Variant report

Variant	rs17825487
Chromosome Location	chr3:56511128-56511129
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10510786	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11708250	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11712094	0.82[EUR][1000 genomes]
rs11923602	0.80[AMR][1000 genomes]
rs1352765	0.85[AMR][1000 genomes]
rs17056833	0.80[AMR][1000 genomes]
rs17056853	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17056854	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17825463	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55783589	0.86[AMR][1000 genomes]
rs55801834	0.91[AMR][1000 genomes]
rs57164168	0.86[AMR][1000 genomes]
rs6800117	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6801539	0.83[EUR][1000 genomes]
rs72875310	0.81[EUR][1000 genomes]
rs72877217	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7611444	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7651181	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs923653	0.80[AMR][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	esv3347557	chr3:56466500-56619322	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56510200-56511600	Enhancers	H1 Cell Line	embryonic stem cell
2	chr3:56510600-56511200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr3:56510600-56511400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:56510600-56511400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:56510600-56511600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:56510800-56511200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr3:56510800-56511200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr3:56510800-56511400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:56511000-56511600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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

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