Variant report

Variant	rs11014631
Chromosome Location	chr10:25874515-25874516
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10458686	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10458706	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10764563	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10764564	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10764565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10764567	0.92[ASN][1000 genomes]
rs10828828	0.84[CHD][hapmap]
rs11014622	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs11014623	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs11014625	0.82[CEU][hapmap];0.85[GIH][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs11014629	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11014630	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12355530	0.87[EUR][1000 genomes]
rs12357174	0.81[GIH][hapmap]
rs12413247	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17557638	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs1855672	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1932147	0.91[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4237372	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs4237374	0.85[GIH][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs4747529	0.82[EUR][1000 genomes]
rs4747532	0.81[GIH][hapmap]
rs4747533	0.85[EUR][1000 genomes]
rs4749050	0.82[CEU][hapmap];0.85[GIH][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs58254885	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7897460	0.93[YRI][hapmap];0.82[AFR][1000 genomes]
rs7914813	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7914821	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7921299	0.81[GIH][hapmap]
rs976361	0.95[CEU][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes];0.99[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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv894972	chr10:25849998-25917909	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 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	chr10:25873800-25875000	Strong transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links