Variant report

Variant	rs60042181
Chromosome Location	chr4:63045728-63045729
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs17226461	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17226496	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17292205	0.88[ASN][1000 genomes]
rs17292254	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2193117	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2193119	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2344676	0.90[ASN][1000 genomes]
rs2344679	0.81[ASN][1000 genomes]
rs2345596	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2881182	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34093205	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35398119	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41452945	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4452459	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4464599	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4508922	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4513599	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4623035	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4860453	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55738302	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56094818	0.91[ASN][1000 genomes]
rs56229538	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56287213	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56373590	0.90[ASN][1000 genomes]
rs56788324	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57737675	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58742242	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60443220	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60732848	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60951852	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61686752	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6817335	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6819199	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6841161	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6854221	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72498878	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7676995	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7698238	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879078	chr4:62923797-63054757	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1013327	chr4:62989426-63149048	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1012093	chr4:63014592-63568580	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537113	chr4:63014592-63568580	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv534618	chr4:63025655-63568620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv997505	chr4:63025663-63575696	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv594333	chr4:63025823-63467034	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv461378	chr4:63037324-63158560	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
9	nsv594334	chr4:63037324-63158560	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr4:63044200-63047400	Weak transcription	Left Ventricle	heart

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