Variant report

Variant	rs17609084
Chromosome Location	chr17:50258956-50258957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10514999	0.82[EUR][1000 genomes]
rs12150318	0.85[YRI][hapmap];0.84[AFR][1000 genomes]
rs1503047	0.86[YRI][hapmap];0.82[AFR][1000 genomes]
rs16951051	0.86[YRI][hapmap]
rs4613111	0.82[AFR][1000 genomes]
rs9910955	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]

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	nsv492317	chr17:50067819-50774475	Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:50258600-50259400	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr17:50258800-50259400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr17:50258800-50259600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr17:50258800-50260000	Enhancers	HUES6 Cell Line	embryonic stem cell

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

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