Variant report

Variant	rs565810
Chromosome Location	chr1:166754536-166754537
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs499528	0.83[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs514494	1.00[YRI][hapmap]
rs525075	0.83[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs529243	1.00[AMR][1000 genomes]
rs542163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs555321	0.82[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs564886	0.96[AFR][1000 genomes]
rs566924	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs572523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs577003	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs577172	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs577252	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs577965	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs580312	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166753600-166754600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:166753600-166755400	Enhancers	H9 Cell Line	embryonic stem cell
3	chr1:166754400-166756400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links