Variant report
Variant | rs73453048 |
---|---|
Chromosome Location | chr7:145499409-145499410 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:145499268..145500796-chr7:145500851..145503015,2 | K562 | blood: | |
2 | chr7:145476367..145479131-chr7:145497414..145500253,2 | K562 | blood: | |
3 | chr7:145498670..145501761-chr7:145504907..145507918,3 | K562 | blood: | |
4 | chr7:145480904..145484102-chr7:145498283..145500839,4 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12113978 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs61472949 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6978041 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73453045 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73453063 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73456924 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73457001 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73458856 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73463786 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73467320 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9918572 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2754040 | chr7:145303352-145698352 | Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | esv2755386 | chr7:145303352-145698352 | Genic enhancers Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv889383 | chr7:145396141-145549570 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv831182 | chr7:145399806-145556489 | Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1019118 | chr7:145483353-145639795 | Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | esv2102367 | chr7:145499022-145499449 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:145495400-145511400 | Weak transcription | K562 | blood |