Variant report

Variant	rs11975661
Chromosome Location	chr7:138073204-138073205
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10236236	1.00[AMR][1000 genomes]
rs10240379	1.00[AMR][1000 genomes]
rs10242949	1.00[AMR][1000 genomes]
rs10258211	1.00[AMR][1000 genomes]
rs10263190	1.00[AMR][1000 genomes]
rs10264150	1.00[AMR][1000 genomes]
rs10264232	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10266093	1.00[AMR][1000 genomes]
rs10271111	1.00[AMR][1000 genomes]
rs11971525	1.00[AMR][1000 genomes]
rs12334219	1.00[AMR][1000 genomes]
rs28455808	1.00[AMR][1000 genomes]
rs28541317	1.00[AMR][1000 genomes]
rs28620635	1.00[AMR][1000 genomes]
rs28678352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28767250	1.00[AMR][1000 genomes]
rs28810494	1.00[AMR][1000 genomes]
rs28874637	1.00[AMR][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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138059400-138081800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:138071600-138081200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:138072200-138074200	Enhancers	Liver	Liver
4	chr7:138072400-138073400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:138072400-138074400	Enhancers	Placenta	Placenta
6	chr7:138072400-138080800	Enhancers	HepG2	liver
7	chr7:138072600-138074400	Enhancers	Hela-S3	cervix
8	chr7:138072800-138073600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:138073000-138074000	Weak transcription	K562	blood

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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

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