Variant report

Variant	rs9822777
Chromosome Location	chr3:69777673-69777674
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs6763056	0.83[YRI][hapmap]
rs7642966	0.82[AFR][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	nsv834723	chr3:69643641-69811601	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr3:69761800-69778400	Weak transcription	Right Atrium	heart
2	chr3:69774400-69778400	Weak transcription	Left Ventricle	heart
3	chr3:69774400-69779800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:69774800-69779800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:69775800-69780000	Weak transcription	Fetal Heart	heart
6	chr3:69776000-69777800	Weak transcription	K562	blood

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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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