Variant report

Variant	rs10259156
Chromosome Location	chr7:126912550-126912551
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-13	chr7:126912402-126913094	NONHSAT123133

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10226369	1.00[ASN][1000 genomes]
rs10226675	1.00[JPT][hapmap]
rs10227769	1.00[JPT][hapmap]
rs10234721	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10234740	1.00[JPT][hapmap]
rs10241965	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10243967	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10259050	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10261152	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10273755	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10280829	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11563676	1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs1419388	1.00[ASN][1000 genomes]
rs17863250	1.00[JPT][hapmap]
rs17864174	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17864176	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17866743	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867800	1.00[ASN][1000 genomes]
rs17867807	1.00[CEU][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17875093	0.85[AMR][1000 genomes]
rs3779537	1.00[JPT][hapmap]
rs6947960	1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs6961760	1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs6961944	1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs7805944	1.00[JPT][hapmap]
rs7806403	1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]

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	nsv889189	chr7:126699088-126963028	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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