Variant report

Variant	rs6733145
Chromosome Location	chr2:209231844-209231845
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10189412	0.94[ASN][1000 genomes]
rs12619470	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12694110	0.95[ASN][1000 genomes]
rs13394289	0.90[ASN][1000 genomes]
rs28386802	0.95[ASN][1000 genomes]
rs4673402	0.95[ASN][1000 genomes]
rs4675762	0.95[ASN][1000 genomes]
rs4675763	0.95[ASN][1000 genomes]
rs4675764	0.94[ASN][1000 genomes]
rs6711995	0.94[ASN][1000 genomes]
rs6728530	0.94[ASN][1000 genomes]
rs6757231	0.94[ASN][1000 genomes]
rs67608809	0.98[ASN][1000 genomes]
rs7590641	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv584297	chr2:209020181-209316760	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv875752	chr2:209141066-209235373	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv437315	chr2:209204714-209249613	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv997721	chr2:209228673-209247209	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1006323	chr2:209228673-209247384	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 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	chr2:209220200-209235200	Weak transcription	K562	blood
2	chr2:209224800-209234200	Weak transcription	Placenta	Placenta
3	chr2:209226000-209234200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:209228800-209234000	Weak transcription	Osteobl	bone
5	chr2:209229200-209234600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:209231400-209232000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr2:209231600-209232200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:209231800-209232000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:209231800-209232200	Enhancers	Primary B cells from peripheral blood	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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