Variant report

Variant	rs9849457
Chromosome Location	chr3:134121421-134121422
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10222468	0.80[EUR][1000 genomes]
rs2133306	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs3846051	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs3913264	0.90[EUR][1000 genomes]
rs4974503	0.99[EUR][1000 genomes]
rs4998531	0.86[EUR][1000 genomes]
rs55875738	0.87[EUR][1000 genomes]
rs6771287	0.86[EUR][1000 genomes]
rs6783899	0.88[EUR][1000 genomes]
rs7624209	1.00[CEU][hapmap]
rs9289470	0.87[CEU][hapmap]
rs9812855	0.87[EUR][1000 genomes]
rs9829949	0.88[EUR][1000 genomes]
rs9842071	0.86[EUR][1000 genomes]
rs9879839	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3522171	chr3:133889405-134156571	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv3522172	chr3:133889405-134156571	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134116000-134125000	Weak transcription	Right Ventricle	heart
2	chr3:134121400-134122000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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