Variant report

Variant	rs7158489
Chromosome Location	chr14:80190707-80190708
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10129446	0.86[CEU][hapmap]
rs11845174	0.86[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs12431759	0.89[CEU][hapmap]
rs12434821	0.81[CHB][hapmap]
rs12435036	0.96[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap]
rs12435099	0.86[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs1861088	0.89[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap]
rs2192422	0.81[CEU][hapmap]
rs2192423	0.81[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2192426	0.86[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs2215839	0.92[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.93[YRI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2215840	0.81[CHB][hapmap]
rs4899749	0.89[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap]
rs55712116	0.84[AFR][1000 genomes]
rs7143192	0.86[CEU][hapmap];0.90[JPT][hapmap]
rs7148264	0.89[CEU][hapmap]
rs7155520	0.89[CEU][hapmap]
rs8018724	0.89[CEU][hapmap];0.89[JPT][hapmap]

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	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv902113	chr14:80172094-80929699	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr14:80171400-80232800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:80178200-80196200	Weak transcription	Aorta	Aorta

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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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