Variant report

Variant	rs4766876
Chromosome Location	chr12:118234710-118234711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10850900	0.85[EUR][1000 genomes]
rs10850902	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10850904	0.90[EUR][1000 genomes]
rs11615079	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2062906	0.87[EUR][1000 genomes]
rs28627182	0.85[EUR][1000 genomes]
rs4766881	0.88[EUR][1000 genomes]
rs4767627	0.82[EUR][1000 genomes]
rs4767629	0.88[EUR][1000 genomes]
rs895472	0.90[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	nsv560387	chr12:118219415-118239673	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118232600-118246400	Weak transcription	Pancreas	Pancrea
2	chr12:118232800-118239400	Weak transcription	Placenta Amnion	Placenta Amnion

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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