| geneid | 197322 |
|---|---|
| ensemblid | ENSG00000176715.17 |
| hgncid | 27288 |
| symbol | ACSF3 |
| name | acyl-CoA synthetase family member 3 |
| refseq_nuc | NM_001243279.3 |
| refseq_prot | NP_001230208.1 |
| ensembl_nuc | ENST00000614302.5 |
| ensembl_prot | ENSP00000479130.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89093852 |
| end | 89156233 |
| strand | + |
| ver | v1.2 |
| region | chr16:89093852-89156233 |
| region5000 | chr16:89088852-89161233 |
| regionname0 | ACSF3_chr16_89093852_89156233 |
| regionname5000 | ACSF3_chr16_89088852_89161233 |
| 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 | 0/0 | 576 | 177 | 55 | 50 | 49 | 10 | 13 | 42 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002 | 1/1 | 576 | 106 | 25 | 14 | 43 | 4 | 18 | 30 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003 | 0/0 | 576 | 35 | 3 | 3 | 23 | 1 | 5 | 11 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004 | 0/0 | 576 | 34 | 0 | 0 | 30 | 0 | 4 | 21 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005 | 0/0 | 576 | 6 | 3 | 1 | 0 | 1 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0006 | 0/0 | 576 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0007 | 0/0 | 229 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0008 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0009 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0010 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0011 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0012 | 0/0 | 576 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1731 | 145 | 48 | 32 | 46 | 6 | 13 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0002 | 1/1 | 1731 | 58 | 6 | 4 | 35 | 0 | 11 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0003 | 0/0 | 1731 | 42 | 18 | 10 | 7 | 2 | 5 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0004 | 0/0 | 1731 | 34 | 0 | 0 | 30 | 0 | 4 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0005 | 0/0 | 1731 | 30 | 6 | 18 | 3 | 3 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0006 | 0/0 | 1731 | 16 | 1 | 0 | 12 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0007 | 0/0 | 1731 | 9 | 0 | 2 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0008 | 0/0 | 1731 | 6 | 2 | 0 | 2 | 1 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0009 | 0/0 | 1731 | 5 | 2 | 1 | 0 | 1 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0010 | 0/0 | 1731 | 4 | 0 | 1 | 2 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0011 | 0/0 | 1731 | 3 | 0 | 0 | 0 | 2 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0012 | 0/0 | 1731 | 3 | 0 | 0 | 3 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0013 | 0/0 | 1731 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0014 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0015 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0016 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0017 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0018 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0019 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0020 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0021 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0022 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0023 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| c0024 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2388 | 70 | 25 | 10 | 27 | 5 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0002 | 0/0 | 2388 | 46 | 2 | 19 | 14 | 2 | 9 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0003 | 0/0 | 2386 | 29 | 0 | 0 | 26 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0004 | 0/0 | 2367 | 28 | 4 | 3 | 12 | 0 | 9 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0005 | 0/0 | 2369 | 28 | 14 | 8 | 2 | 2 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0006 | 0/1 | 2363 | 25 | 0 | 0 | 23 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0007 | 0/0 | 2367 | 25 | 0 | 2 | 20 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0008 | 0/0 | 2369 | 14 | 4 | 0 | 3 | 3 | 4 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0009 | 0/0 | 2388 | 12 | 3 | 6 | 0 | 2 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0010 | 0/0 | 2388 | 11 | 0 | 4 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0011 | 0/0 | 2388 | 10 | 0 | 8 | 0 | 2 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0012 | 0/0 | 2388 | 7 | 7 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0013 | 0/0 | 2388 | 6 | 6 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0014 | 0/0 | 2367 | 3 | 0 | 2 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0015 | 0/0 | 2386 | 2 | 1 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0016 | 0/0 | 2386 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0017 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0018 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0019 | 0/0 | 2363 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0020 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0021 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0022 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0023 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0024 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0025 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0026 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0027 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0028 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0029 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0030 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0031 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0032 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0033 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0034 | 0/0 | 2386 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0035 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0036 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0037 | 0/0 | 2386 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0038 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0039 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0040 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0041 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0042 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0043 | 1/0 | 2365 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0044 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0045 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0046 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0047 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0048 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0049 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0050 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0051 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0052 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0053 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0054 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0055 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0056 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0057 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0058 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0059 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0060 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| t0061 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| 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 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1731 | 145 | 48 | 32 | 46 | 6 | 13 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0005 | 0/0 | 1731 | 30 | 6 | 18 | 3 | 3 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0014 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0018 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002 | 1/1 | 1731 | 58 | 6 | 4 | 35 | 0 | 11 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003 | 0/0 | 1731 | 42 | 18 | 10 | 7 | 2 | 5 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0011 | 0/0 | 1731 | 3 | 0 | 0 | 0 | 2 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0020 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0021 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0023 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0006 | 0/0 | 1731 | 16 | 1 | 0 | 12 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0007 | 0/0 | 1731 | 9 | 0 | 2 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0008 | 0/0 | 1731 | 6 | 2 | 0 | 2 | 1 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0010 | 0/0 | 1731 | 4 | 0 | 1 | 2 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004 | 0/0 | 1731 | 34 | 0 | 0 | 30 | 0 | 4 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0009 | 0/0 | 1731 | 5 | 2 | 1 | 0 | 1 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0017 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0006c0012 | 0/0 | 1731 | 3 | 0 | 0 | 3 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0007c0013 | 0/0 | 1731 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0008c0022 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0009c0024 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0010c0019 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0011c0016 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0012c0015 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4118 | 57 | 22 | 6 | 22 | 4 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0002 | 0/0 | 4118 | 45 | 2 | 19 | 13 | 2 | 9 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0010 | 0/0 | 4118 | 11 | 0 | 4 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0012 | 0/0 | 4118 | 7 | 7 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0013 | 0/0 | 4118 | 6 | 6 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0015 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0016 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0017 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0018 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0023 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0026 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0027 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0028 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0029 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0030 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0032 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0033 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0036 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0051 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0060 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0001t0061 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0005t0001 | 0/0 | 4118 | 11 | 3 | 4 | 3 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0005t0009 | 0/0 | 4118 | 11 | 3 | 6 | 0 | 2 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0005t0011 | 0/0 | 4118 | 8 | 0 | 8 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0014t0024 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0001c0018t0011 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0004 | 0/0 | 4097 | 18 | 3 | 2 | 7 | 0 | 6 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0006 | 0/1 | 4093 | 21 | 0 | 0 | 20 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0007 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0008 | 0/0 | 4099 | 5 | 3 | 0 | 0 | 0 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0014 | 0/0 | 4097 | 3 | 0 | 2 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0019 | 0/0 | 4093 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0041 | 0/0 | 4097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0042 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0043 | 1/0 | 4095 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0044 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0045 | 0/0 | 4097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0054 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0055 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0002t0056 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0004 | 0/0 | 4097 | 6 | 0 | 0 | 4 | 0 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0005 | 0/0 | 4099 | 28 | 14 | 8 | 2 | 2 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0006 | 0/0 | 4093 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0021 | 0/0 | 4099 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0040 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0046 | 0/0 | 4099 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0050 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0052 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0003t0057 | 0/0 | 4099 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0011t0008 | 0/0 | 4099 | 3 | 0 | 0 | 0 | 2 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0020t0008 | 0/0 | 4099 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0021t0004 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0002c0023t0008 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0006t0007 | 0/0 | 4097 | 14 | 0 | 0 | 11 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0006t0048 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0006t0059 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0007t0007 | 0/0 | 4097 | 9 | 0 | 2 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0008t0008 | 0/0 | 4099 | 3 | 0 | 0 | 2 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0008t0020 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0008t0047 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0008t0049 | 0/0 | 4097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0010t0004 | 0/0 | 4097 | 2 | 0 | 1 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0010t0008 | 0/0 | 4099 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0003c0010t0058 | 0/0 | 4099 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004t0003 | 0/0 | 4116 | 29 | 0 | 0 | 26 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004t0022 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004t0025 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004t0031 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004t0037 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0004c0004t0038 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0009t0011 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0009t0015 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0009t0034 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0009t0039 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0009t0053 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0005c0017t0035 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0006c0012t0006 | 0/0 | 4093 | 3 | 0 | 0 | 3 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0007c0013t0001 | 0/0 | 4118 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0008c0022t0007 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0009c0024t0004 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0010c0019t0020 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0011c0016t0002 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| a0012c0015t0009 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | copy fasta | chr16 | 89088852 | 89161233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0018g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0023g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0026g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0027g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0028g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0029g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0030g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0032g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0033g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0036g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0051g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0060g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0061g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0011g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0014t0024g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0018t0011g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0014g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0014g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0014g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0019g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0019g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0041g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0042g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0043g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0044g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0045g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0054g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0055g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0056g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0006g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0021g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0021g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0040g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0046g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0050g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0052g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0057g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0011t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0011t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0011t0008g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0020t0008g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0021t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0023t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0048g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0059g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0020g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0047g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0049g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0058g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0022g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0025g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0031g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0037g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0038g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0011g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0015g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0034g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0039g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0053g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0017t0035g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0006c0012t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0006c0012t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0006c0012t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0007c0013t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0007c0013t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0008c0022t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0009c0024t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0010c0019t0020g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0011c0016t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0012c0015t0009g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0009 | g0327 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0035 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00140 | hp2 | a0005 | c0009 | t0011 | g0310 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | FIN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00323 | hp2 | a0003 | c0008 | t0008 | g0031 | EUR | FIN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00408 | hp1 | a0003 | c0006 | t0007 | g0044 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00408 | hp2 | a0003 | c0007 | t0007 | g0094 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00423 | hp1 | a0002 | c0002 | t0006 | g0066 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00438 | hp1 | a0004 | c0004 | t0003 | g0342 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00438 | hp2 | a0003 | c0007 | t0007 | g0092 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0202 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00544 | hp2 | a0004 | c0004 | t0003 | g0346 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00558 | hp1 | a0002 | c0003 | t0004 | g0061 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00558 | hp2 | a0004 | c0004 | t0025 | g0338 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00621 | hp1 | a0002 | c0002 | t0006 | g0108 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00621 | hp2 | a0004 | c0004 | t0003 | g0348 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00639 | hp1 | a0002 | c0003 | t0005 | g0023 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00642 | hp1 | a0001 | c0005 | t0009 | g0296 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00673 | hp1 | a0003 | c0006 | t0007 | g0050 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00673 | hp2 | a0004 | c0004 | t0003 | g0306 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00735 | hp1 | a0001 | c0005 | t0009 | g0297 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00741 | hp1 | a0005 | c0009 | t0015 | g0258 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0036 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01069 | hp2 | a0001 | c0005 | t0011 | g0312 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01070 | hp1 | a0001 | c0005 | t0011 | g0326 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01071 | hp2 | a0001 | c0005 | t0011 | g0311 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01074 | hp1 | a0001 | c0001 | t0029 | g0243 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01099 | hp2 | a0001 | c0001 | t0023 | g0274 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01109 | hp1 | a0001 | c0005 | t0011 | g0313 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01109 | hp2 | a0002 | c0003 | t0005 | g0015 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01168 | hp2 | a0001 | c0005 | t0011 | g0321 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0039 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01175 | hp2 | a0002 | c0003 | t0005 | g0082 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01192 | hp2 | a0001 | c0005 | t0009 | g0298 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01243 | hp1 | a0001 | c0001 | t0033 | g0271 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0176 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01255 | hp2 | a0001 | c0005 | t0011 | g0322 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01256 | hp2 | a0002 | c0002 | t0004 | g0352 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01257 | hp2 | a0002 | c0002 | t0014 | g0121 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01258 | hp2 | a0002 | c0002 | t0014 | g0122 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01261 | hp1 | a0001 | c0005 | t0009 | g0250 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01261 | hp2 | a0002 | c0003 | t0005 | g0079 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01358 | hp1 | a0001 | c0005 | t0001 | g0037 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01358 | hp2 | a0001 | c0005 | t0009 | g0353 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01361 | hp1 | a0001 | c0005 | t0009 | g0309 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0173 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01433 | hp1 | a0002 | c0003 | t0005 | g0026 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0038 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01516 | hp1 | a0002 | c0003 | t0005 | g0081 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01516 | hp2 | a0002 | c0011 | t0008 | g0131 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01517 | hp1 | a0002 | c0003 | t0005 | g0080 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0249 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0099 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0042 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0361 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01928 | hp1 | a0003 | c0007 | t0007 | g0046 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0177 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01943 | hp1 | a0002 | c0003 | t0046 | g0021 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01952 | hp2 | a0002 | c0003 | t0005 | g0077 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01975 | hp1 | a0001 | c0001 | t0010 | g0168 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01978 | hp1 | a0003 | c0007 | t0007 | g0047 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01978 | hp2 | a0001 | c0005 | t0011 | g0314 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01993 | hp1 | a0002 | c0003 | t0005 | g0078 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02015 | hp1 | a0011 | c0016 | t0002 | g0163 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02015 | hp2 | a0004 | c0004 | t0003 | g0341 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02027 | hp1 | a0002 | c0003 | t0005 | g0071 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02027 | hp2 | a0003 | c0010 | t0008 | g0120 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02040 | hp1 | a0002 | c0002 | t0007 | g0109 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02040 | hp2 | a0001 | c0001 | t0010 | g0221 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0242 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0351 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02056 | hp1 | a0003 | c0006 | t0007 | g0054 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02056 | hp2 | a0002 | c0003 | t0005 | g0087 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02071 | hp1 | a0002 | c0021 | t0004 | g0104 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02071 | hp2 | a0002 | c0003 | t0004 | g0018 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02074 | hp1 | a0003 | c0006 | t0007 | g0001 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02074 | hp2 | a0002 | c0002 | t0006 | g0203 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02080 | hp1 | a0003 | c0006 | t0007 | g0106 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02083 | hp1 | a0003 | c0006 | t0007 | g0001 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02083 | hp2 | a0004 | c0004 | t0003 | g0231 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02129 | hp1 | a0001 | c0001 | t0030 | g0357 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02129 | hp2 | a0002 | c0002 | t0006 | g0211 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02132 | hp2 | a0004 | c0004 | t0003 | g0335 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02145 | hp1 | a0002 | c0003 | t0050 | g0025 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02145 | hp2 | a0002 | c0003 | t0005 | g0090 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02155 | hp1 | a0003 | c0007 | t0007 | g0093 | EAS | CDX | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02155 | hp2 | a0002 | c0002 | t0056 | g0125 | EAS | CDX | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0102 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0251 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0033 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02273 | hp1 | a0002 | c0003 | t0057 | g0116 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02273 | hp2 | a0002 | c0002 | t0004 | g0126 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02280 | hp1 | a0002 | c0003 | t0005 | g0076 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02280 | hp2 | a0010 | c0019 | t0020 | g0244 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02300 | hp1 | a0003 | c0010 | t0004 | g0130 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02451 | hp1 | a0002 | c0002 | t0008 | g0237 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02523 | hp2 | a0003 | c0007 | t0007 | g0048 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02572 | hp1 | a0009 | c0024 | t0004 | g0117 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02572 | hp2 | a0001 | c0005 | t0009 | g0328 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02602 | hp1 | a0002 | c0002 | t0004 | g0214 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02602 | hp2 | a0002 | c0003 | t0006 | g0019 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0105 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0300 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02683 | hp2 | a0002 | c0002 | t0014 | g0143 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02698 | hp1 | a0002 | c0003 | t0005 | g0358 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02698 | hp2 | a0002 | c0002 | t0045 | g0115 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02717 | hp2 | a0002 | c0002 | t0008 | g0236 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02723 | hp2 | a0002 | c0003 | t0005 | g0022 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02738 | hp1 | a0002 | c0002 | t0004 | g0119 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0030 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0043 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02897 | hp2 | a0001 | c0001 | t0060 | g0320 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02965 | hp2 | a0002 | c0003 | t0005 | g0016 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02970 | hp2 | a0002 | c0002 | t0008 | g0239 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0024 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02976 | hp2 | a0003 | c0006 | t0059 | g0350 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0139 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03017 | hp2 | a0002 | c0002 | t0041 | g0127 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03041 | hp2 | a0002 | c0023 | t0008 | g0238 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0034 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03130 | hp1 | a0001 | c0014 | t0024 | g0319 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03139 | hp1 | a0005 | c0009 | t0034 | g0360 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03209 | hp1 | a0002 | c0003 | t0005 | g0091 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03209 | hp2 | a0001 | c0001 | t0051 | g0303 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03225 | hp1 | a0002 | c0003 | t0005 | g0029 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03225 | hp2 | a0001 | c0001 | t0026 | g0006 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03239 | hp1 | a0002 | c0011 | t0008 | g0128 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03239 | hp2 | a0012 | c0015 | t0009 | g0329 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03453 | hp2 | a0002 | c0003 | t0005 | g0075 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03486 | hp1 | a0002 | c0003 | t0005 | g0072 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03490 | hp2 | a0004 | c0004 | t0003 | g0014 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03491 | hp1 | a0002 | c0002 | t0008 | g0144 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03491 | hp2 | a0004 | c0004 | t0037 | g0013 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03492 | hp2 | a0002 | c0002 | t0008 | g0145 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03540 | hp2 | a0001 | c0005 | t0009 | g0308 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03579 | hp2 | a0002 | c0003 | t0005 | g0027 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0225 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03654 | hp2 | a0001 | c0001 | t0032 | g0267 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0118 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03688 | hp1 | a0002 | c0003 | t0005 | g0028 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03704 | hp1 | a0003 | c0010 | t0004 | g0129 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03710 | hp1 | a0005 | c0009 | t0053 | g0217 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03710 | hp2 | a0003 | c0006 | t0007 | g0051 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03927 | hp1 | a0004 | c0004 | t0003 | g0337 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03927 | hp2 | a0002 | c0003 | t0004 | g0096 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0123 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03942 | hp2 | a0003 | c0006 | t0007 | g0017 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04115 | hp1 | a0003 | c0008 | t0049 | g0052 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04184 | hp1 | a0003 | c0006 | t0007 | g0055 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04184 | hp2 | a0002 | c0003 | t0004 | g0020 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04199 | hp2 | a0004 | c0004 | t0003 | g0304 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04228 | hp1 | a0002 | c0020 | t0008 | g0362 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18522 | hp1 | a0003 | c0008 | t0020 | g0245 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18522 | hp2 | a0002 | c0003 | t0052 | g0240 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0005 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18612 | hp2 | a0003 | c0008 | t0008 | g0059 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18747 | hp1 | a0002 | c0003 | t0040 | g0060 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0273 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18939 | hp2 | a0001 | c0005 | t0001 | g0331 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18940 | hp1 | a0006 | c0012 | t0006 | g0204 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18940 | hp2 | a0001 | c0001 | t0028 | g0101 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18941 | hp1 | a0004 | c0004 | t0003 | g0336 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18941 | hp2 | a0002 | c0002 | t0006 | g0213 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18942 | hp1 | a0002 | c0002 | t0019 | g0209 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18942 | hp2 | a0002 | c0002 | t0019 | g0136 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18945 | hp2 | a0006 | c0012 | t0006 | g0206 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18949 | hp2 | a0004 | c0004 | t0003 | g0234 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18950 | hp1 | a0004 | c0004 | t0003 | g0339 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18952 | hp1 | a0002 | c0002 | t0006 | g0210 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18954 | hp1 | a0002 | c0002 | t0055 | g0141 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18954 | hp2 | a0001 | c0001 | t0010 | g0219 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18961 | hp1 | a0003 | c0006 | t0007 | g0069 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18965 | hp1 | a0004 | c0004 | t0003 | g0223 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0222 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18966 | hp1 | a0002 | c0002 | t0004 | g0140 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18967 | hp2 | a0004 | c0004 | t0003 | g0334 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18968 | hp1 | a0004 | c0004 | t0003 | g0333 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18968 | hp2 | a0003 | c0007 | t0007 | g0064 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18969 | hp1 | a0002 | c0002 | t0004 | g0228 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18969 | hp2 | a0004 | c0004 | t0003 | g0230 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18970 | hp1 | a0003 | c0008 | t0008 | g0058 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18970 | hp2 | a0001 | c0005 | t0001 | g0330 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0146 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18973 | hp1 | a0007 | c0013 | t0001 | g0280 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18977 | hp2 | a0002 | c0002 | t0042 | g0152 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18980 | hp1 | a0004 | c0004 | t0003 | g0229 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18980 | hp2 | a0002 | c0002 | t0006 | g0150 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18981 | hp2 | a0004 | c0004 | t0003 | g0307 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18982 | hp1 | a0002 | c0002 | t0054 | g0111 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18985 | hp1 | a0003 | c0007 | t0007 | g0045 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18985 | hp2 | a0003 | c0006 | t0007 | g0067 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18986 | hp1 | a0001 | c0001 | t0036 | g0247 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18986 | hp2 | a0002 | c0003 | t0004 | g0062 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18990 | hp1 | a0003 | c0006 | t0048 | g0056 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18990 | hp2 | a0002 | c0002 | t0006 | g0112 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18992 | hp1 | a0004 | c0004 | t0003 | g0347 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18992 | hp2 | a0002 | c0002 | t0006 | g0151 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18993 | hp2 | a0001 | c0001 | t0027 | g0216 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18994 | hp1 | a0004 | c0004 | t0003 | g0345 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18994 | hp2 | a0002 | c0002 | t0006 | g0153 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18995 | hp2 | a0002 | c0002 | t0006 | g0149 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18998 | hp1 | a0001 | c0001 | t0010 | g0218 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18999 | hp2 | a0002 | c0002 | t0004 | g0133 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19000 | hp2 | a0002 | c0002 | t0006 | g0134 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19003 | hp1 | a0002 | c0002 | t0006 | g0142 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19003 | hp2 | a0004 | c0004 | t0022 | g0103 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19004 | hp1 | a0002 | c0002 | t0006 | g0138 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19005 | hp1 | a0004 | c0004 | t0003 | g0233 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19005 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19007 | hp1 | a0002 | c0002 | t0006 | g0137 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19007 | hp2 | a0001 | c0001 | t0010 | g0166 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19010 | hp1 | a0003 | c0010 | t0058 | g0154 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19010 | hp2 | a0002 | c0002 | t0006 | g0224 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19011 | hp2 | a0004 | c0004 | t0003 | g0340 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19012 | hp1 | a0004 | c0004 | t0003 | g0349 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19030 | hp1 | a0005 | c0009 | t0039 | g0032 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19043 | hp1 | a0001 | c0001 | t0061 | g0260 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19043 | hp2 | a0002 | c0003 | t0021 | g0088 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19057 | hp2 | a0001 | c0005 | t0001 | g0302 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19064 | hp1 | a0002 | c0002 | t0006 | g0135 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19064 | hp2 | a0004 | c0004 | t0003 | g0344 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19065 | hp1 | a0004 | c0004 | t0031 | g0232 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19065 | hp2 | a0002 | c0002 | t0006 | g0212 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19066 | hp1 | a0002 | c0002 | t0004 | g0147 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19066 | hp2 | a0004 | c0004 | t0038 | g0343 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19067 | hp1 | a0007 | c0013 | t0001 | g0292 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19067 | hp2 | a0003 | c0006 | t0007 | g0057 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19068 | hp1 | a0003 | c0007 | t0007 | g0049 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0095 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19070 | hp2 | a0002 | c0002 | t0006 | g0065 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19074 | hp2 | a0004 | c0004 | t0003 | g0005 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19077 | hp1 | a0008 | c0022 | t0007 | g0063 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19077 | hp2 | a0002 | c0002 | t0006 | g0148 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19080 | hp1 | a0004 | c0004 | t0003 | g0332 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19080 | hp2 | a0003 | c0006 | t0007 | g0053 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19083 | hp1 | a0003 | c0006 | t0007 | g0068 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19084 | hp1 | a0002 | c0002 | t0004 | g0201 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19084 | hp2 | a0004 | c0004 | t0003 | g0215 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19085 | hp2 | a0006 | c0012 | t0006 | g0205 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19088 | hp1 | a0001 | c0001 | t0010 | g0169 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19088 | hp2 | a0002 | c0002 | t0044 | g0124 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19240 | hp1 | a0002 | c0003 | t0005 | g0074 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20129 | hp1 | a0002 | c0002 | t0004 | g0226 | AFR | ASW | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20129 | hp2 | a0002 | c0003 | t0005 | g0073 | AFR | ASW | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20752 | hp2 | a0002 | c0011 | t0008 | g0132 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20805 | hp1 | a0001 | c0005 | t0009 | g0199 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20805 | hp2 | a0001 | c0018 | t0011 | g0261 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01123 | hp1 | a0002 | c0003 | t0005 | g0083 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01123 | hp2 | a0001 | c0005 | t0011 | g0323 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02109 | hp1 | a0002 | c0003 | t0021 | g0089 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02109 | hp2 | a0005 | c0017 | t0035 | g0359 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02486 | hp2 | a0001 | c0005 | t0009 | g0246 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0272 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02559 | hp2 | a0001 | c0001 | t0016 | g0241 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0248 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20300 | hp1 | a0002 | c0003 | t0005 | g0255 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA21309 | hp1 | a0003 | c0008 | t0047 | g0012 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0006 | g0235 | REF | REF | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0043 | g0070 | REF | REF | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89100664
|
C | T | 1 | a0001 | 1 | HG03209.hp2 | splice_region_variant | LOW | c.-18C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | chr16 | 89100664 | ||||||
| chr16:89100686
|
T | C | 6 | a0001a0004a0005others(3): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
missense_variant | MODERATE | c.5T>C | p.Leu2Pro | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 343/4095 | 5/1731 | 2/576 | chr16 | 89100686 | ||
| chr16:89100730
|
G | C | 1 | a0004 | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
missense_variant | MODERATE | c.49G>C | p.Ala17Pro | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 387/4095 | 49/1731 | 17/576 | chr16 | 89100730 | ||
| chr16:89101072
|
G | A | 1 | a0010 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.391G>A | p.Ala131Thr | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 729/4095 | 391/1731 | 131/576 | chr16 | 89101072 | ||
| chr16:89101281
|
C | G | 1 | a0009 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.600C>G | p.Ile200Met | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 938/4095 | 600/1731 | 200/576 | chr16 | 89101281 | ||
| chr16:89102626
|
G | A | 1 | a0007 | 2 | NA18973.hp1 NA19067.hp1 |
stop_gained | HIGH | c.689G>A | p.Trp230* | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/11 | 1027/4095 | 689/1731 | 230/576 | chr16 | 89102626 | ||
| chr16:89114475
|
G | A | 7 | a0001a0003a0007others(4): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
missense_variant | MODERATE | c.1114G>A | p.Val372Met | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/11 | 1452/4095 | 1114/1731 | 372/576 | chr16 | 89114475 | ||
| chr16:89133239
|
C | T | 1 | a0011 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1343C>T | p.Thr448Ile | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/11 | 1681/4095 | 1343/1731 | 448/576 | chr16 | 89133239 | ||
| chr16:89145306
|
G | A | 1 | a0012 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1406G>A | p.Arg469Gln | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/11 | 1744/4095 | 1406/1731 | 469/576 | chr16 | 89145306 | ||
| chr16:89145356
|
G | A | 1 | a0006 | 3 | NA18940.hp1 NA18945.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.1456G>A | p.Ala486Thr | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/11 | 1794/4095 | 1456/1731 | 486/576 | chr16 | 89145356 | ||
| chr16:89145998
|
C | G | 1 | a0008 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.1562C>G | p.Thr521Ser | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/11 | 1900/4095 | 1562/1731 | 521/576 | chr16 | 89145998 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89100732
|
G | C | 18 | a0001c0001a0001c0005a0001c0014others(15): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
synonymous_variant | LOW | c.51G>C | p.Ala17Ala | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 389/4095 | 51/1731 | 17/576 | chr16 | 89100732 | ||
| chr16:89100978
|
C | T | 1 | a0003c0007 | 9 | HG00408.hp2 HG00438.hp2 HG01928.hp1 others(6): Show |
synonymous_variant | LOW | c.297C>T | p.Ser99Ser | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 635/4095 | 297/1731 | 99/576 | chr16 | 89100978 | ||
| chr16:89100987
|
C | T | 9 | a0001c0001a0001c0005a0001c0018others(6): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
synonymous_variant | LOW | c.306C>T | p.Cys102Cys | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 644/4095 | 306/1731 | 102/576 | chr16 | 89100987 | ||
| chr16:89100996
|
T | C | 9 | a0001c0001a0001c0005a0001c0018others(6): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
synonymous_variant | LOW | c.315T>C | p.Asp105Asp | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 653/4095 | 315/1731 | 105/576 | chr16 | 89100996 | ||
| chr16:89101023
|
G | C | 10 | a0001c0001a0001c0005a0001c0018others(7): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
synonymous_variant | LOW | c.342G>C | p.Ala114Ala | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 680/4095 | 342/1731 | 114/576 | chr16 | 89101023 | ||
| chr16:89101035
|
T | C | 10 | a0001c0001a0001c0005a0001c0018others(7): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
synonymous_variant | LOW | c.354T>C | p.Ser118Ser | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 692/4095 | 354/1731 | 118/576 | chr16 | 89101035 | ||
| chr16:89101038
|
C | T | 1 | a0001c0018 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.357C>T | p.Gly119Gly | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 695/4095 | 357/1731 | 119/576 | chr16 | 89101038 | ||
| chr16:89101050
|
C | A | 9 | a0001c0001a0001c0005a0001c0018others(6): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
synonymous_variant | LOW | c.369C>A | p.Val123Val | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 707/4095 | 369/1731 | 123/576 | chr16 | 89101050 | ||
| chr16:89114357
|
A | T | 3 | a0003c0006a0003c0007a0008c0022 | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
synonymous_variant | LOW | c.996A>T | p.Ser332Ser | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/11 | 1334/4095 | 996/1731 | 332/576 | chr16 | 89114357 | ||
| chr16:89120808
|
G | A | 1 | a0002c0020 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1134G>A | p.Val378Val | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/11 | 1472/4095 | 1134/1731 | 378/576 | chr16 | 89120808 | ||
| chr16:89133243
|
G | A | 3 | a0001c0005a0002c0011a0012c0015 | 34 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(31): Show |
synonymous_variant | LOW | c.1347G>A | p.Leu449Leu | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/11 | 1685/4095 | 1347/1731 | 449/576 | chr16 | 89133243 | ||
| chr16:89145298
|
C | T | 1 | a0002c0021 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1398C>T | p.Tyr466Tyr | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/11 | 1736/4095 | 1398/1731 | 466/576 | chr16 | 89145298 | ||
| chr16:89145367
|
G | C | 1 | a0005c0017 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1467G>C | p.Val489Val | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/11 | 1805/4095 | 1467/1731 | 489/576 | chr16 | 89145367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89093875
|
C | G | 2 | a0001c0001t0060a0001c0001t0061 | 2 | HG02897.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-315C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/11 | 6807 | chr16 | 89093875 | |||||
| chr16:89093876
|
C | G | 1 | a0003c0006t0059 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-314C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/11 | 6806 | chr16 | 89093876 | |||||
| chr16:89093908
|
C | A | 1 | a0004c0004t0022 | 1 | NA19003.hp2 | 5_prime_UTR_variant | MODIFIER | c.-282C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/11 | 6774 | chr16 | 89093908 | |||||
| chr16:89093921
|
C | G | 10 | a0001c0001t0002a0001c0001t0010a0002c0002t0014others(7): Show | 66 | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(63): Show |
5_prime_UTR_variant | MODIFIER | c.-269C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/11 | 6761 | chr16 | 89093921 | |||||
| chr16:89093923
|
G | C | 1 | a0004c0004t0022 | 1 | NA19003.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/11 | 6759 | chr16 | 89093923 | |||||
| chr16:89098666
|
C | T | 1 | a0002c0003t0052 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/11 | 2016 | chr16 | 89098666 | |||||
| chr16:89100667
|
C | CCCCAGGA others(12): Show |
41 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(38): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-13insCCAGGAGG others(11): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 13 | INFO_REALIGN_3_PRIME | chr16 | 89100667 | ||||
| chr16:89100669
|
G | C | 1 | a0005c0009t0039 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-13G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/11 | 13 | chr16 | 89100669 | |||||
| chr16:89154217
|
C | T | 1 | a0004c0004t0038 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 10 | chr16 | 89154217 | |||||
| chr16:89154273
|
G | T | 1 | a0002c0003t0021 | 2 | HG02109.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*66G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 66 | chr16 | 89154273 | |||||
| chr16:89154280
|
C | T | 2 | a0001c0001t0018a0002c0003t0050 | 3 | HG01884.hp2 HG02145.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*73C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 73 | chr16 | 89154280 | |||||
| chr16:89154403
|
G | T | 1 | a0004c0004t0037 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 196 | chr16 | 89154403 | |||||
| chr16:89154408
|
C | G | 1 | a0001c0001t0036 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*201C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 201 | chr16 | 89154408 | |||||
| chr16:89154438
|
G | A | 5 | a0002c0003t0040a0004c0004t0003a0004c0004t0022others(2): Show | 33 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 231 | chr16 | 89154438 | |||||
| chr16:89154457
|
C | T | 1 | a0005c0017t0035 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 250 | chr16 | 89154457 | |||||
| chr16:89154458
|
G | A | 1 | a0002c0002t0041 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 251 | chr16 | 89154458 | |||||
| chr16:89154472
|
C | A | 1 | a0001c0001t0023 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 265 | chr16 | 89154472 | |||||
| chr16:89154565
|
C | CAAAT | 73 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(70): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*361_*362insTAAA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 362 | INFO_REALIGN_3_PRIME | chr16 | 89154565 | ||||
| chr16:89154578
|
G | A | 6 | a0002c0003t0040a0004c0004t0003a0004c0004t0022others(3): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*371G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 371 | chr16 | 89154578 | |||||
| chr16:89154604
|
C | T | 1 | a0003c0008t0049 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*397C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 397 | chr16 | 89154604 | |||||
| chr16:89154610
|
C | T | 1 | a0005c0009t0034 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 403 | chr16 | 89154610 | |||||
| chr16:89154612
|
C | T | 1 | a0001c0001t0033 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 405 | chr16 | 89154612 | |||||
| chr16:89154637
|
G | A | 2 | a0002c0002t0044a0002c0002t0056 | 2 | HG02155.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*430G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 430 | chr16 | 89154637 | |||||
| chr16:89154646
|
G | A | 19 | a0001c0001t0015a0002c0002t0004a0002c0002t0006others(16): Show | 67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*439G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 439 | chr16 | 89154646 | |||||
| chr16:89154736
|
T | C | 1 | a0002c0002t0045 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 529 | chr16 | 89154736 | |||||
| chr16:89154771
|
G | A | 10 | a0001c0001t0023a0001c0005t0011a0001c0018t0011others(7): Show | 44 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*564G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 564 | chr16 | 89154771 | |||||
| chr16:89154879
|
G | C | 20 | a0001c0001t0015a0002c0002t0004a0002c0002t0006others(17): Show | 68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*672G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 672 | chr16 | 89154879 | |||||
| chr16:89155065
|
G | A | 1 | a0001c0001t0026 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*858G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 858 | chr16 | 89155065 | |||||
| chr16:89155193
|
G | A | 1 | a0001c0001t0027 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*986G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 986 | chr16 | 89155193 | |||||
| chr16:89155220
|
G | C | 3 | a0001c0001t0010a0001c0001t0027a0001c0001t0028 | 13 | HG01255.hp1 HG01361.hp2 HG01934.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1013G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1013 | chr16 | 89155220 | |||||
| chr16:89155224
|
G | A | 2 | a0003c0008t0020a0010c0019t0020 | 2 | HG02280.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1017G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1017 | chr16 | 89155224 | |||||
| chr16:89155324
|
G | A | 1 | a0001c0001t0029 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1117G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1117 | chr16 | 89155324 | |||||
| chr16:89155344
|
C | G | 1 | a0005c0017t0035 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1137 | chr16 | 89155344 | |||||
| chr16:89155355
|
G | A | 1 | a0001c0001t0030 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1148 | chr16 | 89155355 | |||||
| chr16:89155358
|
C | G | 1 | a0002c0003t0046 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1151C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1151 | chr16 | 89155358 | |||||
| chr16:89155371
|
A | C | 1 | a0001c0001t0013 | 6 | HG01891.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1164A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1164 | chr16 | 89155371 | |||||
| chr16:89155380
|
A | C | 7 | a0002c0002t0007a0003c0006t0007a0003c0006t0048others(4): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1173A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1173 | chr16 | 89155380 | |||||
| chr16:89155387
|
G | A | 20 | a0001c0001t0015a0002c0002t0004a0002c0002t0006others(17): Show | 68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1180G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1180 | chr16 | 89155387 | |||||
| chr16:89155462
|
C | T | 2 | a0001c0001t0017a0001c0001t0026 | 3 | HG02258.hp1 HG03225.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1255C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1255 | chr16 | 89155462 | |||||
| chr16:89155537
|
C | T | 1 | a0002c0002t0045 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1330C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1330 | chr16 | 89155537 | |||||
| chr16:89155552
|
C | T | 1 | a0001c0001t0032 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1345 | chr16 | 89155552 | |||||
| chr16:89155620
|
G | A | 2 | a0001c0005t0009a0012c0015t0009 | 12 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1413G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1413 | chr16 | 89155620 | |||||
| chr16:89155776
|
ATC | A | 37 | a0001c0001t0015a0001c0001t0016a0002c0002t0004others(34): Show | 135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1576_*1577delTC | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1576 | INFO_REALIGN_3_PRIME | chr16 | 89155776 | ||||
| chr16:89155807
|
T | G | 1 | a0002c0002t0019 | 2 | NA18942.hp1 NA18942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1600T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1600 | chr16 | 89155807 | |||||
| chr16:89155820
|
A | G | 1 | a0002c0002t0055 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1613A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1613 | chr16 | 89155820 | |||||
| chr16:89155887
|
T | G | 1 | a0002c0002t0042 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1680 | chr16 | 89155887 | |||||
| chr16:89155929
|
A | G | 1 | a0003c0006t0048 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1722A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1722 | chr16 | 89155929 | |||||
| chr16:89155993
|
G | A | 1 | a0002c0003t0052 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1786 | chr16 | 89155993 | |||||
| chr16:89156004
|
G | C | 37 | a0001c0001t0015a0001c0001t0016a0002c0002t0004others(34): Show | 135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1797G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1797 | chr16 | 89156004 | |||||
| chr16:89156036
|
C | T | 29 | a0001c0001t0015a0001c0001t0016a0002c0002t0004others(26): Show | 99 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1829C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1829 | chr16 | 89156036 | |||||
| chr16:89156145
|
T | A | 2 | a0001c0001t0012a0001c0001t0060 | 8 | HG02258.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1938T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 1938 | chr16 | 89156145 | |||||
| chr16:89156227
|
T | C | 1 | a0001c0001t0061 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 2020 | chr16 | 89156227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89094011
|
G | GCCCACGG others(2): Show |
6 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(3): Show | 6 | HG02615.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-194+18_-194+26dup others(9): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 89094011 | |||||
| chr16:89094016
|
C | G | 4 | a0002c0002t0004g0361a0002c0020t0008g0362a0005c0009t0034g0360others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-194+20C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094016 | ||||||
| chr16:89094044
|
A | G | 264 | a0001c0001t0001g0004a0001c0001t0001g0107a0001c0001t0001g0110others(261): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-194+48A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094044 | ||||||
| chr16:89094053
|
G | A | 4 | a0002c0002t0004g0361a0002c0020t0008g0362a0005c0009t0034g0360others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-194+57G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094053 | ||||||
| chr16:89094053
|
G | C | 1 | a0004c0004t0022g0103 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-194+57G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094053 | ||||||
| chr16:89094060
|
C | G | 1 | a0002c0003t0005g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-194+64C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094060 | ||||||
| chr16:89094080
|
T | A | 2 | a0004c0004t0003g0014a0004c0004t0037g0013 | 2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-194+84T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094080 | ||||||
| chr16:89094148
|
G | T | 1 | a0001c0001t0018g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-194+152G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094148 | ||||||
| chr16:89094153
|
G | C | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+157G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094153 | ||||||
| chr16:89094173
|
CCT | C | 5 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(2): Show | 5 | HG02615.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-194+181_-194+182d others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 89094173 | |||||
| chr16:89094271
|
C | G | 1 | a0001c0001t0028g0101 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-194+275C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094271 | ||||||
| chr16:89094299
|
T | A | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+303T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094299 | ||||||
| chr16:89094300
|
C | G | 265 | a0001c0001t0001g0004a0001c0001t0001g0097a0001c0001t0001g0098others(262): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-194+304C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094300 | ||||||
| chr16:89094300
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+304C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094300 | ||||||
| chr16:89094301
|
T | G | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+305T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094301 | ||||||
| chr16:89094304
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-194+308G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094304 | ||||||
| chr16:89094329
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+333C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094329 | ||||||
| chr16:89094339
|
T | C | 138 | a0001c0001t0001g0110a0001c0001t0001g0155a0001c0001t0001g0196others(135): Show | 139 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-194+343T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094339 | ||||||
| chr16:89094438
|
C | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-194+442C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094438 | ||||||
| chr16:89094466
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+470G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094466 | ||||||
| chr16:89094476
|
C | T | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-194+480C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094476 | ||||||
| chr16:89094512
|
A | G | 275 | a0001c0001t0001g0004a0001c0001t0001g0085a0001c0001t0001g0086others(272): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.-194+516A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094512 | ||||||
| chr16:89094624
|
G | T | 9 | a0001c0001t0001g0084a0002c0003t0005g0077a0002c0003t0005g0078others(6): Show | 9 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-194+628G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094624 | ||||||
| chr16:89094695
|
C | G | 2 | a0001c0001t0001g0356a0001c0001t0030g0357 | 2 | HG02129.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-194+699C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094695 | ||||||
| chr16:89094717
|
A | C | 1 | a0004c0004t0022g0103 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-194+721A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094717 | ||||||
| chr16:89094723
|
A | G | 10 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-194+727A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094723 | ||||||
| chr16:89094742
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-194+746A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094742 | ||||||
| chr16:89094809
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(6): Show | 9 | HG02109.hp2 HG02615.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-194+813T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094809 | ||||||
| chr16:89094822
|
G | T | 1 | a0001c0001t0001g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-194+826G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094822 | ||||||
| chr16:89094826
|
C | T | 2 | a0004c0004t0003g0014a0004c0004t0037g0013 | 2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-194+830C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094826 | ||||||
| chr16:89094912
|
A | G | 6 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0354others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-194+916A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094912 | ||||||
| chr16:89094957
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0085a0001c0001t0001g0086others(264): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.-194+961G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094957 | ||||||
| chr16:89094965
|
T | C | 280 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0085others(277): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.-194+969T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094965 | ||||||
| chr16:89095080
|
G | C | 1 | a0002c0002t0006g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-194+1084G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095080 | ||||||
| chr16:89095111
|
C | T | 2 | a0004c0004t0003g0014a0004c0004t0037g0013 | 2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-194+1115C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095111 | ||||||
| chr16:89095113
|
C | T | 9 | a0002c0002t0008g0236a0002c0002t0008g0237a0002c0002t0008g0239others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-194+1117C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095113 | ||||||
| chr16:89095115
|
G | C | 1 | a0001c0001t0029g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-194+1119G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095115 | ||||||
| chr16:89095202
|
A | G | 271 | a0001c0001t0001g0004a0001c0001t0001g0085a0001c0001t0001g0086others(268): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.-194+1206A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095202 | ||||||
| chr16:89095242
|
C | T | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-194+1246C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095242 | ||||||
| chr16:89095276
|
C | T | 144 | a0001c0001t0001g0155a0001c0001t0001g0196a0001c0001t0002g0002others(141): Show | 145 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.-194+1280C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095276 | ||||||
| chr16:89095282
|
A | G | 142 | a0001c0001t0001g0155a0001c0001t0001g0196a0001c0001t0002g0002others(139): Show | 143 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-194+1286A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095282 | ||||||
| chr16:89095296
|
G | C | 1 | a0001c0001t0028g0101 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-194+1300G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095296 | ||||||
| chr16:89095303
|
TGTAA | T | 16 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-194+1310_-194+131 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 89095303 | |||||
| chr16:89095324
|
T | C | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-194+1328T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095324 | ||||||
| chr16:89095329
|
T | G | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-194+1333T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095329 | ||||||
| chr16:89095351
|
C | A | 1 | a0001c0001t0036g0247 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-194+1355C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095351 | ||||||
| chr16:89095392
|
G | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-194+1396G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095392 | ||||||
| chr16:89095460
|
G | A | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-194+1464G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095460 | ||||||
| chr16:89095526
|
C | T | 70 | a0001c0001t0001g0011a0001c0001t0001g0315a0001c0001t0001g0316others(67): Show | 71 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-194+1530C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095526 | ||||||
| chr16:89095601
|
G | C | 6 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0005t0001g0248others(3): Show | 6 | HG01884.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-194+1605G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095601 | ||||||
| chr16:89095602
|
G | C | 4 | a0001c0005t0009g0250a0001c0005t0009g0308a0003c0008t0047g0012others(1): Show | 4 | HG01261.hp1 HG02109.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-194+1606G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095602 | ||||||
| chr16:89095613
|
T | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-194+1617T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095613 | ||||||
| chr16:89095614
|
G | T | 1 | a0005c0009t0053g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-194+1618G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095614 | ||||||
| chr16:89095656
|
G | A | 1 | a0002c0002t0054g0111 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-194+1660G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095656 | ||||||
| chr16:89095715
|
G | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-194+1719G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095715 | ||||||
| chr16:89095749
|
G | A | 1 | a0001c0001t0017g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-194+1753G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095749 | ||||||
| chr16:89095759
|
G | A | 1 | a0001c0001t0018g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-194+1763G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095759 | ||||||
| chr16:89095780
|
G | A | 2 | a0002c0020t0008g0362a0005c0017t0035g0359 | 2 | HG02109.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-194+1784G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095780 | ||||||
| chr16:89095801
|
G | A | 3 | a0001c0001t0016g0241a0001c0001t0016g0242a0005c0017t0035g0359 | 3 | HG02055.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-194+1805G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095801 | ||||||
| chr16:89095844
|
G | A | 114 | a0001c0001t0001g0155a0001c0001t0001g0196a0001c0001t0002g0002others(111): Show | 115 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.-194+1848G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095844 | ||||||
| chr16:89095904
|
C | A | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-194+1908C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095904 | ||||||
| chr16:89095905
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG02622.hp1 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-194+1909G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095905 | ||||||
| chr16:89095940
|
A | G | 43 | a0001c0001t0027g0216a0002c0002t0004g0214a0002c0002t0006g0112others(40): Show | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-194+1944A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095940 | ||||||
| chr16:89095985
|
T | C | 1 | a0002c0002t0045g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-194+1989T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095985 | ||||||
| chr16:89096034
|
G | A | 3 | a0001c0001t0016g0241a0001c0001t0016g0242a0005c0017t0035g0359 | 3 | HG02055.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-194+2038G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096034 | ||||||
| chr16:89096120
|
G | A | 32 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0223others(29): Show | 33 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-194+2124G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096120 | ||||||
| chr16:89096190
|
T | C | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-194+2194T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096190 | ||||||
| chr16:89096214
|
C | T | 2 | a0002c0020t0008g0362a0003c0008t0047g0012 | 2 | HG04228.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-194+2218C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096214 | ||||||
| chr16:89096236
|
C | CTGA | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-194+2241_-194+224 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 89096236 | |||||
| chr16:89096269
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-194+2273G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096269 | ||||||
| chr16:89096330
|
A | G | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-193-2261A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096330 | ||||||
| chr16:89096382
|
C | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-193-2209C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096382 | ||||||
| chr16:89096411
|
G | A | 2 | a0003c0008t0020g0245a0010c0019t0020g0244 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-193-2180G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096411 | ||||||
| chr16:89096436
|
G | A | 4 | a0002c0002t0008g0236a0002c0002t0008g0237a0002c0002t0008g0239others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193-2155G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096436 | ||||||
| chr16:89096507
|
A | G | 1 | a0004c0004t0003g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-193-2084A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096507 | ||||||
| chr16:89096644
|
A | G | 6 | a0001c0001t0013g0040a0001c0001t0013g0041a0001c0001t0013g0042others(3): Show | 6 | HG01891.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-193-1947A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096644 | ||||||
| chr16:89096668
|
G | C | 8 | a0001c0001t0013g0040a0001c0001t0013g0041a0001c0001t0013g0042others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-193-1923G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096668 | ||||||
| chr16:89096677
|
G | T | 1 | a0001c0001t0051g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-193-1914G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096677 | ||||||
| chr16:89096841
|
G | A | 1 | a0003c0010t0058g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-193-1750G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096841 | ||||||
| chr16:89096857
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.-193-1734C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096857 | ||||||
| chr16:89096869
|
C | G | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-193-1722C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096869 | ||||||
| chr16:89096905
|
C | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-193-1686C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096905 | ||||||
| chr16:89096920
|
C | T | 34 | a0002c0002t0006g0112a0004c0004t0003g0005a0004c0004t0003g0014others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-193-1671C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096920 | ||||||
| chr16:89096948
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(173): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-193-1643G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89096948 | ||||||
| chr16:89096984
|
TTGAGTTT others(14): Show |
T | 2 | a0002c0003t0005g0029a0002c0003t0005g0030 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-193-1604_-193-158 others(25): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 89096984 | |||||
| chr16:89097070
|
C | T | 2 | a0001c0005t0001g0248a0001c0005t0001g0249 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-193-1521C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097070 | ||||||
| chr16:89097085
|
C | T | 3 | a0001c0005t0001g0302a0001c0005t0001g0330a0001c0005t0001g0331 | 3 | NA18939.hp2 NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-193-1506C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097085 | ||||||
| chr16:89097094
|
T | C | 223 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-193-1497T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097094 | ||||||
| chr16:89097191
|
C | G | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-193-1400C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097191 | ||||||
| chr16:89097373
|
G | A | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-193-1218G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097373 | ||||||
| chr16:89097380
|
G | T | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-193-1211G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097380 | ||||||
| chr16:89097393
|
G | A | 1 | a0001c0001t0018g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-193-1198G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097393 | ||||||
| chr16:89097421
|
C | T | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-193-1170C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097421 | ||||||
| chr16:89097431
|
A | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-1160A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097431 | ||||||
| chr16:89097438
|
A | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-1153A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097438 | ||||||
| chr16:89097496
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-193-1095C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097496 | ||||||
| chr16:89097502
|
G | C | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-193-1089G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097502 | ||||||
| chr16:89097673
|
G | C | 222 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-193-918G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097673 | ||||||
| chr16:89097749
|
C | G | 1 | a0004c0004t0003g0349 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-193-842C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097749 | ||||||
| chr16:89097773
|
GA | G | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-817delA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097773 | ||||||
| chr16:89097799
|
G | A | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-792G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097799 | ||||||
| chr16:89097800
|
C | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-791C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097800 | ||||||
| chr16:89097899
|
C | T | 1 | a0012c0015t0009g0329 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-193-692C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89097899 | ||||||
| chr16:89098014
|
C | T | 1 | a0002c0002t0006g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-193-577C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098014 | ||||||
| chr16:89098021
|
C | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-570C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098021 | ||||||
| chr16:89098132
|
G | A | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-193-459G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098132 | ||||||
| chr16:89098303
|
T | G | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | NA18967.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-193-288T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098303 | ||||||
| chr16:89098397
|
G | T | 3 | a0001c0001t0001g0299a0001c0001t0029g0243a0001c0005t0001g0300 | 3 | HG01074.hp1 HG02647.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-193-194G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098397 | ||||||
| chr16:89098433
|
C | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(173): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-193-158C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098433 | ||||||
| chr16:89098436
|
G | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-193-155G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098436 | ||||||
| chr16:89098436
|
G | C | 1 | a0001c0001t0018g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-193-155G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098436 | ||||||
| chr16:89098484
|
G | A | 2 | a0002c0002t0006g0210a0002c0002t0019g0209 | 2 | NA18942.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-193-107G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098484 | ||||||
| chr16:89098566
|
C | A | 36 | a0002c0003t0004g0018a0002c0003t0004g0020a0002c0003t0005g0015others(33): Show | 36 | HG00323.hp2 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-193-25C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89098566 | ||||||
| chr16:89098997
|
C | A | 1 | a0002c0003t0005g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-21+234C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89098997 | ||||||
| chr16:89099167
|
G | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-21+404G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099167 | ||||||
| chr16:89099288
|
G | A | 1 | a0004c0004t0003g0332 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-21+525G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099288 | ||||||
| chr16:89099340
|
T | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(218): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-21+577T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099340 | ||||||
| chr16:89099378
|
C | T | 1 | a0001c0001t0002g0200 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-21+615C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099378 | ||||||
| chr16:89099558
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-21+795A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099558 | ||||||
| chr16:89099564
|
G | A | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-21+801G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099564 | ||||||
| chr16:89099572
|
G | A | 1 | a0002c0002t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-21+809G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099572 | ||||||
| chr16:89099576
|
T | C | 23 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(20): Show | 23 | HG00544.hp1 HG01256.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+813T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099576 | ||||||
| chr16:89099640
|
G | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-21+877G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099640 | ||||||
| chr16:89099645
|
G | C | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-21+882G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099645 | ||||||
| chr16:89099714
|
G | A | 1 | a0002c0003t0005g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-20-948G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099714 | ||||||
| chr16:89099831
|
T | C | 2 | a0004c0004t0003g0333a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-20-831T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099831 | ||||||
| chr16:89099854
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-20-808A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099854 | ||||||
| chr16:89099860
|
A | T | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-20-802A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099860 | ||||||
| chr16:89099978
|
CA | C | 6 | a0001c0001t0001g0356a0001c0005t0009g0309a0002c0002t0006g0151others(3): Show | 6 | HG01361.hp1 NA18967.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-668delA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 89099978 | |||||
| chr16:89099978
|
CAA | C | 212 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-20-669_-20-668del others(2): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 89099978 | |||||
| chr16:89099994
|
A | T | 1 | a0008c0022t0007g0063 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-20-668A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89099994 | ||||||
| chr16:89100016
|
T | C | 220 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(217): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-20-646T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100016 | ||||||
| chr16:89100034
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-20-628G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100034 | ||||||
| chr16:89100199
|
C | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-20-463C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100199 | ||||||
| chr16:89100261
|
C | T | 216 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-20-401C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100261 | ||||||
| chr16:89100306
|
T | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-356T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100306 | ||||||
| chr16:89100384
|
G | A | 2 | a0002c0002t0004g0118a0002c0002t0004g0119 | 2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-20-278G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100384 | ||||||
| chr16:89100399
|
A | G | 217 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-20-263A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100399 | ||||||
| chr16:89100424
|
G | A | 243 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(240): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-20-238G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100424 | ||||||
| chr16:89100466
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0159 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-20-196G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100466 | ||||||
| chr16:89100487
|
G | A | 1 | a0002c0003t0005g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-20-175G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100487 | ||||||
| chr16:89100533
|
C | T | 217 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-20-129C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100533 | ||||||
| chr16:89100580
|
G | A | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20-82G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100580 | ||||||
| chr16:89100641
|
C | A | 5 | a0002c0003t0004g0061a0002c0003t0004g0062a0002c0003t0004g0095others(2): Show | 5 | HG00558.hp1 HG02071.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-21C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100641 | ||||||
| chr16:89100658
|
C | G | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
splice_region_variant&intron_variant | LOW | c.-20-4C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2/10 | chr16 | 89100658 | ||||||
| chr16:89101384
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.666+37C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101384 | ||||||
| chr16:89101399
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+52G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101399 | ||||||
| chr16:89101420
|
C | T | 15 | a0001c0005t0001g0302a0001c0005t0001g0330a0001c0005t0001g0331others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+73C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101420 | ||||||
| chr16:89101491
|
G | C | 2 | a0003c0008t0020g0245a0010c0019t0020g0244 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.666+144G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101491 | ||||||
| chr16:89101492
|
G | T | 1 | a0001c0005t0011g0326 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.666+145G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101492 | ||||||
| chr16:89101542
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.666+195G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101542 | ||||||
| chr16:89101546
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.666+199T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101546 | ||||||
| chr16:89101664
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.666+317C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101664 | ||||||
| chr16:89101707
|
G | A | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.666+360G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101707 | ||||||
| chr16:89101807
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+460C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101807 | ||||||
| chr16:89101883
|
G | A | 1 | a0005c0009t0015g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.666+536G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101883 | ||||||
| chr16:89101899
|
G | A | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.666+552G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101899 | ||||||
| chr16:89101915
|
A | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.666+568A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101915 | ||||||
| chr16:89101952
|
C | T | 2 | a0001c0005t0001g0038a0001c0005t0001g0039 | 2 | HG01175.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.666+605C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101952 | ||||||
| chr16:89101988
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.667-616T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89101988 | ||||||
| chr16:89102021
|
T | C | 361 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(358): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.667-583T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102021 | ||||||
| chr16:89102109
|
C | T | 1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.667-495C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102109 | ||||||
| chr16:89102140
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.667-464T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102140 | ||||||
| chr16:89102259
|
A | C | 1 | a0002c0003t0005g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.667-345A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102259 | ||||||
| chr16:89102315
|
C | T | 29 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-289C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102315 | ||||||
| chr16:89102317
|
A | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.667-287A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102317 | ||||||
| chr16:89102391
|
T | C | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.667-213T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102391 | ||||||
| chr16:89102428
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0002g0198 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.667-176G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102428 | ||||||
| chr16:89102493
|
C | G | 2 | a0003c0008t0020g0245a0010c0019t0020g0244 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.667-111C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102493 | ||||||
| chr16:89102503
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.667-101T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102503 | ||||||
| chr16:89102527
|
G | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.667-77G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102527 | ||||||
| chr16:89102528
|
T | C | 3 | a0001c0005t0001g0302a0001c0005t0001g0330a0001c0005t0001g0331 | 3 | NA18939.hp2 NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.667-76T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102528 | ||||||
| chr16:89102573
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.667-31T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102573 | ||||||
| chr16:89102591
|
T | C | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.667-13T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102591 | ||||||
| chr16:89102592
|
C | T | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.667-12C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 3/10 | chr16 | 89102592 | ||||||
| chr16:89102781
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.822+22C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102781 | ||||||
| chr16:89102797
|
C | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+38C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102797 | ||||||
| chr16:89102811
|
CCT | C | 216 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.822+53_822+54delCT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102811 | ||||||
| chr16:89102865
|
T | C | 9 | a0003c0007t0007g0045a0003c0007t0007g0046a0003c0007t0007g0047others(6): Show | 9 | HG00408.hp2 HG00438.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.822+106T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102865 | ||||||
| chr16:89102876
|
G | A | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.822+117G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102876 | ||||||
| chr16:89102904
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+145T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102904 | ||||||
| chr16:89102930
|
A | G | 2 | a0002c0002t0006g0150a0002c0002t0042g0152 | 2 | NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.822+171A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89102930 | ||||||
| chr16:89103007
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+248C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103007 | ||||||
| chr16:89103043
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0325 | 2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.822+284C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103043 | ||||||
| chr16:89103069
|
A | G | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.822+310A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103069 | ||||||
| chr16:89103079
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+320A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103079 | ||||||
| chr16:89103106
|
T | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.822+347T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103106 | ||||||
| chr16:89103109
|
T | G | 1 | a0001c0001t0002g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.822+350T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103109 | ||||||
| chr16:89103196
|
G | C | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.822+437G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103196 | ||||||
| chr16:89103225
|
C | T | 1 | a0002c0002t0007g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.822+466C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103225 | ||||||
| chr16:89103233
|
C | T | 1 | a0009c0024t0004g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.822+474C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103233 | ||||||
| chr16:89103236
|
G | A | 5 | a0001c0005t0011g0311a0001c0005t0011g0312a0001c0005t0011g0313others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+477G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103236 | ||||||
| chr16:89103262
|
C | T | 1 | a0001c0005t0009g0298 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.822+503C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103262 | ||||||
| chr16:89103393
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.822+634C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103393 | ||||||
| chr16:89103619
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+860T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103619 | ||||||
| chr16:89103639
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+880T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103639 | ||||||
| chr16:89103656
|
C | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+897C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103656 | ||||||
| chr16:89103716
|
G | A | 1 | a0004c0004t0003g0336 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.822+957G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103716 | ||||||
| chr16:89103763
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+1004T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103763 | ||||||
| chr16:89103766
|
C | A | 1 | a0001c0001t0002g0160 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.822+1007C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103766 | ||||||
| chr16:89103888
|
C | T | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.822+1129C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103888 | ||||||
| chr16:89103925
|
C | G | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.822+1166C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103925 | ||||||
| chr16:89103960
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+1201C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103960 | ||||||
| chr16:89103977
|
C | T | 2 | a0002c0003t0005g0015a0002c0003t0005g0016 | 2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.822+1218C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89103977 | ||||||
| chr16:89104013
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.822+1254G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104013 | ||||||
| chr16:89104077
|
A | G | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.822+1318A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104077 | ||||||
| chr16:89104162
|
G | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.822+1403G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104162 | ||||||
| chr16:89104228
|
A | G | 1 | a0001c0018t0011g0261 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.822+1469A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104228 | ||||||
| chr16:89104271
|
A | G | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+1512A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104271 | ||||||
| chr16:89104280
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0196a0001c0001t0001g0277others(22): Show | 26 | HG00642.hp2 HG02129.hp1 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.822+1521C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104280 | ||||||
| chr16:89104299
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+1540G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104299 | ||||||
| chr16:89104369
|
A | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+1610A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104369 | ||||||
| chr16:89104448
|
C | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+1689C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104448 | ||||||
| chr16:89104453
|
C | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.822+1694C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104453 | ||||||
| chr16:89104526
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.822+1767C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104526 | ||||||
| chr16:89104566
|
G | T | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+1807G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104566 | ||||||
| chr16:89104609
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.822+1850C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104609 | ||||||
| chr16:89104610
|
C | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+1851C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104610 | ||||||
| chr16:89104634
|
G | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+1875G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104634 | ||||||
| chr16:89104718
|
C | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+1959C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104718 | ||||||
| chr16:89104759
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.822+2000G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104759 | ||||||
| chr16:89104820
|
C | G | 213 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.822+2061C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104820 | ||||||
| chr16:89104859
|
G | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+2100G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104859 | ||||||
| chr16:89104867
|
A | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+2108A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104867 | ||||||
| chr16:89104874
|
C | T | 2 | a0004c0004t0003g0233a0004c0004t0003g0234 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.822+2115C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104874 | ||||||
| chr16:89104895
|
A | C | 1 | a0002c0002t0004g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.822+2136A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104895 | ||||||
| chr16:89104912
|
A | C | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.822+2153A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104912 | ||||||
| chr16:89104976
|
G | A | 35 | a0001c0001t0061g0260a0002c0003t0005g0015a0002c0003t0005g0016others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+2217G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104976 | ||||||
| chr16:89104981
|
T | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+2222T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89104981 | ||||||
| chr16:89105025
|
C | CAGAGCCT others(34): Show |
214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.822+2274_822+2275i others(43): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89105025 | |||||
| chr16:89105034
|
C | T | 4 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0192others(1): Show | 4 | HG01070.hp2 HG01168.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2275C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105034 | ||||||
| chr16:89105045
|
C | CGTCGCCA others(34): Show |
4 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0192others(1): Show | 4 | HG01070.hp2 HG01168.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2326_822+2327i others(43): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89105045 | |||||
| chr16:89105045
|
C | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0189a0001c0001t0002g0193others(2): Show | 6 | HG01071.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+2286C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105045 | ||||||
| chr16:89105086
|
C | T | 32 | a0002c0003t0004g0061a0002c0003t0004g0062a0002c0003t0004g0095others(29): Show | 33 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.822+2327C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105086 | ||||||
| chr16:89105101
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+2342C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105101 | ||||||
| chr16:89105136
|
A | G | 220 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.822+2377A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105136 | ||||||
| chr16:89105211
|
A | G | 1 | a0002c0003t0005g0083 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.822+2452A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105211 | ||||||
| chr16:89105238
|
C | T | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.822+2479C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105238 | ||||||
| chr16:89105253
|
C | T | 32 | a0002c0003t0004g0061a0002c0003t0004g0062a0002c0003t0004g0095others(29): Show | 33 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.822+2494C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105253 | ||||||
| chr16:89105381
|
G | A | 1 | a0001c0005t0011g0326 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.822+2622G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105381 | ||||||
| chr16:89105539
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+2780C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105539 | ||||||
| chr16:89105540
|
G | A | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.822+2781G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105540 | ||||||
| chr16:89105702
|
C | A | 1 | a0003c0010t0008g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.822+2943C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105702 | ||||||
| chr16:89105714
|
C | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.822+2955C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89105714 | ||||||
| chr16:89105805
|
TGAGGGCA others(19): Show |
T | 1 | a0008c0022t0007g0063 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.822+3067_822+3092d others(28): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89105805 | |||||
| chr16:89106029
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.822+3270C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106029 | ||||||
| chr16:89106047
|
G | C | 33 | a0002c0003t0004g0061a0002c0003t0004g0062a0002c0003t0004g0095others(30): Show | 34 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.822+3288G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106047 | ||||||
| chr16:89106132
|
G | A | 2 | a0001c0001t0061g0260a0003c0008t0047g0012 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.822+3373G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106132 | ||||||
| chr16:89106139
|
G | C | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.822+3380G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106139 | ||||||
| chr16:89106209
|
C | T | 2 | a0002c0011t0008g0131a0002c0011t0008g0132 | 2 | HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.822+3450C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106209 | ||||||
| chr16:89106216
|
C | T | 1 | a0002c0003t0005g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.822+3457C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106216 | ||||||
| chr16:89106296
|
A | AT | 215 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.822+3551dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89106296 | |||||
| chr16:89106579
|
A | G | 1 | a0002c0003t0005g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+3820A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106579 | ||||||
| chr16:89106677
|
C | G | 61 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(58): Show | 62 | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.822+3918C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106677 | ||||||
| chr16:89106820
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+4061C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106820 | ||||||
| chr16:89106852
|
G | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.822+4093G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106852 | ||||||
| chr16:89106874
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0301 | 3 | HG03453.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.822+4115G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106874 | ||||||
| chr16:89106931
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.822+4172C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89106931 | ||||||
| chr16:89107001
|
C | G | 1 | a0004c0004t0038g0343 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.822+4242C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107001 | ||||||
| chr16:89107175
|
C | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.822+4416C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107175 | ||||||
| chr16:89107287
|
C | T | 1 | a0002c0002t0054g0111 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.822+4528C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107287 | ||||||
| chr16:89107296
|
C | G | 35 | a0001c0001t0023g0274a0001c0005t0001g0035a0001c0005t0001g0036others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+4537C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107296 | ||||||
| chr16:89107307
|
G | A | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.822+4548G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107307 | ||||||
| chr16:89107407
|
A | ACCTCGGC others(29): Show |
33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-4654_823-4619d others(38): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89107407 | |||||
| chr16:89107442
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.823-4650C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107442 | ||||||
| chr16:89107445
|
C | T | 1 | a0002c0002t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823-4647C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107445 | ||||||
| chr16:89107490
|
G | T | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823-4602G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107490 | ||||||
| chr16:89107602
|
T | C | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.823-4490T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107602 | ||||||
| chr16:89107646
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.823-4446G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107646 | ||||||
| chr16:89107725
|
A | C | 296 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(293): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.823-4367A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107725 | ||||||
| chr16:89107765
|
T | C | 2 | a0002c0002t0014g0121a0002c0002t0014g0122 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.823-4327T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107765 | ||||||
| chr16:89107829
|
G | A | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.823-4263G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107829 | ||||||
| chr16:89107892
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0301 | 3 | HG03453.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.823-4200G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107892 | ||||||
| chr16:89107957
|
A | G | 1 | a0001c0005t0011g0314 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.823-4135A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107957 | ||||||
| chr16:89107995
|
G | T | 1 | a0001c0001t0013g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.823-4097G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89107995 | ||||||
| chr16:89108021
|
G | A | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.823-4071G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108021 | ||||||
| chr16:89108175
|
G | A | 4 | a0002c0002t0008g0236a0002c0002t0008g0237a0002c0002t0008g0239others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-3917G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108175 | ||||||
| chr16:89108262
|
A | G | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.823-3830A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108262 | ||||||
| chr16:89108283
|
C | T | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.823-3809C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108283 | ||||||
| chr16:89108346
|
A | G | 3 | a0001c0001t0012g0008a0001c0001t0012g0009a0001c0001t0012g0010 | 3 | HG02615.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.823-3746A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108346 | ||||||
| chr16:89108523
|
T | C | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-3569T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108523 | ||||||
| chr16:89108525
|
A | G | 3 | a0001c0005t0011g0311a0001c0005t0011g0312a0001c0005t0011g0313 | 3 | HG01069.hp2 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.823-3567A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108525 | ||||||
| chr16:89108567
|
C | T | 1 | a0002c0003t0005g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.823-3525C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108567 | ||||||
| chr16:89108707
|
T | C | 1 | a0004c0004t0037g0013 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.823-3385T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89108707 | ||||||
| chr16:89109166
|
C | T | 1 | a0002c0011t0008g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.823-2926C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109166 | ||||||
| chr16:89109227
|
C | T | 39 | a0002c0003t0004g0018a0002c0003t0004g0020a0002c0003t0005g0015others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.823-2865C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109227 | ||||||
| chr16:89109229
|
C | CA | 19 | a0001c0001t0001g0155a0001c0001t0001g0264a0001c0001t0001g0277others(16): Show | 19 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.823-2842dupA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109229 | |||||
| chr16:89109229
|
CA | C | 38 | a0001c0001t0001g0086a0001c0001t0001g0256a0001c0001t0012g0272others(35): Show | 39 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.823-2842delA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109229 | |||||
| chr16:89109243
|
A | G | 32 | a0001c0001t0016g0241a0001c0001t0016g0242a0002c0003t0004g0061others(29): Show | 33 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-2849A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109243 | ||||||
| chr16:89109245
|
AAAAAAG | A | 66 | a0001c0001t0016g0241a0001c0001t0016g0242a0002c0003t0005g0015others(63): Show | 67 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.823-2842_823-2837d others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109245 | |||||
| chr16:89109246
|
AAAAAG | A | 8 | a0002c0003t0004g0020a0002c0003t0005g0071a0002c0003t0006g0019others(5): Show | 8 | HG00544.hp2 HG02027.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-2832_823-2828d others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109246 | |||||
| chr16:89109247
|
A | G | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.823-2845A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109247 | ||||||
| chr16:89109252
|
A | G | 1 | a0004c0004t0031g0232 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.823-2840A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109252 | ||||||
| chr16:89109393
|
T | C | 34 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-2699T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109393 | ||||||
| chr16:89109403
|
C | CT | 25 | a0002c0002t0004g0119a0002c0002t0004g0123a0002c0002t0004g0146others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-2663dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109403 | |||||
| chr16:89109403
|
CT | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.823-2663delT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109403 | |||||
| chr16:89109403
|
CTT | C | 32 | a0001c0001t0016g0241a0001c0001t0016g0242a0002c0003t0004g0018others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.823-2664_823-2663d others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109403 | |||||
| chr16:89109403
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-2670_823-2663d others(10): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109403 | |||||
| chr16:89109403
|
CTTTTTTT others(8): Show |
C | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823-2677_823-2663d others(17): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89109403 | |||||
| chr16:89109406
|
T | G | 1 | a0002c0003t0005g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.823-2686T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109406 | ||||||
| chr16:89109450
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.823-2642C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109450 | ||||||
| chr16:89109497
|
C | T | 1 | a0001c0001t0051g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.823-2595C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109497 | ||||||
| chr16:89109556
|
C | T | 2 | a0001c0001t0013g0040a0001c0001t0013g0043 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.823-2536C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109556 | ||||||
| chr16:89109596
|
G | T | 1 | a0001c0005t0001g0037 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.823-2496G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109596 | ||||||
| chr16:89109611
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.823-2481C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109611 | ||||||
| chr16:89109612
|
G | A | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.823-2480G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109612 | ||||||
| chr16:89109635
|
C | G | 1 | a0003c0010t0058g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.823-2457C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109635 | ||||||
| chr16:89109697
|
C | T | 4 | a0001c0005t0009g0296a0001c0005t0009g0297a0001c0005t0009g0298others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-2395C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109697 | ||||||
| chr16:89109702
|
C | T | 1 | a0002c0002t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823-2390C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109702 | ||||||
| chr16:89109833
|
C | T | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.823-2259C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109833 | ||||||
| chr16:89109897
|
G | A | 1 | a0001c0001t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823-2195G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109897 | ||||||
| chr16:89109913
|
G | A | 38 | a0001c0001t0016g0241a0001c0001t0016g0242a0002c0003t0052g0240others(35): Show | 39 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.823-2179G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109913 | ||||||
| chr16:89109984
|
T | A | 1 | a0001c0001t0016g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.823-2108T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89109984 | ||||||
| chr16:89110050
|
T | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.823-2042T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110050 | ||||||
| chr16:89110084
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.823-2008T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110084 | ||||||
| chr16:89110131
|
T | TA | 34 | a0001c0001t0002g0207a0004c0004t0003g0005a0004c0004t0003g0014others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-1953dupA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89110131 | |||||
| chr16:89110399
|
A | G | 1 | a0001c0001t0027g0216 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.823-1693A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110399 | ||||||
| chr16:89110470
|
G | A | 225 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.823-1622G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110470 | ||||||
| chr16:89110549
|
G | A | 39 | a0001c0001t0002g0189a0002c0003t0004g0018a0002c0003t0004g0020others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.823-1543G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110549 | ||||||
| chr16:89110563
|
A | T | 20 | a0004c0004t0003g0005a0004c0004t0003g0231a0004c0004t0003g0304others(17): Show | 21 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.823-1529A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110563 | ||||||
| chr16:89110661
|
C | T | 1 | a0004c0004t0003g0341 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.823-1431C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110661 | ||||||
| chr16:89110785
|
G | A | 1 | a0004c0004t0003g0229 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.823-1307G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110785 | ||||||
| chr16:89110940
|
G | T | 1 | a0002c0002t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823-1152G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110940 | ||||||
| chr16:89110958
|
C | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.823-1134C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89110958 | ||||||
| chr16:89111068
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.823-1024C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111068 | ||||||
| chr16:89111098
|
G | T | 223 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.823-994G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111098 | ||||||
| chr16:89111104
|
C | T | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.823-988C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111104 | ||||||
| chr16:89111174
|
T | C | 1 | a0001c0001t0012g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.823-918T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111174 | ||||||
| chr16:89111206
|
G | A | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-886G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111206 | ||||||
| chr16:89111423
|
G | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0325 | 2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.823-669G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111423 | ||||||
| chr16:89111450
|
G | C | 1 | a0003c0008t0008g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.823-642G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111450 | ||||||
| chr16:89111495
|
C | T | 6 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0275others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-597C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111495 | ||||||
| chr16:89111514
|
C | T | 24 | a0004c0004t0003g0005a0004c0004t0003g0223a0004c0004t0003g0231others(21): Show | 25 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.823-578C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111514 | ||||||
| chr16:89111580
|
G | A | 1 | a0005c0009t0011g0310 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.823-512G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111580 | ||||||
| chr16:89111581
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.823-511C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111581 | ||||||
| chr16:89111639
|
T | C | 1 | a0004c0004t0003g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.823-453T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111639 | ||||||
| chr16:89111710
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-382G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111710 | ||||||
| chr16:89111832
|
C | T | 1 | a0001c0001t0012g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.823-260C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111832 | ||||||
| chr16:89111916
|
C | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0301 | 3 | HG03453.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.823-176C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89111916 | ||||||
| chr16:89112040
|
C | T | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-52C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89112040 | ||||||
| chr16:89112047
|
C | T | 1 | a0003c0007t0007g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.823-45C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | chr16 | 89112047 | ||||||
| chr16:89112049
|
G | GTGCCTGC others(46): Show |
256 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(253): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.823-27_823-26insCA others(51): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 89112049 | |||||
| chr16:89112365
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.977+119A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112365 | ||||||
| chr16:89112385
|
C | T | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.977+139C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112385 | ||||||
| chr16:89112431
|
T | C | 255 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.977+185T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112431 | ||||||
| chr16:89112444
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.977+198C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112444 | ||||||
| chr16:89112485
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.977+239C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112485 | ||||||
| chr16:89112513
|
A | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0294 | 3 | NA18949.hp1 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.977+267A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112513 | ||||||
| chr16:89112632
|
C | A | 34 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.977+386C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112632 | ||||||
| chr16:89112641
|
C | CGTCTGTC others(5): Show |
1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.977+399_977+400ins others(12): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 89112641 | |||||
| chr16:89112642
|
G | A | 1 | a0002c0003t0057g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.977+396G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112642 | ||||||
| chr16:89112752
|
G | C | 1 | a0001c0001t0002g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.977+506G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112752 | ||||||
| chr16:89112955
|
C | T | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.977+709C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112955 | ||||||
| chr16:89112983
|
T | C | 4 | a0001c0001t0010g0218a0001c0001t0010g0219a0001c0001t0010g0221others(1): Show | 4 | HG02040.hp2 NA18954.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.977+737T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89112983 | ||||||
| chr16:89113035
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.977+789G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113035 | ||||||
| chr16:89113057
|
G | A | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.977+811G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113057 | ||||||
| chr16:89113159
|
G | A | 37 | a0001c0001t0001g0295a0001c0001t0001g0325a0001c0001t0023g0274others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.977+913G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113159 | ||||||
| chr16:89113270
|
C | T | 1 | a0002c0002t0014g0143 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.977+1024C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113270 | ||||||
| chr16:89113273
|
G | A | 1 | a0001c0005t0009g0353 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.977+1027G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113273 | ||||||
| chr16:89113386
|
T | C | 2 | a0001c0005t0011g0311a0001c0005t0011g0312 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.978-953T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113386 | ||||||
| chr16:89113387
|
G | A | 2 | a0004c0004t0003g0233a0004c0004t0003g0234 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.978-952G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113387 | ||||||
| chr16:89113466
|
A | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(226): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.978-873A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113466 | ||||||
| chr16:89113556
|
G | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.978-783G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113556 | ||||||
| chr16:89113604
|
G | A | 2 | a0002c0002t0006g0150a0002c0002t0042g0152 | 2 | NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.978-735G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113604 | ||||||
| chr16:89113666
|
C | T | 1 | a0004c0004t0003g0349 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.978-673C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113666 | ||||||
| chr16:89113734
|
C | T | 1 | a0011c0016t0002g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.978-605C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113734 | ||||||
| chr16:89113875
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.978-464C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113875 | ||||||
| chr16:89113948
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.978-391C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113948 | ||||||
| chr16:89113998
|
T | C | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.978-341T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89113998 | ||||||
| chr16:89114052
|
G | A | 3 | a0002c0003t0004g0018a0002c0003t0004g0020a0002c0003t0006g0019 | 3 | HG02071.hp2 HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.978-287G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89114052 | ||||||
| chr16:89114256
|
C | G | 289 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.978-83C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89114256 | ||||||
| chr16:89114287
|
C | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(34): Show | 38 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.978-52C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89114287 | ||||||
| chr16:89114288
|
G | A | 1 | a0002c0003t0005g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.978-51G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89114288 | ||||||
| chr16:89114289
|
C | T | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.978-50C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 5/10 | chr16 | 89114289 | ||||||
| chr16:89114491
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1126+4C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114491 | ||||||
| chr16:89114527
|
G | T | 180 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1126+40G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114527 | ||||||
| chr16:89114604
|
G | A | 25 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(22): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1126+117G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114604 | ||||||
| chr16:89114688
|
C | T | 1 | a0002c0003t0005g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1126+201C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114688 | ||||||
| chr16:89114731
|
T | G | 293 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1126+244T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114731 | ||||||
| chr16:89114761
|
A | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+274A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114761 | ||||||
| chr16:89114788
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+301T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114788 | ||||||
| chr16:89114812
|
A | G | 3 | a0002c0011t0008g0128a0002c0011t0008g0131a0002c0011t0008g0132 | 3 | HG01516.hp2 HG03239.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1126+325A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114812 | ||||||
| chr16:89114870
|
G | A | 1 | a0002c0003t0005g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1126+383G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114870 | ||||||
| chr16:89114917
|
G | T | 32 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1126+430G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114917 | ||||||
| chr16:89114955
|
C | T | 1 | a0001c0005t0009g0353 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1126+468C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89114955 | ||||||
| chr16:89115152
|
A | C | 1 | a0003c0010t0058g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1126+665A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115152 | ||||||
| chr16:89115335
|
C | T | 3 | a0001c0001t0012g0008a0001c0001t0012g0009a0001c0001t0012g0010 | 3 | HG02615.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1126+848C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115335 | ||||||
| chr16:89115400
|
G | A | 2 | a0002c0003t0021g0088a0002c0003t0021g0089 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1126+913G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115400 | ||||||
| chr16:89115419
|
C | T | 3 | a0002c0002t0008g0237a0002c0002t0008g0239a0002c0023t0008g0238 | 3 | HG02451.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1126+932C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115419 | ||||||
| chr16:89115462
|
A | G | 8 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(5): Show | 8 | HG01074.hp2 HG01496.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126+975A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115462 | ||||||
| chr16:89115482
|
T | C | 254 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1126+995T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115482 | ||||||
| chr16:89115484
|
C | T | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1126+997C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115484 | ||||||
| chr16:89115696
|
A | G | 252 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1126+1209A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115696 | ||||||
| chr16:89115810
|
A | G | 251 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1126+1323A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115810 | ||||||
| chr16:89115824
|
G | A | 1 | a0004c0004t0003g0307 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1126+1337G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115824 | ||||||
| chr16:89115852
|
T | G | 1 | a0002c0002t0006g0235 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1126+1365T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115852 | ||||||
| chr16:89115887
|
G | A | 188 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1126+1400G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115887 | ||||||
| chr16:89116088
|
T | C | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1126+1601T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116088 | ||||||
| chr16:89116260
|
C | T | 1 | a0002c0002t0041g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1126+1773C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116260 | ||||||
| chr16:89116356
|
A | G | 1 | a0001c0001t0010g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1126+1869A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116356 | ||||||
| chr16:89116464
|
G | C | 1 | a0005c0009t0011g0310 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1126+1977G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116464 | ||||||
| chr16:89116518
|
A | G | 252 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1126+2031A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116518 | ||||||
| chr16:89116530
|
G | A | 25 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(22): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1126+2043G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116530 | ||||||
| chr16:89116673
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1126+2186G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116673 | ||||||
| chr16:89116766
|
C | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1126+2279C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116766 | ||||||
| chr16:89116780
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+2293G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116780 | ||||||
| chr16:89116789
|
G | A | 250 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1126+2302G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116789 | ||||||
| chr16:89116797
|
C | T | 15 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0024others(12): Show | 15 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1126+2310C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116797 | ||||||
| chr16:89116809
|
A | G | 252 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1126+2322A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116809 | ||||||
| chr16:89116821
|
C | T | 1 | a0002c0002t0041g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1126+2334C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116821 | ||||||
| chr16:89116837
|
C | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1126+2350C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89116837 | ||||||
| chr16:89117019
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+2532C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117019 | ||||||
| chr16:89117046
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+2559G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117046 | ||||||
| chr16:89117066
|
C | T | 1 | a0002c0003t0021g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1126+2579C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117066 | ||||||
| chr16:89117256
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+2769C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117256 | ||||||
| chr16:89117271
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1126+2784G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117271 | ||||||
| chr16:89117294
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1126+2807C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117294 | ||||||
| chr16:89117294
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1126+2807C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117294 | ||||||
| chr16:89117298
|
C | T | 5 | a0002c0002t0006g0108a0002c0002t0006g0135a0002c0002t0006g0142others(2): Show | 5 | HG00621.hp1 NA18995.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+2811C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117298 | ||||||
| chr16:89117364
|
A | G | 293 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1126+2877A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117364 | ||||||
| chr16:89117372
|
A | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1126+2885A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117372 | ||||||
| chr16:89117399
|
G | A | 1 | a0002c0002t0004g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1126+2912G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117399 | ||||||
| chr16:89117510
|
A | G | 1 | a0004c0004t0003g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1126+3023A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117510 | ||||||
| chr16:89117565
|
A | G | 292 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(289): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1126+3078A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117565 | ||||||
| chr16:89117683
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-3118G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117683 | ||||||
| chr16:89117727
|
G | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1127-3074G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117727 | ||||||
| chr16:89117752
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1127-3049C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117752 | ||||||
| chr16:89117818
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0012g0007a0001c0001t0012g0008others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1127-2983G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117818 | ||||||
| chr16:89117921
|
T | C | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1127-2880T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117921 | ||||||
| chr16:89117922
|
G | GCTCCCTC others(101): Show |
251 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1127-2852_1127-285 others(112): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 89117922 | |||||
| chr16:89117922
|
G | GCTCCCTC others(101): Show |
1 | a0001c0001t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1127-2853_1127-285 others(112): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 89117922 | |||||
| chr16:89117949
|
C | CGGCAGGT others(47): Show |
1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2852_1127-285 others(58): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117949 | ||||||
| chr16:89117950
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2851A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117950 | ||||||
| chr16:89117952
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2849T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117952 | ||||||
| chr16:89117963
|
A | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0301others(1): Show | 4 | HG03453.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127-2838A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117963 | ||||||
| chr16:89117970
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2831A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117970 | ||||||
| chr16:89117971
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2830A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117971 | ||||||
| chr16:89117977
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2824T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89117977 | ||||||
| chr16:89118006
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2795C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118006 | ||||||
| chr16:89118025
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2776G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118025 | ||||||
| chr16:89118030
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2771G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118030 | ||||||
| chr16:89118030
|
G | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1127-2771G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118030 | ||||||
| chr16:89118058
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2743G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118058 | ||||||
| chr16:89118063
|
GTTCCCTC others(47): Show |
G | 1 | a0002c0003t0005g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1127-2692_1127-263 others(58): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 89118063 | |||||
| chr16:89118070
|
C | T | 36 | a0001c0001t0002g0208a0001c0005t0009g0296a0001c0005t0009g0297others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1127-2731C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118070 | ||||||
| chr16:89118071
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2730G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118071 | ||||||
| chr16:89118078
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2723G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118078 | ||||||
| chr16:89118085
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2716C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118085 | ||||||
| chr16:89118088
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2713T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118088 | ||||||
| chr16:89118117
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2684A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118117 | ||||||
| chr16:89118131
|
C | T | 252 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1127-2670C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118131 | ||||||
| chr16:89118152
|
A | G | 37 | a0001c0001t0002g0208a0001c0005t0009g0296a0001c0005t0009g0297others(34): Show | 38 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1127-2649A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118152 | ||||||
| chr16:89118165
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1127-2636A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118165 | ||||||
| chr16:89118184
|
G | A | 5 | a0002c0002t0006g0108a0002c0002t0006g0135a0002c0002t0006g0142others(2): Show | 5 | HG00621.hp1 NA18995.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127-2617G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118184 | ||||||
| chr16:89118202
|
T | C | 1 | a0002c0003t0046g0021 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1127-2599T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118202 | ||||||
| chr16:89118217
|
A | T | 37 | a0001c0001t0002g0208a0001c0005t0009g0296a0001c0005t0009g0297others(34): Show | 38 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1127-2584A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118217 | ||||||
| chr16:89118244
|
G | T | 1 | a0001c0001t0016g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1127-2557G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118244 | ||||||
| chr16:89118424
|
C | T | 1 | a0002c0003t0005g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1127-2377C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118424 | ||||||
| chr16:89118502
|
C | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1127-2299C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118502 | ||||||
| chr16:89118533
|
C | T | 1 | a0002c0003t0005g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1127-2268C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118533 | ||||||
| chr16:89118534
|
G | A | 36 | a0001c0001t0002g0208a0001c0005t0009g0296a0001c0005t0009g0297others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1127-2267G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118534 | ||||||
| chr16:89118544
|
G | T | 24 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(21): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1127-2257G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118544 | ||||||
| chr16:89118545
|
C | T | 24 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(21): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1127-2256C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118545 | ||||||
| chr16:89118559
|
G | A | 2 | a0002c0003t0005g0015a0002c0003t0005g0016 | 2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1127-2242G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118559 | ||||||
| chr16:89118561
|
A | AAGAG | 252 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1127-2234_1127-223 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 89118561 | |||||
| chr16:89118561
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2240A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118561 | ||||||
| chr16:89118611
|
A | G | 253 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1127-2190A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118611 | ||||||
| chr16:89118626
|
G | A | 1 | a0001c0001t0016g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1127-2175G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118626 | ||||||
| chr16:89118709
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 222 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1127-2092T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118709 | ||||||
| chr16:89118716
|
G | A | 25 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(22): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1127-2085G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118716 | ||||||
| chr16:89118736
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-2065G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118736 | ||||||
| chr16:89118767
|
C | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(61): Show | 65 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1127-2034C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118767 | ||||||
| chr16:89118799
|
CAG | C | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127-1999_1127-199 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 89118799 | |||||
| chr16:89118926
|
C | T | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1127-1875C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118926 | ||||||
| chr16:89118964
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1837C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118964 | ||||||
| chr16:89118975
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1826G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118975 | ||||||
| chr16:89118979
|
G | A | 1 | a0002c0002t0045g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1127-1822G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89118979 | ||||||
| chr16:89119046
|
G | C | 251 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1127-1755G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119046 | ||||||
| chr16:89119068
|
A | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1733A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119068 | ||||||
| chr16:89119093
|
G | C | 352 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(349): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1127-1708G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119093 | ||||||
| chr16:89119132
|
C | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1669C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119132 | ||||||
| chr16:89119157
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1644C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119157 | ||||||
| chr16:89119181
|
A | G | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1127-1620A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119181 | ||||||
| chr16:89119194
|
G | A | 1 | a0003c0010t0058g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1127-1607G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119194 | ||||||
| chr16:89119254
|
C | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1547C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119254 | ||||||
| chr16:89119471
|
G | A | 1 | a0002c0002t0004g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1127-1330G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119471 | ||||||
| chr16:89119511
|
A | C | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1127-1290A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119511 | ||||||
| chr16:89119538
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-1263G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119538 | ||||||
| chr16:89119558
|
A | G | 1 | a0001c0001t0013g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1127-1243A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119558 | ||||||
| chr16:89119677
|
G | A | 12 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0024others(9): Show | 12 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1127-1124G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119677 | ||||||
| chr16:89119692
|
A | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG00323.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1127-1109A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119692 | ||||||
| chr16:89119730
|
A | G | 253 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1127-1071A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119730 | ||||||
| chr16:89119859
|
A | C | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1127-942A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119859 | ||||||
| chr16:89119935
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1127-866C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119935 | ||||||
| chr16:89119946
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1127-855C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119946 | ||||||
| chr16:89119969
|
C | T | 1 | a0001c0005t0009g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1127-832C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89119969 | ||||||
| chr16:89120022
|
G | A | 1 | a0003c0006t0007g0044 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1127-779G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89120022 | ||||||
| chr16:89120121
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1127-680G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89120121 | ||||||
| chr16:89120426
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1127-375G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89120426 | ||||||
| chr16:89120460
|
C | T | 36 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1127-341C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89120460 | ||||||
| chr16:89120526
|
A | T | 1 | a0002c0003t0005g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1127-275A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89120526 | ||||||
| chr16:89120796
|
T | C | 3 | a0001c0005t0001g0302a0001c0005t0001g0330a0001c0005t0001g0331 | 3 | NA18939.hp2 NA18970.hp2 NA19057.hp2 |
splice_region_variant&intron_variant | LOW | c.1127-5T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89120796 | ||||||
| chr16:89120970
|
G | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1239+57G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89120970 | ||||||
| chr16:89120994
|
C | T | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1239+81C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89120994 | ||||||
| chr16:89121024
|
G | T | 1 | a0003c0006t0007g0057 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1239+111G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121024 | ||||||
| chr16:89121101
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+188C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121101 | ||||||
| chr16:89121115
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+202C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121115 | ||||||
| chr16:89121343
|
C | G | 1 | a0003c0006t0007g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1239+430C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121343 | ||||||
| chr16:89121356
|
T | G | 253 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1239+443T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121356 | ||||||
| chr16:89121361
|
G | A | 1 | a0001c0001t0016g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1239+448G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121361 | ||||||
| chr16:89121401
|
T | C | 253 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1239+488T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121401 | ||||||
| chr16:89121416
|
C | A | 1 | a0001c0005t0001g0035 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1239+503C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121416 | ||||||
| chr16:89121440
|
C | A | 2 | a0002c0003t0005g0080a0002c0003t0005g0081 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1239+527C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121440 | ||||||
| chr16:89121546
|
G | T | 32 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1239+633G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121546 | ||||||
| chr16:89121641
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1239+728A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121641 | ||||||
| chr16:89121649
|
G | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1239+736G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121649 | ||||||
| chr16:89121836
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1239+923C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121836 | ||||||
| chr16:89121894
|
T | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1239+981T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89121894 | ||||||
| chr16:89121990
|
CCCCGCAG others(130): Show |
C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1239+1131_1239+126 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89121990 | |||||
| chr16:89122013
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+1100C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122013 | ||||||
| chr16:89122020
|
CTGAAGTG others(254): Show |
C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+1109_1239+136 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89122020 | |||||
| chr16:89122044
|
G | A | 34 | a0001c0005t0009g0296a0001c0005t0009g0297a0002c0020t0008g0362others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1239+1131G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122044 | ||||||
| chr16:89122127
|
ACCCGCAG others(130): Show |
A | 1 | a0001c0005t0009g0328 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1239+1236_1239+137 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89122127 | |||||
| chr16:89122141
|
G | GTTATCCC others(48): Show |
33 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1239+1230_1239+128 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89122141 | |||||
| chr16:89122146
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1239+1233C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122146 | ||||||
| chr16:89122180
|
C | A | 2 | a0002c0011t0008g0131a0002c0011t0008g0132 | 2 | HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1239+1267C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122180 | ||||||
| chr16:89122236
|
G | T | 1 | a0003c0007t0007g0049 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1239+1323G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122236 | ||||||
| chr16:89122264
|
C | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1239+1351C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122264 | ||||||
| chr16:89122282
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+1369T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122282 | ||||||
| chr16:89122284
|
C | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+1371C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122284 | ||||||
| chr16:89122498
|
CT | C | 36 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1239+1586delT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122498 | ||||||
| chr16:89122678
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+1765G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122678 | ||||||
| chr16:89122700
|
G | A | 1 | a0001c0005t0001g0039 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1239+1787G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122700 | ||||||
| chr16:89122721
|
T | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0259 | 2 | HG00140.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1239+1808T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122721 | ||||||
| chr16:89122743
|
C | T | 1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1239+1830C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122743 | ||||||
| chr16:89122786
|
G | A | 35 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1239+1873G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122786 | ||||||
| chr16:89122807
|
A | T | 1 | a0002c0003t0005g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1239+1894A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89122807 | ||||||
| chr16:89123064
|
G | A | 31 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1239+2151G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123064 | ||||||
| chr16:89123148
|
C | T | 31 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1239+2235C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123148 | ||||||
| chr16:89123177
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1239+2264A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123177 | ||||||
| chr16:89123185
|
C | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG02622.hp2 HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1239+2272C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123185 | ||||||
| chr16:89123256
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+2343G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123256 | ||||||
| chr16:89123480
|
A | C | 6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 6 | HG01192.hp1 HG01243.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1239+2567A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123480 | ||||||
| chr16:89123504
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1239+2591C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123504 | ||||||
| chr16:89123521
|
G | T | 1 | a0002c0003t0057g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1239+2608G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123521 | ||||||
| chr16:89123560
|
G | A | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1239+2647G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123560 | ||||||
| chr16:89123592
|
A | G | 1 | a0002c0003t0004g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1239+2679A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123592 | ||||||
| chr16:89123657
|
G | A | 286 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1239+2744G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123657 | ||||||
| chr16:89123709
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1239+2796C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123709 | ||||||
| chr16:89123728
|
G | C | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+2815G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123728 | ||||||
| chr16:89123758
|
C | G | 28 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(25): Show | 29 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.1239+2845C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123758 | ||||||
| chr16:89123775
|
C | T | 1 | a0001c0001t0010g0173 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1239+2862C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123775 | ||||||
| chr16:89123792
|
G | A | 2 | a0004c0004t0003g0332a0004c0004t0003g0337 | 2 | HG03927.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1239+2879G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123792 | ||||||
| chr16:89123799
|
C | A | 213 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1239+2886C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123799 | ||||||
| chr16:89123852
|
G | A | 1 | a0003c0010t0008g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1239+2939G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123852 | ||||||
| chr16:89123886
|
C | T | 1 | a0001c0005t0001g0302 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1239+2973C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123886 | ||||||
| chr16:89123905
|
C | T | 286 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1239+2992C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123905 | ||||||
| chr16:89123923
|
C | T | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1239+3010C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123923 | ||||||
| chr16:89123947
|
G | T | 1 | a0002c0003t0005g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1239+3034G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123947 | ||||||
| chr16:89123971
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+3058G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123971 | ||||||
| chr16:89123980
|
A | G | 1 | a0002c0021t0004g0104 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1239+3067A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89123980 | ||||||
| chr16:89124021
|
GC | G | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1239+3109delC | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124021 | ||||||
| chr16:89124029
|
C | T | 1 | a0002c0003t0004g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1239+3116C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124029 | ||||||
| chr16:89124039
|
TCA | T | 4 | a0003c0006t0007g0067a0003c0006t0007g0068a0003c0006t0007g0069others(1): Show | 4 | NA18961.hp1 NA18985.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+3133_1239+313 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124039 | |||||
| chr16:89124061
|
C | CGGGTATC others(23): Show |
1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1239+3196_1239+322 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124061 | |||||
| chr16:89124061
|
CGGGTATC others(23): Show |
C | 287 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1239+3196_1239+322 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124061 | |||||
| chr16:89124111
|
A | G | 4 | a0001c0005t0009g0246a0001c0005t0009g0250a0001c0005t0009g0308others(1): Show | 4 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+3198A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124111 | ||||||
| chr16:89124118
|
G | A | 36 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1239+3205G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124118 | ||||||
| chr16:89124171
|
A | C | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+3258A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124171 | ||||||
| chr16:89124345
|
A | G | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1239+3432A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124345 | ||||||
| chr16:89124403
|
ATG | A | 213 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1239+3498_1239+349 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124403 | |||||
| chr16:89124421
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1239+3508C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124421 | ||||||
| chr16:89124462
|
C | T | 1 | a0002c0003t0005g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1239+3549C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124462 | ||||||
| chr16:89124478
|
G | T | 2 | a0004c0004t0003g0233a0004c0004t0003g0234 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1239+3565G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124478 | ||||||
| chr16:89124485
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1239+3572C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124485 | ||||||
| chr16:89124491
|
G | GTGTA | 215 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1239+3581_1239+358 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124491 | |||||
| chr16:89124527
|
G | T | 2 | a0001c0001t0002g0158a0001c0001t0002g0159 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1239+3614G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124527 | ||||||
| chr16:89124551
|
A | G | 212 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1239+3638A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124551 | ||||||
| chr16:89124562
|
TGA | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1239+3652_1239+365 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124562 | |||||
| chr16:89124590
|
T | G | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1239+3677T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124590 | ||||||
| chr16:89124599
|
T | C | 1 | a0001c0001t0013g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1239+3686T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124599 | ||||||
| chr16:89124611
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1239+3698G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124611 | ||||||
| chr16:89124645
|
G | A | 1 | a0004c0004t0003g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1239+3732G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124645 | ||||||
| chr16:89124663
|
C | T | 25 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(22): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1239+3750C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124663 | ||||||
| chr16:89124671
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+3758G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124671 | ||||||
| chr16:89124679
|
CAT | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1239+3769_1239+377 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124679 | |||||
| chr16:89124686
|
A | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1239+3773A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124686 | ||||||
| chr16:89124695
|
A | ATG | 285 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(282): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1239+3791_1239+379 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89124695 | |||||
| chr16:89124717
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+3804C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124717 | ||||||
| chr16:89124718
|
G | A | 10 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0275others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1239+3805G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124718 | ||||||
| chr16:89124730
|
C | T | 213 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1239+3817C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124730 | ||||||
| chr16:89124787
|
CAT | C | 210 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1239+3875_1239+387 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124787 | ||||||
| chr16:89124828
|
A | C | 1 | a0001c0001t0001g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1239+3915A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124828 | ||||||
| chr16:89124856
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1239+3943G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124856 | ||||||
| chr16:89124862
|
T | C | 36 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1239+3949T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124862 | ||||||
| chr16:89124889
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1239+3976C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124889 | ||||||
| chr16:89124912
|
G | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+3999G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124912 | ||||||
| chr16:89124947
|
A | G | 212 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1239+4034A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124947 | ||||||
| chr16:89124956
|
G | A | 1 | a0007c0013t0001g0280 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1239+4043G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124956 | ||||||
| chr16:89124967
|
A | T | 1 | a0002c0002t0055g0141 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1239+4054A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89124967 | ||||||
| chr16:89125015
|
C | G | 1 | a0001c0001t0051g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+4102C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125015 | ||||||
| chr16:89125066
|
G | A | 212 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1239+4153G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125066 | ||||||
| chr16:89125120
|
G | C | 1 | a0001c0001t0002g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1239+4207G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125120 | ||||||
| chr16:89125171
|
C | T | 2 | a0003c0008t0020g0245a0010c0019t0020g0244 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1239+4258C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125171 | ||||||
| chr16:89125299
|
C | T | 284 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1239+4386C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125299 | ||||||
| chr16:89125343
|
C | CA | 37 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(34): Show | 37 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1239+4446dupA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89125343 | |||||
| chr16:89125343
|
C | CAA | 36 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1239+4445_1239+444 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89125343 | |||||
| chr16:89125343
|
C | CAAAT | 205 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0085others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1239+4433_1239+443 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89125343 | |||||
| chr16:89125369
|
T | C | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+4456T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125369 | ||||||
| chr16:89125374
|
A | G | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+4461A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125374 | ||||||
| chr16:89125670
|
A | C | 2 | a0002c0002t0006g0210a0002c0002t0019g0209 | 2 | NA18942.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1239+4757A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125670 | ||||||
| chr16:89125698
|
A | AAGAGAG | 136 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(133): Show | 139 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1239+4801_1239+480 others(10): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89125698 | |||||
| chr16:89125698
|
A | AAGAGAGA others(1): Show |
68 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0107others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.1239+4799_1239+480 others(12): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89125698 | |||||
| chr16:89125698
|
A | AAGAGAGA others(3): Show |
3 | a0001c0005t0011g0314a0003c0006t0007g0053a0003c0006t0007g0054 | 3 | HG01978.hp2 HG02056.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1239+4797_1239+480 others(14): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89125698 | |||||
| chr16:89125698
|
A | G | 72 | a0001c0005t0009g0296a0001c0005t0009g0297a0002c0003t0005g0015others(69): Show | 73 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1239+4785A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125698 | ||||||
| chr16:89125731
|
A | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+4818A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125731 | ||||||
| chr16:89125856
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+4943C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125856 | ||||||
| chr16:89125857
|
G | A | 212 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1239+4944G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125857 | ||||||
| chr16:89125870
|
C | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1239+4957C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125870 | ||||||
| chr16:89125975
|
C | T | 1 | a0002c0002t0004g0361 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1239+5062C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89125975 | ||||||
| chr16:89126003
|
T | TTAGATCC others(28): Show |
286 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1239+5112_1239+511 others(39): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89126003 | |||||
| chr16:89126018
|
C | A | 1 | a0002c0003t0040g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1239+5105C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126018 | ||||||
| chr16:89126029
|
T | G | 2 | a0004c0004t0003g0332a0004c0004t0003g0337 | 2 | HG03927.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1239+5116T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126029 | ||||||
| chr16:89126041
|
G | T | 5 | a0002c0002t0008g0236a0002c0002t0008g0237a0002c0002t0008g0239others(2): Show | 5 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+5128G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126041 | ||||||
| chr16:89126053
|
C | T | 1 | a0001c0005t0009g0246 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1239+5140C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126053 | ||||||
| chr16:89126080
|
A | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1239+5167A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126080 | ||||||
| chr16:89126111
|
T | C | 32 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1239+5198T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126111 | ||||||
| chr16:89126186
|
C | G | 1 | a0003c0010t0008g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1239+5273C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126186 | ||||||
| chr16:89126213
|
C | T | 35 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1239+5300C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126213 | ||||||
| chr16:89126307
|
C | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1239+5394C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126307 | ||||||
| chr16:89126335
|
C | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1239+5422C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126335 | ||||||
| chr16:89126394
|
C | A | 74 | a0001c0005t0009g0296a0001c0005t0009g0297a0002c0003t0005g0015others(71): Show | 75 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1239+5481C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126394 | ||||||
| chr16:89126429
|
T | C | 1 | a0004c0004t0003g0307 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1239+5516T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126429 | ||||||
| chr16:89126494
|
C | G | 32 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1239+5581C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126494 | ||||||
| chr16:89126684
|
C | T | 1 | a0002c0003t0005g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1239+5771C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126684 | ||||||
| chr16:89126761
|
T | C | 1 | a0001c0001t0018g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1239+5848T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126761 | ||||||
| chr16:89126794
|
C | G | 1 | a0003c0007t0007g0049 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1239+5881C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126794 | ||||||
| chr16:89126851
|
A | G | 20 | a0002c0003t0005g0022a0002c0003t0005g0023a0002c0003t0005g0026others(17): Show | 20 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1239+5938A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126851 | ||||||
| chr16:89126968
|
A | G | 9 | a0003c0007t0007g0045a0003c0007t0007g0046a0003c0007t0007g0047others(6): Show | 9 | HG00408.hp2 HG00438.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+6055A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126968 | ||||||
| chr16:89126982
|
C | T | 289 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1239+6069C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126982 | ||||||
| chr16:89126987
|
C | T | 36 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1239+6074C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89126987 | ||||||
| chr16:89126999
|
ACTTTT | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1239+6091_1239+609 others(9): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89126999 | |||||
| chr16:89127130
|
CTGAG | C | 35 | a0001c0005t0009g0296a0001c0005t0009g0297a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1240-6004_1240-600 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89127130 | |||||
| chr16:89127269
|
G | A | 190 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1240-5867G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127269 | ||||||
| chr16:89127289
|
G | A | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240-5847G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127289 | ||||||
| chr16:89127307
|
A | G | 191 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1240-5829A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127307 | ||||||
| chr16:89127380
|
T | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-5756T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127380 | ||||||
| chr16:89127441
|
T | G | 1 | a0004c0004t0003g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1240-5695T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127441 | ||||||
| chr16:89127476
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-5660G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127476 | ||||||
| chr16:89127611
|
C | T | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1240-5525C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127611 | ||||||
| chr16:89127613
|
C | G | 1 | a0002c0002t0006g0150 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1240-5523C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127613 | ||||||
| chr16:89127622
|
T | G | 26 | a0003c0006t0007g0001a0003c0006t0007g0017a0003c0006t0007g0044others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1240-5514T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127622 | ||||||
| chr16:89127726
|
T | G | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1240-5410T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127726 | ||||||
| chr16:89127804
|
G | A | 189 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1240-5332G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127804 | ||||||
| chr16:89127842
|
A | G | 72 | a0001c0005t0009g0296a0001c0005t0009g0297a0002c0003t0005g0015others(69): Show | 73 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1240-5294A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127842 | ||||||
| chr16:89127897
|
G | A | 1 | a0005c0009t0053g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1240-5239G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89127897 | ||||||
| chr16:89128051
|
G | A | 1 | a0001c0005t0001g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1240-5085G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128051 | ||||||
| chr16:89128186
|
G | C | 32 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1240-4950G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128186 | ||||||
| chr16:89128222
|
C | T | 7 | a0001c0005t0001g0035a0001c0005t0001g0036a0001c0005t0001g0038others(4): Show | 7 | HG00099.hp2 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-4914C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128222 | ||||||
| chr16:89128247
|
A | T | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1240-4889A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128247 | ||||||
| chr16:89128249
|
A | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(64): Show | 68 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.1240-4887A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128249 | ||||||
| chr16:89128251
|
T | A | 3 | a0002c0003t0005g0087a0002c0003t0040g0060a0006c0012t0006g0204 | 3 | HG02056.hp2 NA18747.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1240-4885T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128251 | ||||||
| chr16:89128264
|
C | CT | 26 | a0002c0003t0005g0074a0003c0006t0007g0001a0003c0006t0007g0017others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1240-4859dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89128264 | |||||
| chr16:89128271
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1240-4865T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128271 | ||||||
| chr16:89128391
|
G | C | 1 | a0001c0001t0001g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1240-4745G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128391 | ||||||
| chr16:89128401
|
T | C | 266 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1240-4735T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128401 | ||||||
| chr16:89128417
|
C | T | 1 | a0001c0001t0027g0216 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1240-4719C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128417 | ||||||
| chr16:89128441
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-4695G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128441 | ||||||
| chr16:89128480
|
G | C | 2 | a0003c0010t0004g0129a0003c0010t0004g0130 | 2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1240-4656G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128480 | ||||||
| chr16:89128507
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-4629A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128507 | ||||||
| chr16:89128617
|
G | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1240-4519G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128617 | ||||||
| chr16:89128730
|
C | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-4406C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128730 | ||||||
| chr16:89128735
|
G | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4401G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128735 | ||||||
| chr16:89128737
|
C | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4399C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128737 | ||||||
| chr16:89128738
|
G | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4398G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128738 | ||||||
| chr16:89128739
|
C | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4397C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128739 | ||||||
| chr16:89128741
|
C | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4395C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128741 | ||||||
| chr16:89128746
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4390T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128746 | ||||||
| chr16:89128748
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4388T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128748 | ||||||
| chr16:89128752
|
T | G | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4384T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128752 | ||||||
| chr16:89128754
|
A | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4382A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128754 | ||||||
| chr16:89128755
|
A | G | 2 | a0002c0003t0005g0073a0002c0003t0005g0075 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240-4381A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128755 | ||||||
| chr16:89128757
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4379T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128757 | ||||||
| chr16:89128761
|
T | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4375T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128761 | ||||||
| chr16:89128765
|
A | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4371A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128765 | ||||||
| chr16:89128767
|
T | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4369T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128767 | ||||||
| chr16:89128768
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4368T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128768 | ||||||
| chr16:89128771
|
T | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4365T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128771 | ||||||
| chr16:89128775
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4361T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128775 | ||||||
| chr16:89128776
|
T | G | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4360T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128776 | ||||||
| chr16:89128778
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4358T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128778 | ||||||
| chr16:89128779
|
G | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4357G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128779 | ||||||
| chr16:89128780
|
T | G | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4356T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128780 | ||||||
| chr16:89128784
|
G | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4352G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128784 | ||||||
| chr16:89128785
|
T | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4351T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128785 | ||||||
| chr16:89128790
|
C | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4346C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128790 | ||||||
| chr16:89128792
|
G | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4344G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128792 | ||||||
| chr16:89128793
|
AATGTGGT others(5): Show |
A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4342_1240-433 others(16): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128793 | ||||||
| chr16:89128810
|
G | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4326G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128810 | ||||||
| chr16:89128811
|
G | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4325G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128811 | ||||||
| chr16:89128815
|
G | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4321G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128815 | ||||||
| chr16:89128820
|
G | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1240-4316G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128820 | ||||||
| chr16:89128854
|
C | T | 1 | a0002c0003t0004g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1240-4282C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128854 | ||||||
| chr16:89128855
|
G | A | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240-4281G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128855 | ||||||
| chr16:89128909
|
A | C | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240-4227A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128909 | ||||||
| chr16:89128933
|
C | G | 4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-4203C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128933 | ||||||
| chr16:89128971
|
G | A | 191 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1240-4165G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128971 | ||||||
| chr16:89128972
|
GA | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(287): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1240-4153delA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89128972 | |||||
| chr16:89128987
|
C | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1240-4149C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89128987 | ||||||
| chr16:89129042
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-4094A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129042 | ||||||
| chr16:89129113
|
G | A | 190 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1240-4023G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129113 | ||||||
| chr16:89129192
|
T | A | 1 | a0001c0001t0001g0324 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1240-3944T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129192 | ||||||
| chr16:89129474
|
A | G | 2 | a0002c0002t0008g0239a0005c0017t0035g0359 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240-3662A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129474 | ||||||
| chr16:89129521
|
T | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1240-3615T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129521 | ||||||
| chr16:89129524
|
T | G | 32 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1240-3612T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129524 | ||||||
| chr16:89129568
|
C | T | 1 | a0004c0004t0003g0345 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1240-3568C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129568 | ||||||
| chr16:89129673
|
C | T | 1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240-3463C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129673 | ||||||
| chr16:89129685
|
A | G | 36 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1240-3451A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129685 | ||||||
| chr16:89129723
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1240-3413C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129723 | ||||||
| chr16:89129789
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-3347G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129789 | ||||||
| chr16:89129796
|
C | T | 196 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1240-3340C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129796 | ||||||
| chr16:89129800
|
A | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0084others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1240-3336A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129800 | ||||||
| chr16:89129856
|
C | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-3280C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129856 | ||||||
| chr16:89129871
|
A | G | 26 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(23): Show | 26 | HG00544.hp1 HG00558.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.1240-3265A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129871 | ||||||
| chr16:89129958
|
G | A | 1 | a0004c0004t0003g0229 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1240-3178G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89129958 | ||||||
| chr16:89130229
|
T | C | 27 | a0002c0002t0006g0210a0002c0002t0019g0209a0003c0006t0007g0001others(24): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240-2907T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130229 | ||||||
| chr16:89130321
|
C | G | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1240-2815C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130321 | ||||||
| chr16:89130358
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1240-2778G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130358 | ||||||
| chr16:89130479
|
CTGGAGGA others(1): Show |
C | 3 | a0002c0003t0005g0082a0002c0003t0005g0358a0005c0009t0053g0217 | 3 | HG01175.hp2 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1240-2654_1240-264 others(12): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89130479 | |||||
| chr16:89130493
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1240-2643T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130493 | ||||||
| chr16:89130540
|
C | T | 1 | a0001c0005t0011g0326 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1240-2596C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130540 | ||||||
| chr16:89130606
|
C | G | 1 | a0003c0006t0007g0044 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1240-2530C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130606 | ||||||
| chr16:89130612
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-2524G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130612 | ||||||
| chr16:89130631
|
G | A | 2 | a0002c0002t0014g0121a0002c0002t0014g0122 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1240-2505G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130631 | ||||||
| chr16:89130806
|
G | A | 1 | a0006c0012t0006g0204 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1240-2330G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130806 | ||||||
| chr16:89130810
|
T | G | 1 | a0003c0008t0008g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1240-2326T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130810 | ||||||
| chr16:89130859
|
G | A | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1240-2277G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130859 | ||||||
| chr16:89130903
|
G | C | 33 | a0004c0004t0003g0005a0004c0004t0003g0014a0004c0004t0003g0215others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1240-2233G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89130903 | ||||||
| chr16:89131005
|
A | G | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1240-2131A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131005 | ||||||
| chr16:89131101
|
CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0016g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1240-2027_1240-201 others(14): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131101 | |||||
| chr16:89131114
|
T | C | 4 | a0001c0005t0011g0321a0001c0005t0011g0322a0001c0005t0011g0323others(1): Show | 4 | HG01070.hp1 HG01123.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-2022T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131114 | ||||||
| chr16:89131121
|
CTTTTTCT others(5): Show |
C | 1 | a0002c0002t0006g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1240-2009_1240-199 others(16): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131121 | |||||
| chr16:89131121
|
CTTTTTCT others(9): Show |
C | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240-2009_1240-199 others(20): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131121 | |||||
| chr16:89131122
|
TTTTTC | T | 38 | a0001c0001t0016g0241a0002c0002t0006g0212a0002c0002t0006g0213others(35): Show | 39 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1240-2009_1240-200 others(9): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131122 | |||||
| chr16:89131123
|
TTTTC | T | 76 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1240-2009_1240-200 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131123 | |||||
| chr16:89131124
|
TTTC | T | 10 | a0002c0002t0004g0225a0002c0002t0006g0065a0002c0002t0006g0134others(7): Show | 10 | HG02300.hp1 HG02683.hp2 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.1240-2009_1240-200 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131124 | |||||
| chr16:89131127
|
C | CT | 42 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(39): Show | 43 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1240-1985dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131127 | |||||
| chr16:89131127
|
C | CTT | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0293others(4): Show | 7 | HG01175.hp1 HG03831.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-1986_1240-198 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131127 | |||||
| chr16:89131127
|
CT | C | 8 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0001g0354others(5): Show | 8 | HG01168.hp2 HG01515.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240-1985delT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131127 | |||||
| chr16:89131127
|
CTTT | C | 32 | a0002c0002t0004g0126a0002c0003t0005g0015a0002c0003t0005g0016others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1240-1987_1240-198 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131127 | |||||
| chr16:89131131
|
T | C | 2 | a0003c0006t0007g0068a0008c0022t0007g0063 | 2 | NA19077.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1240-2005T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131131 | ||||||
| chr16:89131132
|
T | C | 18 | a0003c0006t0007g0017a0003c0006t0007g0044a0003c0006t0007g0050others(15): Show | 18 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240-2004T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131132 | ||||||
| chr16:89131133
|
T | C | 2 | a0003c0006t0007g0053a0003c0006t0007g0054 | 2 | HG02056.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1240-2003T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131133 | ||||||
| chr16:89131160
|
G | T | 22 | a0003c0006t0007g0017a0003c0006t0007g0044a0003c0006t0007g0050others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.1240-1976G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131160 | ||||||
| chr16:89131169
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-1967C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131169 | ||||||
| chr16:89131274
|
G | C | 37 | a0001c0001t0016g0241a0001c0001t0016g0242a0002c0003t0040g0060others(34): Show | 38 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1240-1862G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131274 | ||||||
| chr16:89131285
|
C | G | 1 | a0002c0003t0005g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240-1851C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131285 | ||||||
| chr16:89131607
|
T | TGAGGTGT others(37): Show |
1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-1527_1240-148 others(48): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 89131607 | |||||
| chr16:89131736
|
T | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-1400T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131736 | ||||||
| chr16:89131804
|
G | A | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1240-1332G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89131804 | ||||||
| chr16:89132026
|
C | G | 2 | a0001c0001t0001g0299a0001c0001t0029g0243 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1240-1110C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132026 | ||||||
| chr16:89132041
|
C | G | 122 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(119): Show | 123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1240-1095C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132041 | ||||||
| chr16:89132088
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-1048A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132088 | ||||||
| chr16:89132112
|
G | A | 3 | a0001c0001t0002g0156a0002c0003t0005g0076a0005c0009t0015g0258 | 3 | HG00741.hp1 HG02280.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1240-1024G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132112 | ||||||
| chr16:89132124
|
T | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-1012T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132124 | ||||||
| chr16:89132297
|
G | A | 1 | a0001c0001t0001g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1240-839G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132297 | ||||||
| chr16:89132312
|
G | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-824G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132312 | ||||||
| chr16:89132354
|
C | T | 61 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(58): Show | 61 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1240-782C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132354 | ||||||
| chr16:89132383
|
G | A | 1 | a0002c0003t0004g0096 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1240-753G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132383 | ||||||
| chr16:89132383
|
G | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1240-753G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132383 | ||||||
| chr16:89132418
|
C | T | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1240-718C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132418 | ||||||
| chr16:89132470
|
C | G | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1240-666C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132470 | ||||||
| chr16:89132491
|
C | A | 1 | a0001c0005t0011g0322 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1240-645C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132491 | ||||||
| chr16:89132688
|
A | G | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1240-448A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132688 | ||||||
| chr16:89132700
|
G | A | 61 | a0002c0002t0007g0109a0002c0003t0005g0015a0002c0003t0005g0016others(58): Show | 62 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1240-436G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132700 | ||||||
| chr16:89132794
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1240-342C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132794 | ||||||
| chr16:89132797
|
G | A | 3 | a0002c0011t0008g0128a0002c0011t0008g0131a0002c0011t0008g0132 | 3 | HG01516.hp2 HG03239.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1240-339G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132797 | ||||||
| chr16:89132876
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1240-260C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132876 | ||||||
| chr16:89132937
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1240-199G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89132937 | ||||||
| chr16:89133006
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-130C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89133006 | ||||||
| chr16:89133114
|
C | T | 1 | a0001c0005t0009g0327 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1240-22C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | chr16 | 89133114 | ||||||
| chr16:89133448
|
C | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1366+186C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89133448 | ||||||
| chr16:89133482
|
C | G | 27 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(24): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1366+220C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89133482 | ||||||
| chr16:89133749
|
G | A | 30 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(27): Show | 30 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1366+487G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89133749 | ||||||
| chr16:89133820
|
G | A | 29 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(26): Show | 29 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1366+558G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89133820 | ||||||
| chr16:89133875
|
G | A | 1 | a0001c0005t0009g0298 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1366+613G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89133875 | ||||||
| chr16:89133943
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+681C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89133943 | ||||||
| chr16:89134206
|
G | A | 3 | a0002c0002t0004g0126a0002c0002t0014g0121a0002c0002t0014g0122 | 3 | HG01257.hp2 HG01258.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1366+944G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134206 | ||||||
| chr16:89134299
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+1037G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134299 | ||||||
| chr16:89134404
|
G | A | 95 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(92): Show | 95 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1366+1142G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134404 | ||||||
| chr16:89134465
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+1203G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134465 | ||||||
| chr16:89134545
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+1283G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134545 | ||||||
| chr16:89134636
|
C | T | 1 | a0002c0002t0006g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1366+1374C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134636 | ||||||
| chr16:89134686
|
G | C | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+1424G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134686 | ||||||
| chr16:89134983
|
G | A | 1 | a0005c0009t0053g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1366+1721G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134983 | ||||||
| chr16:89134987
|
C | T | 33 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(30): Show | 33 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1366+1725C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134987 | ||||||
| chr16:89134993
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1366+1731G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89134993 | ||||||
| chr16:89135071
|
G | GT | 28 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0002g0156others(25): Show | 28 | HG00423.hp2 HG01106.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1366+1828dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89135071 | |||||
| chr16:89135071
|
GT | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0196a0001c0001t0001g0277others(133): Show | 139 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1366+1828delT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89135071 | |||||
| chr16:89135360
|
A | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366+2098A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135360 | ||||||
| chr16:89135397
|
A | G | 156 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0196others(153): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1366+2135A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135397 | ||||||
| chr16:89135406
|
C | T | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1366+2144C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135406 | ||||||
| chr16:89135529
|
A | G | 1 | a0003c0008t0008g0059 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1366+2267A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135529 | ||||||
| chr16:89135564
|
C | T | 3 | a0001c0005t0011g0311a0001c0005t0011g0312a0001c0005t0011g0313 | 3 | HG01069.hp2 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1366+2302C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135564 | ||||||
| chr16:89135622
|
C | T | 1 | a0002c0003t0005g0071 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1366+2360C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135622 | ||||||
| chr16:89135633
|
C | T | 96 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0123others(93): Show | 96 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1366+2371C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135633 | ||||||
| chr16:89135762
|
A | C | 1 | a0002c0003t0005g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1366+2500A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135762 | ||||||
| chr16:89135814
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0196a0001c0001t0001g0277others(47): Show | 52 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1366+2552G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135814 | ||||||
| chr16:89135820
|
T | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+2558T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135820 | ||||||
| chr16:89135864
|
T | C | 1 | a0001c0001t0001g0356 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1366+2602T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135864 | ||||||
| chr16:89135935
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+2673C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135935 | ||||||
| chr16:89135936
|
G | A | 1 | a0001c0005t0009g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1366+2674G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135936 | ||||||
| chr16:89135947
|
G | A | 1 | a0002c0002t0008g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1366+2685G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135947 | ||||||
| chr16:89135958
|
A | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+2696A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89135958 | ||||||
| chr16:89136075
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0196a0001c0001t0001g0277others(48): Show | 53 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1366+2813G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136075 | ||||||
| chr16:89136097
|
G | C | 1 | a0002c0002t0004g0126 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1366+2835G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136097 | ||||||
| chr16:89136105
|
C | T | 1 | a0005c0009t0053g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1366+2843C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136105 | ||||||
| chr16:89136132
|
C | T | 1 | a0005c0009t0039g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1366+2870C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136132 | ||||||
| chr16:89136166
|
G | A | 1 | a0002c0002t0006g0212 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1366+2904G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136166 | ||||||
| chr16:89136233
|
A | G | 1 | a0009c0024t0004g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1366+2971A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136233 | ||||||
| chr16:89136479
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+3217C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136479 | ||||||
| chr16:89136497
|
A | G | 1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1366+3235A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136497 | ||||||
| chr16:89136665
|
C | T | 29 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(26): Show | 29 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1366+3403C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136665 | ||||||
| chr16:89136708
|
G | A | 1 | a0001c0001t0010g0173 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1366+3446G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136708 | ||||||
| chr16:89136720
|
C | A | 1 | a0002c0003t0004g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1366+3458C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136720 | ||||||
| chr16:89136767
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1366+3505A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136767 | ||||||
| chr16:89136813
|
GCAAAGGT others(47): Show |
G | 1 | a0001c0001t0001g0257 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1366+3563_1366+361 others(58): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89136813 | |||||
| chr16:89136825
|
TTCAGGTA others(47): Show |
T | 8 | a0001c0001t0001g0011a0001c0001t0001g0325a0001c0001t0012g0007others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+3644_1366+369 others(58): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89136825 | |||||
| chr16:89136995
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+3733G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89136995 | ||||||
| chr16:89137030
|
C | T | 1 | a0002c0003t0004g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1366+3768C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137030 | ||||||
| chr16:89137058
|
C | T | 65 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(62): Show | 65 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1366+3796C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137058 | ||||||
| chr16:89137065
|
C | T | 2 | a0002c0002t0007g0109a0003c0006t0007g0044 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1366+3803C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137065 | ||||||
| chr16:89137076
|
G | A | 1 | a0001c0005t0001g0302 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1366+3814G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137076 | ||||||
| chr16:89137185
|
G | A | 2 | a0001c0005t0001g0248a0001c0005t0001g0249 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1366+3923G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137185 | ||||||
| chr16:89137211
|
C | A | 29 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(26): Show | 30 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1366+3949C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137211 | ||||||
| chr16:89137230
|
A | ATCCCGGG others(103): Show |
1 | a0001c0001t0001g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1366+4075_1366+407 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137230 | |||||
| chr16:89137230
|
A | ATCCCGGG others(821): Show |
1 | a0002c0003t0005g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1366+4046_1366+404 others(832): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137230 | |||||
| chr16:89137230
|
A | ATCCCGGG others(876): Show |
3 | a0002c0003t0005g0072a0002c0003t0005g0074a0002c0003t0005g0075 | 3 | HG03453.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1366+4046_1366+404 others(887): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137230 | |||||
| chr16:89137254
|
T | TGTGGGGA others(598): Show |
1 | a0001c0001t0001g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(609): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137254 | |||||
| chr16:89137259
|
G | GGAAGGAC others(598): Show |
1 | a0001c0001t0029g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(609): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137259 | |||||
| chr16:89137266
|
C | CTGAGGGG others(48): Show |
1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1366+4021_1366+407 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137266 | |||||
| chr16:89137266
|
C | CTGAGGGG others(323): Show |
1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1366+4080_1366+408 others(334): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137266 | |||||
| chr16:89137266
|
C | CTGAGGGG others(103): Show |
3 | a0006c0012t0006g0204a0006c0012t0006g0205a0006c0012t0006g0206 | 3 | NA18940.hp1 NA18945.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1366+4026_1366+413 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137266 | |||||
| chr16:89137266
|
C | CTGAGGGG others(268): Show |
2 | a0003c0006t0007g0051a0003c0006t0007g0055 | 2 | HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1366+4185_1366+418 others(279): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137266 | |||||
| chr16:89137283
|
A | AGGTCTCG others(158): Show |
1 | a0001c0005t0009g0298 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1366+4075_1366+407 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(158): Show |
1 | a0004c0004t0003g0231 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1366+4075_1366+407 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(48): Show |
58 | a0001c0001t0010g0173a0001c0001t0015g0100a0001c0005t0001g0036others(55): Show | 58 | HG00099.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1366+4076_1366+413 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(103): Show |
31 | a0002c0002t0019g0136a0002c0003t0040g0060a0004c0004t0003g0005others(28): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1366+4110_1366+411 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(158): Show |
1 | a0001c0005t0009g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1366+4185_1366+418 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(103): Show |
5 | a0002c0002t0004g0140a0002c0002t0004g0146a0002c0002t0004g0147others(2): Show | 5 | HG04184.hp2 NA18966.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(268): Show |
1 | a0002c0003t0004g0096 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(279): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(158): Show |
1 | a0002c0021t0004g0104 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1366+4127_1366+412 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTCG others(48): Show |
1 | a0003c0010t0004g0129 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1366+4048_1366+404 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137283
|
A | AGGTCTTG others(48): Show |
1 | a0002c0002t0041g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1366+4026_1366+402 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137283 | |||||
| chr16:89137288
|
T | TCGGGAGG others(102): Show |
1 | a0003c0007t0007g0045 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1366+4065_1366+406 others(113): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137288 | |||||
| chr16:89137288
|
T | TCGGGAGG others(103): Show |
15 | a0002c0002t0004g0126a0002c0002t0004g0201a0002c0002t0004g0202others(12): Show | 15 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.1366+4076_1366+418 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137288 | |||||
| chr16:89137288
|
T | TCGGGAGG others(158): Show |
1 | a0002c0002t0006g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137288 | |||||
| chr16:89137288
|
T | TCGGGAGG others(213): Show |
9 | a0002c0002t0007g0109a0003c0006t0007g0044a0003c0006t0007g0053others(6): Show | 9 | HG00408.hp1 HG02040.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+4101_1366+410 others(224): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137288 | |||||
| chr16:89137311
|
C | CGGGGAAG others(764): Show |
2 | a0002c0003t0005g0029a0002c0003t0005g0030 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366+4075_1366+407 others(775): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137311 | |||||
| chr16:89137311
|
C | CGGGGAAG others(1149): Show |
1 | a0002c0003t0005g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1366+4080_1366+408 others(1160): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137311 | |||||
| chr16:89137311
|
C | CGGGGAAG others(103): Show |
1 | a0001c0001t0001g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1366+4080_1366+408 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137311 | |||||
| chr16:89137311
|
C | CGGGGAAG others(710): Show |
1 | a0002c0003t0005g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1366+4080_1366+408 others(721): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137311 | |||||
| chr16:89137311
|
C | CGGGGAAG others(103): Show |
2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1366+4158_1366+415 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137311 | |||||
| chr16:89137311
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366+4049C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137311 | ||||||
| chr16:89137318
|
G | GGATTGAG others(48): Show |
1 | a0003c0010t0008g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1366+4110_1366+411 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137318 | |||||
| chr16:89137321
|
T | C | 1 | a0005c0009t0015g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1366+4059T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137321 | ||||||
| chr16:89137338
|
G | GGGTCCCG others(599): Show |
1 | a0002c0003t0005g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1366+4080_1366+408 others(610): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137338 | |||||
| chr16:89137338
|
G | GGGTCTCG others(378): Show |
1 | a0002c0011t0008g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(389): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137338 | |||||
| chr16:89137338
|
GGGTCTCG others(103): Show |
G | 1 | a0001c0001t0018g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1366+4111_1366+422 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137338 | |||||
| chr16:89137343
|
T | TCGGGAGG others(213): Show |
1 | a0001c0001t0001g0324 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1366+4165_1366+416 others(224): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137343 | |||||
| chr16:89137343
|
T | TCGGGAGG others(103): Show |
3 | a0001c0001t0016g0242a0001c0005t0011g0314a0001c0018t0011g0261 | 3 | HG01978.hp2 HG02055.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137343 | |||||
| chr16:89137343
|
T | TCGGGAGG others(158): Show |
1 | a0001c0001t0016g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137343 | |||||
| chr16:89137343
|
T | TCGGGAGG others(598): Show |
3 | a0001c0005t0001g0302a0001c0005t0001g0330a0001c0005t0001g0331 | 3 | NA18939.hp2 NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(609): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137343 | |||||
| chr16:89137343
|
TCGGGAGG others(48): Show |
T | 17 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0264others(14): Show | 17 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1366+4136_1366+419 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137343 | |||||
| chr16:89137344
|
C | T | 1 | a0002c0003t0005g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1366+4082C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137344 | ||||||
| chr16:89137345
|
G | A | 4 | a0002c0003t0005g0022a0002c0003t0005g0026a0002c0003t0005g0029others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+4083G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137345 | ||||||
| chr16:89137345
|
G | GGGAGGAC others(764): Show |
1 | a0002c0003t0005g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(775): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(874): Show |
1 | a0002c0003t0005g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(885): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(764): Show |
2 | a0002c0003t0005g0023a0002c0003t0046g0021 | 2 | HG00639.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(775): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(599): Show |
1 | a0002c0003t0005g0358 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(610): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(764): Show |
2 | a0002c0003t0005g0071a0005c0009t0039g0032 | 2 | HG02027.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(775): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(709): Show |
7 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0077others(4): Show | 7 | HG01109.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(720): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(654): Show |
1 | a0005c0009t0011g0310 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(665): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(709): Show |
1 | a0002c0003t0005g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(720): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(599): Show |
1 | a0002c0003t0005g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(610): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(819): Show |
2 | a0002c0003t0005g0080a0002c0003t0005g0081 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(830): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAC others(158): Show |
1 | a0002c0003t0005g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137345
|
G | GGGAGGAT others(709): Show |
1 | a0002c0003t0005g0082 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1366+4089_1366+409 others(720): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137345 | |||||
| chr16:89137366
|
C | CGGGGAAA others(323): Show |
2 | a0004c0004t0003g0223a0004c0004t0003g0344 | 2 | NA18965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1366+4110_1366+411 others(334): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137366 | |||||
| chr16:89137366
|
C | CGGGGAAG others(268): Show |
2 | a0001c0001t0023g0274a0001c0005t0011g0323 | 2 | HG01099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(279): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137366 | |||||
| chr16:89137366
|
C | CGGGGAAG others(598): Show |
1 | a0001c0005t0011g0322 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(609): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137366 | |||||
| chr16:89137366
|
CGGGGAAG others(213): Show |
C | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366+4169_1366+438 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137366 | |||||
| chr16:89137373
|
G | A | 1 | a0004c0004t0003g0307 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1366+4111G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137373 | ||||||
| chr16:89137373
|
G | GGATTGAG others(433): Show |
2 | a0001c0001t0002g0160a0001c0001t0002g0170 | 2 | HG01106.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(444): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137373 | |||||
| chr16:89137373
|
G | GGATTGAG others(378): Show |
1 | a0001c0001t0002g0171 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(389): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137373 | |||||
| chr16:89137373
|
G | GGATTGAG others(103): Show |
1 | a0001c0005t0001g0249 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137373 | |||||
| chr16:89137373
|
G | GGATTGAG others(213): Show |
2 | a0002c0011t0008g0128a0002c0011t0008g0131 | 2 | HG01516.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1366+4130_1366+413 others(224): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137373 | |||||
| chr16:89137373
|
G | GGATTGAG others(268): Show |
1 | a0002c0002t0004g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1366+4130_1366+413 others(279): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137373 | |||||
| chr16:89137373
|
GGATTGAG others(103): Show |
G | 2 | a0001c0001t0012g0009a0003c0008t0008g0031 | 2 | HG00323.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1366+4136_1366+424 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137373 | |||||
| chr16:89137376
|
T | TTGAGGGG others(323): Show |
1 | a0003c0006t0007g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1366+4185_1366+418 others(334): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137376 | |||||
| chr16:89137393
|
A | AGGTCCCG others(103): Show |
1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1366+4185_1366+418 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137393 | |||||
| chr16:89137393
|
A | G | 15 | a0001c0001t0002g0183a0001c0001t0012g0010a0001c0001t0016g0242others(12): Show | 15 | HG00099.hp2 HG01358.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366+4131A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137393 | ||||||
| chr16:89137398
|
C | CCGGGAGG others(103): Show |
1 | a0001c0001t0027g0216 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1366+4240_1366+424 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137398 | |||||
| chr16:89137398
|
C | CCGGGAGG others(48): Show |
3 | a0003c0006t0007g0001a0003c0006t0007g0106a0003c0007t0007g0048 | 4 | HG02074.hp1 HG02080.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366+4185_1366+418 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137398 | |||||
| chr16:89137398
|
C | T | 19 | a0001c0001t0002g0174a0001c0001t0023g0274a0001c0001t0032g0267others(16): Show | 19 | HG00099.hp2 HG01099.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1366+4136C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137398 | ||||||
| chr16:89137421
|
C | CGGGGAAG others(433): Show |
1 | a0002c0002t0006g0135 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1366+4190_1366+419 others(444): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137421 | |||||
| chr16:89137421
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0325 | 2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1366+4159C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137421 | ||||||
| chr16:89137422
|
GGGGAAGG others(47): Show |
G | 1 | a0001c0001t0002g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1366+4164_1366+421 others(58): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137422 | |||||
| chr16:89137428
|
G | A | 8 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0301others(5): Show | 8 | HG01099.hp2 HG01255.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+4166G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137428 | ||||||
| chr16:89137428
|
G | GGATTGAG others(48): Show |
51 | a0001c0001t0001g0155a0001c0001t0001g0282a0001c0001t0002g0002others(48): Show | 52 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.1366+4268_1366+432 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137428 | |||||
| chr16:89137428
|
G | GGATTGAG others(103): Show |
2 | a0001c0001t0002g0185a0001c0005t0009g0327 | 2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1366+4213_1366+432 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137428 | |||||
| chr16:89137428
|
G | GGATTGAG others(158): Show |
1 | a0001c0001t0002g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1366+4322_1366+432 others(169): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137428 | |||||
| chr16:89137428
|
G | GGATTGAG others(764): Show |
1 | a0002c0003t0005g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1366+4322_1366+432 others(775): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137428 | |||||
| chr16:89137431
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1366+4169T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137431 | ||||||
| chr16:89137445
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366+4183C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137445 | ||||||
| chr16:89137448
|
A | G | 3 | a0002c0002t0008g0144a0002c0002t0008g0145a0004c0004t0003g0307 | 3 | HG03491.hp1 HG03492.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1366+4186A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137448 | ||||||
| chr16:89137453
|
T | C | 10 | a0001c0001t0001g0299a0001c0001t0016g0241a0001c0001t0016g0242others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1366+4191T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137453 | ||||||
| chr16:89137453
|
T | TCGGGAGG others(48): Show |
1 | a0001c0001t0032g0267 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1366+4245_1366+424 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137453 | |||||
| chr16:89137453
|
T | TCGGGAGG others(269): Show |
1 | a0002c0003t0005g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1366+4322_1366+432 others(280): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137453 | |||||
| chr16:89137453
|
T | TCGGGAGG others(654): Show |
1 | a0002c0003t0005g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1366+4355_1366+435 others(665): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137453 | |||||
| chr16:89137455
|
G | A | 1 | a0002c0002t0014g0143 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1366+4193G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137455 | ||||||
| chr16:89137475
|
A | G | 1 | a0012c0015t0009g0329 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1366+4213A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137475 | ||||||
| chr16:89137476
|
C | T | 1 | a0012c0015t0009g0329 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1366+4214C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137476 | ||||||
| chr16:89137483
|
A | AGATTGAG others(655): Show |
1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1366+4322_1366+432 others(666): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137483 | |||||
| chr16:89137483
|
A | G | 12 | a0001c0001t0016g0241a0001c0001t0016g0242a0001c0005t0001g0035others(9): Show | 12 | HG00099.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366+4221A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137483 | ||||||
| chr16:89137508
|
T | C | 2 | a0002c0002t0008g0144a0002c0002t0008g0145 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1366+4246T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137508 | ||||||
| chr16:89137508
|
T | TCGGGAGG others(103): Show |
2 | a0001c0001t0015g0100a0009c0024t0004g0117 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1366+4321_1366+432 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137508 | |||||
| chr16:89137517
|
C | CCACCAGG others(1537): Show |
1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+4285_1366+428 others(1548): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137517 | |||||
| chr16:89137520
|
C | G | 2 | a0001c0001t0001g0293a0007c0013t0001g0280 | 2 | NA18973.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1366+4258C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137520 | ||||||
| chr16:89137531
|
CGGGGAAA others(48): Show |
C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1366+4276_1366+433 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137531 | |||||
| chr16:89137563
|
TCGGGAGG others(48): Show |
T | 1 | a0001c0001t0002g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1366+4323_1366+437 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89137563 | |||||
| chr16:89137584
|
C | CACGGGGA others(48): Show |
3 | a0002c0002t0006g0210a0002c0002t0019g0209a0002c0002t0044g0124 | 3 | NA18942.hp1 NA18952.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1366+4322_1366+432 others(59): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137584 | ||||||
| chr16:89137584
|
C | T | 121 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(118): Show | 123 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1366+4322C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137584 | ||||||
| chr16:89137585
|
G | A | 2 | a0001c0001t0002g0164a0008c0022t0007g0063 | 2 | NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1366+4323G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137585 | ||||||
| chr16:89137586
|
T | C | 2 | a0001c0001t0002g0164a0008c0022t0007g0063 | 2 | NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1366+4324T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137586 | ||||||
| chr16:89137593
|
G | A | 2 | a0001c0001t0002g0164a0008c0022t0007g0063 | 2 | NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1366+4331G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137593 | ||||||
| chr16:89137593
|
G | C | 1 | a0002c0002t0045g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1366+4331G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137593 | ||||||
| chr16:89137596
|
T | G | 1 | a0002c0002t0045g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1366+4334T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137596 | ||||||
| chr16:89137613
|
A | G | 1 | a0002c0002t0045g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1366+4351A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137613 | ||||||
| chr16:89137618
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1366+4356C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137618 | ||||||
| chr16:89137640
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1366+4378A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137640 | ||||||
| chr16:89137641
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1366+4379C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137641 | ||||||
| chr16:89137642
|
G | A | 3 | a0001c0018t0011g0261a0002c0003t0005g0071a0002c0003t0005g0087 | 3 | HG02027.hp1 HG02056.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1366+4380G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137642 | ||||||
| chr16:89137647
|
A | C | 1 | a0002c0002t0006g0150 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1366+4385A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137647 | ||||||
| chr16:89137648
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1366+4386G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137648 | ||||||
| chr16:89137651
|
C | T | 2 | a0001c0001t0002g0164a0001c0001t0002g0207 | 2 | HG02683.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1366+4389C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137651 | ||||||
| chr16:89137675
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1366+4413A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137675 | ||||||
| chr16:89137737
|
C | T | 26 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1366+4475C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137737 | ||||||
| chr16:89137929
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+4667C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89137929 | ||||||
| chr16:89138152
|
C | T | 1 | a0002c0002t0008g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1366+4890C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138152 | ||||||
| chr16:89138283
|
T | C | 1 | a0002c0003t0005g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1366+5021T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138283 | ||||||
| chr16:89138385
|
G | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366+5123G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138385 | ||||||
| chr16:89138418
|
C | A | 127 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(124): Show | 128 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1366+5156C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138418 | ||||||
| chr16:89138474
|
C | T | 66 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(63): Show | 66 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1366+5212C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138474 | ||||||
| chr16:89138502
|
C | T | 3 | a0002c0002t0004g0139a0002c0002t0004g0225a0002c0002t0014g0143 | 3 | HG02683.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1366+5240C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138502 | ||||||
| chr16:89138935
|
A | G | 1 | a0002c0003t0005g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1366+5673A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138935 | ||||||
| chr16:89138983
|
G | C | 1 | a0002c0002t0006g0135 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1366+5721G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138983 | ||||||
| chr16:89138985
|
G | C | 99 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1366+5723G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138985 | ||||||
| chr16:89138987
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0170a0001c0001t0002g0171 | 3 | HG00735.hp2 HG01106.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1366+5725G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138987 | ||||||
| chr16:89139008
|
G | A | 2 | a0001c0001t0015g0100a0009c0024t0004g0117 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1366+5746G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139008 | ||||||
| chr16:89139088
|
G | A | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1366+5826G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139088 | ||||||
| chr16:89139102
|
T | C | 100 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1366+5840T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139102 | ||||||
| chr16:89139115
|
A | G | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366+5853A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139115 | ||||||
| chr16:89139135
|
G | A | 4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366+5873G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139135 | ||||||
| chr16:89139177
|
C | T | 1 | a0002c0002t0004g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1366+5915C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139177 | ||||||
| chr16:89139274
|
A | G | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(4): Show | 7 | HG01074.hp2 HG01496.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367-5993A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139274 | ||||||
| chr16:89139290
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1367-5977C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139290 | ||||||
| chr16:89139313
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-5954G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139313 | ||||||
| chr16:89139435
|
G | A | 1 | a0001c0001t0033g0271 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1367-5832G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139435 | ||||||
| chr16:89139442
|
C | G | 1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1367-5825C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139442 | ||||||
| chr16:89139465
|
T | C | 100 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1367-5802T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139465 | ||||||
| chr16:89139478
|
G | A | 2 | a0002c0003t0021g0088a0002c0003t0021g0089 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1367-5789G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139478 | ||||||
| chr16:89139480
|
A | G | 1 | a0001c0001t0029g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1367-5787A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139480 | ||||||
| chr16:89139548
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1367-5719G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139548 | ||||||
| chr16:89139591
|
G | GT | 13 | a0001c0001t0001g0295a0001c0001t0001g0305a0001c0001t0001g0325others(10): Show | 13 | HG00639.hp2 HG01099.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367-5657dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89139591 | |||||
| chr16:89139591
|
GT | G | 40 | a0001c0001t0001g0315a0001c0001t0002g0164a0001c0005t0009g0328others(37): Show | 41 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1367-5657delT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89139591 | |||||
| chr16:89139591
|
GTT | G | 90 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0126others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1367-5658_1367-565 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89139591 | |||||
| chr16:89139610
|
T | C | 1 | a0001c0005t0009g0309 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1367-5657T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139610 | ||||||
| chr16:89139618
|
G | T | 3 | a0003c0006t0007g0053a0003c0006t0007g0054a0003c0006t0007g0057 | 3 | HG02056.hp1 NA19067.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1367-5649G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139618 | ||||||
| chr16:89139620
|
G | T | 2 | a0001c0001t0001g0264a0001c0001t0032g0267 | 2 | HG02486.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1367-5647G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139620 | ||||||
| chr16:89139661
|
C | T | 1 | a0002c0002t0006g0211 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1367-5606C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139661 | ||||||
| chr16:89139686
|
G | A | 2 | a0002c0003t0021g0088a0002c0003t0021g0089 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1367-5581G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139686 | ||||||
| chr16:89139784
|
G | C | 1 | a0007c0013t0001g0280 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1367-5483G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139784 | ||||||
| chr16:89139848
|
G | C | 100 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1367-5419G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139848 | ||||||
| chr16:89139893
|
A | G | 1 | a0005c0009t0015g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1367-5374A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139893 | ||||||
| chr16:89139900
|
C | A | 2 | a0002c0002t0006g0210a0002c0002t0019g0209 | 2 | NA18942.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1367-5367C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89139900 | ||||||
| chr16:89140075
|
T | C | 161 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(158): Show | 163 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1367-5192T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140075 | ||||||
| chr16:89140235
|
C | T | 1 | a0001c0001t0017g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1367-5032C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140235 | ||||||
| chr16:89140300
|
T | G | 1 | a0001c0005t0009g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367-4967T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140300 | ||||||
| chr16:89140316
|
C | A | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(1): Show | 4 | HG01243.hp2 HG01952.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-4951C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140316 | ||||||
| chr16:89140433
|
T | G | 160 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(157): Show | 162 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1367-4834T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140433 | ||||||
| chr16:89140454
|
G | A | 1 | a0002c0020t0008g0362 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1367-4813G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140454 | ||||||
| chr16:89140524
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1367-4743A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140524 | ||||||
| chr16:89140533
|
A | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-4734A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140533 | ||||||
| chr16:89140597
|
G | A | 26 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1367-4670G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140597 | ||||||
| chr16:89140667
|
C | T | 2 | a0002c0003t0005g0022a0002c0003t0005g0027 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1367-4600C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140667 | ||||||
| chr16:89140677
|
G | A | 26 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1367-4590G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140677 | ||||||
| chr16:89140718
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1367-4549G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140718 | ||||||
| chr16:89140758
|
C | T | 1 | a0003c0006t0059g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1367-4509C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89140758 | ||||||
| chr16:89141065
|
A | G | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1367-4202A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141065 | ||||||
| chr16:89141318
|
G | A | 1 | a0001c0001t0033g0271 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1367-3949G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141318 | ||||||
| chr16:89141572
|
G | GAAGATGC others(4): Show |
10 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(7): Show | 10 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367-3693_1367-369 others(15): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89141572 | |||||
| chr16:89141593
|
C | T | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1367-3674C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141593 | ||||||
| chr16:89141594
|
G | A | 1 | a0001c0001t0016g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1367-3673G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141594 | ||||||
| chr16:89141668
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1367-3599C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141668 | ||||||
| chr16:89141770
|
T | C | 162 | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(159): Show | 164 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1367-3497T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141770 | ||||||
| chr16:89141872
|
C | T | 4 | a0001c0001t0012g0008a0001c0001t0012g0009a0001c0001t0012g0010others(1): Show | 4 | HG01993.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-3395C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141872 | ||||||
| chr16:89141895
|
C | T | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1367-3372C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141895 | ||||||
| chr16:89141907
|
A | G | 101 | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(98): Show | 101 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1367-3360A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141907 | ||||||
| chr16:89141926
|
A | G | 163 | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(160): Show | 165 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1367-3341A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141926 | ||||||
| chr16:89141982
|
G | A | 1 | a0005c0009t0039g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1367-3285G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141982 | ||||||
| chr16:89141999
|
T | A | 33 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(30): Show | 33 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1367-3268T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141999 | ||||||
| chr16:89142031
|
G | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1367-3236G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142031 | ||||||
| chr16:89142169
|
G | A | 2 | a0001c0005t0011g0311a0001c0005t0011g0312 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1367-3098G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142169 | ||||||
| chr16:89142233
|
C | T | 1 | a0004c0004t0003g0332 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1367-3034C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142233 | ||||||
| chr16:89142237
|
A | G | 1 | a0002c0002t0014g0143 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1367-3030A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142237 | ||||||
| chr16:89142272
|
T | C | 162 | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(159): Show | 164 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1367-2995T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142272 | ||||||
| chr16:89142443
|
G | A | 1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1367-2824G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142443 | ||||||
| chr16:89142486
|
T | TCTGCAGA others(13): Show |
1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1367-2769_1367-275 others(24): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89142486 | |||||
| chr16:89142505
|
G | A | 2 | a0001c0005t0009g0309a0002c0003t0052g0240 | 2 | HG01361.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1367-2762G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142505 | ||||||
| chr16:89142518
|
TACCCACA others(11): Show |
T | 146 | a0001c0001t0001g0098a0001c0001t0001g0256a0001c0001t0001g0262others(143): Show | 147 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1367-2697_1367-268 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89142518 | |||||
| chr16:89142538
|
C | G | 1 | a0003c0008t0049g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1367-2729C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142538 | ||||||
| chr16:89142539
|
C | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1367-2728C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142539 | ||||||
| chr16:89142543
|
A | G | 33 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(30): Show | 33 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1367-2724A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142543 | ||||||
| chr16:89142556
|
C | G | 23 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(20): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.1367-2711C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142556 | ||||||
| chr16:89142561
|
A | G | 33 | a0002c0003t0005g0015a0002c0003t0005g0016a0002c0003t0005g0022others(30): Show | 33 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1367-2706A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142561 | ||||||
| chr16:89142574
|
C | G | 2 | a0003c0006t0007g0068a0003c0006t0007g0069 | 2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1367-2693C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142574 | ||||||
| chr16:89142594
|
GCCACACC others(11): Show |
G | 4 | a0001c0001t0001g0155a0001c0001t0002g0198a0001c0001t0002g0227others(1): Show | 4 | HG03669.hp2 HG04115.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-2656_1367-263 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89142594 | |||||
| chr16:89142667
|
ACACCTGC others(11): Show |
A | 1 | a0002c0003t0005g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1367-2587_1367-257 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89142667 | |||||
| chr16:89142746
|
C | G | 1 | a0003c0008t0047g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1367-2521C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142746 | ||||||
| chr16:89142769
|
A | G | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1367-2498A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142769 | ||||||
| chr16:89142774
|
G | C | 1 | a0001c0014t0024g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1367-2493G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142774 | ||||||
| chr16:89142774
|
GACACCCA others(11): Show |
G | 7 | a0001c0001t0001g0275a0001c0001t0001g0325a0002c0002t0004g0133others(4): Show | 8 | HG02074.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-2462_1367-244 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89142774 | |||||
| chr16:89142965
|
C | T | 1 | a0002c0002t0004g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1367-2302C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89142965 | ||||||
| chr16:89143020
|
G | GTGCTGGT others(24): Show |
2 | a0002c0002t0006g0108a0002c0002t0006g0148 | 2 | HG00621.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1367-2247_1367-224 others(35): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143020 | ||||||
| chr16:89143021
|
G | T | 2 | a0002c0002t0006g0108a0002c0002t0006g0148 | 2 | HG00621.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1367-2246G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143021 | ||||||
| chr16:89143032
|
C | G | 1 | a0001c0001t0016g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1367-2235C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143032 | ||||||
| chr16:89143099
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1367-2168C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143099 | ||||||
| chr16:89143128
|
T | C | 2 | a0002c0003t0052g0240a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1367-2139T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143128 | ||||||
| chr16:89143178
|
G | A | 8 | a0002c0002t0007g0109a0003c0006t0007g0044a0003c0006t0007g0053others(5): Show | 8 | HG00408.hp1 HG02040.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-2089G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143178 | ||||||
| chr16:89143186
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1367-2081A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143186 | ||||||
| chr16:89143202
|
G | A | 1 | a0001c0005t0009g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367-2065G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143202 | ||||||
| chr16:89143208
|
TTGGTGCA others(22): Show |
T | 4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-2050_1367-202 others(33): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89143208 | |||||
| chr16:89143226
|
C | T | 1 | a0002c0002t0006g0142 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1367-2041C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143226 | ||||||
| chr16:89143231
|
G | A | 25 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(22): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1367-2036G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143231 | ||||||
| chr16:89143292
|
A | G | 1 | a0001c0005t0011g0313 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1367-1975A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143292 | ||||||
| chr16:89143525
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1367-1742G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143525 | ||||||
| chr16:89143581
|
C | G | 1 | a0001c0001t0016g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1367-1686C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143581 | ||||||
| chr16:89143586
|
G | T | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1367-1681G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143586 | ||||||
| chr16:89143681
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0002g0198 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1367-1586C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143681 | ||||||
| chr16:89143685
|
C | A | 2 | a0002c0002t0006g0210a0002c0002t0019g0209 | 2 | NA18942.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1367-1582C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143685 | ||||||
| chr16:89143687
|
A | T | 1 | a0002c0002t0042g0152 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1367-1580A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143687 | ||||||
| chr16:89143691
|
G | T | 1 | a0002c0002t0042g0152 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1367-1576G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143691 | ||||||
| chr16:89143704
|
C | A | 1 | a0002c0003t0004g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1367-1563C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143704 | ||||||
| chr16:89143705
|
A | G | 1 | a0002c0003t0004g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1367-1562A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143705 | ||||||
| chr16:89143710
|
C | T | 1 | a0003c0010t0004g0129 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1367-1557C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143710 | ||||||
| chr16:89143745
|
G | A | 1 | a0002c0003t0005g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1367-1522G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143745 | ||||||
| chr16:89143757
|
C | G | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1367-1510C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143757 | ||||||
| chr16:89143813
|
C | CTGGGCAC others(10): Show |
1 | a0002c0002t0006g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1367-1453_1367-143 others(21): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89143813 | |||||
| chr16:89143881
|
TG | T | 162 | a0001c0001t0015g0100a0001c0001t0016g0241a0001c0001t0016g0242others(159): Show | 164 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1367-1384delG | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 89143881 | |||||
| chr16:89143885
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1367-1382T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143885 | ||||||
| chr16:89143903
|
G | A | 2 | a0001c0001t0013g0040a0001c0001t0013g0043 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1367-1364G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143903 | ||||||
| chr16:89143907
|
A | T | 1 | a0002c0003t0004g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1367-1360A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143907 | ||||||
| chr16:89143918
|
G | A | 1 | a0002c0002t0006g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1367-1349G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143918 | ||||||
| chr16:89143969
|
A | G | 2 | a0002c0003t0052g0240a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1367-1298A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143969 | ||||||
| chr16:89143979
|
G | A | 2 | a0002c0003t0052g0240a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1367-1288G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89143979 | ||||||
| chr16:89144038
|
C | T | 2 | a0002c0003t0052g0240a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1367-1229C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144038 | ||||||
| chr16:89144046
|
A | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1367-1221A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144046 | ||||||
| chr16:89144106
|
C | T | 68 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(65): Show | 68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1367-1161C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144106 | ||||||
| chr16:89144134
|
G | A | 2 | a0001c0001t0017g0006a0001c0001t0026g0006 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1367-1133G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144134 | ||||||
| chr16:89144155
|
G | A | 26 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0223others(23): Show | 27 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1367-1112G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144155 | ||||||
| chr16:89144312
|
G | A | 69 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1367-955G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144312 | ||||||
| chr16:89144403
|
C | T | 2 | a0001c0001t0015g0100a0009c0024t0004g0117 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1367-864C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144403 | ||||||
| chr16:89144536
|
G | A | 2 | a0002c0003t0052g0240a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1367-731G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144536 | ||||||
| chr16:89144679
|
G | A | 1 | a0002c0003t0005g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1367-588G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144679 | ||||||
| chr16:89144709
|
C | T | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1367-558C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144709 | ||||||
| chr16:89144710
|
G | A | 1 | a0001c0001t0010g0166 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1367-557G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144710 | ||||||
| chr16:89144713
|
T | C | 1 | a0002c0003t0005g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1367-554T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144713 | ||||||
| chr16:89144816
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1367-451A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144816 | ||||||
| chr16:89144825
|
G | A | 63 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 64 | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1367-442G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144825 | ||||||
| chr16:89144825
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1367-442G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144825 | ||||||
| chr16:89144840
|
C | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-427C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144840 | ||||||
| chr16:89144912
|
C | G | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1367-355C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89144912 | ||||||
| chr16:89145003
|
A | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG00323.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1367-264A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145003 | ||||||
| chr16:89145045
|
G | A | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1367-222G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145045 | ||||||
| chr16:89145058
|
C | A | 1 | a0005c0009t0039g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1367-209C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145058 | ||||||
| chr16:89145072
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0110a0001c0001t0001g0196others(39): Show | 43 | HG00642.hp2 HG01074.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1367-195C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145072 | ||||||
| chr16:89145084
|
G | A | 69 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1367-183G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145084 | ||||||
| chr16:89145142
|
C | G | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1367-125C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145142 | ||||||
| chr16:89145254
|
C | G | 27 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(24): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1367-13C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145254 | ||||||
| chr16:89145261
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1367-6C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89145261 | ||||||
| chr16:89145442
|
G | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1501+41G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145442 | ||||||
| chr16:89145463
|
G | A | 2 | a0002c0002t0006g0212a0002c0002t0006g0213 | 2 | NA18941.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1501+62G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145463 | ||||||
| chr16:89145510
|
G | T | 1 | a0002c0003t0040g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1501+109G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145510 | ||||||
| chr16:89145596
|
A | G | 1 | a0002c0003t0005g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1501+195A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145596 | ||||||
| chr16:89145611
|
A | G | 36 | a0002c0003t0005g0071a0002c0003t0005g0087a0002c0003t0040g0060others(33): Show | 37 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1501+210A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145611 | ||||||
| chr16:89145792
|
A | G | 222 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0085others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1502-146A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145792 | ||||||
| chr16:89145874
|
A | T | 26 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1502-64A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145874 | ||||||
| chr16:89145917
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1502-21A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | chr16 | 89145917 | ||||||
| chr16:89145922
|
GTTC | G | 5 | a0002c0002t0006g0108a0002c0002t0006g0135a0002c0002t0006g0142others(2): Show | 5 | HG00621.hp1 NA18995.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1502-11_1502-9delT others(2): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 89145922 | |||||
| chr16:89146067
|
G | A | 1 | a0001c0005t0001g0302 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1613+18G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146067 | ||||||
| chr16:89146135
|
G | A | 1 | a0004c0004t0003g0349 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1613+86G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146135 | ||||||
| chr16:89146231
|
G | T | 1 | a0002c0003t0005g0077 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1613+182G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146231 | ||||||
| chr16:89146349
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+300C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146349 | ||||||
| chr16:89146351
|
C | T | 12 | a0002c0002t0004g0126a0002c0002t0004g0201a0002c0002t0004g0202others(9): Show | 12 | HG00544.hp1 HG00558.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1613+302C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146351 | ||||||
| chr16:89146417
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+368G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146417 | ||||||
| chr16:89146420
|
G | A | 1 | a0001c0005t0009g0309 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1613+371G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146420 | ||||||
| chr16:89146441
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1613+392G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146441 | ||||||
| chr16:89146730
|
C | T | 5 | a0001c0005t0009g0246a0001c0005t0009g0250a0001c0005t0009g0308others(2): Show | 5 | HG01261.hp1 HG01361.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1613+681C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146730 | ||||||
| chr16:89146810
|
C | T | 1 | a0004c0004t0003g0342 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1613+761C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146810 | ||||||
| chr16:89146875
|
T | A | 1 | a0001c0001t0002g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1613+826T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146875 | ||||||
| chr16:89146886
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+837G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146886 | ||||||
| chr16:89146893
|
C | T | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+844C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146893 | ||||||
| chr16:89146908
|
T | C | 2 | a0002c0002t0044g0124a0002c0002t0056g0125 | 2 | HG02155.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1613+859T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146908 | ||||||
| chr16:89146946
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+897G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146946 | ||||||
| chr16:89146995
|
A | G | 35 | a0002c0003t0005g0071a0002c0003t0005g0087a0002c0003t0040g0060others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1613+946A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89146995 | ||||||
| chr16:89147025
|
C | T | 37 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(34): Show | 37 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1613+976C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147025 | ||||||
| chr16:89147038
|
AGGAAGCG others(15): Show |
A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+990_1613+1011 others(25): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147038 | ||||||
| chr16:89147102
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1613+1053G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147102 | ||||||
| chr16:89147135
|
G | C | 1 | a0002c0003t0040g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1613+1086G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147135 | ||||||
| chr16:89147142
|
G | GCCACAGA others(53): Show |
1 | a0002c0002t0004g0126 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1613+1135_1613+113 others(64): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147142 | |||||
| chr16:89147150
|
G | C | 4 | a0002c0003t0004g0061a0002c0003t0004g0062a0002c0003t0004g0095others(1): Show | 4 | HG00558.hp1 HG02071.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1613+1101G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147150 | ||||||
| chr16:89147172
|
T | G | 1 | a0004c0004t0003g0337 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1613+1123T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147172 | ||||||
| chr16:89147173
|
C | T | 1 | a0004c0004t0003g0337 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1613+1124C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147173 | ||||||
| chr16:89147180
|
G | GGGAGTGA others(4): Show |
70 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(67): Show | 71 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1613+1135_1613+113 others(15): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147180 | |||||
| chr16:89147181
|
G | T | 1 | a0004c0004t0003g0337 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1613+1132G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147181 | ||||||
| chr16:89147181
|
GGAGGGAG others(12): Show |
G | 2 | a0002c0003t0005g0090a0002c0003t0005g0091 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1613+1136_1613+115 others(23): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147181 | |||||
| chr16:89147184
|
GGGAGGGT others(49): Show |
G | 1 | a0004c0004t0003g0337 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1613+1142_1613+119 others(60): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147184 | |||||
| chr16:89147204
|
T | G | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1613+1155T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147204 | ||||||
| chr16:89147208
|
A | AGAGGAGG others(200): Show |
1 | a0001c0005t0009g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1613+1188_1613+118 others(211): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(500): Show |
1 | a0001c0001t0051g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1613+1188_1613+118 others(511): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(110): Show |
2 | a0003c0008t0020g0245a0010c0019t0020g0244 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1613+1202_1613+120 others(121): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(257): Show |
1 | a0001c0001t0002g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1613+1202_1613+120 others(268): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(249): Show |
1 | a0001c0001t0002g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1613+1238_1613+123 others(260): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(83): Show |
1 | a0001c0001t0001g0259 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1613+1238_1613+123 others(94): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(140): Show |
1 | a0001c0001t0001g0098 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1613+1238_1613+123 others(151): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(140): Show |
8 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1613+1239_1613+124 others(151): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(140): Show |
154 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0107others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1613+1301_1613+130 others(151): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(367): Show |
1 | a0001c0001t0002g0114 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1613+1301_1613+130 others(378): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(287): Show |
2 | a0003c0008t0008g0058a0003c0008t0008g0059 | 2 | NA18612.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1613+1301_1613+130 others(298): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(141): Show |
1 | a0001c0001t0002g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1613+1284_1613+128 others(152): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(200): Show |
1 | a0001c0001t0001g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1613+1274_1613+127 others(211): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(230): Show |
4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+1274_1613+127 others(241): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(260): Show |
1 | a0001c0001t0061g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1613+1274_1613+127 others(271): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(260): Show |
1 | a0001c0001t0002g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1613+1231_1613+123 others(271): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | AGAGGAGG others(219): Show |
1 | a0004c0004t0031g0232 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1613+1201_1613+120 others(230): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147208 | |||||
| chr16:89147208
|
A | G | 75 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(72): Show | 76 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1613+1159A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147208 | ||||||
| chr16:89147221
|
T | G | 77 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(74): Show | 78 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1613+1172T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147221 | ||||||
| chr16:89147222
|
C | CACAGAGT others(45): Show |
1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+1173_1613+117 others(56): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147222 | ||||||
| chr16:89147222
|
C | T | 77 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(74): Show | 78 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1613+1173C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147222 | ||||||
| chr16:89147222
|
CCACAGAG others(163): Show |
C | 1 | a0003c0007t0007g0045 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1613+1233_1613+140 others(4): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147222 | |||||
| chr16:89147230
|
T | TGAGTGAG others(136): Show |
1 | a0012c0015t0009g0329 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1613+1301_1613+130 others(147): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147230 | |||||
| chr16:89147233
|
GTGAGGGA | G | 55 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(52): Show | 55 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1613+1185_1613+119 others(11): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147233 | ||||||
| chr16:89147234
|
T | G | 21 | a0002c0003t0005g0071a0002c0003t0005g0087a0002c0003t0040g0060others(18): Show | 22 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1613+1185T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147234 | ||||||
| chr16:89147236
|
A | G | 21 | a0002c0003t0005g0071a0002c0003t0005g0087a0002c0003t0040g0060others(18): Show | 22 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1613+1187A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147236 | ||||||
| chr16:89147243
|
A | AGGGAGGG others(17): Show |
1 | a0002c0002t0054g0111 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1613+1202_1613+120 others(28): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147243 | |||||
| chr16:89147243
|
A | AGGGAGGG others(15): Show |
1 | a0002c0002t0006g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1613+1201_1613+120 others(26): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147243 | |||||
| chr16:89147243
|
A | G | 57 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(54): Show | 57 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1613+1194A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147243 | ||||||
| chr16:89147252
|
T | C | 61 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(58): Show | 61 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1613+1203T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147252 | ||||||
| chr16:89147252
|
T | TCACAGAG others(15): Show |
1 | a0002c0002t0045g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1613+1214_1613+121 others(26): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147252 | |||||
| chr16:89147252
|
T | TCACAGAG others(16): Show |
81 | a0001c0001t0015g0100a0001c0001t0016g0241a0001c0001t0016g0242others(78): Show | 82 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1613+1214_1613+121 others(27): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147252 | |||||
| chr16:89147264
|
T | G | 19 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0230others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1215T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147264 | ||||||
| chr16:89147265
|
G | GC | 13 | a0004c0004t0003g0014a0004c0004t0003g0215a0004c0004t0003g0223others(10): Show | 13 | HG03490.hp2 HG03491.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.1613+1216_1613+121 others(5): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147265 | ||||||
| chr16:89147265
|
G | GGGGGAGG others(17): Show |
19 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0230others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1216_1613+121 others(28): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147265 | ||||||
| chr16:89147266
|
A | AGGGAGGA others(140): Show |
2 | a0003c0010t0004g0129a0003c0010t0004g0130 | 2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1613+1301_1613+130 others(151): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147266 | |||||
| chr16:89147266
|
A | AGGGAGGA others(136): Show |
1 | a0002c0002t0041g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1613+1261_1613+126 others(147): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147266 | |||||
| chr16:89147266
|
A | AGGGAGGA others(46): Show |
3 | a0002c0002t0006g0150a0002c0002t0019g0136a0002c0002t0042g0152 | 3 | NA18942.hp2 NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1613+1232_1613+123 others(57): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147266 | |||||
| chr16:89147266
|
A | C | 130 | a0001c0001t0015g0100a0001c0001t0016g0241a0001c0001t0016g0242others(127): Show | 131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1613+1217A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147266 | ||||||
| chr16:89147266
|
A | G | 32 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(29): Show | 33 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1613+1217A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147266 | ||||||
| chr16:89147273
|
A | G | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1224A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147273 | ||||||
| chr16:89147282
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+1233C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147282 | ||||||
| chr16:89147288
|
T | A | 3 | a0002c0003t0052g0240a0002c0021t0004g0104a0003c0007t0007g0048 | 3 | HG02071.hp1 HG02523.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1613+1239T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147288 | ||||||
| chr16:89147288
|
T | TGTGAGTG others(227): Show |
1 | a0001c0001t0029g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1613+1301_1613+130 others(238): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147288 | |||||
| chr16:89147296
|
A | C | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1247A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147296 | ||||||
| chr16:89147312
|
T | C | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1263T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147312 | ||||||
| chr16:89147318
|
A | T | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1269A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147318 | ||||||
| chr16:89147324
|
C | G | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1275C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147324 | ||||||
| chr16:89147324
|
C | T | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1275C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147324 | ||||||
| chr16:89147325
|
A | C | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1276A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147325 | ||||||
| chr16:89147325
|
A | G | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1276A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147325 | ||||||
| chr16:89147327
|
G | A | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1278G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147327 | ||||||
| chr16:89147330
|
G | A | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1281G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147330 | ||||||
| chr16:89147339
|
C | T | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1290C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147339 | ||||||
| chr16:89147350
|
G | GTGAGGGA | 3 | a0001c0001t0001g0270a0002c0002t0006g0224a0005c0017t0035g0359 | 3 | HG02109.hp2 HG02965.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1613+1301_1613+130 others(11): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147350 | ||||||
| chr16:89147350
|
G | GTGAGGGA others(30): Show |
1 | a0001c0001t0002g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1613+1301_1613+130 others(41): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147350 | ||||||
| chr16:89147351
|
C | G | 4 | a0001c0001t0001g0270a0001c0001t0002g0187a0002c0002t0006g0224others(1): Show | 4 | HG01934.hp2 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+1302C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147351 | ||||||
| chr16:89147351
|
C | T | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1302C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147351 | ||||||
| chr16:89147353
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0002g0187a0002c0002t0006g0224others(1): Show | 4 | HG01934.hp2 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+1304G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147353 | ||||||
| chr16:89147361
|
G | T | 3 | a0001c0001t0001g0270a0002c0002t0006g0224a0002c0003t0004g0095 | 3 | HG02965.hp1 NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1613+1312G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147361 | ||||||
| chr16:89147362
|
C | T | 2 | a0001c0001t0002g0187a0005c0017t0035g0359 | 2 | HG01934.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1613+1313C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147362 | ||||||
| chr16:89147362
|
CCACAGAG others(23): Show |
C | 20 | a0001c0005t0011g0311a0001c0005t0011g0313a0001c0005t0011g0321others(17): Show | 20 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1402_1613+143 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147362 | |||||
| chr16:89147362
|
CCACAGAG others(53): Show |
C | 5 | a0002c0002t0044g0124a0002c0002t0056g0125a0002c0003t0005g0024others(2): Show | 5 | HG02145.hp2 HG02155.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+1372_1613+143 others(64): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147362 | |||||
| chr16:89147376
|
A | AGGGAGGA others(23): Show |
1 | a0004c0004t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1613+1336_1613+133 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147376 | |||||
| chr16:89147381
|
G | C | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1332G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147381 | ||||||
| chr16:89147383
|
A | G | 2 | a0002c0021t0004g0104a0003c0007t0007g0048 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1334A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147383 | ||||||
| chr16:89147392
|
T | C | 3 | a0001c0001t0002g0187a0002c0021t0004g0104a0003c0007t0007g0048 | 3 | HG01934.hp2 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1613+1343T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147392 | ||||||
| chr16:89147392
|
T | TCACAGAG others(103): Show |
1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1372_1613+137 others(114): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147392 | |||||
| chr16:89147398
|
A | T | 1 | a0001c0001t0002g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1613+1349A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147398 | ||||||
| chr16:89147421
|
G | T | 3 | a0002c0003t0005g0029a0002c0003t0005g0030a0002c0003t0005g0091 | 3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1372G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147421 | ||||||
| chr16:89147422
|
T | C | 4 | a0001c0001t0001g0270a0002c0003t0005g0029a0002c0003t0005g0030others(1): Show | 4 | HG02886.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+1373T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147422 | ||||||
| chr16:89147422
|
T | TCACAGAG others(43): Show |
1 | a0001c0001t0002g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1613+1384_1613+138 others(54): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147422 | |||||
| chr16:89147428
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1613+1379A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147428 | ||||||
| chr16:89147445
|
G | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0110a0001c0001t0001g0196others(48): Show | 52 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1613+1396G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147445 | ||||||
| chr16:89147451
|
G | T | 14 | a0001c0001t0023g0274a0001c0005t0011g0312a0001c0005t0011g0314others(11): Show | 14 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1613+1402G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147451 | ||||||
| chr16:89147452
|
T | C | 14 | a0001c0001t0023g0274a0001c0005t0011g0312a0001c0005t0011g0314others(11): Show | 14 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1613+1403T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147452 | ||||||
| chr16:89147452
|
T | TCACAGAG others(43): Show |
1 | a0001c0001t0001g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1613+1414_1613+141 others(54): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147452 | |||||
| chr16:89147452
|
TCACAGAG others(23): Show |
T | 1 | a0002c0002t0006g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1613+1432_1613+146 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147452 | |||||
| chr16:89147464
|
T | C | 3 | a0002c0003t0005g0029a0002c0003t0005g0030a0002c0003t0005g0091 | 3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1415T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147464 | ||||||
| chr16:89147466
|
A | G | 3 | a0002c0003t0005g0029a0002c0003t0005g0030a0002c0003t0005g0091 | 3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1417A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147466 | ||||||
| chr16:89147470
|
A | G | 3 | a0002c0003t0005g0029a0002c0003t0005g0030a0002c0003t0005g0091 | 3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1421A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147470 | ||||||
| chr16:89147473
|
A | G | 3 | a0002c0003t0005g0029a0002c0003t0005g0030a0002c0003t0005g0091 | 3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1424A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147473 | ||||||
| chr16:89147475
|
GGAGGGTC others(42): Show |
G | 2 | a0002c0003t0005g0029a0002c0003t0005g0030 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1428_1613+147 others(53): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147475 | |||||
| chr16:89147476
|
GAGGGTCC others(41): Show |
G | 1 | a0002c0003t0005g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1613+1428_1613+147 others(52): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147476 | ||||||
| chr16:89147481
|
T | G | 14 | a0001c0001t0001g0270a0001c0001t0023g0274a0001c0005t0011g0312others(11): Show | 14 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1613+1432T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147481 | ||||||
| chr16:89147482
|
C | T | 14 | a0001c0001t0001g0270a0001c0001t0023g0274a0001c0005t0011g0312others(11): Show | 14 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1613+1433C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147482 | ||||||
| chr16:89147482
|
CCACAGAG others(23): Show |
C | 4 | a0002c0002t0004g0201a0002c0002t0004g0202a0002c0002t0004g0228others(1): Show | 4 | HG00544.hp1 HG02074.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+1445_1613+147 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147482 | |||||
| chr16:89147493
|
G | A | 2 | a0004c0004t0003g0234a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1613+1444G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147493 | ||||||
| chr16:89147493
|
G | GTGAGGGA others(23): Show |
13 | a0004c0004t0003g0014a0004c0004t0003g0215a0004c0004t0003g0223others(10): Show | 13 | HG03490.hp2 HG03491.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.1613+1461_1613+146 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147493 | |||||
| chr16:89147494
|
T | C | 12 | a0001c0001t0023g0274a0001c0005t0011g0312a0001c0005t0011g0314others(9): Show | 12 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1613+1445T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147494 | ||||||
| chr16:89147496
|
A | G | 12 | a0001c0001t0023g0274a0001c0005t0011g0312a0001c0005t0011g0314others(9): Show | 12 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1613+1447A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147496 | ||||||
| chr16:89147499
|
GAGGA | G | 5 | a0002c0003t0005g0026a0002c0003t0005g0027a0002c0003t0005g0082others(2): Show | 5 | HG01175.hp2 HG01433.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+1451_1613+145 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147499 | ||||||
| chr16:89147500
|
A | G | 7 | a0001c0001t0023g0274a0001c0005t0011g0312a0001c0005t0011g0314others(4): Show | 7 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613+1451A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147500 | ||||||
| chr16:89147503
|
A | G | 7 | a0001c0001t0023g0274a0001c0005t0011g0312a0001c0005t0011g0314others(4): Show | 7 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613+1454A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147503 | ||||||
| chr16:89147505
|
GGAGGGGT others(12): Show |
G | 3 | a0001c0001t0023g0274a0001c0005t0011g0312a0002c0003t0005g0077 | 3 | HG01069.hp2 HG01099.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1613+1458_1613+147 others(23): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147505 | |||||
| chr16:89147506
|
GAGGGGTC others(11): Show |
G | 3 | a0001c0005t0011g0314a0005c0009t0011g0310a0005c0009t0053g0217 | 3 | HG00140.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1613+1458_1613+147 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147506 | ||||||
| chr16:89147507
|
A | G | 6 | a0002c0003t0004g0061a0002c0003t0005g0026a0002c0003t0005g0027others(3): Show | 6 | HG00558.hp1 HG01175.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1613+1458A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147507 | ||||||
| chr16:89147510
|
GGTCACAG others(7): Show |
G | 1 | a0002c0003t0004g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1613+1463_1613+147 others(18): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147510 | |||||
| chr16:89147511
|
G | T | 20 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(17): Show | 21 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1613+1462G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147511 | ||||||
| chr16:89147511
|
GTCACAGA others(6): Show |
G | 5 | a0002c0003t0005g0026a0002c0003t0005g0027a0002c0003t0005g0082others(2): Show | 5 | HG01175.hp2 HG01433.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+1463_1613+147 others(17): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147511 | ||||||
| chr16:89147512
|
T | C | 20 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(17): Show | 21 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1613+1463T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147512 | ||||||
| chr16:89147521
|
G | GAATGAGG others(17): Show |
19 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0230others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1473_1613+147 others(28): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147521 | |||||
| chr16:89147522
|
A | AGGCGGGG others(10): Show |
1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1474_1613+147 others(21): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147522 | |||||
| chr16:89147522
|
AGCGGGG | A | 14 | a0004c0004t0003g0014a0004c0004t0003g0215a0004c0004t0003g0223others(11): Show | 14 | HG02109.hp2 HG03490.hp2 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.1613+1475_1613+148 others(10): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147522 | |||||
| chr16:89147524
|
C | A | 19 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0230others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1475C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147524 | ||||||
| chr16:89147524
|
C | CG | 41 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0001g0262others(38): Show | 41 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1613+1487dupG | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGG | 46 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0268others(43): Show | 46 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1613+1486_1613+148 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGG | 30 | a0001c0001t0001g0155a0001c0001t0001g0276a0001c0001t0001g0316others(27): Show | 30 | HG00099.hp2 HG01074.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.1613+1485_1613+148 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGG | 29 | a0001c0001t0001g0259a0001c0001t0001g0318a0001c0001t0002g0003others(26): Show | 31 | HG00140.hp1 HG00438.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1613+1484_1613+148 others(8): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(3): Show |
24 | a0001c0001t0001g0107a0001c0001t0001g0252a0001c0001t0001g0354others(21): Show | 24 | HG00639.hp1 HG01109.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1613+1478_1613+148 others(14): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(4): Show |
17 | a0001c0001t0001g0253a0001c0001t0033g0271a0002c0002t0004g0118others(14): Show | 17 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1613+1477_1613+148 others(15): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(5): Show |
5 | a0001c0001t0001g0254a0002c0002t0004g0214a0002c0002t0004g0225others(2): Show | 5 | HG02602.hp1 HG02602.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+1476_1613+148 others(16): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(6): Show |
6 | a0002c0002t0006g0108a0002c0002t0006g0112a0002c0002t0006g0134others(3): Show | 6 | HG00621.hp1 NA18941.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1613+1487_1613+148 others(17): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(7): Show |
3 | a0002c0002t0004g0123a0002c0002t0004g0226a0006c0012t0006g0205 | 3 | HG03942.hp1 NA19085.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1613+1487_1613+148 others(18): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(10): Show |
2 | a0002c0002t0006g0212a0002c0002t0006g0224 | 2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1613+1487_1613+148 others(21): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | CGGGGGGG others(15): Show |
1 | a0002c0002t0055g0141 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1613+1487_1613+148 others(26): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147524 | |||||
| chr16:89147524
|
C | G | 1 | a0002c0003t0004g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1613+1475C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147524 | ||||||
| chr16:89147524
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+1475C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147524 | ||||||
| chr16:89147526
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+1477G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147526 | ||||||
| chr16:89147526
|
G | T | 19 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0230others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1477G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147526 | ||||||
| chr16:89147528
|
G | A | 19 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0230others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1613+1479G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147528 | ||||||
| chr16:89147528
|
G | GGAGGAGG others(47): Show |
1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+1480_1613+148 others(58): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89147528 | |||||
| chr16:89147530
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0196a0001c0001t0001g0277others(21): Show | 25 | HG00642.hp2 HG02129.hp1 HG02523.hp1 others(22): Show |
intron_variant | MODIFIER | c.1613+1481G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147530 | ||||||
| chr16:89147534
|
G | T | 1 | a0004c0004t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1613+1485G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147534 | ||||||
| chr16:89147535
|
G | T | 34 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1613+1486G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147535 | ||||||
| chr16:89147536
|
G | A | 1 | a0004c0004t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1613+1487G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147536 | ||||||
| chr16:89147537
|
A | G | 1 | a0004c0004t0003g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1613+1488A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147537 | ||||||
| chr16:89147594
|
T | G | 114 | a0001c0001t0001g0011a0001c0001t0001g0098a0001c0001t0001g0107others(111): Show | 115 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1613+1545T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147594 | ||||||
| chr16:89147599
|
C | T | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1613+1550C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147599 | ||||||
| chr16:89147600
|
G | A | 2 | a0002c0003t0052g0240a0005c0017t0035g0359 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1613+1551G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147600 | ||||||
| chr16:89147699
|
G | A | 2 | a0002c0003t0005g0029a0002c0003t0005g0030 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+1650G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147699 | ||||||
| chr16:89147723
|
A | G | 1 | a0004c0004t0003g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1613+1674A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147723 | ||||||
| chr16:89147756
|
C | G | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1613+1707C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147756 | ||||||
| chr16:89147796
|
G | A | 39 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1613+1747G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147796 | ||||||
| chr16:89147861
|
G | C | 1 | a0002c0003t0005g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1613+1812G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147861 | ||||||
| chr16:89148033
|
C | T | 1 | a0002c0003t0021g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1613+1984C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148033 | ||||||
| chr16:89148101
|
G | GT | 59 | a0001c0001t0001g0110a0001c0001t0001g0253a0001c0001t0001g0265others(56): Show | 59 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1613+2073dupT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89148101 | |||||
| chr16:89148101
|
G | GTT | 58 | a0001c0001t0001g0011a0001c0001t0001g0098a0001c0001t0001g0107others(55): Show | 59 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1613+2072_1613+207 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89148101 | |||||
| chr16:89148101
|
G | GTTT | 11 | a0001c0001t0015g0100a0002c0002t0006g0065a0002c0002t0006g0134others(8): Show | 11 | HG00673.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1613+2071_1613+207 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89148101 | |||||
| chr16:89148101
|
GT | G | 39 | a0001c0001t0001g0283a0001c0001t0001g0288a0001c0001t0002g0180others(36): Show | 39 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1613+2073delT | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89148101 | |||||
| chr16:89148182
|
A | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+2133A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148182 | ||||||
| chr16:89148193
|
C | G | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1613+2144C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148193 | ||||||
| chr16:89148345
|
C | A | 75 | a0001c0001t0001g0011a0001c0001t0001g0098a0001c0001t0001g0107others(72): Show | 75 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1613+2296C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148345 | ||||||
| chr16:89148380
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1613+2331G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148380 | ||||||
| chr16:89148448
|
A | T | 39 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1613+2399A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148448 | ||||||
| chr16:89148546
|
C | CTGCTGTT others(23): Show |
1 | a0001c0005t0009g0246 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1613+2498_1613+252 others(34): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89148546 | |||||
| chr16:89148564
|
A | G | 183 | a0001c0001t0001g0011a0001c0001t0001g0098a0001c0001t0001g0107others(180): Show | 185 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1613+2515A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148564 | ||||||
| chr16:89148625
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1613+2576C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148625 | ||||||
| chr16:89148880
|
G | A | 1 | a0001c0001t0010g0169 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1613+2831G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148880 | ||||||
| chr16:89148965
|
C | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1613+2916C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148965 | ||||||
| chr16:89148996
|
A | G | 39 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1613+2947A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89148996 | ||||||
| chr16:89149058
|
G | A | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+3009G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149058 | ||||||
| chr16:89149072
|
T | G | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1613+3023T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149072 | ||||||
| chr16:89149073
|
C | G | 1 | a0004c0004t0003g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1613+3024C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149073 | ||||||
| chr16:89149097
|
A | G | 35 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1613+3048A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149097 | ||||||
| chr16:89149127
|
A | G | 35 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1613+3078A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149127 | ||||||
| chr16:89149136
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+3087C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149136 | ||||||
| chr16:89149171
|
C | T | 1 | a0001c0001t0001g0356 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1613+3122C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149171 | ||||||
| chr16:89149172
|
G | A | 1 | a0001c0001t0013g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1613+3123G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149172 | ||||||
| chr16:89149281
|
G | C | 1 | a0004c0004t0003g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1613+3232G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149281 | ||||||
| chr16:89149341
|
C | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+3292C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149341 | ||||||
| chr16:89149430
|
C | T | 1 | a0004c0004t0003g0334 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1613+3381C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149430 | ||||||
| chr16:89149443
|
A | ACC | 67 | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(64): Show | 67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1613+3398_1613+339 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89149443 | |||||
| chr16:89149513
|
CTGG | C | 69 | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1613+3465_1613+346 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149513 | ||||||
| chr16:89149545
|
C | G | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(1): Show | 4 | HG01243.hp2 HG01952.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+3496C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149545 | ||||||
| chr16:89149568
|
C | T | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1613+3519C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149568 | ||||||
| chr16:89149646
|
A | G | 2 | a0001c0005t0001g0330a0001c0005t0001g0331 | 2 | NA18939.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1613+3597A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149646 | ||||||
| chr16:89149716
|
T | C | 35 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1613+3667T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149716 | ||||||
| chr16:89149786
|
G | A | 68 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(65): Show | 68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1613+3737G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149786 | ||||||
| chr16:89149905
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0002g0198a0001c0001t0002g0227 | 3 | HG03669.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1613+3856G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89149905 | ||||||
| chr16:89150125
|
C | G | 1 | a0002c0003t0052g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1614-3965C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150125 | ||||||
| chr16:89150240
|
A | G | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-3850A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150240 | ||||||
| chr16:89150300
|
A | G | 4 | a0001c0005t0009g0246a0001c0005t0009g0250a0001c0005t0009g0308others(1): Show | 4 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614-3790A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150300 | ||||||
| chr16:89150533
|
C | T | 72 | a0001c0001t0015g0100a0001c0001t0016g0241a0001c0001t0016g0242others(69): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1614-3557C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150533 | ||||||
| chr16:89150622
|
C | T | 2 | a0001c0001t0016g0241a0001c0001t0016g0242 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1614-3468C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150622 | ||||||
| chr16:89150658
|
A | G | 35 | a0002c0003t0040g0060a0002c0003t0052g0240a0004c0004t0003g0005others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1614-3432A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150658 | ||||||
| chr16:89150686
|
T | C | 34 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(31): Show | 35 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1614-3404T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150686 | ||||||
| chr16:89150711
|
C | T | 66 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(63): Show | 66 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1614-3379C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150711 | ||||||
| chr16:89150712
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0325 | 2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1614-3378G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150712 | ||||||
| chr16:89150765
|
G | A | 68 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(65): Show | 69 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1614-3325G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89150765 | ||||||
| chr16:89151016
|
A | G | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(1): Show | 4 | HG01243.hp2 HG01952.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-3074A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151016 | ||||||
| chr16:89151086
|
C | T | 1 | a0002c0002t0004g0118 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1614-3004C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151086 | ||||||
| chr16:89151087
|
G | A | 1 | a0002c0002t0014g0143 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1614-3003G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151087 | ||||||
| chr16:89151099
|
C | T | 26 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(23): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1614-2991C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151099 | ||||||
| chr16:89151278
|
C | T | 66 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(63): Show | 66 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1614-2812C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151278 | ||||||
| chr16:89151290
|
G | C | 1 | a0005c0017t0035g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1614-2800G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151290 | ||||||
| chr16:89151346
|
A | G | 67 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(64): Show | 67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1614-2744A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151346 | ||||||
| chr16:89151397
|
G | A | 4 | a0002c0003t0005g0072a0002c0003t0005g0073a0002c0003t0005g0074others(1): Show | 4 | HG03453.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-2693G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151397 | ||||||
| chr16:89151606
|
CAT | C | 69 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1614-2479_1614-247 others(6): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89151606 | |||||
| chr16:89151609
|
ATAT | A | 31 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(28): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1614-2479_1614-247 others(7): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 89151609 | |||||
| chr16:89151610
|
TA | T | 69 | a0001c0001t0016g0241a0001c0001t0016g0242a0001c0001t0023g0274others(66): Show | 70 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.1614-2479delA | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151610 | ||||||
| chr16:89151611
|
A | T | 2 | a0002c0003t0005g0082a0005c0009t0039g0032 | 2 | HG01175.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1614-2479A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151611 | ||||||
| chr16:89151613
|
T | A | 1 | a0001c0001t0012g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1614-2477T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151613 | ||||||
| chr16:89151616
|
T | G | 1 | a0002c0002t0008g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1614-2474T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151616 | ||||||
| chr16:89151670
|
G | A | 1 | a0001c0001t0060g0320 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1614-2420G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151670 | ||||||
| chr16:89151699
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1614-2391C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151699 | ||||||
| chr16:89151795
|
C | T | 1 | a0004c0004t0037g0013 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1614-2295C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151795 | ||||||
| chr16:89151858
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1614-2232C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151858 | ||||||
| chr16:89151886
|
C | T | 1 | a0003c0008t0020g0245 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1614-2204C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151886 | ||||||
| chr16:89151902
|
T | A | 4 | a0002c0003t0004g0061a0002c0003t0004g0062a0002c0003t0004g0095others(1): Show | 4 | HG00558.hp1 HG02071.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614-2188T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89151902 | ||||||
| chr16:89152202
|
G | A | 2 | a0004c0004t0003g0333a0004c0004t0003g0339 | 2 | NA18950.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1614-1888G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152202 | ||||||
| chr16:89152275
|
G | A | 2 | a0001c0001t0016g0241a0005c0017t0035g0359 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1614-1815G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152275 | ||||||
| chr16:89152450
|
A | T | 1 | a0001c0001t0001g0285 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1614-1640A>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152450 | ||||||
| chr16:89152523
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1614-1567G>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152523 | ||||||
| chr16:89152532
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1614-1558C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152532 | ||||||
| chr16:89152541
|
G | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1614-1549G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152541 | ||||||
| chr16:89152557
|
G | A | 1 | a0004c0004t0003g0333 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1614-1533G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152557 | ||||||
| chr16:89152697
|
T | A | 11 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0275others(8): Show | 11 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1614-1393T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152697 | ||||||
| chr16:89152720
|
A | G | 1 | a0005c0009t0015g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1614-1370A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152720 | ||||||
| chr16:89152747
|
A | G | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(1): Show | 4 | HG01243.hp2 HG01952.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-1343A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152747 | ||||||
| chr16:89152776
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0293a0007c0013t0001g0280 | 3 | NA18973.hp1 NA18998.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1614-1314G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89152776 | ||||||
| chr16:89153009
|
C | A | 1 | a0005c0009t0034g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1614-1081C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153009 | ||||||
| chr16:89153021
|
G | A | 3 | a0006c0012t0006g0204a0006c0012t0006g0205a0006c0012t0006g0206 | 3 | NA18940.hp1 NA18945.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1614-1069G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153021 | ||||||
| chr16:89153116
|
G | C | 39 | a0001c0001t0023g0274a0001c0005t0011g0311a0001c0005t0011g0312others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1614-974G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153116 | ||||||
| chr16:89153147
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1614-943A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153147 | ||||||
| chr16:89153183
|
T | A | 134 | a0001c0001t0015g0100a0001c0001t0016g0241a0001c0001t0016g0242others(131): Show | 136 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1614-907T>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153183 | ||||||
| chr16:89153210
|
T | C | 2 | a0001c0001t0012g0034a0001c0001t0061g0260 | 2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1614-880T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153210 | ||||||
| chr16:89153449
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1614-641G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153449 | ||||||
| chr16:89153465
|
G | A | 24 | a0001c0001t0015g0100a0002c0002t0004g0118a0002c0002t0004g0119others(21): Show | 24 | HG00544.hp1 HG00558.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1614-625G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153465 | ||||||
| chr16:89153490
|
C | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0325 | 2 | HG00639.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1614-600C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153490 | ||||||
| chr16:89153540
|
G | A | 1 | a0004c0004t0003g0345 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1614-550G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153540 | ||||||
| chr16:89153593
|
C | T | 2 | a0004c0004t0003g0333a0004c0004t0003g0339 | 2 | NA18950.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1614-497C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153593 | ||||||
| chr16:89153752
|
C | G | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1614-338C>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153752 | ||||||
| chr16:89153769
|
G | A | 28 | a0002c0002t0007g0109a0002c0002t0055g0141a0003c0006t0007g0001others(25): Show | 29 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.1614-321G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153769 | ||||||
| chr16:89153831
|
G | A | 1 | a0004c0004t0038g0343 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1614-259G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153831 | ||||||
| chr16:89153870
|
T | C | 27 | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(24): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1614-220T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89153870 | ||||||
| chr16:89154065
|
C | T | 33 | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(30): Show | 34 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1614-25C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89154065 |