Variant report

Variant	rs706553
Chromosome Location	chr7:136855232-136855233
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10488605	1.00[ASN][1000 genomes]
rs10488606	1.00[JPT][hapmap]
rs11982570	0.92[ASN][1000 genomes]
rs12707345	0.92[ASN][1000 genomes]
rs17168934	0.92[ASN][1000 genomes]
rs17168947	0.92[ASN][1000 genomes]
rs17168990	1.00[JPT][hapmap]
rs17169018	1.00[JPT][hapmap]
rs1839780	1.00[JPT][hapmap]
rs2017578	1.00[CHB][hapmap]
rs33914231	1.00[ASN][1000 genomes]
rs35119148	0.92[ASN][1000 genomes]
rs35655262	0.92[ASN][1000 genomes]
rs35695483	0.92[ASN][1000 genomes]
rs36110794	0.92[ASN][1000 genomes]
rs4338046	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs66483613	1.00[ASN][1000 genomes]
rs66709830	1.00[ASN][1000 genomes]
rs67751562	0.92[ASN][1000 genomes]
rs6956523	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs727185	1.00[JPT][hapmap]
rs73450814	0.92[ASN][1000 genomes]
rs73450817	0.92[ASN][1000 genomes]
rs7804134	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1028902	chr7:136727136-136858804	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv464730	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv608463	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv831149	chr7:136831665-137006468	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1034546	chr7:136832263-136858804	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136855000-136860600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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