Variant report
Variant | rs58959891 |
---|---|
Chromosome Location | chr19:40085980-40085981 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:2 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | REST | chr19:40085751-40092211 | PANC-1 | pancreas: | n/a | chr19:40089953-40089973 chr19:40089956-40089969 chr19:40089958-40089967 chr19:40089953-40089973 chr19:40089953-40089966 chr19:40089954-40089972 chr19:40089959-40089973 chr19:40089953-40089962 chr19:40089961-40089971 chr19:40089956-40089969 chr19:40089953-40089973 |
2 | REST | chr19:40085749-40093889 | PANC-1 | pancreas: | n/a | chr19:40089953-40089973 chr19:40089956-40089969 chr19:40089958-40089967 chr19:40089953-40089973 chr19:40092973-40092991 chr19:40089953-40089966 chr19:40089954-40089972 chr19:40093618-40093636 chr19:40089959-40089973 chr19:40089953-40089962 chr19:40089961-40089971 chr19:40089956-40089969 chr19:40089953-40089973 |
No data |
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No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
RPS29P26 | TF binding region |
ENSG00000105198 | Chromatin interaction |
ENSG00000239320 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs59586385 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73553853 | 0.81[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1060251 | chr19:39982988-40099773 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
2 | nsv579509 | chr19:40004640-40133438 | Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
3 | esv34120 | chr19:40044635-40131820 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |