Variant report

Variant	rs6955524
Chromosome Location	chr7:14296948-14296949
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10263173	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12536803	0.90[ASN][1000 genomes]
rs12536819	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17710027	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1859729	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35198760	0.90[ASN][1000 genomes]
rs36095426	0.90[ASN][1000 genomes]
rs38261	0.82[ASN][1000 genomes]
rs38264	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs38265	0.82[ASN][1000 genomes]
rs38267	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs38268	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs38269	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs38270	0.82[ASN][1000 genomes]
rs38271	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs38272	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs38275	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs38276	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs38277	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs38278	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs38284	0.90[ASN][1000 genomes]
rs38285	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs38289	0.90[ASN][1000 genomes]
rs38290	0.90[ASN][1000 genomes]
rs40236	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs40450	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4719396	0.90[ASN][1000 genomes]
rs4721316	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6966405	0.82[ASN][1000 genomes]
rs6972707	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv8054	chr7:14294529-14299547	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6955524	VWDE	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14292400-14299400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:14293400-14297000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr7:14295400-14298000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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