Variant report

Variant	rs929243
Chromosome Location	chr7:27453712-27453713
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10232941	0.97[ASN][1000 genomes]
rs10252971	0.91[ASN][1000 genomes]
rs10268859	0.96[ASN][1000 genomes]
rs10951165	1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[ASN][1000 genomes]
rs11520770	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs11563380	1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs11563567	1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs11978918	1.00[CHB][hapmap];0.84[CHD][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs12667419	0.92[ASN][1000 genomes]
rs12668112	0.86[ASN][1000 genomes]
rs12672272	0.96[ASN][1000 genomes]
rs17429361	0.91[CHB][hapmap]
rs17429641	1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs17429648	1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs17439000	0.91[CHB][hapmap]
rs17439221	1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs17439235	1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs17439374	0.94[ASN][1000 genomes]
rs2074336	0.93[ASN][1000 genomes]
rs2074337	0.91[ASN][1000 genomes]
rs2074338	0.91[ASN][1000 genomes]
rs2893286	0.96[ASN][1000 genomes]
rs4298409	1.00[CHB][hapmap];0.84[CHD][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs4470906	1.00[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs4529360	0.89[ASN][1000 genomes]
rs4719891	0.88[ASN][1000 genomes]
rs58842477	0.93[ASN][1000 genomes]
rs6953463	0.90[ASN][1000 genomes]
rs6957441	1.00[CHB][hapmap];0.88[CHD][hapmap];0.91[ASN][1000 genomes]
rs6957649	1.00[CHB][hapmap];0.91[CHD][hapmap];0.91[ASN][1000 genomes]
rs7798437	0.90[ASN][1000 genomes]
rs929242	1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[ASN][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	nsv531024	chr7:27194426-27461954	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
2	nsv830930	chr7:27395838-27587355	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27444800-27458000	Weak transcription	Pancreas	Pancrea
2	chr7:27444800-27458000	Weak transcription	Stomach Mucosa	stomach
3	chr7:27453200-27454200	Enhancers	Fetal Lung	lung

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