Variant report

Variant	rs11947636
Chromosome Location	chr4:85258731-85258732
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10005772	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2083665	0.95[AFR][1000 genomes]
rs2119793	0.86[AFR][1000 genomes]
rs28558705	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28656956	0.92[AFR][1000 genomes]
rs28894761	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60097326	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6826424	0.86[AFR][1000 genomes]
rs6828383	0.89[AFR][1000 genomes]
rs6843960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7668554	0.91[AFR][1000 genomes]
rs7688976	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9993950	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9999113	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879514	chr4:85057124-85272572	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv829997	chr4:85244076-85409405	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85257600-85260600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:85257800-85258800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:85258000-85259200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:85258200-85259000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr4:85258400-85258800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr4:85258600-85258800	Enhancers	H1 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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