Variant report

Variant	rs57119946
Chromosome Location	chr2:21926948-21926949
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs11885530	0.81[EUR][1000 genomes]
rs11890428	0.85[EUR][1000 genomes]
rs11893913	0.81[EUR][1000 genomes]
rs11894171	0.81[EUR][1000 genomes]
rs11897479	0.85[EUR][1000 genomes]
rs11901833	0.85[EUR][1000 genomes]
rs17042814	0.85[EUR][1000 genomes]
rs17042818	0.85[EUR][1000 genomes]
rs17042879	0.81[EUR][1000 genomes]
rs1901343	0.83[AMR][1000 genomes]
rs1901345	0.83[AMR][1000 genomes]
rs1901347	0.83[AMR][1000 genomes]
rs2006198	0.85[EUR][1000 genomes]
rs2218882	0.83[AMR][1000 genomes]
rs4082172	0.83[AMR][1000 genomes]
rs4082173	0.83[AMR][1000 genomes]
rs4355148	0.85[EUR][1000 genomes]
rs56259583	0.81[EUR][1000 genomes]
rs57064261	0.85[EUR][1000 genomes]
rs57994839	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59464527	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59660521	0.81[EUR][1000 genomes]
rs60029510	0.85[EUR][1000 genomes]
rs60061690	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60445840	1.00[AMR][1000 genomes]
rs60451450	0.81[EUR][1000 genomes]
rs61350387	0.81[EUR][1000 genomes]
rs6547804	0.85[EUR][1000 genomes]
rs6708716	0.85[EUR][1000 genomes]
rs6714387	0.81[EUR][1000 genomes]
rs6719475	0.85[EUR][1000 genomes]
rs6722505	0.81[EUR][1000 genomes]
rs6731548	0.81[EUR][1000 genomes]
rs6737021	0.85[EUR][1000 genomes]
rs6737862	0.85[EUR][1000 genomes]
rs6750094	0.85[EUR][1000 genomes]
rs6751535	0.81[EUR][1000 genomes]
rs6754905	0.85[EUR][1000 genomes]
rs6758775	0.85[EUR][1000 genomes]
rs6759533	0.85[EUR][1000 genomes]
rs72897836	0.81[EUR][1000 genomes]
rs72897840	0.81[EUR][1000 genomes]
rs72897842	0.81[EUR][1000 genomes]
rs72897853	0.81[EUR][1000 genomes]
rs72897876	0.85[EUR][1000 genomes]
rs72897882	0.83[AMR][1000 genomes]
rs72897891	0.83[AMR][1000 genomes]
rs72897892	0.83[AMR][1000 genomes]
rs72897894	0.83[AMR][1000 genomes]
rs72897896	0.83[AMR][1000 genomes]
rs72897899	0.83[AMR][1000 genomes]
rs72897902	0.83[AMR][1000 genomes]
rs72898229	0.85[EUR][1000 genomes]
rs72898237	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72898238	0.85[EUR][1000 genomes]
rs72898259	0.81[EUR][1000 genomes]
rs72898265	0.81[EUR][1000 genomes]
rs72899865	0.83[AMR][1000 genomes]
rs72899867	0.83[AMR][1000 genomes]
rs72899871	0.83[AMR][1000 genomes]
rs72899873	0.83[AMR][1000 genomes]
rs72899877	0.83[AMR][1000 genomes]
rs72899878	0.83[AMR][1000 genomes]
rs72899881	0.83[AMR][1000 genomes]
rs72899883	0.83[AMR][1000 genomes]
rs72899885	1.00[AMR][1000 genomes]
rs72899889	1.00[AMR][1000 genomes]
rs72899891	1.00[AMR][1000 genomes]
rs72899893	0.83[AMR][1000 genomes]
rs72899896	1.00[AMR][1000 genomes]
rs72899898	1.00[AMR][1000 genomes]
rs72899901	1.00[AMR][1000 genomes]
rs72901713	1.00[AMR][1000 genomes]
rs72901720	1.00[AMR][1000 genomes]
rs72901721	1.00[AMR][1000 genomes]
rs72901727	1.00[AMR][1000 genomes]
rs72901729	1.00[AMR][1000 genomes]
rs72901731	1.00[AMR][1000 genomes]
rs72901736	1.00[AMR][1000 genomes]
rs72901741	1.00[AMR][1000 genomes]
rs72901767	1.00[AMR][1000 genomes]
rs72901774	1.00[AMR][1000 genomes]
rs72909015	1.00[AMR][1000 genomes]
rs73919125	0.81[EUR][1000 genomes]
rs73919132	0.85[EUR][1000 genomes]
rs9679075	0.81[EUR][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	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	nsv1004702	chr2:21874266-21934331	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv581171	chr2:21897192-21952204	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	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	chr2:21923400-21927400	Enhancers	Fetal Heart	heart

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