Variant report

Variant	rs6734821
Chromosome Location	chr2:181692213-181692214
allele	A/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:13)

rs_ID	r²[population]
rs12619585	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12693262	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs13387820	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13426990	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4128869	0.80[CEU][hapmap]
rs4359601	0.80[AMR][1000 genomes]
rs4666608	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4666643	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4666946	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4666957	0.80[AMR][1000 genomes]
rs7590308	0.81[ASN][1000 genomes]
rs9677524	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9677649	0.84[AMR][1000 genomes];0.82[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	nsv834475	chr2:181537463-181724891	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181688800-181694200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:181689000-181693400	Weak transcription	NHEK	skin
3	chr2:181689000-181693600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:181689000-181693600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:181689000-181693800	Weak transcription	HMEC	breast

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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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