Variant report

Variant	rs59753430
Chromosome Location	chr2:100157691-100157692
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs17022741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022788	0.83[EUR][1000 genomes]
rs2167339	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3087387	1.00[AMR][1000 genomes]
rs56684522	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57093686	1.00[AMR][1000 genomes]
rs57599963	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57668619	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs57969550	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58226642	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58780429	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59311105	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59859749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60633946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6707685	1.00[AMR][1000 genomes]
rs6723062	1.00[AMR][1000 genomes]
rs6745673	0.83[EUR][1000 genomes]
rs6761053	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6761507	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964150	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964151	0.83[AMR][1000 genomes]
rs73964152	1.00[AMR][1000 genomes]
rs73964155	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964157	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964158	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73964166	0.83[EUR][1000 genomes]
rs7568990	1.00[AMR][1000 genomes]
rs7570405	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7571186	1.00[AMR][1000 genomes]
rs7595242	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv962113	chr2:100022168-100317461	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100154600-100161000	Weak transcription	Primary B cells from cord blood	blood
2	chr2:100155000-100160200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:100155200-100158200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr2:100156000-100158800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:100157400-100162200	Enhancers	Fetal Heart	heart
6	chr2:100157600-100161400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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