Variant report
Variant | rs72700847 |
---|---|
Chromosome Location | chr4:171810899-171810900 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs72696893 | 0.86[EUR][1000 genomes] |
rs72698830 | 0.86[EUR][1000 genomes] |
rs72698837 | 0.86[EUR][1000 genomes] |
rs72698861 | 0.86[EUR][1000 genomes] |
rs72698875 | 1.00[EUR][1000 genomes] |
rs72698878 | 1.00[EUR][1000 genomes] |
rs72698881 | 1.00[EUR][1000 genomes] |
rs72700821 | 1.00[EUR][1000 genomes] |
rs72700825 | 1.00[EUR][1000 genomes] |
rs72700830 | 1.00[EUR][1000 genomes] |
rs72700833 | 1.00[EUR][1000 genomes] |
rs72700834 | 1.00[EUR][1000 genomes] |
rs72700839 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72700840 | 1.00[EUR][1000 genomes] |
rs72700842 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72700843 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72700846 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72700850 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72702533 | 1.00[EUR][1000 genomes] |
rs72702562 | 1.00[EUR][1000 genomes] |
rs72704647 | 1.00[EUR][1000 genomes] |
rs7693814 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv881345 | chr4:171673765-172228547 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv881415 | chr4:171694739-171842726 | Active TSS ZNF genes & repeats Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv881334 | chr4:171713039-171842726 | Weak transcription Enhancers ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv521422 | chr4:171808256-171824549 | Enhancers ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1018793 | chr4:171808272-172395180 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:171809000-171813600 | Weak transcription | H1 Cell Line | embryonic stem cell |