Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MPPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0002 | 1/1 | 576 | 106 | 25 | 14 | 43 | 4 | 18 | 30 | ACSF3_chr16_89088852_89161233 | ACSF3 | MLPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0003 | 0/0 | 576 | 35 | 3 | 3 | 23 | 1 | 5 | 11 | ACSF3_chr16_89088852_89161233 | ACSF3 | MLPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0004 | 0/0 | 576 | 34 | 0 | 0 | 30 | 0 | 4 | 21 | ACSF3_chr16_89088852_89161233 | ACSF3 | MPPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0005 | 0/0 | 576 | 6 | 3 | 1 | 0 | 1 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | MPPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0006 | 0/0 | 576 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | MLPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0007 | 0/0 | 229 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | MPPHV others(224): Show |
chr16 | 89088852 | 89161233 |
| a0008 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | MPPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0009 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | MLPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0010 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | MLPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0011 | 0/0 | 576 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | MPPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| a0012 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | MLPHV others(571): Show |
chr16 | 89088852 | 89161233 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1728 | 145 | 48 | 32 | 46 | 6 | 13 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0001c0005 | 0/0 | 1728 | 30 | 6 | 18 | 3 | 3 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0001c0014 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0001c0018 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0002c0002 | 1/1 | 1728 | 58 | 6 | 4 | 35 | 0 | 11 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0002c0003 | 0/0 | 1728 | 42 | 18 | 10 | 7 | 2 | 5 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0002c0011 | 0/0 | 1728 | 3 | 0 | 0 | 0 | 2 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0002c0020 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0002c0021 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0002c0023 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0003c0006 | 0/0 | 1728 | 16 | 1 | 0 | 12 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0003c0007 | 0/0 | 1728 | 9 | 0 | 2 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0003c0008 | 0/0 | 1728 | 6 | 2 | 0 | 2 | 1 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0003c0010 | 0/0 | 1728 | 4 | 0 | 1 | 2 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0004c0004 | 0/0 | 1728 | 34 | 0 | 0 | 30 | 0 | 4 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0005c0009 | 0/0 | 1728 | 5 | 2 | 1 | 0 | 1 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0005c0017 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0006c0012 | 0/0 | 1728 | 3 | 0 | 0 | 3 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0007c0013 | 0/0 | 1728 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0008c0016 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0009c0019 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0010c0024 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0011c0015 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCC others(1723): Show |
chr16 | 89088852 | 89161233 | ||
| a0012c0022 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | ATGCT others(1723): Show |
chr16 | 89088852 | 89161233 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4118 | 58 | 22 | 6 | 23 | 4 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0002 | 0/0 | 4118 | 56 | 2 | 23 | 20 | 2 | 9 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0011 | 0/0 | 4118 | 7 | 7 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0012 | 0/0 | 4118 | 6 | 6 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0014 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0015 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0016 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0017 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0022 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0025 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0026 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0027 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0028 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0030 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0031 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0034 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0049 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0058 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0001t0059 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0005t0001 | 0/0 | 4118 | 11 | 3 | 4 | 3 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0005t0009 | 0/0 | 4118 | 11 | 3 | 6 | 0 | 2 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0005t0010 | 0/0 | 4118 | 8 | 0 | 8 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0001c0014t0023 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4109): Show |
chr16 | 89088852 | 89161233 |
| a0001c0018t0010 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0004 | 0/0 | 4097 | 18 | 3 | 2 | 7 | 0 | 6 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0006 | 0/1 | 4093 | 21 | 0 | 0 | 20 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0007 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0008 | 0/0 | 4099 | 5 | 3 | 0 | 0 | 0 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0013 | 0/0 | 4097 | 3 | 0 | 2 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0018 | 0/0 | 4093 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0039 | 0/0 | 4097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0040 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0041 | 1/0 | 4095 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4090): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0042 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0043 | 0/0 | 4097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0052 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0053 | 0/0 | 4093 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0002c0002t0054 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0004 | 0/0 | 4097 | 6 | 0 | 0 | 4 | 0 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0005 | 0/0 | 4099 | 28 | 14 | 8 | 2 | 2 | 2 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0006 | 0/0 | 4093 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0020 | 0/0 | 4099 | 2 | 2 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0038 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0044 | 0/0 | 4099 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0048 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0050 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0002c0003t0055 | 0/0 | 4099 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0011t0008 | 0/0 | 4099 | 3 | 0 | 0 | 0 | 2 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0020t0008 | 0/0 | 4099 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0002c0021t0004 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0002c0023t0008 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0003c0006t0007 | 0/0 | 4097 | 14 | 0 | 0 | 11 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0006t0046 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0006t0057 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0007t0007 | 0/0 | 4097 | 9 | 0 | 2 | 7 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0008t0008 | 0/0 | 4099 | 3 | 0 | 0 | 2 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0003c0008t0019 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0003c0008t0045 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0008t0047 | 0/0 | 4097 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0010t0004 | 0/0 | 4097 | 2 | 0 | 1 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0003c0010t0008 | 0/0 | 4099 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0003c0010t0056 | 0/0 | 4099 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0004c0004t0003 | 0/0 | 4116 | 29 | 0 | 0 | 26 | 0 | 3 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0004c0004t0021 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0004c0004t0024 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0004c0004t0029 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0004c0004t0035 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0004c0004t0036 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0005c0009t0010 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0005c0009t0014 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0005c0009t0032 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4111): Show |
chr16 | 89088852 | 89161233 |
| a0005c0009t0037 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0005c0009t0051 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0005c0017t0033 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4107): Show |
chr16 | 89088852 | 89161233 |
| a0006c0012t0006 | 0/0 | 4093 | 3 | 0 | 0 | 3 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4088): Show |
chr16 | 89088852 | 89161233 |
| a0007c0013t0001 | 0/0 | 4118 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0008c0016t0002 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0009c0019t0019 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4094): Show |
chr16 | 89088852 | 89161233 |
| a0010c0024t0004 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| a0011c0015t0009 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4113): Show |
chr16 | 89088852 | 89161233 |
| a0012c0022t0007 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | GTTGG others(4092): Show |
chr16 | 89088852 | 89161233 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0280 | 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 |
| 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 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0014g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0015g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0015g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0016g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0017g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0022g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0025g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0026g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0027g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0028g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0030g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0031g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0034g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0049g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0058g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0001t0059g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0009g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0005t0010g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0014t0023g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0001c0018t0010g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0002c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0117 | 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 |
| a0002c0002t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0145 | 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 |
| a0002c0002t0006g0152 | 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 |
| a0002c0002t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0209 | 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 |
| a0002c0002t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0006g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0013g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0013g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0018g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0039g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0040g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0041g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0042g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0043g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0052g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0053g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0002t0054g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0021 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 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 |
| a0002c0003t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0002c0003t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0005g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0020g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0038g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0044g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0048g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0050g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0003t0055g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0011t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0011t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0011t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0020t0008g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0021t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0002c0023t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0046g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0006t0057g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0007t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0008g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0045g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0008t0047g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0003c0010t0056g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0228 | 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 |
| a0004c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0003g0331 | 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 |
| 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 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0021g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0024g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0029g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0035g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0004c0004t0036g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0010g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0014g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0032g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0037g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0009t0051g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0005c0017t0033g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0006c0012t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0006c0012t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0006c0012t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0007c0013t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0007c0013t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0008c0016t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0009c0019t0019g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0010c0024t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0011c0015t0009g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| a0012c0022t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0320 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0040 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00140 | hp2 | a0005 | c0009 | t0010 | g0303 | EUR | GBR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0176 | EUR | FIN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00323 | hp2 | a0003 | c0008 | t0008 | g0036 | EUR | FIN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00408 | hp1 | a0003 | c0006 | t0007 | g0049 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00408 | hp2 | a0003 | c0007 | t0007 | g0099 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00423 | hp1 | a0002 | c0002 | t0006 | g0071 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00438 | hp1 | a0004 | c0004 | t0003 | g0333 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00438 | hp2 | a0003 | c0007 | t0007 | g0097 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0199 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00544 | hp2 | a0004 | c0004 | t0003 | g0001 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00558 | hp1 | a0002 | c0003 | t0004 | g0066 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00558 | hp2 | a0004 | c0004 | t0024 | g0329 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00621 | hp1 | a0002 | c0002 | t0006 | g0113 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00621 | hp2 | a0004 | c0004 | t0003 | g0001 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00639 | hp1 | a0002 | c0003 | t0005 | g0028 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00642 | hp1 | a0001 | c0005 | t0009 | g0289 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00673 | hp1 | a0003 | c0006 | t0007 | g0055 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00673 | hp2 | a0004 | c0004 | t0003 | g0299 | EAS | CHS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00735 | hp1 | a0001 | c0005 | t0009 | g0290 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00741 | hp1 | a0005 | c0009 | t0014 | g0253 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0041 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01069 | hp2 | a0001 | c0005 | t0010 | g0305 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01070 | hp1 | a0001 | c0005 | t0010 | g0319 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01071 | hp2 | a0001 | c0005 | t0010 | g0304 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01074 | hp1 | a0001 | c0001 | t0027 | g0238 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01099 | hp2 | a0001 | c0001 | t0022 | g0269 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01109 | hp1 | a0001 | c0005 | t0010 | g0306 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01109 | hp2 | a0002 | c0003 | t0005 | g0020 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01168 | hp2 | a0001 | c0005 | t0010 | g0316 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0044 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01175 | hp2 | a0002 | c0003 | t0005 | g0087 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01192 | hp2 | a0001 | c0005 | t0009 | g0291 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01243 | hp1 | a0001 | c0001 | t0031 | g0265 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01255 | hp2 | a0001 | c0005 | t0010 | g0314 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01256 | hp2 | a0002 | c0002 | t0004 | g0340 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01257 | hp2 | a0002 | c0002 | t0013 | g0006 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01258 | hp2 | a0002 | c0002 | t0013 | g0006 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01261 | hp1 | a0001 | c0005 | t0009 | g0245 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01261 | hp2 | a0002 | c0003 | t0005 | g0084 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01358 | hp1 | a0001 | c0005 | t0001 | g0042 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01358 | hp2 | a0001 | c0005 | t0009 | g0341 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01361 | hp1 | a0001 | c0005 | t0009 | g0302 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01433 | hp1 | a0002 | c0003 | t0005 | g0031 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0043 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0175 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01516 | hp1 | a0002 | c0003 | t0005 | g0086 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01516 | hp2 | a0002 | c0011 | t0008 | g0134 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01517 | hp1 | a0002 | c0003 | t0005 | g0085 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0244 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0104 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0349 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01928 | hp1 | a0003 | c0007 | t0007 | g0051 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01943 | hp1 | a0002 | c0003 | t0044 | g0026 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01952 | hp2 | a0002 | c0003 | t0005 | g0082 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01978 | hp1 | a0003 | c0007 | t0007 | g0052 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01978 | hp2 | a0001 | c0005 | t0010 | g0307 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01993 | hp1 | a0002 | c0003 | t0005 | g0083 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02015 | hp1 | a0008 | c0016 | t0002 | g0167 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02015 | hp2 | a0004 | c0004 | t0003 | g0332 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02027 | hp1 | a0002 | c0003 | t0005 | g0076 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02027 | hp2 | a0003 | c0010 | t0008 | g0125 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02040 | hp1 | a0002 | c0002 | t0007 | g0114 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0237 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0339 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02056 | hp1 | a0003 | c0006 | t0007 | g0059 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02056 | hp2 | a0002 | c0003 | t0005 | g0092 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02071 | hp1 | a0002 | c0021 | t0004 | g0109 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02071 | hp2 | a0002 | c0003 | t0004 | g0023 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02074 | hp1 | a0003 | c0006 | t0007 | g0005 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02074 | hp2 | a0002 | c0002 | t0006 | g0200 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02080 | hp1 | a0003 | c0006 | t0007 | g0111 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02083 | hp1 | a0003 | c0006 | t0007 | g0005 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02083 | hp2 | a0004 | c0004 | t0003 | g0226 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02129 | hp1 | a0001 | c0001 | t0028 | g0345 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02129 | hp2 | a0002 | c0002 | t0006 | g0208 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02132 | hp2 | a0004 | c0004 | t0003 | g0326 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02145 | hp1 | a0002 | c0003 | t0048 | g0030 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02145 | hp2 | a0002 | c0003 | t0005 | g0095 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02155 | hp1 | a0003 | c0007 | t0007 | g0098 | EAS | CDX | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02155 | hp2 | a0002 | c0002 | t0054 | g0127 | EAS | CDX | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0107 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0246 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02273 | hp1 | a0002 | c0003 | t0055 | g0121 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02273 | hp2 | a0002 | c0002 | t0004 | g0129 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02280 | hp1 | a0002 | c0003 | t0005 | g0081 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02280 | hp2 | a0009 | c0019 | t0019 | g0239 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02300 | hp1 | a0003 | c0010 | t0004 | g0132 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02451 | hp1 | a0002 | c0002 | t0008 | g0233 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02523 | hp2 | a0003 | c0007 | t0007 | g0053 | EAS | KHV | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02572 | hp1 | a0010 | c0024 | t0004 | g0122 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02572 | hp2 | a0001 | c0005 | t0009 | g0321 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02602 | hp1 | a0002 | c0002 | t0004 | g0211 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02602 | hp2 | a0002 | c0003 | t0006 | g0024 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0110 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0293 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02683 | hp2 | a0002 | c0002 | t0013 | g0146 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02698 | hp1 | a0002 | c0003 | t0005 | g0346 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02698 | hp2 | a0002 | c0002 | t0043 | g0120 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02717 | hp2 | a0002 | c0002 | t0008 | g0231 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0046 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02723 | hp2 | a0002 | c0003 | t0005 | g0027 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02738 | hp1 | a0002 | c0002 | t0004 | g0124 | 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 | g0309 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0035 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0048 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02897 | hp2 | a0001 | c0001 | t0058 | g0313 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02965 | hp2 | a0002 | c0003 | t0005 | g0021 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02970 | hp2 | a0002 | c0002 | t0008 | g0234 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0029 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02976 | hp2 | a0003 | c0006 | t0057 | g0338 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0142 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03017 | hp2 | a0002 | c0002 | t0039 | g0130 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03041 | hp2 | a0002 | c0023 | t0008 | g0232 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0105 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03130 | hp1 | a0001 | c0014 | t0023 | g0312 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03139 | hp1 | a0005 | c0009 | t0032 | g0348 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03209 | hp1 | a0002 | c0003 | t0005 | g0096 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03209 | hp2 | a0001 | c0001 | t0049 | g0296 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03225 | hp1 | a0002 | c0003 | t0005 | g0034 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03225 | hp2 | a0001 | c0001 | t0025 | g0011 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03239 | hp1 | a0002 | c0011 | t0008 | g0131 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03239 | hp2 | a0011 | c0015 | t0009 | g0322 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03453 | hp2 | a0002 | c0003 | t0005 | g0080 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03486 | hp1 | a0002 | c0003 | t0005 | g0077 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03490 | hp2 | a0004 | c0004 | t0003 | g0019 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03491 | hp1 | a0002 | c0002 | t0008 | g0147 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03491 | hp2 | a0004 | c0004 | t0035 | g0018 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03492 | hp2 | a0002 | c0002 | t0008 | g0148 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03540 | hp2 | a0001 | c0005 | t0009 | g0301 | AFR | GWD | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03579 | hp2 | a0002 | c0003 | t0005 | g0032 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0220 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03654 | hp2 | a0001 | c0001 | t0030 | g0262 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0123 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03688 | hp1 | a0002 | c0003 | t0005 | g0033 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03704 | hp1 | a0003 | c0010 | t0004 | g0133 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03710 | hp1 | a0005 | c0009 | t0051 | g0214 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03710 | hp2 | a0003 | c0006 | t0007 | g0056 | SAS | PJL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03927 | hp1 | a0004 | c0004 | t0003 | g0328 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03927 | hp2 | a0002 | c0003 | t0004 | g0101 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0126 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03942 | hp2 | a0003 | c0006 | t0007 | g0022 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04115 | hp1 | a0003 | c0008 | t0047 | g0057 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04184 | hp1 | a0003 | c0006 | t0007 | g0060 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04184 | hp2 | a0002 | c0003 | t0004 | g0025 | SAS | BEB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04199 | hp2 | a0004 | c0004 | t0003 | g0297 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04228 | hp1 | a0002 | c0020 | t0008 | g0350 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18522 | hp1 | a0003 | c0008 | t0019 | g0240 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18522 | hp2 | a0002 | c0003 | t0050 | g0235 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0001 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18612 | hp2 | a0003 | c0008 | t0008 | g0064 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18747 | hp1 | a0002 | c0003 | t0038 | g0065 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0268 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18939 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18940 | hp1 | a0006 | c0012 | t0006 | g0201 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18941 | hp1 | a0004 | c0004 | t0003 | g0327 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18941 | hp2 | a0002 | c0002 | t0006 | g0210 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18942 | hp1 | a0002 | c0002 | t0018 | g0206 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18942 | hp2 | a0002 | c0002 | t0018 | g0139 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18945 | hp2 | a0006 | c0012 | t0006 | g0203 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18949 | hp2 | a0004 | c0004 | t0003 | g0229 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18950 | hp1 | a0004 | c0004 | t0003 | g0330 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18952 | hp1 | a0002 | c0002 | t0006 | g0207 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18954 | hp1 | a0002 | c0002 | t0053 | g0144 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18961 | hp1 | a0003 | c0006 | t0007 | g0074 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18965 | hp1 | a0004 | c0004 | t0003 | g0218 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18966 | hp1 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18967 | hp2 | a0004 | c0004 | t0003 | g0325 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18968 | hp1 | a0004 | c0004 | t0003 | g0324 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18968 | hp2 | a0003 | c0007 | t0007 | g0069 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18969 | hp1 | a0002 | c0002 | t0004 | g0223 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18969 | hp2 | a0004 | c0004 | t0003 | g0225 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18970 | hp1 | a0003 | c0008 | t0008 | g0063 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18970 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0149 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18973 | hp1 | a0007 | c0013 | t0001 | g0275 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18977 | hp2 | a0002 | c0002 | t0040 | g0155 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18980 | hp1 | a0004 | c0004 | t0003 | g0224 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18980 | hp2 | a0002 | c0002 | t0006 | g0153 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18981 | hp2 | a0004 | c0004 | t0003 | g0300 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18982 | hp1 | a0002 | c0002 | t0052 | g0116 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18985 | hp1 | a0003 | c0007 | t0007 | g0050 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18985 | hp2 | a0003 | c0006 | t0007 | g0072 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18986 | hp1 | a0001 | c0001 | t0034 | g0242 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18986 | hp2 | a0002 | c0003 | t0004 | g0067 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18990 | hp1 | a0003 | c0006 | t0046 | g0061 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18990 | hp2 | a0002 | c0002 | t0006 | g0117 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18992 | hp1 | a0004 | c0004 | t0003 | g0001 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18992 | hp2 | a0002 | c0002 | t0006 | g0154 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18993 | hp2 | a0001 | c0001 | t0026 | g0213 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18994 | hp1 | a0004 | c0004 | t0003 | g0336 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18994 | hp2 | a0002 | c0002 | t0006 | g0156 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18995 | hp2 | a0002 | c0002 | t0006 | g0151 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA18999 | hp2 | a0002 | c0002 | t0004 | g0136 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19000 | hp2 | a0002 | c0002 | t0006 | g0137 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19003 | hp1 | a0002 | c0002 | t0006 | g0145 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19003 | hp2 | a0004 | c0004 | t0021 | g0108 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19004 | hp1 | a0002 | c0002 | t0006 | g0141 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19005 | hp1 | a0004 | c0004 | t0003 | g0228 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19007 | hp1 | a0002 | c0002 | t0006 | g0140 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19010 | hp1 | a0003 | c0010 | t0056 | g0157 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19010 | hp2 | a0002 | c0002 | t0006 | g0219 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19011 | hp2 | a0004 | c0004 | t0003 | g0331 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19012 | hp1 | a0004 | c0004 | t0003 | g0337 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19030 | hp1 | a0005 | c0009 | t0037 | g0037 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19043 | hp1 | a0001 | c0001 | t0059 | g0255 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19043 | hp2 | a0002 | c0003 | t0020 | g0094 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19057 | hp2 | a0001 | c0005 | t0001 | g0295 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19064 | hp1 | a0002 | c0002 | t0006 | g0138 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19064 | hp2 | a0004 | c0004 | t0003 | g0335 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19065 | hp1 | a0004 | c0004 | t0029 | g0227 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19065 | hp2 | a0002 | c0002 | t0006 | g0209 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19066 | hp1 | a0002 | c0002 | t0004 | g0150 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19066 | hp2 | a0004 | c0004 | t0036 | g0334 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19067 | hp1 | a0007 | c0013 | t0001 | g0285 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19067 | hp2 | a0003 | c0006 | t0007 | g0062 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19068 | hp1 | a0003 | c0007 | t0007 | g0054 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0100 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19070 | hp2 | a0002 | c0002 | t0006 | g0070 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19074 | hp2 | a0004 | c0004 | t0003 | g0001 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19077 | hp1 | a0012 | c0022 | t0007 | g0068 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19077 | hp2 | a0002 | c0002 | t0006 | g0152 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19080 | hp1 | a0004 | c0004 | t0003 | g0323 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19080 | hp2 | a0003 | c0006 | t0007 | g0058 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19083 | hp1 | a0003 | c0006 | t0007 | g0073 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19084 | hp1 | a0002 | c0002 | t0004 | g0198 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19084 | hp2 | a0004 | c0004 | t0003 | g0212 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19085 | hp2 | a0006 | c0012 | t0006 | g0202 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19088 | hp2 | a0002 | c0002 | t0042 | g0128 | EAS | JPT | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19240 | hp1 | a0002 | c0003 | t0005 | g0079 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA19240 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | YRI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20129 | hp1 | a0002 | c0002 | t0004 | g0221 | AFR | ASW | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20129 | hp2 | a0002 | c0003 | t0005 | g0078 | AFR | ASW | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20752 | hp2 | a0002 | c0011 | t0008 | g0135 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20805 | hp1 | a0001 | c0005 | t0009 | g0196 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20805 | hp2 | a0001 | c0018 | t0010 | g0256 | EUR | TSI | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01123 | hp1 | a0002 | c0003 | t0005 | g0088 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG01123 | hp2 | a0001 | c0005 | t0010 | g0315 | AMR | CLM | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02109 | hp1 | a0002 | c0003 | t0020 | g0093 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02109 | hp2 | a0005 | c0017 | t0033 | g0347 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02486 | hp2 | a0001 | c0005 | t0009 | g0241 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0267 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0236 | AFR | ACB | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0243 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0015 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20300 | hp1 | a0002 | c0003 | t0005 | g0250 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | USA | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA21309 | hp1 | a0003 | c0008 | t0045 | g0017 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | LWK | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0006 | g0230 | REF | REF | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0041 | g0075 | REF | REF | ACSF3_chr16_89088852_89161233 | ACSF3 | chr16 | 89088852 | 89161233 |
| view | 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 | a0001 a0004 a0005 others(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 | a0009 | 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 | a0010 | 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 | a0001 a0003 a0007 others(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 | a0008 | 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 | a0011 | 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 | a0012 | 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 |
| view | 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 | a0001c0001 a0001c0005 a0001c0014 others(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 | a0001c0001 a0001c0005 a0001c0018 others(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 | a0001c0001 a0001c0005 a0001c0018 others(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 | a0001c0001 a0001c0005 a0001c0018 others(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 | a0001c0001 a0001c0005 a0001c0018 others(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 | a0001c0001 a0001c0005 a0001c0018 others(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 | a0003c0006 a0003c0007 a0012c0022 |
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 | a0001c0005 a0002c0011 a0011c0015 |
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 |
| view | 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 | a0001c0001t0058 a0001c0001t0059 |
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 | a0003c0006t0057 | 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 | a0004c0004t0021 | 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 | 9 | a0001c0001t0002 a0002c0002t0013 a0002c0002t0052 others(6): 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 | a0004c0004t0021 | 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 | a0002c0003t0050 | 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 |
39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(36): 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 | a0005c0009t0037 | 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 | a0004c0004t0036 | 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 | a0002c0003t0020 | 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 | a0001c0001t0017 a0002c0003t0048 |
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 | a0004c0004t0035 | 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 | a0001c0001t0034 | 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 | a0002c0003t0038 a0004c0004t0003 a0004c0004t0021 others(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 | a0005c0017t0033 | 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 | a0002c0002t0039 | 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 | a0001c0001t0022 | 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 | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(68): 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 | a0002c0003t0038 a0004c0004t0003 a0004c0004t0021 others(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 | a0003c0008t0047 | 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 | a0005c0009t0032 | 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 | a0001c0001t0031 | 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 | a0002c0002t0042 a0002c0002t0054 |
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 | a0001c0001t0014 a0002c0002t0004 a0002c0002t0006 others(16): Show |
66 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(63): 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 | a0002c0002t0043 | 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 | a0001c0001t0022 a0001c0005t0010 a0001c0018t0010 others(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 | a0001c0001t0014 a0002c0002t0004 a0002c0002t0006 others(17): Show |
67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): 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 | a0001c0001t0025 | 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 | a0001c0001t0026 | 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0026 |
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 | a0003c0008t0019 a0009c0019t0019 |
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 | a0001c0001t0027 | 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 | a0005c0017t0033 | 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 | a0001c0001t0028 | 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 | a0002c0003t0044 | 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 | a0001c0001t0012 | 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 | a0002c0002t0007 a0003c0006t0007 a0003c0006t0046 others(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 | a0001c0001t0014 a0002c0002t0004 a0002c0002t0006 others(17): Show |
67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): 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 | a0001c0001t0016 a0001c0001t0025 |
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 | a0002c0002t0043 | 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 | a0001c0001t0030 | 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 | a0001c0005t0009 a0011c0015t0009 |
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 | a0001c0001t0014 a0001c0001t0015 a0002c0002t0004 others(34): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): 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 | a0002c0002t0018 | 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 | a0002c0002t0053 | 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 | a0002c0002t0040 | 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 | a0003c0006t0046 | 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 | a0002c0003t0050 | 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 | a0001c0001t0014 a0001c0001t0015 a0002c0002t0004 others(34): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): 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 | a0001c0001t0014 a0001c0001t0015 a0002c0002t0004 others(26): Show |
98 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(95): 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 | a0001c0001t0011 a0001c0001t0058 |
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 | a0001c0001t0059 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 11/11 | 2020 | chr16 | 89156227 |
| view | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0002c0002t0004g0349 a0002c0020t0008g0350 a0005c0009t0032g0348 others(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 | 250 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0115 others(247): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): 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 | a0002c0002t0004g0349 a0002c0020t0008g0350 a0005c0009t0032g0348 others(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 | a0004c0004t0021g0108 | 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 | a0002c0003t0005g0346 | 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 | a0004c0004t0003g0019 a0004c0004t0035g0018 |
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 | a0001c0001t0017g0107 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | 251 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(248): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | 130 | a0001c0001t0001g0115 a0001c0001t0001g0158 a0001c0001t0001g0194 others(127): Show |
138 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(135): 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 | a0002c0003t0004g0100 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0002c0020t0008g0350 | 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 | 261 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0091 others(258): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): 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 | a0001c0001t0001g0089 a0002c0003t0005g0082 a0002c0003t0005g0083 others(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 | a0001c0001t0001g0344 a0001c0001t0028g0345 |
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 | a0004c0004t0021g0108 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0001g0343 | 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 | a0004c0004t0003g0019 a0004c0004t0035g0018 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0342 others(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 | 253 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0091 others(250): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-194+961G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89094957 | |||||||
| chr16:89094965 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0090 others(263): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): 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 | a0002c0002t0006g0113 | 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 | a0004c0004t0003g0019 a0004c0004t0035g0018 |
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 | a0002c0002t0008g0231 a0002c0002t0008g0233 a0002c0002t0008g0234 others(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 | a0001c0001t0027g0238 | 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 | 257 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0091 others(254): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): 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 | a0002c0020t0008g0350 | 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 | 136 | a0001c0001t0001g0158 a0001c0001t0001g0194 a0001c0001t0002g0003 others(133): Show |
144 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.-194+1280C>T | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1/10 | chr16 | 89095276 | |||||||
| chr16:89095282 | A | G | 134 | a0001c0001t0001g0158 a0001c0001t0001g0194 a0001c0001t0002g0003 others(131): Show |
142 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(139): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0005c0009t0032g0348 | 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 | a0001c0001t0034g0242 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0020t0008g0350 | 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 | 65 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(62): Show |
70 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(67): 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 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0005t0001g0243 others(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 | a0001c0005t0009g0245 a0001c0005t0009g0301 a0003c0008t0045g0017 others(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 | 304 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(301): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): 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 | a0005c0009t0051g0214 | 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 | a0002c0002t0052g0116 | 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 | a0005c0017t0033g0347 | 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 | a0001c0001t0016g0246 | 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 | a0001c0001t0017g0107 | 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 | a0002c0020t0008g0350 a0005c0017t0033g0347 |
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 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0005c0017t0033g0347 |
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 | 107 | a0001c0001t0001g0158 a0001c0001t0001g0194 a0001c0001t0002g0003 others(104): 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 | a0005c0017t0033g0347 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
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 | 39 | a0001c0001t0026g0213 a0002c0002t0004g0211 a0002c0002t0006g0117 others(36): Show |
44 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(41): 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 | a0002c0002t0043g0120 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0005c0017t0033g0347 |
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 | 29 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0218 others(26): 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 | a0003c0006t0057g0338 | 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 | a0002c0020t0008g0350 a0003c0008t0045g0017 |
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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | a0001c0001t0001g0251 | 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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | 177 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(174): 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 | a0003c0008t0019g0240 a0009c0019t0019g0239 |
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 | a0002c0002t0008g0231 a0002c0002t0008g0233 a0002c0002t0008g0234 others(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 | a0004c0004t0003g0335 | 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 | a0001c0001t0012g0045 a0001c0001t0012g0046 a0001c0001t0012g0047 others(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 | a0001c0001t0012g0045 a0001c0001t0012g0046 a0001c0001t0012g0047 others(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 | a0001c0001t0049g0296 | 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 | a0003c0010t0056g0157 | 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 | 175 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(172): 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 | a0003c0008t0045g0017 | 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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | 31 | a0002c0002t0006g0117 a0004c0004t0003g0001 a0004c0004t0003g0019 others(28): 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 | 167 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(164): 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 | a0002c0003t0005g0034 a0002c0003t0005g0035 |
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 | a0001c0005t0001g0243 a0001c0005t0001g0244 |
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 | 2 | a0001c0005t0001g0010 a0001c0005t0001g0295 |
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 | 211 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(208): 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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | a0005c0017t0033g0347 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0001c0001t0017g0107 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0001c0001t0001g0294 | 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 | a0002c0020t0008g0350 | 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 | 210 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(207): 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 | a0004c0004t0003g0337 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0011c0015t0009g0322 | 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 | a0002c0002t0006g0156 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
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 | a0001c0001t0001g0292 a0001c0001t0027g0238 a0001c0005t0001g0293 |
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 | 167 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(164): 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 | 233 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(230): 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 | a0001c0001t0017g0107 | 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 | a0002c0002t0006g0207 a0002c0002t0018g0206 |
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 | a0002c0003t0004g0023 a0002c0003t0004g0025 a0002c0003t0005g0020 others(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 | a0002c0003t0005g0020 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0004c0004t0003g0323 | 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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(206): 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 | a0001c0001t0002g0197 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0002c0002t0004g0339 | 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 | 22 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(19): 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0005c0009t0032g0348 | 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 | a0002c0003t0005g0083 | 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 | a0004c0004t0003g0324 a0005c0017t0033g0347 |
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 | 172 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(169): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0001c0001t0001g0344 a0001c0005t0009g0302 a0002c0002t0006g0154 others(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 | 200 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(197): 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 | a0012c0022t0007g0068 | 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 | 208 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(205): 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 | a0001c0001t0001g0252 | 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 | 173 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(170): 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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(201): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0002t0004g0123 a0002c0002t0004g0124 |
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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | 231 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(228): 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | a0002c0003t0005g0092 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0002c0003t0004g0066 a0002c0003t0004g0067 a0002c0003t0004g0100 others(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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 202 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(199): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 14 | a0001c0005t0001g0010 a0001c0005t0001g0295 a0001c0005t0009g0196 others(11): 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 | a0003c0008t0019g0240 a0009c0019t0019g0239 |
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 | a0001c0005t0010g0319 | 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 | 175 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(172): 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 | 174 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(171): 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 | a0001c0001t0001g0112 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0005c0009t0014g0253 | 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 | a0003c0008t0045g0017 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0001c0005t0001g0043 a0001c0005t0001g0044 |
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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 347 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(344): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): 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 | a0001c0001t0059g0255 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0005g0033 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0003c0008t0045g0017 | 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 | a0001c0001t0001g0158 a0001c0001t0002g0195 |
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 | a0003c0008t0019g0240 a0009c0019t0019g0239 |
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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | 2 | a0001c0005t0001g0010 a0001c0005t0001g0295 |
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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0003c0006t0057g0338 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0005c0009t0032g0348 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(201): 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 | a0003c0007t0007g0050 a0003c0007t0007g0051 a0003c0007t0007g0052 others(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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0002c0002t0006g0153 a0002c0002t0040g0155 |
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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0288 a0001c0001t0001g0318 |
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 | a0002c0020t0008g0350 | 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 | a0002c0003t0050g0235 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0001c0001t0002g0163 | 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 | a0003c0008t0045g0017 | 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 | a0002c0002t0007g0114 | 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 | a0010c0024t0004g0122 | 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 | a0001c0005t0010g0304 a0001c0005t0010g0305 a0001c0005t0010g0306 others(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 | a0001c0005t0009g0291 | 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 | a0005c0009t0032g0348 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0004c0004t0003g0327 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0001c0001t0002g0164 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
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 | a0002c0003t0050g0235 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 |
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 | 175 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(172): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | 173 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(170): 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 | a0001c0018t0010g0256 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 23 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0272 others(20): 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 | a0002c0003t0050g0235 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0001c0001t0001g0271 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0001c0001t0001g0270 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0318 | 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 | 201 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(198): 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0002c0003t0050g0235 | 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 | a0004c0004t0003g0228 a0004c0004t0003g0229 |
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 | a0002c0002t0004g0221 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0001c0001t0059g0255 a0002c0003t0005g0020 a0002c0003t0005g0021 others(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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 |
203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | a0001c0001t0002g0004 a0001c0001t0002g0163 a0001c0001t0002g0189 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0163 a0001c0001t0002g0189 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0188 a0001c0001t0002g0191 others(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 | a0002c0003t0004g0066 a0002c0003t0004g0067 a0002c0003t0004g0100 others(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 | a0002c0003t0050g0235 | 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 | 208 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(205): 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 | a0002c0003t0005g0088 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0002c0003t0004g0066 a0002c0003t0004g0067 a0002c0003t0004g0100 others(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 | a0001c0005t0010g0319 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0003c0010t0008g0125 | 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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | a0012c0022t0007g0068 | 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 | a0005c0017t0033g0347 | 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 | a0002c0003t0004g0066 a0002c0003t0004g0067 a0002c0003t0004g0100 others(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 | a0001c0001t0059g0255 a0003c0008t0045g0017 |
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 | a0003c0008t0045g0017 | 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 | a0002c0011t0008g0134 a0002c0011t0008g0135 |
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 | a0002c0003t0005g0031 | 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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | a0002c0003t0005g0032 | 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 | 55 | a0001c0001t0001g0106 a0001c0001t0001g0158 a0001c0001t0002g0003 others(52): 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 | a0002c0003t0050g0235 | 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 | 171 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(168): 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0294 |
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 | a0001c0001t0001g0089 | 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 | a0004c0004t0036g0334 | 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 | 212 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(209): 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 | a0002c0002t0052g0116 | 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 | 34 | a0001c0001t0022g0269 a0001c0005t0001g0010 a0001c0005t0001g0040 others(31): 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 | a0003c0008t0045g0017 | 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 |
30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0005c0009t0032g0348 | 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 | a0002c0002t0004g0339 | 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 | a0003c0008t0045g0017 | 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 | a0005c0009t0032g0348 | 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 | a0002c0003t0050g0235 | 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 | 284 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(281): 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 | 1 | a0002c0002t0013g0006 | 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 | a0001c0014t0023g0312 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0294 |
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 | a0001c0005t0010g0307 | 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 | a0001c0001t0012g0268 | 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 | a0001c0014t0023g0312 | 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 | a0002c0002t0008g0231 a0002c0002t0008g0233 a0002c0002t0008g0234 others(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 | a0003c0006t0057g0338 | 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 | a0002c0020t0008g0350 | 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 | a0001c0001t0011g0013 a0001c0001t0011g0014 a0001c0001t0011g0015 |
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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0001c0005t0010g0304 a0001c0005t0010g0305 a0001c0005t0010g0306 |
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 | a0002c0003t0005g0033 | 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 | a0004c0004t0035g0018 | 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 | a0002c0011t0008g0135 | 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 | a0002c0003t0004g0023 a0002c0003t0004g0025 a0002c0003t0005g0020 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0259 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0251 a0001c0001t0011g0267 others(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 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0002c0003t0004g0066 others(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 | 64 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0002c0003t0005g0020 others(61): 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 | a0002c0003t0004g0025 a0002c0003t0005g0076 a0002c0003t0006g0024 others(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 | a0002c0020t0008g0350 | 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 | a0004c0004t0029g0227 | 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 | 31 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(28): 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 | 24 | a0002c0002t0004g0124 a0002c0002t0004g0126 a0002c0002t0004g0149 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(21): 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 | 179 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0002c0003t0004g0023 others(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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0003c0008t0045g0017 | 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 | a0002c0003t0005g0346 | 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 | a0005c0017t0033g0347 | 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 | a0001c0001t0049g0296 | 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 | a0001c0001t0012g0045 a0001c0001t0012g0048 |
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 | a0001c0005t0001g0042 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0003c0010t0056g0157 | 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 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0001c0005t0009g0291 others(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 | a0002c0002t0004g0339 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0001c0001t0011g0267 | 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 | 35 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0002c0003t0050g0235 others(32): 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 | a0001c0001t0015g0237 | 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 | 181 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(178): 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 | a0002c0003t0050g0235 | 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 | 31 | a0001c0001t0002g0204 a0004c0004t0003g0001 a0004c0004t0003g0019 others(28): 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 | a0001c0001t0026g0213 | 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 | 213 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(210): 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 | a0001c0001t0002g0188 a0002c0003t0004g0023 a0002c0003t0004g0025 others(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 | 17 | a0004c0004t0003g0001 a0004c0004t0003g0226 a0004c0004t0003g0297 others(14): 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 | a0004c0004t0003g0332 | 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 | a0004c0004t0003g0224 | 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 | a0002c0002t0004g0339 | 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 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
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 | a0002c0003t0050g0235 | 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 | 211 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(208): 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 | a0003c0006t0057g0338 | 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 | a0001c0001t0011g0038 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0001c0001t0001g0288 a0001c0001t0001g0318 |
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 | a0003c0008t0008g0036 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0270 others(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 | 21 | a0004c0004t0003g0001 a0004c0004t0003g0218 a0004c0004t0003g0226 others(18): 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 | a0005c0009t0010g0303 | 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 | a0005c0017t0033g0347 | 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 | a0004c0004t0003g0218 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0001c0001t0011g0038 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0294 |
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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0003c0007t0007g0099 | 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 |
244 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(241): 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 | 183 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(180): 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 | a0002c0020t0008g0350 | 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 | 243 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(240): 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 | a0002c0003t0050g0235 | 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 | a0005c0009t0032g0348 | 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 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0287 |
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 | 31 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(28): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0055g0121 | 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 | a0001c0001t0002g0204 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | 3 | a0001c0001t0002g0009 a0001c0001t0002g0215 a0001c0001t0002g0216 |
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 | a0001c0001t0002g0160 | 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 | a0001c0014t0023g0312 | 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 | 36 | a0001c0001t0001g0288 a0001c0001t0001g0318 a0001c0001t0022g0269 others(33): 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 | a0002c0002t0013g0146 | 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 | a0001c0005t0009g0341 | 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 | a0001c0005t0010g0304 a0001c0005t0010g0305 |
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 | a0004c0004t0003g0228 a0004c0004t0003g0229 |
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 | 217 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(214): 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 | a0005c0017t0033g0347 | 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 | a0002c0002t0006g0153 a0002c0002t0040g0155 |
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 | a0004c0004t0003g0337 | 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 | a0008c0016t0002g0167 | 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 | a0005c0017t0033g0347 | 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 | a0001c0001t0002g0182 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0003t0004g0023 a0002c0003t0004g0025 a0002c0003t0006g0024 |
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 | 277 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(274): 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 | 35 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(32): 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 | a0002c0003t0005g0084 | 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 | a0003c0008t0045g0017 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 171 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(168): 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0002c0003t0005g0032 | 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 | 281 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(278): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0011t0008g0131 a0002c0011t0008g0134 a0002c0011t0008g0135 |
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 | a0002c0003t0005g0031 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0005t0009g0341 | 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 | a0003c0010t0056g0157 | 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 | a0001c0001t0011g0013 a0001c0001t0011g0014 a0001c0001t0011g0015 |
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 | a0002c0003t0020g0093 a0002c0003t0020g0094 |
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 | a0002c0002t0008g0233 a0002c0002t0008g0234 a0002c0023t0008g0232 |
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 | 7 | a0001c0001t0002g0008 a0001c0001t0002g0178 a0001c0001t0002g0179 others(4): 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 | 242 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(239): 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 | a0003c0006t0057g0338 | 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 | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(237): 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 | 239 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(236): 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 | a0004c0004t0003g0300 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1126+1337G>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 6/10 | chr16 | 89115824 | |||||||
| chr16:89115887 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(176): 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 | a0001c0014t0023g0312 | 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 | a0002c0002t0039g0130 | 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 | a0001c0001t0002g0177 | 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 | a0005c0009t0010g0303 | 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 | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(237): 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
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 | a0002c0003t0050g0235 | 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(235): 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0029 others(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 | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(237): 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 | a0002c0002t0039g0130 | 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 | a0005c0009t0032g0348 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0020g0094 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0251 | 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 | a0005c0017t0033g0347 | 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 | a0002c0002t0006g0113 a0002c0002t0006g0138 a0002c0002t0006g0145 others(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 | 281 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(278): 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(235): 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 | a0002c0002t0004g0220 | 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 | a0004c0004t0003g0335 | 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 | 280 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(277): 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 | a0002c0003t0050g0235 | 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 | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(237): 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 | a0001c0001t0002g0163 | 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 | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(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 | a0005c0009t0032g0348 | 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 |
239 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(236): 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 | a0001c0001t0011g0267 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0294 others(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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | 178 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(175): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0005g0033 | 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 | 33 | a0001c0001t0002g0205 a0001c0005t0009g0289 a0001c0005t0009g0290 others(30): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(237): 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 | 34 | a0001c0001t0002g0205 a0001c0005t0009g0289 a0001c0005t0009g0290 others(31): 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 | a0001c0001t0001g0115 | 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 | a0002c0002t0006g0113 a0002c0002t0006g0138 a0002c0002t0006g0145 others(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 | a0002c0003t0044g0026 | 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 | 34 | a0001c0001t0002g0205 a0001c0005t0009g0289 a0001c0005t0009g0290 others(31): 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 | a0001c0001t0015g0236 | 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 | a0002c0003t0005g0035 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0002c0003t0005g0034 | 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 | 33 | a0001c0001t0002g0205 a0001c0005t0009g0289 a0001c0005t0009g0290 others(30): 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0002c0003t0005g0020 a0002c0003t0005g0021 |
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 | 240 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(237): 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 | a0002c0003t0050g0235 | 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 | 241 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(238): 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 | a0001c0001t0015g0236 | 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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(204): 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0002c0003t0050g0235 | 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 | 62 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(59): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0020t0008g0350 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0002t0043g0120 | 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 | 239 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(236): 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 | a0002c0003t0050g0235 | 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 | 339 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(336): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0003c0010t0056g0157 | 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 | a0002c0003t0050g0235 | 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 | a0002c0002t0004g0220 | 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 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
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 | a0002c0003t0050g0235 | 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 | a0001c0001t0012g0110 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0029 others(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 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
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 | 241 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(238): 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 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
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 | a0005c0017t0033g0347 | 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 | a0001c0001t0002g0205 | 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 | a0001c0005t0009g0196 | 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 | a0003c0006t0007g0049 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0002c0003t0050g0235 | 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 | 33 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(30): 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 | a0002c0003t0005g0031 | 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 | 2 | a0001c0005t0001g0010 a0001c0005t0001g0295 |
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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0003c0006t0007g0062 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0003c0006t0007g0022 | 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 | 241 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(238): 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 | a0001c0001t0015g0237 | 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 | 241 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(238): 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 | a0001c0005t0001g0040 | 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 | a0002c0003t0005g0085 a0002c0003t0005g0086 |
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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0001t0001g0112 | 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 | a0005c0009t0032g0348 | 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 | a0001c0001t0002g0181 | 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 | 208 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(205): 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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(206): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | 31 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0002c0020t0008g0350 others(28): 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 | a0001c0005t0009g0321 | 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 |
30 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(27): 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 | a0001c0001t0002g0204 | 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 | a0002c0011t0008g0134 a0002c0011t0008g0135 |
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 | a0003c0007t0007g0054 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | 33 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(30): 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 | a0002c0003t0050g0235 | 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 | a0001c0005t0001g0044 | 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 | a0001c0001t0001g0252 a0001c0001t0001g0254 |
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 | a0001c0001t0059g0255 | 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 | 32 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(29): 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 | a0002c0003t0005g0346 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0001t0002g0204 | 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 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 |
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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(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 | 174 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(171): 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 | a0002c0003t0055g0121 | 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 | a0002c0020t0008g0350 | 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 | a0002c0003t0004g0025 | 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 | 274 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(271): 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 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
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 | a0005c0017t0033g0347 | 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0001c0001t0002g0174 | 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 | a0004c0004t0003g0323 a0004c0004t0003g0328 |
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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(201): 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 | a0003c0010t0008g0125 | 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 | a0001c0005t0001g0295 | 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 | 274 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(271): 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 | a0001c0014t0023g0312 | 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 | a0002c0003t0005g0028 | 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 | a0002c0003t0050g0235 | 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 | a0002c0021t0004g0109 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0002c0003t0004g0025 | 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 | a0003c0006t0007g0072 a0003c0006t0007g0073 a0003c0006t0007g0074 others(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 | a0002c0020t0008g0350 | 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 | 275 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(272): 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 | a0001c0005t0009g0241 a0001c0005t0009g0245 a0001c0005t0009g0301 others(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 | 33 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(30): 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 | a0005c0017t0033g0347 | 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 | a0005c0009t0032g0348 | 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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(201): 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 | a0005c0009t0032g0348 | 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 | a0002c0003t0005g0033 | 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 | a0004c0004t0003g0228 a0004c0004t0003g0229 |
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 | a0005c0009t0032g0348 | 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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(203): 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0001c0001t0012g0268 | 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 | a0001c0001t0001g0089 | 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 | a0004c0004t0003g0218 | 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0002c0003t0050g0235 | 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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(201): 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(235): 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 | 273 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(270): 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0270 others(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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(201): 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 | 202 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(199): 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 | a0001c0001t0001g0271 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(202): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | a0007c0013t0001g0275 | 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 | a0002c0002t0053g0144 | 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 | a0001c0001t0049g0296 | 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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | a0001c0001t0002g0205 | 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 | a0003c0008t0019g0240 a0009c0019t0019g0239 |
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 | 272 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(269): 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | 33 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(30): 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 | 196 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0090 others(193): 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 | a0005c0017t0033g0347 | 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 | a0005c0017t0033g0347 | 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 | a0002c0002t0006g0207 a0002c0002t0018g0206 |
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 | 129 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(126): 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 |
66 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0112 others(63): 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 | a0001c0005t0010g0307 a0003c0006t0007g0058 a0003c0006t0007g0059 |
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 | 69 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0002c0003t0005g0020 others(66): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0005c0017t0033g0347 | 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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(200): 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 | a0002c0002t0004g0349 | 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 |
274 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(271): 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 | a0002c0003t0038g0065 | 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 | a0004c0004t0003g0323 a0004c0004t0003g0328 |
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 | a0002c0002t0008g0231 a0002c0002t0008g0233 a0002c0002t0008g0234 others(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 | a0001c0005t0009g0241 | 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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(206): 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0003c0010t0008g0125 | 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 | 32 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(29): 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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | a0002c0003t0050g0235 | 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 | 71 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0002c0003t0005g0020 others(68): 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 | a0004c0004t0003g0300 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0002c0003t0005g0079 | 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 | a0001c0001t0017g0107 | 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 | a0003c0007t0007g0054 | 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 | a0002c0003t0005g0027 a0002c0003t0005g0028 a0002c0003t0005g0031 others(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 | a0003c0007t0007g0050 a0003c0007t0007g0051 a0003c0007t0007g0052 others(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 | 277 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(274): 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(173): 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 | 32 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0004c0004t0003g0001 others(29): 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 | 181 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(178): 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 | a0005c0017t0033g0347 | 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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(179): 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 | a0002c0003t0050g0235 | 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 | a0004c0004t0003g0297 | 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 | a0002c0003t0050g0235 | 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 | a0001c0014t0023g0312 | 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 | a0002c0002t0006g0153 | 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 | a0003c0006t0007g0005 a0003c0006t0007g0022 a0003c0006t0007g0049 others(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 | a0005c0009t0032g0348 | 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 | 180 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(177): 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 | 69 | a0001c0005t0009g0289 a0001c0005t0009g0290 a0002c0003t0005g0020 others(66): 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 | a0005c0009t0051g0214 | 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 | a0001c0005t0001g0293 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0043 others(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 | a0003c0008t0045g0017 | 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 | 65 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(62): 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 | a0002c0003t0005g0092 a0002c0003t0038g0065 a0006c0012t0006g0201 |
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 | a0002c0003t0005g0079 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | 183 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(180): 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 | a0001c0001t0001g0271 | 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 | 254 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(251): 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 | a0001c0001t0026g0213 | 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 | a0002c0003t0050g0235 | 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 | a0003c0010t0004g0132 a0003c0010t0004g0133 |
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 | a0002c0003t0050g0235 | 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 | 183 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(180): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0005g0078 a0002c0003t0005g0080 |
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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0004g0025 | 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 | a0005c0017t0033g0347 | 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 | a0005c0017t0033g0347 | 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 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(179): 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 | 278 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(275): 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 | 178 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(175): 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 | a0002c0003t0050g0235 | 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 | 181 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(178): 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 | a0001c0001t0001g0317 | 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 | a0002c0002t0008g0234 a0005c0017t0033g0347 |
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 | 187 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(184): 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0004c0004t0003g0336 | 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 | a0001c0001t0059g0255 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0001t0001g0251 | 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 | a0002c0003t0050g0235 | 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 | 187 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(184): 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 | 188 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(185): 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 | a0002c0003t0050g0235 | 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 | 25 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(22): 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 | a0004c0004t0003g0224 | 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 | a0002c0002t0006g0207 a0002c0002t0018g0206 a0003c0006t0007g0005 others(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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0001c0001t0001g0271 | 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 | a0002c0003t0005g0087 a0002c0003t0005g0346 a0005c0009t0051g0214 |
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 | a0001c0001t0002g0175 | 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 | a0001c0005t0010g0319 | 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 | a0003c0006t0007g0049 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 1 | a0002c0002t0013g0006 | 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 | a0006c0012t0006g0201 | 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 | a0003c0008t0008g0036 | 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | 30 | a0004c0004t0003g0001 a0004c0004t0003g0019 a0004c0004t0003g0212 others(27): 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 | a0005c0009t0032g0348 | 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 | a0001c0001t0015g0237 | 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 | a0001c0005t0010g0314 a0001c0005t0010g0315 a0001c0005t0010g0316 others(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 | a0002c0002t0006g0113 | 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 | a0005c0017t0033g0347 | 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 | 37 | a0001c0001t0015g0236 a0002c0002t0006g0209 a0002c0002t0006g0210 others(34): 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 | 75 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(72): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(72): 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 | a0002c0002t0004g0220 a0002c0002t0006g0070 a0002c0002t0006g0137 others(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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(38): 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 | a0001c0001t0001g0002 a0001c0001t0001g0278 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0001g0342 others(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 | a0002c0002t0004g0129 a0002c0003t0005g0020 a0002c0003t0005g0021 others(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 | a0003c0006t0007g0073 a0012c0022t0007g0068 |
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 | a0003c0006t0007g0022 a0003c0006t0007g0049 a0003c0006t0007g0055 others(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 | a0003c0006t0007g0058 a0003c0006t0007g0059 |
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 | a0003c0006t0007g0022 a0003c0006t0007g0049 a0003c0006t0007g0055 others(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 | a0002c0003t0050g0235 | 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 | 34 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0002c0003t0038g0065 others(31): 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 | a0002c0003t0005g0021 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0001c0001t0001g0292 a0001c0001t0027g0238 |
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 | 120 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(117): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0002g0159 a0002c0003t0005g0081 a0005c0009t0014g0253 |
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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0343 | 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 | a0002c0003t0050g0235 | 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 | 59 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(56): Show |
60 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(57): 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 | a0002c0003t0004g0101 | 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 | a0002c0003t0050g0235 | 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 | a0002c0020t0008g0350 | 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 | a0003c0006t0057g0338 | 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 | a0001c0005t0010g0314 | 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 | a0003c0008t0045g0017 | 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 | a0002c0002t0007g0114 a0002c0003t0005g0020 a0002c0003t0005g0021 others(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 | a0001c0001t0001g0280 | 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 | a0002c0011t0008g0131 a0002c0011t0008g0134 a0002c0011t0008g0135 |
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 | a0005c0009t0032g0348 | 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 | a0001c0001t0001g0254 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0001c0005t0009g0320 | 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 | a0005c0017t0033g0347 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0005t0009g0291 | 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 | a0002c0003t0050g0235 | 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 | 2 | a0002c0002t0004g0129 a0002c0002t0013g0006 |
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 | a0002c0003t0050g0235 | 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 | 93 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(90): Show |
94 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(91): 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | a0002c0002t0006g0117 | 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 | a0002c0003t0050g0235 | 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 | a0005c0009t0051g0214 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0001t0002g0192 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0002g0159 others(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 | 129 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0272 others(126): Show |
138 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(135): 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 | a0005c0009t0032g0348 | 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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0194 others(149): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0003c0008t0008g0064 | 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 | a0001c0005t0010g0304 a0001c0005t0010g0305 a0001c0005t0010g0306 |
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 | a0002c0003t0005g0076 | 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 | 94 | a0002c0002t0004g0123 a0002c0002t0004g0124 a0002c0002t0004g0126 others(91): Show |
95 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(92): 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 | a0002c0003t0005g0021 | 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 | 48 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0272 others(45): 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0344 | 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 | a0002c0003t0050g0235 | 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 | a0001c0005t0009g0196 | 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 | a0002c0002t0008g0231 | 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 | a0002c0003t0050g0235 | 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 | 49 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0272 others(46): 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 | a0002c0002t0004g0129 | 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 | a0005c0009t0051g0214 | 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 | a0005c0009t0037g0037 | 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 | a0002c0002t0006g0209 | 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 | a0010c0024t0004g0122 | 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0059g0255 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0001c0001t0002g0174 | 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 | a0002c0003t0004g0025 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0318 a0001c0001t0011g0012 others(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 | a0002c0003t0050g0235 | 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 | a0002c0003t0004g0067 | 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 | 63 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(60): Show |
64 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(61): 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 | a0002c0002t0007g0114 a0003c0006t0007g0049 |
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 | a0001c0005t0001g0295 | 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 | a0001c0005t0001g0243 a0001c0005t0001g0244 |
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 | 26 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(23): 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 | a0001c0001t0001g0102 | 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 | a0002c0003t0005g0078 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0079 a0002c0003t0005g0080 |
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 | a0001c0001t0001g0292 | 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 | a0001c0001t0027g0238 | 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 | a0001c0001t0002g0168 | 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 | a0003c0008t0045g0017 | 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 | a0006c0012t0006g0201 a0006c0012t0006g0202 a0006c0012t0006g0203 |
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 | a0003c0006t0007g0056 a0003c0006t0007g0060 |
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 | a0001c0005t0009g0291 | 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 | a0004c0004t0003g0226 | 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 |
57 | a0001c0001t0002g0174 a0001c0001t0014g0105 a0001c0005t0001g0041 others(54): Show |
57 | HG00099.hp1 HG00423.hp1 HG00642.hp1 others(54): 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 |
28 | a0002c0002t0018g0139 a0002c0003t0038g0065 a0004c0004t0003g0001 others(25): 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 | a0001c0005t0009g0245 | 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 | a0002c0002t0004g0143 a0002c0002t0004g0149 a0002c0002t0004g0150 others(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 | a0002c0003t0004g0101 | 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 | a0002c0021t0004g0109 | 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 | a0003c0010t0004g0133 | 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 | a0002c0002t0039g0130 | 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 | a0003c0007t0007g0050 | 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 |
14 | a0002c0002t0004g0129 a0002c0002t0004g0198 a0002c0002t0004g0199 others(11): 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 | a0002c0002t0006g0113 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0049 a0003c0006t0007g0058 others(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 | a0002c0003t0005g0034 a0002c0003t0005g0035 |
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 | a0002c0003t0005g0027 | 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 | a0001c0001t0001g0294 | 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 | a0002c0003t0005g0031 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0003c0010t0008g0125 | 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 | a0005c0009t0014g0253 | 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 | a0002c0003t0005g0250 | 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 | a0002c0011t0008g0135 | 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 | a0001c0001t0017g0107 | 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0015g0237 a0001c0005t0010g0307 a0001c0018t0010g0256 |
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 | a0001c0001t0015g0236 | 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 |
2 | a0001c0005t0001g0010 a0001c0005t0001g0295 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0259 others(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 | a0002c0003t0005g0250 | 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 | a0002c0003t0005g0027 a0002c0003t0005g0031 a0002c0003t0005g0034 others(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 | a0002c0003t0005g0032 | 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 | a0002c0003t0005g0033 | 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 | a0002c0003t0005g0028 a0002c0003t0044g0026 |
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 | a0002c0003t0005g0346 | 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 | a0002c0003t0005g0076 a0005c0009t0037g0037 |
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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0082 others(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 | a0005c0009t0010g0303 | 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 | a0002c0003t0005g0029 | 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 | a0002c0003t0005g0081 | 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 | a0002c0003t0005g0085 a0002c0003t0005g0086 |
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 | a0002c0003t0005g0092 | 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 | a0002c0003t0005g0087 | 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 | a0004c0004t0003g0218 a0004c0004t0003g0335 |
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 | a0001c0001t0022g0269 a0001c0005t0010g0315 |
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 | a0001c0005t0010g0314 | 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 | a0005c0009t0032g0348 | 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 | a0004c0004t0003g0300 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0164 |
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 | a0001c0001t0002g0007 | 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 | a0001c0005t0001g0244 | 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 | a0002c0011t0008g0131 a0002c0011t0008g0134 |
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 | a0002c0002t0004g0220 | 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 | a0001c0001t0011g0013 a0003c0008t0008g0036 |
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 | a0003c0006t0007g0022 | 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 | a0003c0006t0057g0338 | 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 | 14 | a0001c0001t0002g0182 a0001c0001t0011g0015 a0001c0001t0015g0237 others(11): 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 | a0001c0001t0026g0213 | 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 | a0003c0006t0007g0005 a0003c0006t0007g0111 a0003c0007t0007g0053 |
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 | 18 | a0001c0001t0002g0175 a0001c0001t0022g0269 a0001c0001t0030g0262 others(15): 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 | a0002c0002t0006g0138 | 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 | a0001c0001t0001g0288 a0001c0001t0001g0318 |
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 | a0001c0001t0002g0175 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0294 others(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 |
46 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0001g0158 others(43): 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 | a0001c0001t0002g0185 a0001c0005t0009g0320 |
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 | a0001c0001t0002g0173 | 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 | a0002c0003t0005g0083 | 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 | a0001c0001t0001g0261 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0002t0008g0147 a0002c0002t0008g0148 a0004c0004t0003g0300 |
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 | 9 | a0001c0001t0001g0292 a0001c0001t0015g0236 a0001c0001t0015g0237 others(6): 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 | a0001c0001t0030g0262 | 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 | a0002c0003t0005g0095 | 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 | a0002c0003t0005g0096 | 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 | a0002c0002t0013g0146 | 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 | a0011c0015t0009g0322 | 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 | a0011c0015t0009g0322 | 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 | a0005c0017t0033g0347 | 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 | 11 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0001c0005t0001g0010 others(8): 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 | a0002c0002t0008g0147 a0002c0002t0008g0148 |
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 | a0001c0001t0014g0105 a0010c0024t0004g0122 |
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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0286 a0007c0013t0001g0275 |
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 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
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 | a0001c0001t0002g0204 | 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 | a0002c0002t0006g0207 a0002c0002t0018g0206 a0002c0002t0042g0128 |
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 | 116 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(113): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): 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 | a0001c0001t0002g0168 a0012c0022t0007g0068 |
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 | a0001c0001t0002g0168 a0012c0022t0007g0068 |
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 | a0001c0001t0002g0168 a0012c0022t0007g0068 |
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 | a0002c0002t0043g0120 | 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 | a0002c0002t0043g0120 | 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 | a0002c0002t0043g0120 | 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 | a0001c0001t0002g0168 | 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 | a0001c0001t0002g0168 | 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 | a0001c0001t0002g0168 | 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 | a0001c0018t0010g0256 a0002c0003t0005g0076 a0002c0003t0005g0092 |
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 | a0002c0002t0006g0153 | 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 | a0001c0001t0002g0204 | 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 | a0001c0001t0002g0168 a0001c0001t0002g0204 |
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 | a0001c0001t0002g0168 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0002c0003t0050g0235 | 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 | a0002c0002t0008g0233 | 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 | a0002c0003t0005g0028 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 125 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(122): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1366+5156C>A | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138418 | |||||||
| chr16:89138474 | C | T | 64 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(61): Show |
65 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(62): 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 | a0002c0002t0004g0142 a0002c0002t0004g0220 a0002c0002t0013g0146 |
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 | a0002c0003t0005g0021 | 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 | a0002c0002t0006g0138 | 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 | 97 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(94): Show |
98 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1366+5723G>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89138985 | |||||||
| chr16:89138987 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0164 |
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 | a0001c0001t0014g0105 a0010c0024t0004g0122 |
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 | a0003c0008t0045g0017 | 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 | 98 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(95): Show |
99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): 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 | a0005c0009t0032g0348 | 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 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(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 | a0002c0002t0004g0126 | 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 | 6 | a0001c0001t0002g0008 a0001c0001t0002g0179 a0001c0001t0002g0180 others(3): 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 | a0001c0001t0001g0252 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0001c0001t0031g0265 | 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 | a0001c0001t0059g0255 | 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 | 98 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(95): Show |
99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): 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 | a0002c0003t0020g0093 a0002c0003t0020g0094 |
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 | a0001c0001t0027g0238 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0288 a0001c0001t0001g0298 a0001c0001t0001g0318 others(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 | 37 | a0001c0001t0001g0308 a0001c0001t0002g0168 a0001c0005t0009g0321 others(34): 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 | 88 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0129 others(85): Show |
89 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(86): 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 | a0001c0005t0009g0302 | 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 | a0003c0006t0007g0058 a0003c0006t0007g0059 a0003c0006t0007g0062 |
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 | a0001c0001t0001g0259 a0001c0001t0030g0262 |
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 | a0002c0002t0006g0208 | 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 | a0002c0003t0020g0093 a0002c0003t0020g0094 |
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 | a0007c0013t0001g0275 | 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 | 98 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(95): Show |
99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): 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 | a0005c0009t0014g0253 | 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 | a0002c0002t0006g0207 a0002c0002t0018g0206 |
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 | 156 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(153): Show |
162 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(159): 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 | a0001c0001t0016g0246 | 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 | a0001c0005t0009g0196 | 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0165 others(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 | 155 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(152): Show |
161 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(158): 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 | a0002c0020t0008g0350 | 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 | a0001c0001t0001g0264 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0002c0003t0005g0027 a0002c0003t0005g0032 |
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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0001c0001t0001g0115 | 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 | a0003c0006t0057g0338 | 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | a0001c0001t0031g0265 | 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0005c0009t0032g0348 | 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 | a0001c0001t0015g0236 | 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 | a0001c0001t0001g0270 | 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 | 157 | a0001c0001t0001g0103 a0001c0001t0014g0105 a0002c0002t0004g0123 others(154): Show |
163 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(160): 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 | a0001c0001t0011g0013 a0001c0001t0011g0014 a0001c0001t0011g0015 others(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 | a0003c0008t0045g0017 | 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 | 99 | a0001c0001t0001g0103 a0001c0001t0014g0105 a0002c0002t0004g0123 others(96): Show |
100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1367-3360A>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 8/10 | chr16 | 89141907 | |||||||
| chr16:89141926 | A | G | 158 | a0001c0001t0001g0103 a0001c0001t0014g0105 a0002c0002t0004g0123 others(155): Show |
164 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(161): 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 | a0005c0009t0037g0037 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0005c0009t0032g0348 | 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 | a0001c0005t0010g0304 a0001c0005t0010g0305 |
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 | a0004c0004t0003g0323 | 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 | a0002c0002t0013g0146 | 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 | 157 | a0001c0001t0001g0103 a0001c0001t0014g0105 a0002c0002t0004g0123 others(154): Show |
163 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(160): 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 | a0001c0001t0059g0255 | 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 | a0005c0017t0033g0347 | 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 | a0001c0005t0009g0302 a0002c0003t0050g0235 |
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 | 141 | a0001c0001t0001g0103 a0001c0001t0001g0251 a0001c0001t0001g0257 others(138): Show |
146 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(143): 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 | a0003c0008t0047g0057 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0027 others(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 | a0003c0006t0007g0073 a0003c0006t0007g0074 |
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 | a0001c0001t0001g0158 a0001c0001t0002g0195 a0001c0001t0002g0222 others(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 | a0002c0003t0005g0031 | 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 | a0003c0008t0045g0017 | 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 | a0001c0014t0023g0312 | 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 | a0001c0014t0023g0312 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0318 a0002c0002t0004g0136 others(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 | a0002c0002t0004g0124 | 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 | a0002c0002t0006g0113 a0002c0002t0006g0152 |
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 | a0002c0002t0006g0113 a0002c0002t0006g0152 |
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 | a0001c0001t0015g0237 | 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 | a0001c0001t0002g0179 | 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 | a0002c0003t0050g0235 a0005c0017t0033g0347 |
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 | a0002c0002t0007g0114 a0003c0006t0007g0049 a0003c0006t0007g0058 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
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 | a0001c0005t0009g0196 | 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 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(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 | a0002c0002t0006g0145 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0001c0005t0010g0306 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0015g0237 | 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 | a0005c0017t0033g0347 | 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 | a0001c0001t0001g0158 a0001c0001t0002g0195 |
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 | a0002c0002t0006g0207 a0002c0002t0018g0206 |
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 | a0002c0002t0040g0155 | 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 | a0002c0002t0040g0155 | 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 | a0002c0003t0004g0067 | 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 | a0002c0003t0004g0067 | 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 | a0003c0010t0004g0133 | 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 | a0002c0003t0005g0029 | 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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | a0002c0002t0006g0156 | 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 | 157 | a0001c0001t0014g0105 a0001c0001t0015g0236 a0001c0001t0015g0237 others(154): Show |
163 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(160): 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0012g0045 a0001c0001t0012g0048 |
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 | a0002c0003t0004g0067 | 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 | a0002c0002t0006g0140 | 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 | a0002c0003t0050g0235 a0005c0017t0033g0347 |
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 | a0002c0003t0050g0235 a0005c0017t0033g0347 |
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 | a0002c0003t0050g0235 a0005c0017t0033g0347 |
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 | a0002c0003t0050g0235 | 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 | 66 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(63): Show |
67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): 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 | a0001c0001t0016g0011 a0001c0001t0025g0011 |
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 | 23 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0218 others(20): 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 | 67 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(64): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): 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 | a0001c0001t0014g0105 a0010c0024t0004g0122 |
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 | a0002c0003t0050g0235 a0005c0017t0033g0347 |
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 | a0002c0003t0005g0033 | 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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | a0001c0001t0002g0170 | 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 | a0002c0003t0005g0250 | 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 | a0001c0001t0001g0249 | 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 | 57 | a0001c0001t0001g0106 a0001c0001t0001g0158 a0001c0001t0002g0003 others(54): 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 | a0001c0001t0001g0270 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0005c0009t0032g0348 | 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 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | a0005c0009t0037g0037 | 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 | 40 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0194 others(37): 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 | 67 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(64): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): 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 | a0005c0017t0033g0347 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0005c0009t0032g0348 | 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 | a0002c0002t0006g0209 a0002c0002t0006g0210 |
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 | a0002c0003t0038g0065 | 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 | a0002c0003t0005g0029 | 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 | 33 | a0002c0003t0005g0076 a0002c0003t0005g0092 a0002c0003t0038g0065 others(30): 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 | 216 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0090 others(213): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | a0001c0001t0002g0168 | 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 | a0002c0002t0006g0113 a0002c0002t0006g0138 a0002c0002t0006g0145 others(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 | a0001c0005t0001g0295 | 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 | a0004c0004t0003g0337 | 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 | a0002c0003t0005g0082 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 11 | a0002c0002t0004g0129 a0002c0002t0004g0198 a0002c0002t0004g0199 others(8): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0001c0005t0009g0302 | 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 | a0001c0001t0002g0193 | 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 | a0001c0005t0009g0241 a0001c0005t0009g0245 a0001c0005t0009g0301 others(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 | a0004c0004t0003g0333 | 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 | a0001c0001t0002g0189 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0002c0002t0042g0128 a0002c0002t0054g0127 |
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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 32 | a0002c0003t0005g0076 a0002c0003t0005g0092 a0002c0003t0038g0065 others(29): 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0002c0003t0004g0100 | 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 | a0001c0001t0002g0189 | 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 | a0002c0003t0038g0065 | 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 | a0002c0002t0004g0129 | 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 | a0002c0003t0004g0066 a0002c0003t0004g0067 a0002c0003t0004g0100 others(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 | a0004c0004t0003g0328 | 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 | a0004c0004t0003g0328 | 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 |
67 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(64): 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 | a0004c0004t0003g0328 | 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 | a0002c0003t0005g0095 a0002c0003t0005g0096 |
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 | a0004c0004t0003g0328 | 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 | a0005c0017t0033g0347 | 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 | a0001c0005t0009g0196 | 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 | a0001c0001t0049g0296 | 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 | a0003c0008t0019g0240 a0009c0019t0019g0239 |
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 | a0001c0001t0002g0168 | 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 | a0001c0001t0002g0171 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 |
145 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0106 others(142): 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 | a0001c0001t0002g0119 | 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 | a0003c0008t0008g0063 a0003c0008t0008g0064 |
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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(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 | a0001c0001t0059g0255 | 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 | a0001c0001t0002g0189 | 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 | a0004c0004t0029g0227 | 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 | 72 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(69): 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 | 74 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(71): 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 | a0002c0003t0050g0235 | 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 | 74 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(71): 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 | a0003c0007t0007g0050 | 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 | a0011c0015t0009g0322 | 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | 18 | a0002c0003t0005g0076 a0002c0003t0005g0092 a0002c0003t0038g0065 others(15): 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 | 18 | a0002c0003t0005g0076 a0002c0003t0005g0092 a0002c0003t0038g0065 others(15): 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 | a0002c0002t0052g0116 | 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 | a0002c0002t0006g0156 | 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0002c0002t0043g0120 | 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 |
79 | a0001c0001t0014g0105 a0001c0001t0015g0236 a0001c0001t0015g0237 others(76): Show |
81 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(78): 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 | 16 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0225 others(13): 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 | a0004c0004t0003g0019 a0004c0004t0003g0212 a0004c0004t0003g0218 others(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 |
16 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0225 others(13): 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 | a0003c0010t0004g0132 a0003c0010t0004g0133 |
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 | a0002c0002t0039g0130 | 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 | a0002c0002t0006g0153 a0002c0002t0018g0139 a0002c0002t0040g0155 |
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 | 128 | a0001c0001t0014g0105 a0001c0001t0015g0236 a0001c0001t0015g0237 others(125): Show |
130 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1613+1217A>C | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147266 | |||||||
| chr16:89147266 | A | G | 29 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(26): 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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0001c0001t0027g0238 | 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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0003t0004g0100 | 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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0003t0004g0100 | 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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0003t0004g0100 | 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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0001c0001t0001g0266 a0002c0002t0006g0219 a0005c0017t0033g0347 |
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 | a0001c0001t0002g0186 | 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 | a0001c0001t0001g0266 a0001c0001t0002g0186 a0002c0002t0006g0219 others(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 | a0002c0003t0004g0100 | 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 | a0001c0001t0001g0266 a0001c0001t0002g0186 a0002c0002t0006g0219 others(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 | a0001c0001t0001g0266 a0002c0002t0006g0219 a0002c0003t0004g0100 |
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 | a0001c0001t0002g0186 a0005c0017t0033g0347 |
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 | a0001c0005t0010g0304 a0001c0005t0010g0306 a0001c0005t0010g0314 others(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 | a0002c0002t0042g0128 a0002c0002t0054g0127 a0002c0003t0005g0029 others(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 | a0004c0004t0003g0229 | 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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0001c0001t0002g0186 a0002c0021t0004g0109 a0003c0007t0007g0053 |
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 | a0002c0003t0004g0100 | 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 | a0001c0001t0002g0186 | 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 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0096 |
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 | a0001c0001t0001g0266 a0002c0003t0005g0034 a0002c0003t0005g0035 others(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 | a0001c0001t0002g0186 | 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 | a0001c0001t0001g0266 | 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 | 49 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0194 others(46): 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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0001c0005t0010g0307 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0001c0005t0010g0307 others(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 | a0001c0001t0001g0266 | 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 | a0002c0002t0006g0113 | 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 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0096 |
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 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0096 |
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 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0096 |
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 | a0002c0003t0005g0034 a0002c0003t0005g0035 a0002c0003t0005g0096 |
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 | a0002c0003t0005g0034 a0002c0003t0005g0035 |
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 | a0002c0003t0005g0096 | 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 | a0001c0001t0001g0266 a0001c0001t0022g0269 a0001c0005t0010g0305 others(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 | a0001c0001t0001g0266 a0001c0001t0022g0269 a0001c0005t0010g0305 others(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 | a0002c0002t0004g0198 a0002c0002t0004g0199 a0002c0002t0004g0223 others(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 | a0004c0004t0003g0229 a0005c0017t0033g0347 |
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 | a0004c0004t0003g0019 a0004c0004t0003g0212 a0004c0004t0003g0218 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0001c0005t0010g0307 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0001c0005t0010g0307 others(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 | a0002c0003t0005g0031 a0002c0003t0005g0032 a0002c0003t0005g0087 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0001c0005t0010g0307 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0001c0005t0010g0307 others(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 | a0001c0001t0022g0269 a0001c0005t0010g0305 a0002c0003t0005g0082 |
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 | a0001c0005t0010g0307 a0005c0009t0010g0303 a0005c0009t0051g0214 |
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 | a0002c0003t0004g0066 a0002c0003t0005g0031 a0002c0003t0005g0032 others(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 | a0002c0003t0004g0066 | 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 | 17 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(14): 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 | a0002c0003t0005g0031 a0002c0003t0005g0032 a0002c0003t0005g0087 others(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 | 17 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(14): 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 |
16 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0225 others(13): 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 | a0002c0003t0004g0100 | 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 | a0004c0004t0003g0019 a0004c0004t0003g0212 a0004c0004t0003g0218 others(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 | 16 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0225 others(13): 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 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0001g0257 others(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 | 45 | a0001c0001t0001g0106 a0001c0001t0001g0252 a0001c0001t0001g0261 others(42): 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 | a0001c0001t0001g0158 a0001c0001t0001g0271 a0001c0001t0001g0309 others(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 | a0001c0001t0001g0254 a0001c0001t0001g0311 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0248 a0001c0001t0001g0342 others(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 | a0001c0001t0001g0247 a0001c0001t0031g0265 a0002c0002t0004g0123 others(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 | a0001c0001t0001g0249 a0002c0002t0004g0211 a0002c0002t0004g0220 others(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 |
5 | a0002c0002t0006g0113 a0002c0002t0006g0117 a0002c0002t0006g0137 others(2): Show |
5 | HG00621.hp1 NA18941.hp2 NA18977.hp2 others(2): 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 | a0002c0002t0004g0126 a0002c0002t0004g0221 a0006c0012t0006g0202 |
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 | a0002c0002t0006g0209 a0002c0002t0006g0219 |
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 | a0002c0002t0053g0144 | 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 | a0002c0003t0004g0100 | 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 | a0002c0003t0050g0235 | 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 | a0002c0003t0050g0235 | 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 | 16 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0225 others(13): 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 | 16 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0225 others(13): 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 | a0002c0003t0050g0235 | 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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0272 others(19): 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 | a0004c0004t0003g0229 | 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 | 31 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(28): 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 | a0004c0004t0003g0229 | 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 | a0004c0004t0003g0229 | 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 | 109 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0112 others(106): Show |
114 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1613+1545T>G | ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | 89147594 | |||||||
| chr16:89147599 | C | T | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | a0002c0003t0050g0235 a0005c0017t0033g0347 |
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 | a0002c0003t0005g0034 a0002c0003t0005g0035 |
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 | a0004c0004t0003g0019 | 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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0002c0003t0005g0028 | 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 | a0002c0003t0020g0093 | 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 | 57 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0247 others(54): Show |
58 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(55): 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 | 55 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0112 others(52): 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 | a0001c0001t0014g0105 a0002c0002t0006g0070 a0002c0002t0006g0137 others(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 | a0001c0001t0001g0277 a0001c0001t0001g0281 a0001c0001t0002g0179 others(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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | 73 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0112 others(70): Show |
74 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(71): 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0001c0005t0009g0241 | 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 | 178 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0112 others(175): Show |
184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0002g0172 | 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 | a0005c0009t0032g0348 | 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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0002c0003t0050g0235 | 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 | a0005c0017t0033g0347 | 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 | a0004c0004t0003g0019 | 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 | 32 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(29): 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 | 32 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(29): 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 | a0002c0003t0050g0235 | 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 | a0001c0001t0001g0344 | 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 | a0001c0001t0012g0268 | 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 | a0004c0004t0003g0019 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0004c0004t0003g0325 | 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 | 65 | a0001c0001t0001g0103 a0001c0001t0014g0105 a0002c0002t0004g0123 others(62): Show |
66 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(63): 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 | 67 | a0001c0001t0001g0103 a0001c0001t0014g0105 a0002c0002t0004g0123 others(64): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0165 others(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 | a0002c0003t0050g0235 | 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 | 1 | a0001c0005t0001g0010 | 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 | 32 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(29): 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 | 66 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(63): Show |
67 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(64): 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 | a0001c0001t0001g0158 a0001c0001t0002g0195 a0001c0001t0002g0222 |
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 | a0002c0003t0050g0235 | 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | a0001c0005t0009g0241 a0001c0005t0009g0245 a0001c0005t0009g0301 others(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 | 70 | a0001c0001t0014g0105 a0001c0001t0015g0236 a0001c0001t0015g0237 others(67): Show |
71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 |
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 | 32 | a0002c0003t0038g0065 a0002c0003t0050g0235 a0004c0004t0003g0001 others(29): 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 | 31 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(28): 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 | 64 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(61): Show |
65 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(62): 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 | a0001c0001t0001g0288 a0001c0001t0001g0318 |
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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0165 others(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 | a0002c0002t0004g0123 | 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 | a0002c0002t0013g0146 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | 64 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(61): Show |
65 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(62): 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 | a0005c0017t0033g0347 | 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 | 65 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(62): Show |
66 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(63): 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 | a0002c0003t0005g0077 a0002c0003t0005g0078 a0002c0003t0005g0079 others(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 | 67 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(64): Show |
68 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(65): 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 | 28 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(25): 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 | a0001c0001t0015g0236 a0001c0001t0015g0237 a0001c0001t0022g0269 others(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 | a0002c0003t0005g0087 a0005c0009t0037g0037 |
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 | a0001c0001t0011g0038 | 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 | a0002c0002t0008g0231 | 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 | a0001c0001t0058g0313 | 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 | a0001c0001t0001g0270 | 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 | a0004c0004t0035g0018 | 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 | a0001c0001t0001g0279 | 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 | a0003c0008t0019g0240 | 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 | a0002c0003t0004g0066 a0002c0003t0004g0067 a0002c0003t0004g0100 others(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 | a0004c0004t0003g0324 a0004c0004t0003g0330 |
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 | a0001c0001t0015g0236 a0005c0017t0033g0347 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0002g0217 | 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 | a0005c0009t0032g0348 | 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 | a0004c0004t0003g0324 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0270 others(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 | a0005c0009t0014g0253 | 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 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0165 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0286 a0007c0013t0001g0275 |
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 | a0005c0009t0032g0348 | 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 | a0006c0012t0006g0201 a0006c0012t0006g0202 a0006c0012t0006g0203 |
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 | a0001c0001t0022g0269 a0001c0005t0010g0304 a0001c0005t0010g0305 others(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 | a0001c0001t0001g0258 | 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 | 130 | a0001c0001t0014g0105 a0001c0001t0015g0236 a0001c0001t0015g0237 others(127): 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 | a0001c0001t0011g0039 a0001c0001t0059g0255 |
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 | a0001c0001t0001g0112 | 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 | 23 | a0001c0001t0014g0105 a0002c0002t0004g0123 a0002c0002t0004g0124 others(20): 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 | a0001c0001t0001g0288 a0001c0001t0001g0318 |
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 | a0004c0004t0003g0336 | 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 | a0004c0004t0003g0324 a0004c0004t0003g0330 |
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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 | a0002c0002t0007g0114 a0002c0002t0053g0144 a0003c0006t0007g0005 others(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 | a0004c0004t0036g0334 | 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 | a0002c0002t0007g0114 a0003c0006t0007g0005 a0003c0006t0007g0022 others(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 | 30 | a0002c0003t0038g0065 a0004c0004t0003g0001 a0004c0004t0003g0019 others(27): 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 |