Variant report

Variant	rs1934849
Chromosome Location	chr13:62277021-62277022
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10507672	0.92[ASN][1000 genomes]
rs10507673	0.92[ASN][1000 genomes]
rs12583397	0.92[ASN][1000 genomes]
rs12585168	0.83[ASN][1000 genomes]
rs12864912	0.92[ASN][1000 genomes]
rs12868112	0.83[ASN][1000 genomes]
rs12868360	0.83[ASN][1000 genomes]
rs12868573	0.83[ASN][1000 genomes]
rs12870568	0.88[ASN][1000 genomes]
rs12873399	0.92[ASN][1000 genomes]
rs1340799	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1340800	0.89[EUR][1000 genomes]
rs1417463	0.87[EUR][1000 genomes]
rs1417464	0.92[ASN][1000 genomes]
rs17060246	0.92[ASN][1000 genomes]
rs2153566	0.88[EUR][1000 genomes]
rs2153567	0.86[EUR][1000 genomes]
rs2153568	0.89[EUR][1000 genomes]
rs2323482	0.92[EUR][1000 genomes]
rs2875069	0.86[EUR][1000 genomes]
rs34266436	0.92[ASN][1000 genomes]
rs34289387	0.92[ASN][1000 genomes]
rs34580180	0.86[ASN][1000 genomes]
rs34690958	0.92[ASN][1000 genomes]
rs4483753	0.87[EUR][1000 genomes]
rs4884396	0.92[EUR][1000 genomes]
rs4886366	0.87[EUR][1000 genomes]
rs4886367	0.92[EUR][1000 genomes]
rs4886368	0.92[ASN][1000 genomes]
rs4886371	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs4886372	0.84[EUR][1000 genomes]
rs4886373	0.87[EUR][1000 genomes]
rs4886374	0.89[EUR][1000 genomes]
rs67276133	0.92[ASN][1000 genomes]
rs73217927	0.92[ASN][1000 genomes]
rs7328627	0.87[EUR][1000 genomes]
rs7328967	0.87[EUR][1000 genomes]
rs7333956	0.85[EUR][1000 genomes]
rs7988690	0.88[EUR][1000 genomes]
rs7994543	0.89[EUR][1000 genomes]
rs7995118	0.89[EUR][1000 genomes]
rs7995227	0.89[EUR][1000 genomes]
rs7998919	0.84[EUR][1000 genomes]
rs9528394	0.89[EUR][1000 genomes]
rs9539271	0.92[EUR][1000 genomes]
rs9539275	0.92[EUR][1000 genomes]
rs9539298	0.89[EUR][1000 genomes]
rs9539299	0.89[EUR][1000 genomes]
rs9598348	0.91[EUR][1000 genomes]
rs9598356	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv900250	chr13:62147535-62321073	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62271800-62277800	Weak transcription	Left Ventricle	heart

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