Variant report

Variant	rs7015635
Chromosome Location	chr8:63113328-63113329
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10957215	0.88[CEU][hapmap];1.00[YRI][hapmap]
rs10957216	0.87[CEU][hapmap];1.00[YRI][hapmap]
rs12542544	0.85[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs13252146	0.80[EUR][1000 genomes]
rs13264311	0.81[EUR][1000 genomes]
rs1601056	0.95[ASN][1000 genomes]
rs16928600	0.80[EUR][1000 genomes]
rs16928602	0.80[EUR][1000 genomes]
rs16928605	0.80[EUR][1000 genomes]
rs34250977	0.84[ASN][1000 genomes]
rs4268118	0.86[ASN][1000 genomes]
rs4383956	0.86[ASN][1000 genomes]
rs4562310	0.84[ASN][1000 genomes]
rs4610738	0.84[ASN][1000 genomes]
rs4738938	0.86[ASN][1000 genomes]
rs6983440	0.81[EUR][1000 genomes]
rs7832144	0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016883	chr8:63110741-63171354	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr8:63112600-63115000	Weak transcription	Brain Germinal Matrix	brain
2	chr8:63112800-63113600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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

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