Variant report

Variant	rs12062605
Chromosome Location	chr1:70460835-70460836
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10889863	1.00[CEU][hapmap];0.85[GIH][hapmap]
rs11802766	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs12060100	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12066962	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12074727	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap]
rs12088269	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17131039	0.85[GIH][hapmap]
rs17131125	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41440946	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap]
rs55858638	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56278841	0.95[EUR][1000 genomes]
rs58574417	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66724614	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67032718	1.00[EUR][1000 genomes]
rs72676873	0.95[EUR][1000 genomes]
rs72676875	0.95[EUR][1000 genomes]
rs72676880	0.95[EUR][1000 genomes]
rs7554827	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes]
rs7556220	0.85[GIH][hapmap];1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531879	chr1:70386455-70644617	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv871018	chr1:70450024-70496379	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv526839	chr1:70459886-70475794	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70450800-70481200	Weak transcription	Fetal Brain Female	brain
2	chr1:70457800-70464600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:70458600-70461000	Enhancers	HUVEC	blood vessel

Quick Search:

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

what's new

Quick links