Variant report

Variant	rs2895471
Chromosome Location	chr11:93282840-93282841
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10501807	1.00[AMR][1000 genomes]
rs11820244	1.00[AMR][1000 genomes]
rs16918984	1.00[AMR][1000 genomes]
rs1939558	1.00[AMR][1000 genomes]
rs2399678	1.00[AMR][1000 genomes]
rs2399687	1.00[AMR][1000 genomes]
rs4753087	1.00[AMR][1000 genomes]
rs4753469	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4753479	1.00[AMR][1000 genomes]
rs6483252	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7111644	1.00[AMR][1000 genomes]
rs7127955	1.00[AMR][1000 genomes]

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	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1039623	chr11:93141461-93328739	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	esv3337063	chr11:93282606-93282890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93277200-93293000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:93281400-93283400	Enhancers	Fetal Intestine Large	intestine
3	chr11:93282400-93285800	Weak transcription	HepG2	liver
4	chr11:93282600-93286000	Weak transcription	Liver	Liver

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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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