Variant report

Variant	rs72909023
Chromosome Location	chr2:22003053-22003054
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs13415187	1.00[AFR][1000 genomes]
rs13415274	1.00[AFR][1000 genomes]
rs1901343	1.00[EUR][1000 genomes]
rs1901345	1.00[EUR][1000 genomes]
rs1901347	1.00[EUR][1000 genomes]
rs2218882	0.93[EUR][1000 genomes]
rs4082172	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4082173	1.00[EUR][1000 genomes]
rs59102304	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60445840	1.00[EUR][1000 genomes]
rs72897882	1.00[EUR][1000 genomes]
rs72897891	1.00[EUR][1000 genomes]
rs72897892	1.00[EUR][1000 genomes]
rs72897894	1.00[EUR][1000 genomes]
rs72897896	1.00[EUR][1000 genomes]
rs72897899	1.00[EUR][1000 genomes]
rs72897902	1.00[EUR][1000 genomes]
rs72899865	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899867	1.00[EUR][1000 genomes]
rs72899871	1.00[EUR][1000 genomes]
rs72899873	1.00[EUR][1000 genomes]
rs72899875	1.00[EUR][1000 genomes]
rs72899877	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899878	1.00[EUR][1000 genomes]
rs72899881	1.00[EUR][1000 genomes]
rs72899883	1.00[EUR][1000 genomes]
rs72899885	1.00[EUR][1000 genomes]
rs72899889	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899891	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899893	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899896	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899898	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72899901	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901713	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901720	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901721	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901727	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901729	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901731	1.00[EUR][1000 genomes]
rs72901736	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901741	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72901767	1.00[EUR][1000 genomes]
rs72901774	1.00[EUR][1000 genomes]
rs72909015	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011486	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv535602	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3406784	chr2:21805088-22160765	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv430602	chr2:21910981-22221206	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21994600-22016400	Weak transcription	Aorta	Aorta

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