Variant report

Variant	rs11984237
Chromosome Location	chr7:147890403-147890404
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12333907	1.00[EUR][1000 genomes]
rs55810799	1.00[EUR][1000 genomes]
rs58572035	1.00[EUR][1000 genomes]
rs6952849	1.00[EUR][1000 genomes]
rs73472292	1.00[EUR][1000 genomes]
rs73474225	1.00[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	nsv428189	chr7:147885525-148051226	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147888600-147891000	Weak transcription	Fetal Intestine Large	intestine
2	chr7:147889200-147890600	Weak transcription	Fetal Intestine Small	intestine
3	chr7:147890400-147891000	Enhancers	K562	blood

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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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