 | ||||||
| chr4:184811019
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-32-7473C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811019 | ||||||
| chr4:184811067
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-32-7521A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811067 | ||||||
| chr4:184811147
|
C | T | 1 | a0001c0002t0002g0123 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-32-7601G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811147 | ||||||
| chr4:184811148
|
G | A | 1 | a0001c0002t0002g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-32-7602C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811148 | ||||||
| chr4:184811171
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 95 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.-32-7625A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811171 | ||||||
| chr4:184811177
|
C | T | 7 | a0001c0001t0004g0346a0001c0001t0004g0347a0001c0001t0004g0360others(4): Show | 7 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-7631G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811177 | ||||||
| chr4:184811209
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0023others(60): Show | 68 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-32-7663G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811209 | ||||||
| chr4:184811213
|
A | G | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-7667T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811213 | ||||||
| chr4:184811220
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0301others(19): Show | 24 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32-7674G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811220 | ||||||
| chr4:184811221
|
A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0173others(32): Show | 38 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-32-7675T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811221 | ||||||
| chr4:184811232
|
C | G | 1 | a0001c0002t0002g0045 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-32-7686G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811232 | ||||||
| chr4:184811233
|
G | C | 4 | a0001c0001t0001g0019a0001c0002t0002g0020a0001c0002t0002g0021others(1): Show | 4 | NA18967.hp2 NA18971.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-7687C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811233 | ||||||
| chr4:184811254
|
A | G | 14 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0191others(11): Show | 14 | HG01099.hp1 HG02486.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-7708T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811254 | ||||||
| chr4:184811264
|
A | G | 7 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0354others(4): Show | 7 | HG02486.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-7718T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811264 | ||||||
| chr4:184811265
|
C | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0186others(39): Show | 44 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-32-7719G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811265 | ||||||
| chr4:184811266
|
G | T | 1 | a0001c0002t0002g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-32-7720C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811266 | ||||||
| chr4:184811269
|
T | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0301a0001c0001t0001g0303others(6): Show | 10 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-7723A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811269 | ||||||
| chr4:184811275
|
AT | A | 12 | a0001c0001t0001g0171a0001c0001t0001g0228a0001c0001t0002g0150others(9): Show | 12 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-7730delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811275 | ||||||
| chr4:184811304
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-32-7758C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811304 | ||||||
| chr4:184811313
|
C | T | 2 | a0001c0002t0002g0007a0001c0008t0004g0304 | 3 | HG00639.hp2 NA18975.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-32-7767G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811313 | ||||||
| chr4:184811314
|
G | A | 4 | a0001c0001t0001g0328a0001c0002t0002g0201a0001c0002t0002g0244others(1): Show | 4 | HG01361.hp1 HG02976.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-7768C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811314 | ||||||
| chr4:184811319
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0118a0001c0001t0001g0119others(7): Show | 11 | HG00639.hp2 HG02071.hp2 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-7773C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811319 | ||||||
| chr4:184811319
|
G | C | 1 | a0001c0010t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-32-7773C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811319 | ||||||
| chr4:184811324
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0305a0001c0001t0004g0146others(4): Show | 8 | HG01106.hp2 HG01109.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32-7778C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811324 | ||||||
| chr4:184811326
|
A | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0305a0001c0001t0004g0140others(16): Show | 20 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-7780T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811326 | ||||||
| chr4:184811333
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0305others(19): Show | 23 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-32-7787G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811333 | ||||||
| chr4:184811334
|
G | A | 1 | a0001c0001t0002g0372 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-7788C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811334 | ||||||
| chr4:184811334
|
G | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0305others(19): Show | 23 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-32-7788C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811334 | ||||||
| chr4:184811341
|
C | T | 2 | a0001c0007t0002g0154a0001c0007t0002g0155 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-7795G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811341 | ||||||
| chr4:184811354
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-32-7808A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811354 | ||||||
| chr4:184811363
|
T | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(40): Show | 45 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-32-7817A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811363 | ||||||
| chr4:184811363
|
TGGCCTCC others(8898): Show |
T | 1 | a0001c0002t0002g0201 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-33+5648_-32-7818d others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811363 | ||||||
| chr4:184811370
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-32-7824G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811370 | ||||||
| chr4:184811391
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 72 | HG00544.hp2 HG00673.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-32-7845A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811391 | ||||||
| chr4:184811397
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32-7851G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811397 | ||||||
| chr4:184811401
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-32-7855G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811401 | ||||||
| chr4:184811402
|
G | A | 7 | a0001c0001t0001g0212a0001c0002t0002g0031a0001c0002t0002g0123others(4): Show | 8 | HG00544.hp1 HG02015.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-7856C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811402 | ||||||
| chr4:184811403
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-32-7857G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811403 | ||||||
| chr4:184811404
|
G | A | 17 | a0001c0001t0001g0322a0001c0001t0004g0140a0001c0001t0004g0141others(14): Show | 17 | HG00735.hp1 HG01069.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-32-7858C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811404 | ||||||
| chr4:184811407
|
C | T | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-7861G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811407 | ||||||
| chr4:184811408
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 287 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(284): Show |
intron_variant | MODIFIER | c.-32-7862T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811408 | ||||||
| chr4:184811486
|
A | G | 2 | a0001c0001t0001g0354a0001c0001t0002g0353 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-32-7940T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811486 | ||||||
| chr4:184811504
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(147): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-32-7958T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811504 | ||||||
| chr4:184812030
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-8484G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812030 | ||||||
| chr4:184812054
|
C | T | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.-32-8508G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812054 | ||||||
| chr4:184812182
|
T | C | 2 | a0001c0001t0005g0330a0001c0001t0005g0331 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-32-8636A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812182 | ||||||
| chr4:184812454
|
C | T | 1 | a0001c0001t0002g0353 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-32-8908G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812454 | ||||||
| chr4:184812455
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-32-8909C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812455 | ||||||
| chr4:184812470
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-8924G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812470 | ||||||
| chr4:184812572
|
GCT | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-9028_-32-9027d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812572 | ||||||
| chr4:184812588
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-32-9042A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812588 | ||||||
| chr4:184812637
|
A | T | 5 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0002g0225others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-9091T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812637 | ||||||
| chr4:184812816
|
C | T | 6 | a0001c0001t0004g0346a0001c0001t0004g0347a0001c0001t0004g0360others(3): Show | 6 | HG01358.hp1 HG01433.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-9270G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812816 | ||||||
| chr4:184813009
|
A | G | 18 | a0001c0001t0004g0140a0001c0001t0004g0145a0001c0001t0004g0146others(15): Show | 18 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32-9463T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813009 | ||||||
| chr4:184813029
|
C | CAAACA | 8 | a0001c0001t0001g0171a0001c0001t0001g0228a0001c0001t0001g0234others(5): Show | 8 | HG02027.hp1 HG02071.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-9488_-32-9484d others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813029 | ||||||
| chr4:184813128
|
G | A | 1 | a0001c0002t0002g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-32-9582C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813128 | ||||||
| chr4:184813130
|
T | C | 1 | a0001c0003t0003g0335 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32-9584A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813130 | ||||||
| chr4:184813159
|
T | A | 1 | a0001c0003t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-32-9613A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813159 | ||||||
| chr4:184813208
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-9662C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813208 | ||||||
| chr4:184813221
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-9675C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813221 | ||||||
| chr4:184813430
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-9884C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813430 | ||||||
| chr4:184813473
|
A | G | 1 | a0001c0003t0003g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-32-9927T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813473 | ||||||
| chr4:184813519
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-32-9973G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813519 | ||||||
| chr4:184813559
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-32-10013C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813559 | ||||||
| chr4:184813578
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32-10032G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813578 | ||||||
| chr4:184813579
|
G | A | 3 | a0001c0001t0001g0173a0001c0001t0002g0009a0001c0001t0002g0172 | 4 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-10033C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813579 | ||||||
| chr4:184813631
|
C | T | 1 | a0001c0003t0003g0267 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-32-10085G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813631 | ||||||
| chr4:184813632
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-10086C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813632 | ||||||
| chr4:184813637
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-32-10091C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813637 | ||||||
| chr4:184813644
|
C | T | 1 | a0001c0003t0003g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-32-10098G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813644 | ||||||
| chr4:184813718
|
A | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-10172T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813718 | ||||||
| chr4:184813727
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-10181G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813727 | ||||||
| chr4:184813900
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 139 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-32-10354C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813900 | ||||||
| chr4:184813980
|
A | G | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-10434T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813980 | ||||||
| chr4:184813988
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 20 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-10442T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813988 | ||||||
| chr4:184814061
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-32-10515G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814061 | ||||||
| chr4:184814168
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-32-10622C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814168 | ||||||
| chr4:184814190
|
C | G | 1 | a0001c0003t0003g0260 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-32-10644G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814190 | ||||||
| chr4:184814208
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0133others(1): Show | 4 | NA18955.hp2 NA19010.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-10662T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814208 | ||||||
| chr4:184814209
|
T | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0133others(1): Show | 4 | NA18955.hp2 NA19010.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-10663A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814209 | ||||||
| chr4:184814256
|
T | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(301): Show | 318 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.-32-10710A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814256 | ||||||
| chr4:184814277
|
C | A | 1 | a0001c0001t0004g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-32-10731G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814277 | ||||||
| chr4:184814286
|
G | A | 11 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(8): Show | 11 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-10740C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814286 | ||||||
| chr4:184814290
|
C | CA | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(198): Show | 212 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-32-10745dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | ||||||
| chr4:184814290
|
C | CAA | 21 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0129others(18): Show | 22 | HG00738.hp1 HG01167.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32-10746_-32-1074 others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | ||||||
| chr4:184814290
|
CA | C | 12 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0002g0150others(9): Show | 12 | HG01069.hp1 HG01081.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-10745delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | ||||||
| chr4:184814290
|
CAAA | C | 8 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0354others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-10747_-32-1074 others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | ||||||
| chr4:184814339
|
C | T | 2 | a0001c0002t0002g0107a0001c0004t0001g0106 | 2 | HG01928.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-32-10793G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814339 | ||||||
| chr4:184814400
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-32-10854C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814400 | ||||||
| chr4:184814400
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-10854C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814400 | ||||||
| chr4:184814420
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-10874C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814420 | ||||||
| chr4:184814524
|
G | A | 9 | a0001c0001t0004g0140a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-10978C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814524 | ||||||
| chr4:184814533
|
G | C | 3 | a0001c0001t0001g0173a0001c0001t0002g0009a0001c0001t0002g0172 | 4 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-10987C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814533 | ||||||
| chr4:184814547
|
T | C | 10 | a0001c0001t0004g0346a0001c0001t0004g0347a0001c0001t0004g0360others(7): Show | 10 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-11001A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814547 | ||||||
| chr4:184814837
|
G | A | 2 | a0001c0001t0001g0104a0001c0002t0002g0105 | 2 | HG02135.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-33+11079C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814837 | ||||||
| chr4:184814959
|
G | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 181 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.-33+10957C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814959 | ||||||
| chr4:184815001
|
G | A | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+10915C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815001 | ||||||
| chr4:184815005
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-33+10911A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815005 | ||||||
| chr4:184815076
|
G | C | 1 | a0001c0002t0002g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-33+10840C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815076 | ||||||
| chr4:184815160
|
T | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 18 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33+10756A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815160 | ||||||
| chr4:184815163
|
G | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-33+10753C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815163 | ||||||
| chr4:184815255
|
G | A | 1 | a0001c0003t0003g0008 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-33+10661C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815255 | ||||||
| chr4:184815299
|
C | T | 15 | a0001c0001t0004g0140a0001c0001t0004g0145a0001c0001t0004g0146others(12): Show | 15 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+10617G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815299 | ||||||
| chr4:184815337
|
C | T | 1 | a0001c0002t0002g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-33+10579G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815337 | ||||||
| chr4:184815489
|
T | TG | 34 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0002g0150others(31): Show | 34 | HG00639.hp1 HG01069.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+10426dupC | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815489 | ||||||
| chr4:184815495
|
G | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+10421C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815495 | ||||||
| chr4:184815535
|
G | A | 9 | a0001c0001t0002g0373a0001c0001t0002g0374a0001c0001t0002g0375others(6): Show | 9 | HG01081.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33+10381C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815535 | ||||||
| chr4:184815547
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-33+10369G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815547 | ||||||
| chr4:184816050
|
G | A | 1 | a0001c0001t0002g0348 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-33+9866C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816050 | ||||||
| chr4:184816053
|
C | T | 9 | a0001c0001t0004g0140a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33+9863G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816053 | ||||||
| chr4:184816059
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-33+9857C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816059 | ||||||
| chr4:184816208
|
A | C | 1 | a0001c0002t0002g0371 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-33+9708T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816208 | ||||||
| chr4:184816247
|
T | C | 2 | a0001c0002t0002g0220a0001c0002t0002g0221 | 2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-33+9669A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816247 | ||||||
| chr4:184816471
|
T | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(20): Show | 25 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-33+9445A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816471 | ||||||
| chr4:184816516
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+9400C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816516 | ||||||
| chr4:184816684
|
T | C | 1 | a0001c0001t0004g0366 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-33+9232A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816684 | ||||||
| chr4:184816689
|
G | A | 80 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0173others(77): Show | 83 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+9227C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816689 | ||||||
| chr4:184816711
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-33+9205T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816711 | ||||||
| chr4:184816800
|
C | T | 21 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(18): Show | 22 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-33+9116G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816800 | ||||||
| chr4:184816820
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-33+9096C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816820 | ||||||
| chr4:184816975
|
T | C | 1 | a0001c0001t0010g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33+8941A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816975 | ||||||
| chr4:184817007
|
G | C | 1 | a0001c0001t0004g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-33+8909C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817007 | ||||||
| chr4:184817092
|
A | T | 5 | a0001c0001t0002g0150a0001c0001t0002g0235a0001c0005t0012g0151others(2): Show | 5 | HG02258.hp2 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+8824T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817092 | ||||||
| chr4:184817122
|
T | A | 1 | a0001c0001t0004g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-33+8794A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817122 | ||||||
| chr4:184817269
|
G | T | 1 | a0001c0003t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-33+8647C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817269 | ||||||
| chr4:184817406
|
A | G | 2 | a0001c0001t0001g0239a0001c0003t0003g0358 | 2 | HG01255.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-33+8510T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817406 | ||||||
| chr4:184817456
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0010g0159 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-33+8460C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817456 | ||||||
| chr4:184817468
|
C | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-33+8448G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817468 | ||||||
| chr4:184817581
|
G | A | 5 | a0001c0001t0002g0150a0001c0001t0002g0235a0001c0005t0012g0151others(2): Show | 5 | HG02258.hp2 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+8335C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817581 | ||||||
| chr4:184817625
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-33+8291C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817625 | ||||||
| chr4:184817625
|
G | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-33+8291C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817625 | ||||||
| chr4:184817650
|
C | G | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33+8266G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817650 | ||||||
| chr4:184817756
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-33+8160C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817756 | ||||||
| chr4:184817768
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+8148G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817768 | ||||||
| chr4:184817772
|
G | A | 1 | a0001c0003t0003g0349 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-33+8144C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817772 | ||||||
| chr4:184818092
|
C | T | 5 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0002g0009others(2): Show | 6 | HG00733.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+7824G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818092 | ||||||
| chr4:184818099
|
G | C | 1 | a0001c0002t0002g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-33+7817C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818099 | ||||||
| chr4:184818556
|
C | T | 2 | a0001c0001t0001g0238a0001c0003t0003g0237 | 2 | NA19002.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-33+7360G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818556 | ||||||
| chr4:184818663
|
C | T | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33+7253G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818663 | ||||||
| chr4:184818740
|
G | C | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+7176C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818740 | ||||||
| chr4:184818814
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-33+7102G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818814 | ||||||
| chr4:184818910
|
T | C | 23 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(20): Show | 24 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-33+7006A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818910 | ||||||
| chr4:184818912
|
T | A | 1 | a0001c0002t0002g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+7004A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818912 | ||||||
| chr4:184819060
|
G | A | 1 | a0001c0001t0002g0357 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-33+6856C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819060 | ||||||
| chr4:184819061
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 20 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-33+6855G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819061 | ||||||
| chr4:184819140
|
C | CT | 12 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0202others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33+6775dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819140 | ||||||
| chr4:184819140
|
CT | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0135a0001c0001t0001g0171others(41): Show | 46 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-33+6775delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819140 | ||||||
| chr4:184819140
|
CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0002g0150a0001c0001t0002g0160a0001c0001t0002g0372others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33+6766_-33+6775d others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819140 | ||||||
| chr4:184819142
|
T | C | 21 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(18): Show | 22 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-33+6774A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819142 | ||||||
| chr4:184819169
|
G | T | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+6747C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819169 | ||||||
| chr4:184819211
|
T | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(27): Show | 32 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-33+6705A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819211 | ||||||
| chr4:184819535
|
C | T | 1 | a0001c0006t0002g0033 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-33+6381G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819535 | ||||||
| chr4:184819602
|
TAC | T | 7 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+6312_-33+6313d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819602 | ||||||
| chr4:184819618
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33+6298G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819618 | ||||||
| chr4:184819969
|
G | C | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5947C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819969 | ||||||
| chr4:184820035
|
A | AACAGGC | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5875_-33+5880d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820035 | ||||||
| chr4:184820121
|
C | T | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5795G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820121 | ||||||
| chr4:184820212
|
T | G | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+5704A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820212 | ||||||
| chr4:184820306
|
T | C | 1 | a0001c0002t0002g0351 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-33+5610A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820306 | ||||||
| chr4:184820324
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0010g0159 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-33+5592G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820324 | ||||||
| chr4:184820327
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-33+5589G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820327 | ||||||
| chr4:184820443
|
C | A | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5473G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820443 | ||||||
| chr4:184820607
|
C | CT | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0002g0226others(4): Show | 8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5308dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820607 | ||||||
| chr4:184820609
|
T | C | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01516.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+5307A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820609 | ||||||
| chr4:184820642
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-33+5274A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820642 | ||||||
| chr4:184820665
|
C | T | 1 | a0001c0002t0002g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33+5251G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820665 | ||||||
| chr4:184820704
|
A | T | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33+5212T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820704 | ||||||
| chr4:184820708
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(5): Show | 10 | HG01891.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+5208C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820708 | ||||||
| chr4:184820793
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+5123G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820793 | ||||||
| chr4:184820860
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(10): Show | 14 | HG01074.hp1 HG01109.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+5056G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820860 | ||||||
| chr4:184821255
|
C | T | 2 | a0001c0001t0002g0200a0001c0002t0002g0158 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+4661G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821255 | ||||||
| chr4:184821305
|
G | C | 3 | a0001c0005t0012g0151a0001c0005t0014g0153a0003c0012t0002g0152 | 3 | HG02258.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33+4611C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821305 | ||||||
| chr4:184821422
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(6): Show | 10 | HG01074.hp1 HG01109.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+4494G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821422 | ||||||
| chr4:184821956
|
C | T | 1 | a0001c0001t0004g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-33+3960G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821956 | ||||||
| chr4:184822194
|
C | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 221 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.-33+3722G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822194 | ||||||
| chr4:184822537
|
G | A | 1 | a0001c0002t0002g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-33+3379C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822537 | ||||||
| chr4:184822564
|
G | A | 1 | a0001c0003t0003g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-33+3352C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822564 | ||||||
| chr4:184822584
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 222 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(219): Show |
intron_variant | MODIFIER | c.-33+3332G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822584 | ||||||
| chr4:184822672
|
G | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0002g0004others(3): Show | 7 | HG02074.hp2 NA18941.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+3244C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822672 | ||||||
| chr4:184822834
|
T | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 19 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+3082A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822834 | ||||||
| chr4:184822860
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-33+3056T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822860 | ||||||
| chr4:184822916
|
C | A | 1 | a0001c0002t0002g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-33+3000G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822916 | ||||||
| chr4:184822949
|
T | C | 3 | a0001c0007t0002g0154a0001c0007t0002g0155a0001c0007t0002g0156 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33+2967A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822949 | ||||||
| chr4:184823177
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-33+2739G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823177 | ||||||
| chr4:184823270
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-33+2646T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823270 | ||||||
| chr4:184823508
|
T | C | 1 | a0001c0005t0003g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+2408A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823508 | ||||||
| chr4:184823649
|
A | T | 1 | a0001c0003t0003g0025 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-33+2267T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823649 | ||||||
| chr4:184823666
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 134 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.-33+2250G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823666 | ||||||
| chr4:184823741
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-33+2175T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823741 | ||||||
| chr4:184823768
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+2148A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823768 | ||||||
| chr4:184823875
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 221 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.-33+2041G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823875 | ||||||
| chr4:184824257
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0002t0002g0018others(4): Show | 8 | NA18965.hp2 NA18967.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+1659G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824257 | ||||||
| chr4:184824283
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+1633C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824283 | ||||||
| chr4:184824286
|
TG | T | 10 | a0001c0001t0004g0140a0001c0001t0004g0141a0001c0001t0004g0145others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+1629delC | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824286 | ||||||
| chr4:184824416
|
G | A | 1 | a0001c0002t0002g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-33+1500C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824416 | ||||||
| chr4:184824456
|
T | C | 55 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0171others(52): Show | 58 | HG00733.hp2 HG01074.hp1 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-33+1460A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824456 | ||||||
| chr4:184824486
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 221 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.-33+1430A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824486 | ||||||
| chr4:184824835
|
AAAAG | A | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG02647.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+1077_-33+1080d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824835 | ||||||
| chr4:184824934
|
G | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 223 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.-33+982C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824934 | ||||||
| chr4:184825019
|
G | A | 9 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | HG01167.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33+897C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825019 | ||||||
| chr4:184825103
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 143 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-33+813A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825103 | ||||||
| chr4:184825147
|
C | A | 1 | a0001c0003t0003g0358 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+769G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825147 | ||||||
| chr4:184825173
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-33+743C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825173 | ||||||
| chr4:184825341
|
T | C | 7 | a0001c0001t0004g0360a0001c0001t0004g0361a0001c0001t0004g0362others(4): Show | 7 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+575A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825341 | ||||||
| chr4:184825411
|
C | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 136 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.-33+505G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825411 | ||||||
| chr4:184825673
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 142 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.-33+243G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825673 | ||||||
| chr4:184825735
|
G | A | 4 | a0001c0001t0001g0367a0001c0001t0001g0368a0001c0001t0001g0369others(1): Show | 4 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+181C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825735 | ||||||
| chr4:184825788
|
G | A | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG02647.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+128C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825788 |