Variant report

Variant	rs9302358
Chromosome Location	chr15:92895457-92895458
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11074063	0.90[EUR][1000 genomes]
rs11634097	0.89[EUR][1000 genomes]
rs11637546	0.90[ASN][1000 genomes]
rs11857313	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16946777	0.89[EUR][1000 genomes]
rs17521083	0.89[EUR][1000 genomes]
rs17600009	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4777963	0.84[EUR][1000 genomes]
rs58243974	0.89[EUR][1000 genomes]
rs62019829	0.94[EUR][1000 genomes]
rs6496926	0.82[EUR][1000 genomes]
rs7166312	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7176079	0.84[EUR][1000 genomes]
rs7176571	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7181854	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7181934	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7183115	0.87[EUR][1000 genomes]
rs8027941	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1049561	chr15:92758434-93097965	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv1041582	chr15:92879844-92910306	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv869844	chr15:92881526-92935448	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3397348	chr15:92895384-92895669	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92888200-92899400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:92890400-92911800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:92894600-92895800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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