Variant report

Variant	rs62510300
Chromosome Location	chr8:79064648-79064649
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs62508008	1.00[AMR][1000 genomes]
rs62508010	1.00[AMR][1000 genomes]
rs62508216	1.00[AMR][1000 genomes]
rs62510267	1.00[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	nsv831364	chr8:79034769-79223319	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:79063200-79066400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr8:79063200-79067200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr8:79063400-79067200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr8:79063400-79067200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:79063600-79065200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:79063600-79065200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:79063600-79067200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:79064400-79066800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr8:79064600-79065800	Enhancers	iPS-20b 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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