Variant report

Variant	rs13430619
Chromosome Location	chr2:213332570-213332571
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10166052	0.96[EUR][1000 genomes]
rs10168850	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10194811	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11675580	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11678974	0.96[EUR][1000 genomes]
rs11894208	0.87[EUR][1000 genomes]
rs13015808	0.83[ASN][1000 genomes]
rs13389790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1354617	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1505369	0.89[EUR][1000 genomes]
rs1505372	0.84[ASN][1000 genomes]
rs1505376	0.89[EUR][1000 genomes]
rs16848556	0.87[ASN][1000 genomes]
rs16848564	0.87[ASN][1000 genomes]
rs16848571	0.87[ASN][1000 genomes]
rs16848593	1.00[ASN][1000 genomes]
rs17259208	0.91[ASN][1000 genomes]
rs17325821	0.83[ASN][1000 genomes]
rs17325842	0.96[EUR][1000 genomes]
rs1842767	0.95[EUR][1000 genomes]
rs1847671	0.89[EUR][1000 genomes]
rs2062930	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2101152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2128318	0.96[EUR][1000 genomes]
rs2170529	0.95[EUR][1000 genomes]
rs2220024	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2371576	0.88[EUR][1000 genomes]
rs2860080	0.96[EUR][1000 genomes]
rs55992489	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56009609	0.85[EUR][1000 genomes]
rs62186293	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6711080	0.82[EUR][1000 genomes]
rs6723878	0.90[EUR][1000 genomes]
rs6731193	0.86[EUR][1000 genomes]
rs6735807	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73079459	0.95[ASN][1000 genomes]
rs73079470	0.95[ASN][1000 genomes]
rs7575120	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs974968	0.81[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	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	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
3	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
4	nsv432024	chr2:213314899-213446726	Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:213328800-213334000	Weak transcription	Fetal Heart	heart

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