Variant report

Variant	rs4263293
Chromosome Location	chr3:86286959-86286960
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12487935	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12636329	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1512919	0.85[CEU][hapmap]
rs1512934	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1512935	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34090744	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34151490	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4688891	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7611502	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs932058	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877113	chr3:86205676-86298087	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv877114	chr3:86257272-86328961	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv877115	chr3:86278951-86554319	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86283800-86287000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr3:86283800-86287000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:86285400-86287000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:86285400-86289000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:86286400-86287000	Enhancers	Fetal Heart	heart
6	chr3:86286600-86287800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr3:86286600-86288800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:86286800-86288600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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