Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10166052	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs10168850	0.85[CEU][hapmap]
rs10194811	0.86[CEU][hapmap]
rs11675580	0.84[CEU][hapmap]
rs11678974	0.80[EUR][1000 genomes]
rs11894208	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs12694281	0.89[CEU][hapmap]
rs13389790	0.85[CEU][hapmap]
rs1354617	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs1505369	0.95[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1505376	0.96[CEU][hapmap];0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1546371	0.89[CEU][hapmap]
rs17325842	0.89[CEU][hapmap]
rs1847671	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2062930	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs2170529	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs2220024	0.83[EUR][1000 genomes]
rs2371576	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2860080	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs55992489	0.86[EUR][1000 genomes]
rs6435705	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6723878	0.92[CEU][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6731193	0.96[CEU][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6735807	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs974968	1.00[CEU][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834527	chr2:213115966-213334308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1014680	chr2:213142147-213301614	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	esv34076	chr2:213298576-213306627	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213299400-213302200	Weak transcription	Fetal Heart	heart

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