Variant report

Variant	rs62467886
Chromosome Location	chr7:108181617-108181618
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11982329	1.00[AFR][1000 genomes]
rs62467877	1.00[AFR][1000 genomes]
rs62467879	1.00[AFR][1000 genomes]
rs62467881	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62467898	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 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	chr7:108181000-108181800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr7:108181600-108181800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:108181600-108181800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr7:108181600-108182200	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr7:108181600-108182600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr7:108181600-108182800	Enhancers	HUES64 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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