Variant report

Variant	rs73836025
Chromosome Location	chr3:70099917-70099918
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:70047678..70050413-chr3:70099154..70100827,2	K562	blood:

Variant related genes	Relation type
ENSG00000240405	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs55906238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56086555	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57240203	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59761935	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60327342	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60618858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61545912	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61678936	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836019	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836029	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836030	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836031	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836032	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836034	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836035	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836037	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836039	1.00[AMR][1000 genomes]
rs73836041	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836042	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836043	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836044	0.81[AFR][1000 genomes]
rs73836046	1.00[AMR][1000 genomes]
rs73836049	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836053	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836054	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836056	1.00[AMR][1000 genomes]
rs73836057	1.00[AMR][1000 genomes]
rs73836058	1.00[AMR][1000 genomes]
rs73836059	1.00[AMR][1000 genomes]
rs73836089	1.00[AMR][1000 genomes]
rs73836091	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836092	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836094	1.00[AMR][1000 genomes]
rs73836095	1.00[AMR][1000 genomes]
rs73838685	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7620183	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7631251	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7633610	1.00[AMR][1000 genomes]
rs9814696	1.00[AMR][1000 genomes]
rs9839441	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9840427	1.00[AMR][1000 genomes]
rs9843425	0.80[AFR][1000 genomes];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	nsv533396	chr3:69964029-70538306	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70092000-70105000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:70098600-70103400	Weak transcription	Aorta	Aorta
3	chr3:70099200-70102400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:70099600-70105000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr3:70099800-70102000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links