Variant report

Variant	rs72901767
Chromosome Location	chr2:21964077-21964078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1901343	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1901345	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1901347	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2218882	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4082172	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4082173	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57119946	1.00[AMR][1000 genomes]
rs57994839	1.00[AMR][1000 genomes]
rs59102304	1.00[EUR][1000 genomes]
rs59464527	1.00[AMR][1000 genomes]
rs60061690	0.83[AMR][1000 genomes]
rs60445840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897882	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897891	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897892	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897894	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897896	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897899	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72897902	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898237	0.83[AMR][1000 genomes]
rs72899865	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899867	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899871	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899873	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899875	1.00[EUR][1000 genomes]
rs72899877	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899878	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899881	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899883	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899885	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899889	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899891	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899893	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899896	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899898	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72899901	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901713	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901720	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901727	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901729	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901731	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901736	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72901774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72909015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72909023	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	chr2:21964000-21971000	Weak transcription	NHLF	lung

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