Variant report

Variant	rs6719714
Chromosome Location	chr2:11186020-11186021
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13422602	1.00[EUR][1000 genomes]
rs16857096	1.00[EUR][1000 genomes]
rs16857110	1.00[EUR][1000 genomes]
rs16857139	1.00[EUR][1000 genomes]
rs16857295	1.00[CEU][hapmap]
rs2037105	1.00[CEU][hapmap]
rs57881743	1.00[EUR][1000 genomes]
rs73177189	1.00[EUR][1000 genomes]
rs7591945	1.00[CEU][hapmap]
rs868393	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833392	chr2:11054580-11235239	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv580971	chr2:11175395-11226507	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11183800-11188800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:11184200-11187800	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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