Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2181 |
|---|---|
| ensemblid | ENSG00000123983.15 |
| hgncid | 3570 |
| symbol | ACSL3 |
| name | acyl-CoA synthetase long chain family member 3 |
| refseq_nuc | NM_004457.5 |
| refseq_prot | NP_004448.2 |
| ensembl_nuc | ENST00000357430.8 |
| ensembl_prot | ENSP00000350012.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 222861036 |
| end | 222944639 |
| strand | + |
| ver | v1.2 |
| region | chr2:222861036-222944639 |
| region5000 | chr2:222856036-222949639 |
| regionname0 | ACSL3_chr2_222861036_222944639 |
| regionname5000 | ACSL3_chr2_222856036_222949639 |
| 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 | 720 | 249 | 84 | 55 | 70 | 14 | 24 | 52 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0002 | 0/0 | 720 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0003 | 0/0 | 720 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0004 | 0/0 | 720 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2163 | 240 | 83 | 51 | 70 | 13 | 21 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| c0002 | 0/0 | 2163 | 8 | 1 | 3 | 0 | 1 | 3 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| c0003 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| c0004 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| c0005 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| c0006 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| 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 | 0/1 | 3425 | 81 | 20 | 21 | 27 | 5 | 7 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0002 | 0/0 | 3425 | 75 | 11 | 17 | 35 | 3 | 9 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0003 | 0/0 | 3425 | 26 | 24 | 2 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0004 | 1/0 | 3415 | 16 | 3 | 6 | 1 | 4 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0005 | 0/0 | 3421 | 9 | 2 | 3 | 0 | 1 | 3 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0006 | 0/0 | 3418 | 5 | 1 | 2 | 0 | 1 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0007 | 0/0 | 3425 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0008 | 0/0 | 3421 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0009 | 0/0 | 3425 | 4 | 3 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0010 | 0/0 | 3425 | 3 | 3 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0011 | 0/0 | 3425 | 3 | 0 | 0 | 3 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0012 | 0/0 | 3425 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0013 | 0/0 | 3425 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0014 | 0/0 | 3414 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0015 | 0/0 | 3426 | 2 | 0 | 1 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0016 | 0/0 | 3425 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0017 | 0/0 | 3426 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0018 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0019 | 0/0 | 3418 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0020 | 0/0 | 3418 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0021 | 0/0 | 3415 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0022 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0023 | 0/0 | 3425 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0024 | 0/0 | 3425 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0025 | 0/0 | 3425 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0026 | 0/0 | 3425 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| t0027 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2163 | 240 | 83 | 51 | 70 | 13 | 21 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0002 | 0/0 | 2163 | 8 | 1 | 3 | 0 | 1 | 3 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0006 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0002c0003 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0003c0004 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0004c0005 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5587 | 80 | 20 | 20 | 27 | 5 | 7 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0002 | 0/0 | 5587 | 75 | 11 | 17 | 35 | 3 | 9 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0003 | 0/0 | 5587 | 25 | 23 | 2 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0004 | 1/0 | 5577 | 16 | 3 | 6 | 1 | 4 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0005 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0006 | 0/0 | 5580 | 5 | 1 | 2 | 0 | 1 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0007 | 0/0 | 5587 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0008 | 0/0 | 5583 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0009 | 0/0 | 5587 | 4 | 3 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0010 | 0/0 | 5587 | 3 | 3 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0011 | 0/0 | 5587 | 3 | 0 | 0 | 3 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0012 | 0/0 | 5587 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0013 | 0/0 | 5587 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0014 | 0/0 | 5576 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0015 | 0/0 | 5588 | 2 | 0 | 1 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0016 | 0/0 | 5587 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0017 | 0/0 | 5588 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0018 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0019 | 0/0 | 5580 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0021 | 0/0 | 5577 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0023 | 0/0 | 5587 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0024 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0025 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0026 | 0/0 | 5587 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0001t0027 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0002t0005 | 0/0 | 5583 | 8 | 1 | 3 | 0 | 1 | 3 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0001c0006t0001 | 0/0 | 5587 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0002c0003t0020 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0003c0004t0003 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| a0004c0005t0022 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | copy fasta | chr2 | 222856036 | 222949639 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0010g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0011g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0014g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0015g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0016g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0017g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0017g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0018g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0019g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0021g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0023g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0024g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0025g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0026g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0002t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0001c0006t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0002c0003t0020g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0003c0004t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| a0004c0005t0022g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0036 | EUR | GBR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0194 | EUR | GBR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0246 | EUR | FIN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0136 | EUR | FIN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0124 | EUR | FIN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00438 | hp1 | a0001 | c0001 | t0025 | g0086 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01081 | hp1 | a0001 | c0001 | t0021 | g0040 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01106 | hp1 | a0001 | c0006 | t0001 | g0095 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01109 | hp1 | a0002 | c0003 | t0020 | g0012 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0118 | AMR | PUR | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0121 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0126 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0134 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01358 | hp1 | a0001 | c0001 | t0015 | g0221 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0169 | EUR | IBS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0088 | EUR | IBS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0100 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01978 | hp1 | a0001 | c0002 | t0005 | g0122 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02083 | hp1 | a0001 | c0001 | t0011 | g0150 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CDX | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02273 | hp1 | a0001 | c0001 | t0026 | g0232 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02615 | hp1 | a0004 | c0005 | t0022 | g0205 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02622 | hp1 | a0001 | c0002 | t0005 | g0127 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0216 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02698 | hp1 | a0001 | c0001 | t0023 | g0175 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02698 | hp2 | a0001 | c0002 | t0005 | g0125 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02723 | hp2 | a0003 | c0004 | t0003 | g0010 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02738 | hp1 | a0001 | c0002 | t0005 | g0128 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0104 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0113 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0202 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02976 | hp1 | a0001 | c0001 | t0010 | g0141 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0243 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0214 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | ESN | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03579 | hp2 | a0001 | c0001 | t0027 | g0137 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03688 | hp2 | a0001 | c0002 | t0005 | g0123 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | BEB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG04199 | hp1 | a0001 | c0001 | t0015 | g0156 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0133 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18940 | hp2 | a0001 | c0001 | t0024 | g0071 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18977 | hp2 | a0001 | c0001 | t0011 | g0231 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18989 | hp2 | a0001 | c0001 | t0017 | g0066 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0200 | AFR | LWK | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0178 | AFR | LWK | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19063 | hp2 | a0001 | c0001 | t0017 | g0025 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19080 | hp2 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | YRI | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0117 | AFR | ASW | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ASW | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0037 | EUR | TSI | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | GIH | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA20905 | hp2 | a0001 | c0001 | t0019 | g0131 | SAS | GIH | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | USA | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | USA | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| NA21309 | hp2 | a0001 | c0001 | t0016 | g0101 | AFR | LWK | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0044 | REF | REF | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0217 | REF | REF | ACSL3_chr2_222856036_222949639 | ACSL3 | chr2 | 222856036 | 222949639 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222919163
|
A | G | 1 | a0004 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.766A>G | p.Met256Val | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/17 | 1195/5577 | 766/2163 | 256/720 | chr2 | 222919163 | ||
| chr2:222919191
|
A | G | 1 | a0003 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.794A>G | p.Lys265Arg | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/17 | 1223/5577 | 794/2163 | 265/720 | chr2 | 222919191 | ||
| chr2:222934623
|
G | C | 1 | a0002 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1941G>C | p.Glu647Asp | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/17 | 2370/5577 | 1941/2163 | 647/720 | chr2 | 222934623 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222916468
|
A | G | 1 | a0001c0006 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.528A>G | p.Ala176Ala | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/17 | 957/5577 | 528/2163 | 176/720 | chr2 | 222916468 | ||
| chr2:222919123
|
G | A | 1 | a0001c0002 | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
synonymous_variant | LOW | c.726G>A | p.Pro242Pro | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/17 | 1155/5577 | 726/2163 | 242/720 | chr2 | 222919123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222861073
|
G | C | 1 | a0001c0001t0007 | 4 | HG02257.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-392G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/17 | 47700 | chr2 | 222861073 | |||||
| chr2:222861098
|
C | G | 1 | a0001c0001t0027 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-367C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/17 | 47675 | chr2 | 222861098 | |||||
| chr2:222861241
|
C | T | 1 | a0001c0001t0011 | 3 | HG02083.hp1 NA18977.hp2 NA19080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-224C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/17 | 47532 | chr2 | 222861241 | |||||
| chr2:222900773
|
C | T | 6 | a0001c0001t0001a0001c0001t0017a0001c0001t0024others(3): Show | 86 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/17 | chr2 | 222900773 | ||||||
| chr2:222941770
|
C | T | 1 | a0001c0001t0023 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 116 | chr2 | 222941770 | |||||
| chr2:222942403
|
A | G | 1 | a0001c0001t0016 | 2 | HG01891.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*749A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 749 | chr2 | 222942403 | |||||
| chr2:222942538
|
C | T | 3 | a0001c0001t0009a0001c0001t0010a0004c0005t0022 | 8 | HG01243.hp2 HG02615.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*884C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 884 | chr2 | 222942538 | |||||
| chr2:222942539
|
G | A | 6 | a0001c0001t0001a0001c0001t0012a0001c0001t0017others(3): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 885 | chr2 | 222942539 | |||||
| chr2:222942604
|
C | T | 6 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(3): Show | 86 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*950C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 950 | chr2 | 222942604 | |||||
| chr2:222942605
|
T | C | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*951T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 951 | chr2 | 222942605 | |||||
| chr2:222942662
|
C | A | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1008C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1008 | chr2 | 222942662 | |||||
| chr2:222942912
|
T | TAGTA | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*1261_*1262insAAGT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1262 | INFO_REALIGN_3_PRIME | chr2 | 222942912 | ||||
| chr2:222943085
|
CA | C | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0014others(1): Show | 15 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1445delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1445 | INFO_REALIGN_3_PRIME | chr2 | 222943085 | ||||
| chr2:222943094
|
A | C | 1 | a0001c0001t0021 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1440 | chr2 | 222943094 | |||||
| chr2:222943096
|
A | AAAC | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 216 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1444_*1445insCAA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1445 | INFO_REALIGN_3_PRIME | chr2 | 222943096 | ||||
| chr2:222943100
|
C | A | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 216 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1446C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1446 | chr2 | 222943100 | |||||
| chr2:222943102
|
A | AAAAC | 2 | a0001c0001t0015a0001c0001t0017 | 4 | HG01358.hp1 HG04199.hp1 NA18989.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1452_*1455dupCAAA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1456 | INFO_REALIGN_3_PRIME | chr2 | 222943102 | ||||
| chr2:222943102
|
A | C | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 216 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1448A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1448 | chr2 | 222943102 | |||||
| chr2:222943251
|
A | ATTC | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*1599_*1600insCTT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1600 | INFO_REALIGN_3_PRIME | chr2 | 222943251 | ||||
| chr2:222943398
|
G | A | 1 | a0004c0005t0022 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1744G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1744 | chr2 | 222943398 | |||||
| chr2:222943402
|
G | T | 1 | a0002c0003t0020 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1748G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1748 | chr2 | 222943402 | |||||
| chr2:222943484
|
G | T | 1 | a0001c0001t0009 | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1830G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 1830 | chr2 | 222943484 | |||||
| chr2:222943683
|
A | C | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2029A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2029 | chr2 | 222943683 | |||||
| chr2:222943684
|
G | A | 1 | a0001c0001t0018 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2030G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2030 | chr2 | 222943684 | |||||
| chr2:222943719
|
G | C | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2065G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2065 | chr2 | 222943719 | |||||
| chr2:222943807
|
A | G | 1 | a0001c0001t0025 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2153A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2153 | chr2 | 222943807 | |||||
| chr2:222944152
|
C | T | 1 | a0001c0001t0013 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2498C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2498 | chr2 | 222944152 | |||||
| chr2:222944297
|
T | A | 1 | a0001c0001t0024 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2643 | chr2 | 222944297 | |||||
| chr2:222944353
|
G | A | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2699G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2699 | chr2 | 222944353 | |||||
| chr2:222944371
|
A | G | 1 | a0001c0001t0019 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2717A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 17/17 | 2717 | chr2 | 222944371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222861606
|
C | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0008g0006others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-207+348C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861606 | ||||||
| chr2:222861607
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-207+349C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861607 | ||||||
| chr2:222861644
|
T | A | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+386T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861644 | ||||||
| chr2:222861704
|
C | G | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-207+446C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861704 | ||||||
| chr2:222861723
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-207+465G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861723 | ||||||
| chr2:222861836
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-207+578C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861836 | ||||||
| chr2:222861858
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-207+600C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861858 | ||||||
| chr2:222861868
|
A | G | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-207+610A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861868 | ||||||
| chr2:222861971
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-207+713A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222861971 | ||||||
| chr2:222862082
|
A | G | 1 | a0001c0001t0007g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-207+824A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222862082 | ||||||
| chr2:222862185
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-207+927T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222862185 | ||||||
| chr2:222862281
|
C | A | 4 | a0001c0001t0004g0246a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 4 | HG00280.hp1 HG01109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+1023C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222862281 | ||||||
| chr2:222862467
|
T | A | 4 | a0001c0001t0004g0246a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 4 | HG00280.hp1 HG01109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+1209T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222862467 | ||||||
| chr2:222862495
|
T | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 94 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-207+1237T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222862495 | ||||||
| chr2:222862523
|
G | GT | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-207+1267dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222862523 | |||||
| chr2:222862714
|
A | AG | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-207+1456_-207+145 others(5): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222862714 | ||||||
| chr2:222863084
|
A | T | 9 | a0001c0001t0002g0129a0001c0002t0005g0121a0001c0002t0005g0122others(6): Show | 9 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207+1826A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863084 | ||||||
| chr2:222863292
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-207+2034T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863292 | ||||||
| chr2:222863297
|
G | A | 9 | a0001c0001t0002g0129a0001c0002t0005g0121a0001c0002t0005g0122others(6): Show | 9 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207+2039G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863297 | ||||||
| chr2:222863431
|
C | T | 4 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(1): Show | 4 | HG02080.hp2 NA18966.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+2173C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863431 | ||||||
| chr2:222863568
|
C | G | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+2310C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863568 | ||||||
| chr2:222863574
|
T | G | 9 | a0001c0001t0002g0129a0001c0002t0005g0121a0001c0002t0005g0122others(6): Show | 9 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207+2316T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863574 | ||||||
| chr2:222863619
|
A | C | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-207+2361A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863619 | ||||||
| chr2:222863635
|
T | TG | 10 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235others(7): Show | 10 | HG00558.hp2 HG02080.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-207+2378dupG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222863635 | |||||
| chr2:222863727
|
C | T | 3 | a0001c0001t0004g0246a0001c0001t0014g0013a0001c0001t0014g0014 | 3 | HG00280.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-207+2469C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863727 | ||||||
| chr2:222863830
|
A | G | 1 | a0001c0001t0026g0232 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-207+2572A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863830 | ||||||
| chr2:222863852
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-207+2594G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863852 | ||||||
| chr2:222863873
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-207+2615G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222863873 | ||||||
| chr2:222864171
|
C | G | 1 | a0001c0001t0011g0231 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-207+2913C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222864171 | ||||||
| chr2:222864231
|
G | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-207+2973G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222864231 | ||||||
| chr2:222864397
|
A | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+3139A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222864397 | ||||||
| chr2:222864402
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 96 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-207+3144A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222864402 | ||||||
| chr2:222864444
|
T | C | 4 | a0001c0001t0004g0246a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 4 | HG00280.hp1 HG01109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+3186T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222864444 | ||||||
| chr2:222864547
|
T | C | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+3289T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222864547 | ||||||
| chr2:222865049
|
C | T | 1 | a0001c0001t0011g0231 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-207+3791C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865049 | ||||||
| chr2:222865255
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-207+3997G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865255 | ||||||
| chr2:222865312
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-207+4054A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865312 | ||||||
| chr2:222865337
|
A | G | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-207+4079A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865337 | ||||||
| chr2:222865356
|
C | T | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-207+4098C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865356 | ||||||
| chr2:222865531
|
A | C | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-207+4273A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865531 | ||||||
| chr2:222865562
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-207+4304G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865562 | ||||||
| chr2:222865571
|
G | T | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-207+4313G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865571 | ||||||
| chr2:222865663
|
G | A | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-207+4405G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865663 | ||||||
| chr2:222865777
|
C | T | 1 | a0001c0001t0011g0231 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-207+4519C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865777 | ||||||
| chr2:222865794
|
C | CTG | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-207+4566_-207+456 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865794
|
C | CTGTG | 15 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-207+4564_-207+456 others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865794
|
C | CTGTGTG | 3 | a0001c0001t0006g0134a0001c0001t0006g0135a0001c0001t0006g0136 | 3 | HG00280.hp2 HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-207+4562_-207+456 others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865794
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0014g0013others(1): Show | 4 | HG02717.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207+4558_-207+456 others(14): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865794
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-207+4556_-207+456 others(16): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865794
|
CTG | C | 38 | a0001c0001t0001g0021a0001c0001t0002g0129a0001c0001t0002g0215others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-207+4566_-207+456 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865794
|
CTGTG | C | 90 | a0001c0001t0001g0159a0001c0001t0001g0167a0001c0001t0001g0177others(87): Show | 90 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-207+4564_-207+456 others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222865794 | |||||
| chr2:222865810
|
G | A | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | NA18952.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-207+4552G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222865810 | ||||||
| chr2:222866184
|
C | G | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+4926C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866184 | ||||||
| chr2:222866185
|
C | G | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+4927C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866185 | ||||||
| chr2:222866189
|
T | A | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+4931T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866189 | ||||||
| chr2:222866193
|
T | G | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+4935T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866193 | ||||||
| chr2:222866208
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-207+4950T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866208 | ||||||
| chr2:222866240
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0026others(3): Show | 6 | HG00639.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-207+4982G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866240 | ||||||
| chr2:222866326
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-207+5068C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866326 | ||||||
| chr2:222866347
|
A | G | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-207+5089A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866347 | ||||||
| chr2:222866366
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207+5108T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866366 | ||||||
| chr2:222866396
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-207+5138C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866396 | ||||||
| chr2:222866410
|
A | G | 6 | a0001c0001t0007g0243a0001c0001t0009g0117a0001c0001t0009g0118others(3): Show | 6 | HG01243.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-207+5152A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866410 | ||||||
| chr2:222866438
|
G | T | 8 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(5): Show | 8 | HG00558.hp2 HG02080.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+5180G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866438 | ||||||
| chr2:222866440
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-207+5182T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866440 | ||||||
| chr2:222866470
|
A | G | 4 | a0001c0001t0004g0246a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 4 | HG00280.hp1 HG01109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+5212A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866470 | ||||||
| chr2:222866585
|
T | G | 8 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+5327T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866585 | ||||||
| chr2:222866586
|
A | G | 8 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+5328A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866586 | ||||||
| chr2:222866588
|
C | A | 8 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+5330C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866588 | ||||||
| chr2:222866593
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-207+5335G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866593 | ||||||
| chr2:222866657
|
G | A | 20 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0004g0022others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-207+5399G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866657 | ||||||
| chr2:222866712
|
C | G | 1 | a0001c0001t0011g0231 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-207+5454C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866712 | ||||||
| chr2:222866740
|
C | G | 1 | a0001c0001t0002g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-207+5482C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866740 | ||||||
| chr2:222866744
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-207+5486G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866744 | ||||||
| chr2:222866744
|
G | GCCCCCTC others(4): Show |
1 | a0001c0001t0001g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-207+5491_-207+549 others(15): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866744 | |||||
| chr2:222866750
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(60): Show | 65 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-207+5492C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866750 | ||||||
| chr2:222866753
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-207+5495G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866753 | ||||||
| chr2:222866753
|
G | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0002g0233 | 3 | HG01081.hp2 HG01255.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-207+5495G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866753 | ||||||
| chr2:222866753
|
GC | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(14): Show | 17 | HG01099.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-207+5519delC | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCC | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 18 | HG00639.hp2 HG01168.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.-207+5517_-207+551 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCC | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-207+5516_-207+551 others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCCC | G | 30 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0027others(27): Show | 30 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-207+5515_-207+551 others(9): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCCCC | G | 29 | a0001c0001t0001g0028a0001c0001t0001g0084a0001c0001t0001g0188others(26): Show | 29 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-207+5514_-207+551 others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCCCCC | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0097others(28): Show | 31 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-207+5513_-207+551 others(11): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCCCCC others(1): Show |
G | 23 | a0001c0001t0001g0085a0001c0001t0002g0145a0001c0001t0002g0198others(20): Show | 23 | HG01071.hp2 HG01169.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-207+5512_-207+551 others(12): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCCCCC others(4): Show |
G | 2 | a0001c0001t0003g0247a0003c0004t0003g0010 | 2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-207+5509_-207+551 others(15): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866753
|
GCCCCCCC others(5): Show |
G | 1 | a0001c0001t0003g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-207+5508_-207+551 others(16): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866753 | |||||
| chr2:222866755
|
C | A | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-207+5497C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866755 | ||||||
| chr2:222866756
|
C | G | 1 | a0001c0001t0003g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-207+5498C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866756 | ||||||
| chr2:222866757
|
C | A | 1 | a0001c0002t0005g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-207+5499C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866757 | ||||||
| chr2:222866757
|
C | G | 1 | a0001c0001t0002g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-207+5499C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866757 | ||||||
| chr2:222866758
|
C | A | 1 | a0001c0001t0004g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-207+5500C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866758 | ||||||
| chr2:222866758
|
C | G | 4 | a0001c0001t0002g0132a0001c0001t0006g0133a0001c0001t0006g0136others(1): Show | 4 | HG00280.hp2 HG01192.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+5500C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866758 | ||||||
| chr2:222866759
|
C | G | 3 | a0001c0001t0002g0225a0001c0002t0005g0127a0004c0005t0022g0205 | 3 | HG00558.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-207+5501C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866759 | ||||||
| chr2:222866760
|
C | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-207+5502C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866760 | ||||||
| chr2:222866760
|
C | G | 3 | a0001c0001t0004g0042a0001c0001t0006g0135a0001c0001t0019g0131 | 3 | HG01433.hp2 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-207+5502C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866760 | ||||||
| chr2:222866761
|
C | G | 4 | a0001c0001t0002g0204a0001c0001t0003g0115a0001c0001t0006g0130others(1): Show | 4 | HG00642.hp2 HG01346.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207+5503C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866761 | ||||||
| chr2:222866766
|
C | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+5508C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866766 | ||||||
| chr2:222866769
|
C | G | 1 | a0001c0001t0003g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-207+5511C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866769 | ||||||
| chr2:222866770
|
C | G | 6 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(3): Show | 6 | HG01496.hp2 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-207+5512C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866770 | ||||||
| chr2:222866773
|
C | G | 18 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(15): Show | 18 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-207+5515C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866773 | ||||||
| chr2:222866779
|
C | G | 1 | a0001c0002t0005g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-207+5521C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866779 | ||||||
| chr2:222866820
|
ATTTTCTT others(2): Show |
A | 3 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009 | 3 | HG02896.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-207+5573_-207+558 others(13): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866820 | |||||
| chr2:222866840
|
C | CT | 30 | a0001c0001t0001g0064a0001c0001t0002g0132a0001c0001t0002g0179others(27): Show | 30 | HG00280.hp2 HG01192.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.-207+5594dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222866840 | |||||
| chr2:222866894
|
G | A | 1 | a0001c0006t0001g0095 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-207+5636G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222866894 | ||||||
| chr2:222867035
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207+5777A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867035 | ||||||
| chr2:222867565
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.-207+6307G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867565 | ||||||
| chr2:222867598
|
A | G | 11 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 11 | HG00280.hp2 HG01192.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.-207+6340A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867598 | ||||||
| chr2:222867628
|
G | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(14): Show | 17 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-207+6370G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867628 | ||||||
| chr2:222867657
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 80 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-207+6399A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867657 | ||||||
| chr2:222867843
|
C | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-207+6585C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867843 | ||||||
| chr2:222867859
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-207+6601G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867859 | ||||||
| chr2:222867928
|
C | T | 7 | a0001c0001t0002g0132a0001c0001t0006g0130a0001c0001t0006g0133others(4): Show | 7 | HG00280.hp2 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207+6670C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867928 | ||||||
| chr2:222867936
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0188 | 2 | NA18942.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-207+6678C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867936 | ||||||
| chr2:222867965
|
A | G | 1 | a0001c0002t0005g0127 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-207+6707A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867965 | ||||||
| chr2:222867980
|
C | CT | 5 | a0001c0001t0001g0063a0001c0001t0001g0081a0001c0001t0001g0097others(2): Show | 5 | HG02886.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-207+6735dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222867980 | |||||
| chr2:222867980
|
CT | C | 55 | a0001c0001t0002g0223a0001c0001t0002g0242a0001c0001t0003g0011others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-207+6735delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222867980 | |||||
| chr2:222867993
|
T | A | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+6735T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867993 | ||||||
| chr2:222867993
|
T | G | 34 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(31): Show | 34 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-207+6735T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222867993 | ||||||
| chr2:222868364
|
C | T | 1 | a0001c0001t0015g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-207+7106C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868364 | ||||||
| chr2:222868400
|
A | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+7142A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868400 | ||||||
| chr2:222868462
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-207+7204G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868462 | ||||||
| chr2:222868463
|
T | C | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-207+7205T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868463 | ||||||
| chr2:222868512
|
G | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(14): Show | 17 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-207+7254G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868512 | ||||||
| chr2:222868589
|
C | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-207+7331C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868589 | ||||||
| chr2:222868680
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0017g0025 | 4 | HG00544.hp2 HG02040.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207+7422C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868680 | ||||||
| chr2:222868757
|
G | A | 1 | a0001c0001t0003g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-207+7499G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868757 | ||||||
| chr2:222868793
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-207+7535G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868793 | ||||||
| chr2:222868839
|
G | C | 9 | a0001c0001t0002g0161a0001c0001t0002g0235a0001c0001t0002g0236others(6): Show | 9 | HG00423.hp1 HG00558.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-207+7581G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868839 | ||||||
| chr2:222868942
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | NA18940.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-207+7684C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868942 | ||||||
| chr2:222868965
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0245 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-207+7707G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868965 | ||||||
| chr2:222868969
|
C | CA | 53 | a0001c0001t0001g0046a0001c0001t0001g0072a0001c0001t0002g0168others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-207+7727dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222868969 | |||||
| chr2:222868969
|
CA | C | 8 | a0001c0001t0002g0225a0001c0001t0003g0138a0001c0001t0003g0139others(5): Show | 8 | HG00558.hp1 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+7727delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222868969 | |||||
| chr2:222868977
|
A | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0076 | 3 | HG01891.hp1 HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-207+7719A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222868977 | ||||||
| chr2:222869032
|
T | A | 62 | a0001c0001t0002g0132a0001c0001t0003g0011a0001c0001t0003g0099others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-207+7774T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869032 | ||||||
| chr2:222869325
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-207+8067T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869325 | ||||||
| chr2:222869364
|
C | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+8106C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869364 | ||||||
| chr2:222869422
|
C | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+8164C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869422 | ||||||
| chr2:222869423
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-207+8165C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869423 | ||||||
| chr2:222869428
|
C | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-207+8170C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869428 | ||||||
| chr2:222869467
|
A | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-207+8209A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869467 | ||||||
| chr2:222869588
|
G | C | 2 | a0001c0001t0003g0107a0001c0001t0003g0116 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-207+8330G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869588 | ||||||
| chr2:222869874
|
C | G | 1 | a0001c0001t0002g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-207+8616C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869874 | ||||||
| chr2:222869880
|
G | A | 28 | a0001c0001t0003g0203a0001c0001t0003g0208a0001c0001t0003g0209others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-207+8622G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222869880 | ||||||
| chr2:222870103
|
G | GT | 8 | a0001c0001t0001g0072a0001c0001t0001g0188a0001c0001t0002g0152others(5): Show | 8 | HG01109.hp2 HG01978.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+8860dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222870103 | |||||
| chr2:222870103
|
GT | G | 62 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-207+8860delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222870103 | |||||
| chr2:222870103
|
GTT | G | 7 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 7 | HG01433.hp1 HG02818.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207+8859_-207+886 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222870103 | |||||
| chr2:222870143
|
G | T | 10 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(7): Show | 10 | HG01361.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-207+8885G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870143 | ||||||
| chr2:222870155
|
G | A | 4 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+8897G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870155 | ||||||
| chr2:222870238
|
T | C | 17 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(14): Show | 17 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-207+8980T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870238 | ||||||
| chr2:222870287
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-207+9029A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870287 | ||||||
| chr2:222870526
|
G | A | 26 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(23): Show | 26 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.-207+9268G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870526 | ||||||
| chr2:222870532
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-207+9274G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870532 | ||||||
| chr2:222870552
|
G | A | 17 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(14): Show | 17 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-207+9294G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870552 | ||||||
| chr2:222870601
|
A | G | 1 | a0001c0001t0005g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-207+9343A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870601 | ||||||
| chr2:222870653
|
A | T | 1 | a0001c0001t0002g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-207+9395A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870653 | ||||||
| chr2:222870704
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-207+9446G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870704 | ||||||
| chr2:222870856
|
T | G | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-207+9598T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870856 | ||||||
| chr2:222870901
|
A | G | 2 | a0001c0001t0004g0106a0001c0001t0026g0232 | 2 | HG02273.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-207+9643A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870901 | ||||||
| chr2:222870942
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207+9684A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222870942 | ||||||
| chr2:222871171
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-207+9913C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871171 | ||||||
| chr2:222871249
|
G | GA | 63 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-207+9994dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222871249 | |||||
| chr2:222871283
|
G | T | 5 | a0001c0001t0006g0133a0001c0001t0006g0134a0001c0001t0006g0135others(2): Show | 5 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-207+10025G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871283 | ||||||
| chr2:222871412
|
G | T | 1 | a0001c0001t0010g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-207+10154G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871412 | ||||||
| chr2:222871604
|
A | G | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-207+10346A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871604 | ||||||
| chr2:222871628
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-207+10370G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871628 | ||||||
| chr2:222871959
|
C | G | 37 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(34): Show | 37 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.-207+10701C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871959 | ||||||
| chr2:222871965
|
C | T | 13 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(10): Show | 13 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-207+10707C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222871965 | ||||||
| chr2:222872007
|
A | G | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-207+10749A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872007 | ||||||
| chr2:222872023
|
G | A | 1 | a0001c0001t0008g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-207+10765G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872023 | ||||||
| chr2:222872053
|
A | C | 1 | a0001c0001t0002g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-207+10795A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872053 | ||||||
| chr2:222872141
|
TG | T | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+10884delG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872141 | ||||||
| chr2:222872198
|
C | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-207+10940C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872198 | ||||||
| chr2:222872404
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-207+11146G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872404 | ||||||
| chr2:222872431
|
T | C | 3 | a0001c0001t0010g0141a0001c0001t0016g0100a0001c0001t0016g0101 | 3 | HG01891.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-207+11173T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872431 | ||||||
| chr2:222872480
|
A | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-207+11222A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872480 | ||||||
| chr2:222872504
|
A | G | 1 | a0001c0001t0023g0175 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-207+11246A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872504 | ||||||
| chr2:222872506
|
C | T | 1 | a0001c0001t0023g0175 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-207+11248C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872506 | ||||||
| chr2:222872508
|
G | A | 1 | a0001c0001t0007g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-207+11250G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872508 | ||||||
| chr2:222872510
|
T | C | 1 | a0001c0001t0023g0175 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-207+11252T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872510 | ||||||
| chr2:222872516
|
A | G | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-207+11258A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872516 | ||||||
| chr2:222872552
|
A | G | 7 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207+11294A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872552 | ||||||
| chr2:222872703
|
T | A | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-207+11445T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872703 | ||||||
| chr2:222872897
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-207+11639A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222872897 | ||||||
| chr2:222873025
|
G | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(33): Show | 38 | HG00544.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-207+11767G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873025 | ||||||
| chr2:222873220
|
C | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-207+11962C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873220 | ||||||
| chr2:222873225
|
A | G | 2 | a0001c0001t0004g0035a0001c0001t0004g0036 | 2 | HG00099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-207+11967A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873225 | ||||||
| chr2:222873331
|
T | TA | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-207+12075dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222873331 | |||||
| chr2:222873473
|
A | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0009 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-207+12215A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873473 | ||||||
| chr2:222873548
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-207+12290C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873548 | ||||||
| chr2:222873644
|
T | C | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-207+12386T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873644 | ||||||
| chr2:222873767
|
C | T | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-207+12509C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873767 | ||||||
| chr2:222873880
|
G | A | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-207+12622G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222873880 | ||||||
| chr2:222873885
|
G | GT | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-207+12630dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222873885 | |||||
| chr2:222874113
|
C | T | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-207+12855C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874113 | ||||||
| chr2:222874148
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-207+12890G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874148 | ||||||
| chr2:222874172
|
A | G | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-207+12914A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874172 | ||||||
| chr2:222874308
|
G | A | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-207+13050G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874308 | ||||||
| chr2:222874428
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-207+13170C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874428 | ||||||
| chr2:222874445
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-207+13187C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874445 | ||||||
| chr2:222874553
|
G | A | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0027g0137 | 3 | HG02922.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-206-13277G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874553 | ||||||
| chr2:222874674
|
GA | G | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0074others(5): Show | 8 | HG01106.hp1 HG01433.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-206-13143delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222874674 | |||||
| chr2:222874685
|
A | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-206-13145A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874685 | ||||||
| chr2:222874812
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-206-13018A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874812 | ||||||
| chr2:222874814
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0026others(3): Show | 6 | HG00639.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-13016A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874814 | ||||||
| chr2:222874834
|
A | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-206-12996A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874834 | ||||||
| chr2:222874927
|
T | G | 37 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(34): Show | 37 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.-206-12903T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874927 | ||||||
| chr2:222874948
|
A | G | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-206-12882A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874948 | ||||||
| chr2:222874961
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-206-12869A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222874961 | ||||||
| chr2:222875092
|
CTAATGTT others(5): Show |
C | 1 | a0001c0006t0001g0095 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-206-12733_-206-12 others(18): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222875092 | |||||
| chr2:222875102
|
G | A | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-206-12728G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222875102 | ||||||
| chr2:222875244
|
TTTTATCA others(10): Show |
T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-12573_-206-12 others(23): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222875244 | |||||
| chr2:222875335
|
A | G | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-206-12495A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222875335 | ||||||
| chr2:222875683
|
A | G | 1 | a0001c0001t0007g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-206-12147A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222875683 | ||||||
| chr2:222875771
|
C | A | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-206-12059C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222875771 | ||||||
| chr2:222875796
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-206-12034A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222875796 | ||||||
| chr2:222875964
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-206-11866A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222875964 | ||||||
| chr2:222876311
|
G | T | 4 | a0001c0001t0001g0059a0001c0001t0002g0190a0001c0001t0002g0191others(1): Show | 4 | NA18941.hp2 NA18945.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-206-11519G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876311 | ||||||
| chr2:222876413
|
C | T | 5 | a0001c0001t0002g0179a0001c0001t0002g0183a0001c0001t0002g0190others(2): Show | 5 | NA18945.hp1 NA18967.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-206-11417C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876413 | ||||||
| chr2:222876592
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-206-11238G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876592 | ||||||
| chr2:222876742
|
A | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0152 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-206-11088A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876742 | ||||||
| chr2:222876787
|
A | G | 20 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-206-11043A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876787 | ||||||
| chr2:222876876
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-206-10954T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876876 | ||||||
| chr2:222876897
|
C | A | 1 | a0001c0001t0002g0184 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-206-10933C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222876897 | ||||||
| chr2:222877042
|
G | A | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-206-10788G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222877042 | ||||||
| chr2:222877733
|
A | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-206-10097A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222877733 | ||||||
| chr2:222877984
|
A | T | 7 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-206-9846A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222877984 | ||||||
| chr2:222878005
|
TTTAA | T | 16 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-206-9822_-206-981 others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222878005 | |||||
| chr2:222878304
|
A | G | 34 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(31): Show | 34 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-206-9526A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222878304 | ||||||
| chr2:222878329
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-206-9501A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222878329 | ||||||
| chr2:222878469
|
C | A | 34 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(31): Show | 34 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-206-9361C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222878469 | ||||||
| chr2:222878661
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-206-9169C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222878661 | ||||||
| chr2:222878699
|
T | G | 1 | a0001c0001t0017g0025 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-206-9131T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222878699 | ||||||
| chr2:222878726
|
A | T | 1 | a0001c0001t0002g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-206-9104A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222878726 | ||||||
| chr2:222878752
|
GTTC | G | 7 | a0001c0001t0002g0161a0001c0001t0002g0218a0001c0001t0002g0219others(4): Show | 7 | HG00423.hp1 HG01358.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-206-9072_-206-907 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222878752 | |||||
| chr2:222879002
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-206-8828T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222879002 | ||||||
| chr2:222879092
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 214 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-206-8738G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222879092 | ||||||
| chr2:222879304
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-206-8526C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222879304 | ||||||
| chr2:222879406
|
T | TC | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-8418dupC | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222879406 | |||||
| chr2:222879413
|
A | G | 34 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(31): Show | 34 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-206-8417A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222879413 | ||||||
| chr2:222879896
|
C | CT | 9 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0002g0223others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-206-7920dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222879896 | |||||
| chr2:222880034
|
G | A | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-206-7796G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880034 | ||||||
| chr2:222880200
|
T | G | 34 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(31): Show | 34 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.-206-7630T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880200 | ||||||
| chr2:222880433
|
A | C | 2 | a0001c0001t0003g0209a0001c0001t0003g0213 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-206-7397A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880433 | ||||||
| chr2:222880672
|
A | C | 1 | a0001c0001t0005g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-206-7158A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880672 | ||||||
| chr2:222880722
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0017g0025 | 3 | HG02040.hp2 HG02083.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-206-7108C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880722 | ||||||
| chr2:222880754
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-206-7076C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880754 | ||||||
| chr2:222880769
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.-206-7061A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880769 | ||||||
| chr2:222880831
|
C | CA | 48 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0064others(45): Show | 48 | HG00323.hp1 HG00642.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-6985dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222880831 | |||||
| chr2:222880831
|
C | CAA | 8 | a0001c0001t0003g0011a0001c0001t0003g0248a0001c0001t0007g0110others(5): Show | 8 | HG01978.hp1 HG02257.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-206-6986_-206-698 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222880831 | |||||
| chr2:222880839
|
A | C | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-206-6991A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880839 | ||||||
| chr2:222880846
|
C | A | 2 | a0001c0001t0001g0072a0001c0001t0002g0142 | 2 | NA18967.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-206-6984C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880846 | ||||||
| chr2:222880855
|
A | C | 7 | a0001c0001t0003g0103a0001c0001t0006g0130a0001c0001t0006g0133others(4): Show | 7 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.-206-6975A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880855 | ||||||
| chr2:222880955
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-206-6875G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222880955 | ||||||
| chr2:222881008
|
T | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-206-6822T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881008 | ||||||
| chr2:222881016
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.-206-6814A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881016 | ||||||
| chr2:222881091
|
A | G | 1 | a0001c0001t0002g0184 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-206-6739A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881091 | ||||||
| chr2:222881117
|
A | T | 1 | a0001c0001t0002g0249 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-206-6713A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881117 | ||||||
| chr2:222881223
|
C | G | 40 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.-206-6607C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881223 | ||||||
| chr2:222881308
|
T | TG | 3 | a0001c0001t0001g0159a0001c0001t0001g0177a0001c0001t0001g0188 | 3 | HG00423.hp2 NA18942.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-206-6521dupG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222881308 | |||||
| chr2:222881330
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-206-6500A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881330 | ||||||
| chr2:222881419
|
A | C | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-206-6411A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881419 | ||||||
| chr2:222881455
|
T | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01346.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-206-6375T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881455 | ||||||
| chr2:222881556
|
G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0009 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-206-6274G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881556 | ||||||
| chr2:222881602
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-206-6228C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881602 | ||||||
| chr2:222881609
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 122 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-206-6221C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881609 | ||||||
| chr2:222881816
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-206-6014A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222881816 | ||||||
| chr2:222882014
|
C | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-206-5816C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882014 | ||||||
| chr2:222882323
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-206-5507C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882323 | ||||||
| chr2:222882364
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-206-5466C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882364 | ||||||
| chr2:222882399
|
C | T | 85 | a0001c0001t0002g0132a0001c0001t0002g0142a0001c0001t0002g0143others(82): Show | 85 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-206-5431C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882399 | ||||||
| chr2:222882474
|
C | CAGT | 7 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-206-5355_-206-535 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882474 | |||||
| chr2:222882508
|
C | T | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-206-5322C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882508 | ||||||
| chr2:222882509
|
T | A | 102 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(99): Show | 102 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-206-5321T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882509 | ||||||
| chr2:222882761
|
G | GTT | 22 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0004g0106others(19): Show | 22 | HG00280.hp2 HG00323.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.-206-5051_-206-505 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882761
|
G | GTTTT | 58 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0145others(55): Show | 58 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-206-5053_-206-505 others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882761
|
G | GTTTTT | 43 | a0001c0001t0002g0132a0001c0001t0002g0144a0001c0001t0002g0146others(40): Show | 43 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-206-5054_-206-505 others(9): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882761
|
G | GTTTTTT | 8 | a0001c0001t0002g0129a0001c0001t0002g0152a0001c0001t0002g0153others(5): Show | 8 | HG01099.hp1 HG01358.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-206-5055_-206-505 others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882761
|
GT | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG00642.hp1 HG01099.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-206-5050delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882761
|
GTT | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 78 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-206-5051_-206-505 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882761
|
GTTTTTTT others(2): Show |
G | 10 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0105others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-206-5058_-206-505 others(13): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882761 | |||||
| chr2:222882794
|
C | T | 4 | a0001c0001t0002g0145a0001c0001t0002g0189a0001c0001t0002g0223others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-206-5036C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882794 | ||||||
| chr2:222882880
|
G | A | 138 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(135): Show | 138 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-206-4950G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882880 | ||||||
| chr2:222882965
|
C | T | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-206-4865C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882965 | ||||||
| chr2:222882966
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-206-4864G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222882966 | ||||||
| chr2:222882989
|
GA | G | 145 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(142): Show | 145 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-206-4839delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222882989 | |||||
| chr2:222883040
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-206-4790T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883040 | ||||||
| chr2:222883067
|
C | G | 1 | a0001c0001t0012g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-206-4763C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883067 | ||||||
| chr2:222883167
|
G | GT | 38 | a0001c0001t0001g0097a0001c0001t0003g0011a0001c0001t0003g0099others(35): Show | 38 | HG00280.hp2 HG00323.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-206-4649dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222883167 | |||||
| chr2:222883456
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-206-4374T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883456 | ||||||
| chr2:222883473
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-206-4357A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883473 | ||||||
| chr2:222883522
|
T | C | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-206-4308T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883522 | ||||||
| chr2:222883544
|
C | T | 1 | a0001c0001t0006g0135 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-206-4286C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883544 | ||||||
| chr2:222883605
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-206-4225T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883605 | ||||||
| chr2:222883709
|
C | CTTTT | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 236 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-206-4120_-206-411 others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222883709 | |||||
| chr2:222883801
|
A | G | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-206-4029A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883801 | ||||||
| chr2:222883824
|
A | G | 138 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(135): Show | 138 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-206-4006A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883824 | ||||||
| chr2:222883868
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-206-3962C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222883868 | ||||||
| chr2:222884065
|
G | A | 1 | a0001c0001t0010g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-206-3765G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884065 | ||||||
| chr2:222884368
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-206-3462C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884368 | ||||||
| chr2:222884406
|
A | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-206-3424A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884406 | ||||||
| chr2:222884439
|
G | A | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-3391G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884439 | ||||||
| chr2:222884595
|
C | T | 31 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(28): Show | 31 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.-206-3235C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884595 | ||||||
| chr2:222884844
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-206-2986T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884844 | ||||||
| chr2:222884994
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-206-2836C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222884994 | ||||||
| chr2:222885325
|
T | C | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-206-2505T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222885325 | ||||||
| chr2:222885407
|
G | T | 1 | a0001c0001t0001g0075 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-206-2423G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222885407 | ||||||
| chr2:222885703
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0097 | 2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-206-2127A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222885703 | ||||||
| chr2:222885750
|
C | CT | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-2070dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222885750 | |||||
| chr2:222885891
|
C | T | 138 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(135): Show | 138 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-206-1939C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222885891 | ||||||
| chr2:222886024
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | NA18940.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-206-1806T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886024 | ||||||
| chr2:222886101
|
G | A | 1 | a0001c0001t0004g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-206-1729G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886101 | ||||||
| chr2:222886138
|
A | T | 138 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(135): Show | 138 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-206-1692A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886138 | ||||||
| chr2:222886163
|
CCAT | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-206-1659_-206-165 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222886163 | |||||
| chr2:222886437
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0021g0040 | 3 | HG01081.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-206-1393C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886437 | ||||||
| chr2:222886461
|
A | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-206-1369A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886461 | ||||||
| chr2:222886493
|
T | A | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-206-1337T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886493 | ||||||
| chr2:222886700
|
C | T | 1 | a0001c0001t0012g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-206-1130C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886700 | ||||||
| chr2:222886712
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-206-1118A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886712 | ||||||
| chr2:222886738
|
C | T | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-206-1092C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886738 | ||||||
| chr2:222886789
|
C | A | 27 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(24): Show | 27 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.-206-1041C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886789 | ||||||
| chr2:222886795
|
T | C | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-206-1035T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886795 | ||||||
| chr2:222886920
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-206-910C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886920 | ||||||
| chr2:222886925
|
C | T | 6 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(3): Show | 6 | HG01361.hp2 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-905C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886925 | ||||||
| chr2:222886982
|
C | T | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-206-848C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222886982 | ||||||
| chr2:222887230
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-206-600C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222887230 | ||||||
| chr2:222887367
|
T | C | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-206-463T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222887367 | ||||||
| chr2:222887415
|
A | G | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-206-415A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222887415 | ||||||
| chr2:222887569
|
C | G | 1 | a0001c0001t0002g0241 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-206-261C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222887569 | ||||||
| chr2:222887747
|
G | C | 149 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(146): Show | 149 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-206-83G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | chr2 | 222887747 | ||||||
| chr2:222887765
|
CATTCGGC others(4): Show |
C | 2 | a0001c0001t0001g0159a0001c0001t0001g0188 | 2 | NA18942.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-206-61_-206-51del others(11): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 222887765 | |||||
| chr2:222888359
|
G | A | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-148+471G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222888359 | ||||||
| chr2:222888813
|
T | C | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-148+925T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222888813 | ||||||
| chr2:222888860
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-148+972C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222888860 | ||||||
| chr2:222888907
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-148+1019C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222888907 | ||||||
| chr2:222888940
|
T | A | 1 | a0001c0001t0002g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-148+1052T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222888940 | ||||||
| chr2:222889186
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-148+1298T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889186 | ||||||
| chr2:222889351
|
C | A | 1 | a0001c0001t0003g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-148+1463C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889351 | ||||||
| chr2:222889369
|
A | T | 143 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-148+1481A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889369 | ||||||
| chr2:222889426
|
C | T | 2 | a0001c0001t0007g0108a0001c0001t0007g0110 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-148+1538C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889426 | ||||||
| chr2:222889435
|
A | C | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-148+1547A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889435 | ||||||
| chr2:222889454
|
C | T | 2 | a0001c0001t0010g0200a0004c0005t0022g0205 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-148+1566C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889454 | ||||||
| chr2:222889644
|
A | G | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-148+1756A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889644 | ||||||
| chr2:222889670
|
C | T | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-148+1782C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889670 | ||||||
| chr2:222889813
|
A | C | 1 | a0001c0001t0006g0134 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-148+1925A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222889813 | ||||||
| chr2:222890161
|
T | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-148+2273T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890161 | ||||||
| chr2:222890275
|
A | G | 1 | a0001c0001t0006g0135 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-148+2387A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890275 | ||||||
| chr2:222890320
|
G | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+2432G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890320 | ||||||
| chr2:222890525
|
T | C | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | NA18952.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-148+2637T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890525 | ||||||
| chr2:222890633
|
G | C | 136 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-148+2745G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890633 | ||||||
| chr2:222890768
|
A | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-148+2880A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890768 | ||||||
| chr2:222890897
|
C | T | 136 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-148+3009C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222890897 | ||||||
| chr2:222891637
|
T | C | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-148+3749T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222891637 | ||||||
| chr2:222891653
|
A | G | 1 | a0001c0001t0005g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-148+3765A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222891653 | ||||||
| chr2:222892243
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-148+4355A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892243 | ||||||
| chr2:222892480
|
ACT | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-148+4595_-148+459 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222892480 | |||||
| chr2:222892563
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-148+4675C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892563 | ||||||
| chr2:222892662
|
CT | C | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-148+4780delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222892662 | |||||
| chr2:222892684
|
G | A | 136 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-148+4796G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892684 | ||||||
| chr2:222892800
|
G | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-148+4912G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892800 | ||||||
| chr2:222892841
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-148+4953A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892841 | ||||||
| chr2:222892894
|
T | C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-148+5006T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892894 | ||||||
| chr2:222892933
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-148+5045T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892933 | ||||||
| chr2:222892947
|
A | G | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-148+5059A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222892947 | ||||||
| chr2:222893058
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-148+5170A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893058 | ||||||
| chr2:222893084
|
G | A | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0027g0137 | 3 | HG02922.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-148+5196G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893084 | ||||||
| chr2:222893352
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 228 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.-148+5464C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893352 | ||||||
| chr2:222893444
|
G | T | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-148+5556G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893444 | ||||||
| chr2:222893465
|
G | A | 4 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(1): Show | 4 | HG00558.hp2 NA18942.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+5577G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893465 | ||||||
| chr2:222893508
|
T | C | 1 | a0001c0001t0014g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-148+5620T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893508 | ||||||
| chr2:222893639
|
C | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-148+5751C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893639 | ||||||
| chr2:222893951
|
C | T | 2 | a0001c0001t0012g0202a0001c0001t0012g0216 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-148+6063C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222893951 | ||||||
| chr2:222894096
|
A | G | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0027g0137 | 3 | HG02922.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-148+6208A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894096 | ||||||
| chr2:222894136
|
C | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-148+6248C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894136 | ||||||
| chr2:222894147
|
A | G | 1 | a0001c0001t0015g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-148+6259A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894147 | ||||||
| chr2:222894323
|
C | T | 1 | a0001c0001t0019g0131 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-147-6351C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894323 | ||||||
| chr2:222894404
|
C | A | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-147-6270C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894404 | ||||||
| chr2:222894415
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-147-6259C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894415 | ||||||
| chr2:222894701
|
T | C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-5973T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894701 | ||||||
| chr2:222894732
|
C | A | 1 | a0001c0001t0002g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-147-5942C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894732 | ||||||
| chr2:222894892
|
A | G | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-147-5782A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894892 | ||||||
| chr2:222894951
|
C | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-147-5723C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894951 | ||||||
| chr2:222894953
|
T | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-147-5721T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894953 | ||||||
| chr2:222894966
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-147-5708C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894966 | ||||||
| chr2:222894977
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-147-5697G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222894977 | ||||||
| chr2:222895020
|
A | C | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-147-5654A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222895020 | ||||||
| chr2:222895077
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-147-5597C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222895077 | ||||||
| chr2:222895329
|
C | G | 7 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-147-5345C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222895329 | ||||||
| chr2:222895460
|
TTACTTTG others(2486): Show |
T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-147-5200_-147-270 others(4): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222895460 | |||||
| chr2:222895470
|
CTTT | C | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-5178_-147-517 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222895470 | |||||
| chr2:222895470
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-5190_-147-517 others(19): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222895470 | |||||
| chr2:222895523
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-147-5151G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222895523 | ||||||
| chr2:222896151
|
C | CG | 9 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(6): Show | 9 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147-4520dupG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222896151 | |||||
| chr2:222896155
|
T | G | 9 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(6): Show | 9 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147-4519T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896155 | ||||||
| chr2:222896168
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-4506A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896168 | ||||||
| chr2:222896197
|
A | AC | 14 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0035others(11): Show | 14 | HG00280.hp1 HG00735.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-147-4466dupC | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222896197 | |||||
| chr2:222896211
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-4463C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896211 | ||||||
| chr2:222896293
|
C | A | 1 | a0001c0001t0004g0039 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-147-4381C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896293 | ||||||
| chr2:222896447
|
C | T | 1 | a0001c0001t0006g0135 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-147-4227C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896447 | ||||||
| chr2:222896491
|
C | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-4183C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896491 | ||||||
| chr2:222896554
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-4120C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896554 | ||||||
| chr2:222896566
|
CG | C | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-4101delG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222896566 | |||||
| chr2:222896614
|
G | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-4060G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896614 | ||||||
| chr2:222896812
|
T | C | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-3862T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896812 | ||||||
| chr2:222896820
|
CG | C | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-3847delG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222896820 | |||||
| chr2:222896867
|
G | GGGCAGAG others(71): Show |
6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3804_-147-380 others(82): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222896867 | |||||
| chr2:222896871
|
G | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3803G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896871 | ||||||
| chr2:222896873
|
G | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3801G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896873 | ||||||
| chr2:222896877
|
C | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3797C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896877 | ||||||
| chr2:222896878
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3796C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896878 | ||||||
| chr2:222896881
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3793C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896881 | ||||||
| chr2:222896882
|
A | C | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3792A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896882 | ||||||
| chr2:222896883
|
T | C | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3791T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896883 | ||||||
| chr2:222896886
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3788C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896886 | ||||||
| chr2:222896890
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3784C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896890 | ||||||
| chr2:222896895
|
T | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3779T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896895 | ||||||
| chr2:222896896
|
C | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3778C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896896 | ||||||
| chr2:222896897
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3777C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896897 | ||||||
| chr2:222896898
|
C | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3776C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896898 | ||||||
| chr2:222896903
|
C | G | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3771C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896903 | ||||||
| chr2:222896916
|
A | G | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-3758A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896916 | ||||||
| chr2:222896922
|
G | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3752G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896922 | ||||||
| chr2:222896931
|
C | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3743C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896931 | ||||||
| chr2:222896940
|
C | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3734C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896940 | ||||||
| chr2:222896950
|
C | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3724C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896950 | ||||||
| chr2:222896951
|
T | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3723T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896951 | ||||||
| chr2:222896964
|
G | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3710G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896964 | ||||||
| chr2:222896978
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3696C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896978 | ||||||
| chr2:222896995
|
T | C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3679T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222896995 | ||||||
| chr2:222897006
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3668A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897006 | ||||||
| chr2:222897008
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3666C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897008 | ||||||
| chr2:222897040
|
G | A | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-3634G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897040 | ||||||
| chr2:222897059
|
A | C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3615A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897059 | ||||||
| chr2:222897077
|
C | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3597C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897077 | ||||||
| chr2:222897091
|
G | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3583G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897091 | ||||||
| chr2:222897105
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3569C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897105 | ||||||
| chr2:222897106
|
C | CCCCCCAC others(40): Show |
1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3563_-147-356 others(51): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222897106 | |||||
| chr2:222897114
|
A | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3560A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897114 | ||||||
| chr2:222897117
|
T | C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3557T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897117 | ||||||
| chr2:222897290
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-147-3384C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897290 | ||||||
| chr2:222897464
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3210C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897464 | ||||||
| chr2:222897666
|
T | C | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-3008T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897666 | ||||||
| chr2:222897728
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-2946C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897728 | ||||||
| chr2:222897834
|
C | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-2840C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897834 | ||||||
| chr2:222897913
|
A | AGAGGGG | 5 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(2): Show | 5 | HG00280.hp2 HG01346.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147-2756_-147-275 others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222897913 | |||||
| chr2:222897919
|
A | AGAGGGGG others(5): Show |
1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-147-2733_-147-272 others(16): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222897919 | |||||
| chr2:222897919
|
A | G | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-2755A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897919 | ||||||
| chr2:222897986
|
G | A | 18 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(15): Show | 18 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-147-2688G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222897986 | ||||||
| chr2:222898064
|
G | A | 3 | a0001c0001t0010g0141a0001c0001t0016g0100a0001c0001t0016g0101 | 3 | HG01891.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-147-2610G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222898064 | ||||||
| chr2:222898259
|
A | T | 1 | a0001c0001t0002g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-147-2415A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222898259 | ||||||
| chr2:222898278
|
C | T | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147-2396C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222898278 | ||||||
| chr2:222898591
|
G | A | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0027g0137 | 3 | HG02922.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-147-2083G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222898591 | ||||||
| chr2:222898688
|
G | A | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-147-1986G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222898688 | ||||||
| chr2:222899163
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-147-1511T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899163 | ||||||
| chr2:222899273
|
A | G | 136 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-147-1401A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899273 | ||||||
| chr2:222899335
|
C | CGTG | 27 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(24): Show | 27 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.-147-1334_-147-133 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222899335 | |||||
| chr2:222899344
|
A | G | 1 | a0001c0001t0021g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-147-1330A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899344 | ||||||
| chr2:222899455
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-147-1219C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899455 | ||||||
| chr2:222899544
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-147-1130C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899544 | ||||||
| chr2:222899570
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-147-1104G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899570 | ||||||
| chr2:222899638
|
G | A | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0027g0137 | 3 | HG02922.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-147-1036G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899638 | ||||||
| chr2:222899848
|
C | G | 27 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(24): Show | 27 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.-147-826C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899848 | ||||||
| chr2:222899931
|
C | T | 1 | a0001c0001t0006g0134 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-147-743C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899931 | ||||||
| chr2:222899939
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-147-735C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222899939 | ||||||
| chr2:222900231
|
GAAT | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-147-441_-147-439d others(5): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 222900231 | |||||
| chr2:222900259
|
C | T | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-147-415C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222900259 | ||||||
| chr2:222900553
|
G | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 236 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-147-121G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222900553 | ||||||
| chr2:222900619
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-147-55C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | chr2 | 222900619 | ||||||
| chr2:222900816
|
C | G | 1 | a0001c0001t0002g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-41+36C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222900816 | ||||||
| chr2:222900884
|
T | C | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+104T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222900884 | ||||||
| chr2:222900922
|
A | G | 2 | a0001c0001t0012g0202a0001c0001t0012g0216 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-41+142A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222900922 | ||||||
| chr2:222900948
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-41+168A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222900948 | ||||||
| chr2:222901084
|
C | G | 1 | a0001c0001t0001g0019 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-41+304C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901084 | ||||||
| chr2:222901096
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-41+316A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901096 | ||||||
| chr2:222901193
|
C | G | 2 | a0001c0001t0012g0202a0001c0001t0012g0216 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-41+413C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901193 | ||||||
| chr2:222901200
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-41+420A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901200 | ||||||
| chr2:222901224
|
T | C | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-41+444T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901224 | ||||||
| chr2:222901409
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-41+629A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901409 | ||||||
| chr2:222901487
|
A | G | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+707A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901487 | ||||||
| chr2:222901501
|
G | GTTC | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-41+724_-41+726dup others(3): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222901501 | |||||
| chr2:222901561
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-41+781A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901561 | ||||||
| chr2:222901599
|
A | T | 93 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(90): Show | 93 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-41+819A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901599 | ||||||
| chr2:222901625
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-41+845C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901625 | ||||||
| chr2:222901679
|
G | A | 93 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(90): Show | 93 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-41+899G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901679 | ||||||
| chr2:222901732
|
G | GTC | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41+953_-41+954dup others(2): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222901732 | |||||
| chr2:222901811
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-41+1031T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901811 | ||||||
| chr2:222901951
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-41+1171A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901951 | ||||||
| chr2:222901963
|
A | T | 4 | a0001c0001t0002g0144a0001c0001t0002g0192a0001c0001t0016g0100others(1): Show | 4 | HG01106.hp2 HG01891.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+1183A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901963 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(8): Show |
7 | a0001c0001t0002g0155a0001c0001t0002g0164a0001c0001t0002g0169others(4): Show | 7 | HG00558.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(17): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(7): Show |
4 | a0001c0001t0002g0157a0001c0001t0002g0185a0001c0001t0002g0196others(1): Show | 4 | HG01109.hp2 HG02738.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(16): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(6): Show |
29 | a0001c0001t0002g0132a0001c0001t0002g0148a0001c0001t0002g0160others(26): Show | 29 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(15): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(5): Show |
39 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0146others(36): Show | 39 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(14): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(4): Show |
17 | a0001c0001t0002g0129a0001c0001t0002g0142a0001c0001t0002g0173others(14): Show | 17 | HG01256.hp2 HG01257.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(13): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(3): Show |
6 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0003g0103others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(12): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAA others(2): Show |
8 | a0001c0001t0002g0186a0001c0001t0003g0011a0001c0001t0003g0102others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(11): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAAAT others(1): Show |
31 | a0001c0001t0001g0026a0001c0001t0001g0056a0001c0001t0001g0063others(28): Show | 31 | HG00423.hp2 HG01081.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | AAAAAATG | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 79 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-41+1184_-41+1185i others(9): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222901964
|
A | G | 5 | a0001c0001t0002g0144a0001c0001t0002g0192a0001c0001t0016g0100others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+1184A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222901964 | ||||||
| chr2:222902048
|
TGTTACTT others(13): Show |
T | 1 | a0001c0001t0003g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-41+1271_-41+1290d others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222902048 | |||||
| chr2:222902112
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-41+1332A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222902112 | ||||||
| chr2:222902269
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-41+1489A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222902269 | ||||||
| chr2:222902437
|
A | G | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41+1657A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222902437 | ||||||
| chr2:222902889
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-41+2109G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222902889 | ||||||
| chr2:222902959
|
A | G | 136 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-41+2179A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222902959 | ||||||
| chr2:222902961
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-41+2181C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222902961 | ||||||
| chr2:222903139
|
A | T | 1 | a0001c0001t0002g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-41+2359A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903139 | ||||||
| chr2:222903199
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-41+2419A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903199 | ||||||
| chr2:222903385
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-41+2605A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903385 | ||||||
| chr2:222903482
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-41+2702T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903482 | ||||||
| chr2:222903491
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-41+2711C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903491 | ||||||
| chr2:222903671
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-41+2891A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903671 | ||||||
| chr2:222903814
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-41+3034C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903814 | ||||||
| chr2:222903828
|
A | G | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+3048A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222903828 | ||||||
| chr2:222903942
|
TA | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-41+3173delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222903942 | |||||
| chr2:222904288
|
C | CA | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 79 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-41+3512dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222904288 | |||||
| chr2:222904293
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-41+3513C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222904293 | ||||||
| chr2:222904293
|
C | CA | 143 | a0001c0001t0001g0049a0001c0001t0002g0129a0001c0001t0002g0132others(140): Show | 143 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.-41+3519dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222904293 | |||||
| chr2:222904957
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-40-3776G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222904957 | ||||||
| chr2:222905134
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-40-3599T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222905134 | ||||||
| chr2:222905258
|
T | C | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0027g0137 | 3 | HG02922.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-40-3475T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222905258 | ||||||
| chr2:222905285
|
C | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG00639.hp2 HG01099.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-3448C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222905285 | ||||||
| chr2:222905514
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-40-3219G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222905514 | ||||||
| chr2:222905525
|
G | C | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-40-3208G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222905525 | ||||||
| chr2:222905866
|
C | CT | 16 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0057others(13): Show | 16 | HG00323.hp2 HG00423.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40-2854dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222905866 | |||||
| chr2:222906080
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-40-2653A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906080 | ||||||
| chr2:222906335
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(33): Show | 38 | HG00544.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-40-2398A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906335 | ||||||
| chr2:222906344
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-40-2389C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906344 | ||||||
| chr2:222906618
|
AT | A | 141 | a0001c0001t0001g0031a0001c0001t0001g0159a0001c0001t0002g0129others(138): Show | 141 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-40-2099delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222906618 | |||||
| chr2:222906745
|
G | T | 1 | a0001c0001t0001g0003 | 2 | HG02040.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-40-1988G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906745 | ||||||
| chr2:222906789
|
A | G | 31 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(28): Show | 31 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.-40-1944A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906789 | ||||||
| chr2:222906890
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-1843C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906890 | ||||||
| chr2:222906995
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-40-1738A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222906995 | ||||||
| chr2:222907071
|
G | A | 1 | a0001c0001t0003g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-40-1662G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907071 | ||||||
| chr2:222907116
|
G | T | 1 | a0001c0001t0003g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-1617G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907116 | ||||||
| chr2:222907119
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-1614C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907119 | ||||||
| chr2:222907145
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-40-1588G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907145 | ||||||
| chr2:222907154
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-40-1579G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907154 | ||||||
| chr2:222907309
|
A | G | 1 | a0001c0001t0004g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-40-1424A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907309 | ||||||
| chr2:222907460
|
T | G | 7 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-1273T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907460 | ||||||
| chr2:222907552
|
G | A | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-40-1181G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907552 | ||||||
| chr2:222907649
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-40-1084C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907649 | ||||||
| chr2:222907736
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-40-997C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222907736 | ||||||
| chr2:222907756
|
T | TA | 7 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-960dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222907756 | |||||
| chr2:222907756
|
TA | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-40-960delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 222907756 | |||||
| chr2:222908026
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-707C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908026 | ||||||
| chr2:222908059
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 228 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.-40-674T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908059 | ||||||
| chr2:222908108
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-40-625G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908108 | ||||||
| chr2:222908113
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-620C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908113 | ||||||
| chr2:222908117
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-40-616C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908117 | ||||||
| chr2:222908184
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-40-549C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908184 | ||||||
| chr2:222908185
|
G | A | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-548G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 3/16 | chr2 | 222908185 | ||||||
| chr2:222909397
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.378+247T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909397 | ||||||
| chr2:222909639
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 228 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.378+489C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909639 | ||||||
| chr2:222909647
|
G | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.378+497G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909647 | ||||||
| chr2:222909687
|
A | G | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+537A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909687 | ||||||
| chr2:222909921
|
TG | T | 134 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.378+772delG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909921 | ||||||
| chr2:222909948
|
A | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0215 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.378+798A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909948 | ||||||
| chr2:222909959
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.378+809C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222909959 | ||||||
| chr2:222910083
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378+933T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910083 | ||||||
| chr2:222910171
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.378+1021A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910171 | ||||||
| chr2:222910189
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.378+1039G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910189 | ||||||
| chr2:222910454
|
A | G | 1 | a0001c0001t0004g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.378+1304A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910454 | ||||||
| chr2:222910552
|
A | G | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+1402A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910552 | ||||||
| chr2:222910573
|
C | T | 31 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(28): Show | 31 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+1423C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910573 | ||||||
| chr2:222910672
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.378+1522T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910672 | ||||||
| chr2:222910948
|
A | T | 1 | a0001c0001t0017g0025 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.378+1798A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222910948 | ||||||
| chr2:222911045
|
C | CT | 7 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+1916dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222911045 | |||||
| chr2:222911056
|
T | TC | 93 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(90): Show | 93 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.378+1906_378+1907i others(3): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911056 | ||||||
| chr2:222911057
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.378+1907T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911057 | ||||||
| chr2:222911083
|
C | T | 7 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+1933C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911083 | ||||||
| chr2:222911126
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.378+1976C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911126 | ||||||
| chr2:222911268
|
C | T | 100 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.378+2118C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911268 | ||||||
| chr2:222911397
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.378+2247C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911397 | ||||||
| chr2:222911722
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.378+2572T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222911722 | ||||||
| chr2:222912033
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.378+2883G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912033 | ||||||
| chr2:222912043
|
A | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0097 | 2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.378+2893A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912043 | ||||||
| chr2:222912083
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 86 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.378+2933C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912083 | ||||||
| chr2:222912200
|
C | T | 1 | a0001c0002t0005g0124 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.378+3050C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912200 | ||||||
| chr2:222912291
|
G | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.378+3141G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912291 | ||||||
| chr2:222912303
|
A | G | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+3153A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912303 | ||||||
| chr2:222912343
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.378+3193C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912343 | ||||||
| chr2:222912451
|
A | G | 1 | a0001c0001t0002g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.378+3301A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912451 | ||||||
| chr2:222912532
|
G | T | 1 | a0001c0001t0010g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.378+3382G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912532 | ||||||
| chr2:222912726
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.378+3576C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912726 | ||||||
| chr2:222912809
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.379-3510C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912809 | ||||||
| chr2:222912822
|
G | A | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.379-3497G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912822 | ||||||
| chr2:222912833
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.379-3486G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912833 | ||||||
| chr2:222912988
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0105others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.379-3331G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912988 | ||||||
| chr2:222912995
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.379-3324C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222912995 | ||||||
| chr2:222913211
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.379-3108A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913211 | ||||||
| chr2:222913554
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.379-2765C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913554 | ||||||
| chr2:222913602
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.379-2717C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913602 | ||||||
| chr2:222913604
|
C | T | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-2715C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913604 | ||||||
| chr2:222913705
|
G | T | 8 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2614G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913705 | ||||||
| chr2:222913888
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0045 | 3 | HG01074.hp1 HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.379-2431G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913888 | ||||||
| chr2:222913955
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.379-2364A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222913955 | ||||||
| chr2:222914200
|
G | C | 1 | a0001c0001t0001g0065 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.379-2119G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914200 | ||||||
| chr2:222914234
|
C | CGT | 14 | a0001c0001t0002g0157a0001c0001t0002g0174a0001c0001t0003g0116others(11): Show | 14 | HG00099.hp1 HG01109.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-2042_379-2041d others(4): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
C | CGTGT | 9 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-2044_379-2041d others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379-2050_379-2041d others(12): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGT | C | 47 | a0001c0001t0002g0132a0001c0001t0002g0143a0001c0001t0002g0146others(44): Show | 47 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.379-2042_379-2041d others(4): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGT | C | 22 | a0001c0001t0002g0129a0001c0001t0002g0144a0001c0001t0002g0165others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-2044_379-2041d others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGT | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(21): Show | 25 | HG00639.hp1 HG00642.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.379-2046_379-2041d others(8): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGTG others(1): Show |
C | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 67 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.379-2048_379-2041d others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGTG others(3): Show |
C | 8 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0081others(5): Show | 8 | HG01515.hp1 HG01517.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2050_379-2041d others(12): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGTG others(5): Show |
C | 3 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0052 | 3 | HG00639.hp2 HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.379-2052_379-2041d others(14): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0031a0001c0001t0001g0033 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.379-2054_379-2041d others(16): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379-2056_379-2041d others(18): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914234
|
CGTGTGTG others(11): Show |
C | 8 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2058_379-2041d others(20): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222914234 | |||||
| chr2:222914259
|
G | A | 8 | a0001c0001t0002g0146a0001c0001t0002g0148a0001c0001t0002g0152others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2060G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914259 | ||||||
| chr2:222914288
|
CAG | C | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2030_379-2029d others(4): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914288 | ||||||
| chr2:222914303
|
G | T | 2 | a0001c0002t0005g0121a0001c0002t0005g0126 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.379-2016G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914303 | ||||||
| chr2:222914402
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 228 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.379-1917G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914402 | ||||||
| chr2:222914462
|
G | C | 2 | a0001c0001t0004g0022a0001c0001t0004g0023 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.379-1857G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914462 | ||||||
| chr2:222914560
|
C | T | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.379-1759C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914560 | ||||||
| chr2:222914856
|
A | G | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-1463A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914856 | ||||||
| chr2:222914997
|
A | G | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379-1322A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222914997 | ||||||
| chr2:222915319
|
C | CTTAAATG others(174): Show |
1 | a0001c0001t0002g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.379-997_379-817dup others(181): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222915319 | |||||
| chr2:222915534
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.379-785G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222915534 | ||||||
| chr2:222915731
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.379-588A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222915731 | ||||||
| chr2:222915734
|
A | G | 4 | a0001c0001t0002g0145a0001c0001t0002g0189a0001c0001t0002g0223others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-585A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222915734 | ||||||
| chr2:222915984
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.379-335G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222915984 | ||||||
| chr2:222916064
|
T | TTTTTGAA others(3): Show |
1 | a0001c0001t0001g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.379-247_379-246ins others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222916064 | |||||
| chr2:222916203
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.379-116G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222916203 | ||||||
| chr2:222916242
|
C | G | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-77C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222916242 | ||||||
| chr2:222916299
|
AT | A | 92 | a0001c0001t0001g0056a0001c0001t0002g0129a0001c0001t0002g0132others(89): Show | 92 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.379-11delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 222916299 | |||||
| chr2:222916300
|
T | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 122 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.379-19T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222916300 | ||||||
| chr2:222916301
|
T | A | 1 | a0001c0001t0017g0025 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.379-18T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 4/16 | chr2 | 222916301 | ||||||
| chr2:222916850
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01346.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.556+354C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222916850 | ||||||
| chr2:222916983
|
G | C | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+487G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222916983 | ||||||
| chr2:222917257
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.556+761T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917257 | ||||||
| chr2:222917343
|
C | T | 2 | a0001c0001t0004g0035a0001c0001t0004g0036 | 2 | HG00099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.557-703C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917343 | ||||||
| chr2:222917455
|
C | A | 8 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-591C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917455 | ||||||
| chr2:222917569
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.557-477A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917569 | ||||||
| chr2:222917588
|
A | G | 101 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.557-458A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917588 | ||||||
| chr2:222917649
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.557-397C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917649 | ||||||
| chr2:222917666
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(33): Show | 38 | HG00544.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.557-380G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917666 | ||||||
| chr2:222917671
|
T | C | 30 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0102others(27): Show | 30 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.557-375T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917671 | ||||||
| chr2:222917679
|
T | C | 95 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0083others(92): Show | 95 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.557-367T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917679 | ||||||
| chr2:222917948
|
G | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.557-98G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 5/16 | chr2 | 222917948 | ||||||
| chr2:222918164
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.666+9T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918164 | ||||||
| chr2:222918175
|
TCTAA | T | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+23_666+26delAA others(2): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 222918175 | |||||
| chr2:222918199
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.666+44T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918199 | ||||||
| chr2:222918232
|
G | C | 1 | a0001c0001t0005g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666+77G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918232 | ||||||
| chr2:222918313
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666+158A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918313 | ||||||
| chr2:222918404
|
TTC | T | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+253_666+254del others(2): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 222918404 | |||||
| chr2:222918461
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.666+306A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918461 | ||||||
| chr2:222918537
|
G | A | 7 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+382G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918537 | ||||||
| chr2:222918579
|
A | AG | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.666+425dupG | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 222918579 | |||||
| chr2:222918774
|
T | C | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-290T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918774 | ||||||
| chr2:222918905
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.667-159A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 6/16 | chr2 | 222918905 | ||||||
| chr2:222919350
|
T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.805+148T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222919350 | ||||||
| chr2:222919446
|
A | T | 5 | a0001c0001t0004g0034a0001c0001t0004g0038a0001c0001t0004g0039others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+244A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222919446 | ||||||
| chr2:222919759
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0245 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.805+557C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222919759 | ||||||
| chr2:222920027
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.805+825A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920027 | ||||||
| chr2:222920423
|
G | A | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-857G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920423 | ||||||
| chr2:222920465
|
A | G | 4 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0126others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-815A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920465 | ||||||
| chr2:222920553
|
T | A | 18 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(15): Show | 18 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.806-727T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920553 | ||||||
| chr2:222920644
|
C | T | 14 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0105others(11): Show | 14 | HG01361.hp2 HG01496.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-636C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920644 | ||||||
| chr2:222920662
|
C | CT | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.806-610dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 222920662 | |||||
| chr2:222920689
|
C | G | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.806-591C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920689 | ||||||
| chr2:222920759
|
A | G | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-521A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920759 | ||||||
| chr2:222920786
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 235 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.806-494T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222920786 | ||||||
| chr2:222921022
|
A | G | 112 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0083others(109): Show | 112 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.806-258A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222921022 | ||||||
| chr2:222921128
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.806-152G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 7/16 | chr2 | 222921128 | ||||||
| chr2:222921528
|
CT | C | 3 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206 | 3 | HG02258.hp1 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.956+99delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222921528 | ||||||
| chr2:222921545
|
G | A | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+115G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222921545 | ||||||
| chr2:222921550
|
C | T | 1 | a0001c0001t0005g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.956+120C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222921550 | ||||||
| chr2:222921789
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.956+359T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222921789 | ||||||
| chr2:222921854
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.956+424G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222921854 | ||||||
| chr2:222921949
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.956+519C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222921949 | ||||||
| chr2:222922209
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.957-499T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922209 | ||||||
| chr2:222922217
|
A | T | 2 | a0001c0001t0003g0209a0001c0001t0003g0213 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.957-491A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922217 | ||||||
| chr2:222922348
|
A | G | 92 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0083others(89): Show | 92 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.957-360A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922348 | ||||||
| chr2:222922426
|
C | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.957-282C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922426 | ||||||
| chr2:222922535
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.957-173C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922535 | ||||||
| chr2:222922554
|
G | GTCTC | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.957-141_957-138dup others(4): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 222922554 | |||||
| chr2:222922610
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.957-98G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922610 | ||||||
| chr2:222922614
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.957-94C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922614 | ||||||
| chr2:222922619
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.957-89C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922619 | ||||||
| chr2:222922690
|
G | A | 3 | a0001c0001t0010g0141a0001c0001t0010g0200a0004c0005t0022g0205 | 3 | HG02615.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.957-18G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 8/16 | chr2 | 222922690 | ||||||
| chr2:222922841
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1080+10G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 9/16 | chr2 | 222922841 | ||||||
| chr2:222922870
|
A | G | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1080+39A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 9/16 | chr2 | 222922870 | ||||||
| chr2:222922973
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1081-105G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 9/16 | chr2 | 222922973 | ||||||
| chr2:222923021
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1081-57C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 9/16 | chr2 | 222923021 | ||||||
| chr2:222923291
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1152+142G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923291 | ||||||
| chr2:222923594
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+445C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923594 | ||||||
| chr2:222923742
|
C | T | 2 | a0001c0001t0002g0219a0001c0001t0002g0222 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1152+593C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923742 | ||||||
| chr2:222923789
|
A | AGTAGTTT others(1): Show |
224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1152+641_1152+648d others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 222923789 | |||||
| chr2:222923861
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1153-595C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923861 | ||||||
| chr2:222923914
|
A | G | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153-542A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923914 | ||||||
| chr2:222923944
|
C | T | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-512C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923944 | ||||||
| chr2:222923999
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1153-457T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222923999 | ||||||
| chr2:222924033
|
A | G | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1153-423A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222924033 | ||||||
| chr2:222924074
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1153-382T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222924074 | ||||||
| chr2:222924130
|
G | T | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-326G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222924130 | ||||||
| chr2:222924336
|
A | G | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1153-120A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222924336 | ||||||
| chr2:222924362
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 217 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1153-94C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222924362 | ||||||
| chr2:222924371
|
T | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0225 | 2 | HG00558.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1153-85T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 10/16 | chr2 | 222924371 | ||||||
| chr2:222924778
|
C | A | 2 | a0001c0001t0013g0104a0001c0001t0013g0113 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1292+183C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222924778 | ||||||
| chr2:222924808
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 217 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292+213G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222924808 | ||||||
| chr2:222924923
|
G | A | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1292+328G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222924923 | ||||||
| chr2:222924941
|
G | A | 12 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0105others(9): Show | 12 | HG01361.hp2 HG01496.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292+346G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222924941 | ||||||
| chr2:222924958
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1292+363G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222924958 | ||||||
| chr2:222925030
|
CA | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 229 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1292+451delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 222925030 | |||||
| chr2:222925108
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1292+513G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222925108 | ||||||
| chr2:222925342
|
C | CA | 16 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0002g0173others(13): Show | 16 | HG00323.hp1 HG00544.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1292+769dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 222925342 | |||||
| chr2:222925342
|
CA | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 100 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1292+769delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 222925342 | |||||
| chr2:222925424
|
T | C | 1 | a0001c0001t0026g0232 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1292+829T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222925424 | ||||||
| chr2:222925567
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0026others(3): Show | 6 | HG00639.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292+972A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222925567 | ||||||
| chr2:222925590
|
T | G | 1 | a0001c0001t0001g0017 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1292+995T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222925590 | ||||||
| chr2:222926042
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1293-975C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222926042 | ||||||
| chr2:222926149
|
T | C | 1 | a0001c0001t0006g0136 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1293-868T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222926149 | ||||||
| chr2:222926684
|
C | T | 3 | a0001c0001t0010g0141a0001c0001t0010g0200a0004c0005t0022g0205 | 3 | HG02615.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1293-333C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222926684 | ||||||
| chr2:222926757
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1293-260A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222926757 | ||||||
| chr2:222926796
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1293-221C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 11/16 | chr2 | 222926796 | ||||||
| chr2:222927238
|
T | C | 1 | a0001c0001t0006g0134 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1465+49T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222927238 | ||||||
| chr2:222927332
|
T | C | 26 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(23): Show | 26 | HG00323.hp2 HG00423.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1465+143T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222927332 | ||||||
| chr2:222927686
|
A | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1465+497A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222927686 | ||||||
| chr2:222927926
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0188 | 2 | NA18942.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1465+737G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222927926 | ||||||
| chr2:222928120
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | NA18940.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1466-742T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928120 | ||||||
| chr2:222928139
|
A | G | 4 | a0001c0001t0010g0141a0001c0001t0010g0200a0001c0001t0010g0214others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1466-723A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928139 | ||||||
| chr2:222928324
|
G | A | 2 | a0001c0001t0004g0037a0001c0001t0004g0042 | 2 | HG03927.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1466-538G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928324 | ||||||
| chr2:222928384
|
A | G | 8 | a0001c0001t0002g0146a0001c0001t0002g0148a0001c0001t0002g0152others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1466-478A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928384 | ||||||
| chr2:222928431
|
A | G | 90 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(87): Show | 90 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1466-431A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928431 | ||||||
| chr2:222928497
|
G | A | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1466-365G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928497 | ||||||
| chr2:222928652
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1466-210T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928652 | ||||||
| chr2:222928652
|
T | TA | 34 | a0001c0001t0002g0168a0001c0001t0003g0102a0001c0001t0003g0103others(31): Show | 34 | HG00323.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1466-194dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 222928652 | |||||
| chr2:222928652
|
TA | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0053others(5): Show | 9 | HG00099.hp2 HG01515.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466-194delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 222928652 | |||||
| chr2:222928665
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0245 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1466-197A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928665 | ||||||
| chr2:222928753
|
C | T | 130 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(127): Show | 130 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1466-109C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928753 | ||||||
| chr2:222928762
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 235 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1466-100C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 12/16 | chr2 | 222928762 | ||||||
| chr2:222929073
|
C | T | 1 | a0001c0001t0010g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1540+137C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929073 | ||||||
| chr2:222929198
|
A | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1540+262A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929198 | ||||||
| chr2:222929291
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1540+355A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929291 | ||||||
| chr2:222929304
|
CT | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1540+377delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222929304 | |||||
| chr2:222929310
|
T | G | 1 | a0001c0001t0003g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1540+374T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929310 | ||||||
| chr2:222929331
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540+395G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929331 | ||||||
| chr2:222929480
|
TAAGTA | T | 6 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235others(3): Show | 6 | HG00558.hp2 HG02523.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540+548_1540+552d others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222929480 | |||||
| chr2:222929494
|
G | A | 6 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235others(3): Show | 6 | HG00558.hp2 HG02523.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540+558G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929494 | ||||||
| chr2:222929662
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1540+726C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929662 | ||||||
| chr2:222929737
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1540+801C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929737 | ||||||
| chr2:222929792
|
TAAAG | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541-823_1541-820d others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222929792 | |||||
| chr2:222929836
|
C | T | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1541-785C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929836 | ||||||
| chr2:222929923
|
CT | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 199 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1541-677delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222929923 | |||||
| chr2:222929923
|
CTT | C | 16 | a0001c0001t0001g0004a0001c0001t0002g0148a0001c0001t0002g0164others(13): Show | 16 | HG01516.hp1 HG01517.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.1541-678_1541-677d others(4): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222929923 | |||||
| chr2:222929923
|
CTTT | C | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1541-679_1541-677d others(5): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222929923 | |||||
| chr2:222929926
|
T | G | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1541-695T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929926 | ||||||
| chr2:222929949
|
C | T | 2 | a0001c0001t0003g0163a0001c0001t0003g0206 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1541-672C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222929949 | ||||||
| chr2:222930031
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1541-590T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222930031 | ||||||
| chr2:222930089
|
C | T | 6 | a0001c0001t0006g0133a0001c0001t0006g0134a0001c0001t0006g0135others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541-532C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222930089 | ||||||
| chr2:222930168
|
G | A | 25 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(22): Show | 25 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1541-453G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | chr2 | 222930168 | ||||||
| chr2:222930345
|
AT | A | 9 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541-273delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 222930345 | |||||
| chr2:222930845
|
G | T | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1732+33G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930845 | ||||||
| chr2:222930847
|
T | G | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1732+35T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930847 | ||||||
| chr2:222930849
|
C | G | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1732+37C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930849 | ||||||
| chr2:222930851
|
G | A | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1732+39G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930851 | ||||||
| chr2:222930854
|
A | C | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1732+42A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930854 | ||||||
| chr2:222930857
|
G | T | 1 | a0001c0001t0027g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1732+45G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930857 | ||||||
| chr2:222930985
|
T | C | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1732+173T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222930985 | ||||||
| chr2:222931133
|
TTGCCC | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1732+327_1732+331d others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 222931133 | |||||
| chr2:222931152
|
A | G | 2 | a0001c0001t0002g0219a0001c0001t0002g0222 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1732+340A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931152 | ||||||
| chr2:222931305
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1732+493T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931305 | ||||||
| chr2:222931408
|
T | A | 8 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(5): Show | 8 | HG01243.hp2 HG02615.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1732+596T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931408 | ||||||
| chr2:222931412
|
T | TA | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 99 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1732+615dupA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 222931412 | |||||
| chr2:222931412
|
TA | T | 9 | a0001c0001t0002g0132a0001c0001t0002g0157a0001c0001t0002g0164others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1732+615delA | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 222931412 | |||||
| chr2:222931468
|
T | C | 1 | a0001c0001t0025g0086 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1732+656T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931468 | ||||||
| chr2:222931508
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0076 | 3 | HG01891.hp1 HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1732+696A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931508 | ||||||
| chr2:222931655
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1732+843C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931655 | ||||||
| chr2:222931712
|
C | G | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1732+900C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931712 | ||||||
| chr2:222931728
|
C | T | 4 | a0001c0001t0010g0141a0001c0001t0010g0200a0001c0001t0010g0214others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732+916C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931728 | ||||||
| chr2:222931751
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1732+939G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931751 | ||||||
| chr2:222931752
|
C | T | 4 | a0001c0001t0010g0141a0001c0001t0010g0200a0001c0001t0010g0214others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732+940C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931752 | ||||||
| chr2:222931787
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1732+975G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931787 | ||||||
| chr2:222931805
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1732+993C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931805 | ||||||
| chr2:222931894
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1732+1082C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222931894 | ||||||
| chr2:222932058
|
T | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1733-1108T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932058 | ||||||
| chr2:222932151
|
T | C | 18 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(15): Show | 18 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1733-1015T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932151 | ||||||
| chr2:222932195
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1733-971G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932195 | ||||||
| chr2:222932369
|
C | A | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1733-797C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932369 | ||||||
| chr2:222932448
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1733-718C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932448 | ||||||
| chr2:222932470
|
A | G | 105 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(102): Show | 105 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1733-696A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932470 | ||||||
| chr2:222932478
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1733-688A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932478 | ||||||
| chr2:222932607
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1733-559A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222932607 | ||||||
| chr2:222932640
|
TAAAAGCA others(310): Show |
T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1733-516_1733-200d others(2): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 222932640 | |||||
| chr2:222933079
|
G | A | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1733-87G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 14/16 | chr2 | 222933079 | ||||||
| chr2:222933423
|
A | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1847+143A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222933423 | ||||||
| chr2:222933455
|
T | TC | 18 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(15): Show | 18 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1847+179dupC | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 222933455 | |||||
| chr2:222933526
|
A | G | 10 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1847+246A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222933526 | ||||||
| chr2:222933712
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1847+432A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222933712 | ||||||
| chr2:222933783
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 202 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1847+503G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222933783 | ||||||
| chr2:222933829
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1847+549C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222933829 | ||||||
| chr2:222934015
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1848-515T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222934015 | ||||||
| chr2:222934204
|
G | A | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1848-326G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222934204 | ||||||
| chr2:222934235
|
ACTTT | A | 80 | a0001c0001t0002g0132a0001c0001t0002g0142a0001c0001t0002g0143others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1848-290_1848-287d others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 222934235 | |||||
| chr2:222934331
|
A | G | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848-199A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222934331 | ||||||
| chr2:222934412
|
A | G | 1 | a0001c0001t0005g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1848-118A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222934412 | ||||||
| chr2:222934436
|
T | G | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1848-94T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222934436 | ||||||
| chr2:222934489
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1848-41C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 15/16 | chr2 | 222934489 | ||||||
| chr2:222934746
|
A | T | 3 | a0001c0002t0005g0121a0001c0002t0005g0126a0001c0002t0005g0128 | 3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2005+59A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222934746 | ||||||
| chr2:222934781
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2005+94T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222934781 | ||||||
| chr2:222934854
|
C | T | 2 | a0001c0001t0003g0163a0001c0001t0003g0206 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2005+167C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222934854 | ||||||
| chr2:222934906
|
G | T | 18 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(15): Show | 18 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2005+219G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222934906 | ||||||
| chr2:222935698
|
G | T | 1 | a0001c0001t0007g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2005+1011G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935698 | ||||||
| chr2:222935828
|
CAGTAATG others(3): Show |
C | 1 | a0001c0001t0006g0135 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2005+1145_2005+115 others(14): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222935828 | |||||
| chr2:222935903
|
A | G | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2005+1216A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935903 | ||||||
| chr2:222935909
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2005+1222A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935909 | ||||||
| chr2:222935929
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2005+1242C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935929 | ||||||
| chr2:222935930
|
T | A | 1 | a0001c0001t0002g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2005+1243T>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935930 | ||||||
| chr2:222935931
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2005+1244C>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935931 | ||||||
| chr2:222935986
|
A | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.2005+1299A>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222935986 | ||||||
| chr2:222936006
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2005+1319A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936006 | ||||||
| chr2:222936191
|
T | C | 1 | a0001c0001t0010g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2005+1504T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936191 | ||||||
| chr2:222936215
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 217 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2005+1528T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936215 | ||||||
| chr2:222936254
|
A | G | 1 | a0001c0001t0010g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2005+1567A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936254 | ||||||
| chr2:222936436
|
A | C | 80 | a0001c0001t0002g0132a0001c0001t0002g0142a0001c0001t0002g0143others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2005+1749A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936436 | ||||||
| chr2:222936454
|
G | A | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2005+1767G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936454 | ||||||
| chr2:222936608
|
T | TC | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 179 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2005+1929dupC | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222936608 | |||||
| chr2:222936608
|
T | TCC | 35 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0033others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2005+1928_2005+192 others(6): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222936608 | |||||
| chr2:222936627
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2005+1940C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936627 | ||||||
| chr2:222936846
|
G | A | 1 | a0001c0001t0004g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2005+2159G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936846 | ||||||
| chr2:222936929
|
C | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2005+2242C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936929 | ||||||
| chr2:222936935
|
G | A | 6 | a0001c0001t0003g0099a0001c0001t0003g0105a0001c0001t0003g0112others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2005+2248G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936935 | ||||||
| chr2:222936952
|
A | G | 2 | a0001c0001t0004g0035a0001c0001t0004g0036 | 2 | HG00099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2005+2265A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936952 | ||||||
| chr2:222936997
|
C | T | 2 | a0001c0001t0002g0173a0001c0001t0002g0174 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2005+2310C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222936997 | ||||||
| chr2:222937125
|
G | C | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2005+2438G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222937125 | ||||||
| chr2:222937200
|
ATTG | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.2005+2516_2005+251 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222937200 | |||||
| chr2:222937228
|
AGTTATT | A | 90 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(87): Show | 90 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2005+2546_2005+255 others(10): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222937228 | |||||
| chr2:222937342
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.2005+2655C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222937342 | ||||||
| chr2:222937353
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2005+2666C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222937353 | ||||||
| chr2:222937514
|
TATC | T | 7 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(4): Show | 7 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2005+2831_2005+283 others(7): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222937514 | |||||
| chr2:222937668
|
C | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2005+2981C>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222937668 | ||||||
| chr2:222937873
|
TTGCTGCC | T | 10 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2005+3188_2005+319 others(11): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222937873 | |||||
| chr2:222937897
|
A | AT | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2005+3216dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222937897 | |||||
| chr2:222938036
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.2005+3349G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938036 | ||||||
| chr2:222938217
|
G | C | 4 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0119others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2006-3280G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938217 | ||||||
| chr2:222938387
|
G | A | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2006-3110G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938387 | ||||||
| chr2:222938516
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2006-2981G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938516 | ||||||
| chr2:222938665
|
C | T | 1 | a0002c0003t0020g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2006-2832C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938665 | ||||||
| chr2:222938883
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2006-2614C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938883 | ||||||
| chr2:222938895
|
G | A | 2 | a0001c0001t0016g0100a0001c0001t0016g0101 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2006-2602G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222938895 | ||||||
| chr2:222939016
|
G | GT | 10 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0002t0005g0121others(7): Show | 10 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2006-2473dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222939016 | |||||
| chr2:222939072
|
C | T | 1 | a0001c0001t0010g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2006-2425C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939072 | ||||||
| chr2:222939078
|
T | G | 1 | a0001c0001t0002g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2006-2419T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939078 | ||||||
| chr2:222939118
|
G | A | 1 | a0001c0002t0005g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2006-2379G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939118 | ||||||
| chr2:222939168
|
A | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(1): Show | 4 | HG00558.hp2 NA18942.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2006-2329A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939168 | ||||||
| chr2:222939351
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2006-2146A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939351 | ||||||
| chr2:222939413
|
T | C | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0206others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2006-2084T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939413 | ||||||
| chr2:222939489
|
T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.2006-2008T>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939489 | ||||||
| chr2:222939613
|
C | T | 6 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2006-1884C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939613 | ||||||
| chr2:222939620
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2006-1877G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939620 | ||||||
| chr2:222939980
|
A | G | 1 | a0001c0001t0002g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2006-1517A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222939980 | ||||||
| chr2:222940033
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.2006-1464A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940033 | ||||||
| chr2:222940065
|
C | T | 9 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2006-1432C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940065 | ||||||
| chr2:222940111
|
A | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.2006-1386A>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940111 | ||||||
| chr2:222940199
|
A | G | 8 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2006-1298A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940199 | ||||||
| chr2:222940439
|
T | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG00735.hp2 HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2006-1058T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940439 | ||||||
| chr2:222940475
|
CT | C | 21 | a0001c0001t0001g0027a0001c0001t0002g0161a0001c0001t0002g0169others(18): Show | 21 | HG00323.hp1 HG00423.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2006-1004delT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222940475 | |||||
| chr2:222940557
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2006-940C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940557 | ||||||
| chr2:222940691
|
C | T | 24 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0107others(21): Show | 24 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.2006-806C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940691 | ||||||
| chr2:222940711
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0045 | 3 | HG01074.hp1 HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2006-786C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940711 | ||||||
| chr2:222940777
|
A | G | 106 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(103): Show | 106 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.2006-720A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940777 | ||||||
| chr2:222940783
|
T | C | 1 | a0003c0004t0003g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2006-714T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940783 | ||||||
| chr2:222940860
|
G | A | 2 | a0001c0001t0007g0109a0001c0001t0007g0243 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2006-637G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940860 | ||||||
| chr2:222940867
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2006-630T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940867 | ||||||
| chr2:222940922
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2006-575A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222940922 | ||||||
| chr2:222941047
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2006-450G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941047 | ||||||
| chr2:222941047
|
G | C | 8 | a0001c0001t0003g0011a0001c0001t0003g0099a0001c0001t0003g0105others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2006-450G>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941047 | ||||||
| chr2:222941137
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2006-360C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941137 | ||||||
| chr2:222941138
|
G | T | 1 | a0001c0001t0002g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2006-359G>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941138 | ||||||
| chr2:222941226
|
G | A | 1 | a0001c0001t0017g0025 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2006-271G>A | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941226 | ||||||
| chr2:222941256
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 87 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2006-241A>G | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941256 | ||||||
| chr2:222941342
|
T | C | 1 | a0001c0001t0002g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2006-155T>C | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941342 | ||||||
| chr2:222941471
|
C | CT | 105 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0142others(102): Show | 105 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.2006-22dupT | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222941471 | |||||
| chr2:222941471
|
C | CTT | 3 | a0001c0001t0009g0117a0001c0001t0009g0118a0001c0001t0009g0120 | 3 | HG01243.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2006-23_2006-22dup others(2): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 222941471 | |||||
| chr2:222941475
|
TC | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0079 | 3 | HG01069.hp1 HG01515.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.2006-21delC | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941475 | ||||||
| chr2:222941476
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2006-21C>T | ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | chr2 | 222941476 |