Variant report

Variant	rs11012602
Chromosome Location	chr10:21526369-21526370
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11012603	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012604	1.00[ASN][1000 genomes]
rs11012605	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11012609	0.83[ASN][1000 genomes]
rs11012610	0.83[ASN][1000 genomes]
rs11527738	0.84[EUR][1000 genomes]
rs11592695	0.97[EUR][1000 genomes]
rs11594881	0.97[EUR][1000 genomes]
rs11594971	0.97[EUR][1000 genomes]
rs11595400	0.97[EUR][1000 genomes]
rs11595448	0.97[EUR][1000 genomes]
rs11596876	0.97[EUR][1000 genomes]
rs11596900	0.97[EUR][1000 genomes]
rs1350787	0.84[EUR][1000 genomes]
rs35120966	0.97[EUR][1000 genomes]
rs35240427	0.97[EUR][1000 genomes]
rs35273599	0.97[EUR][1000 genomes]
rs7077481	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7085480	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7094627	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72798578	0.97[EUR][1000 genomes]
rs72798581	0.97[EUR][1000 genomes]
rs72798582	0.97[EUR][1000 genomes]
rs72798584	0.91[EUR][1000 genomes]
rs72798585	0.97[EUR][1000 genomes]
rs72798586	0.97[EUR][1000 genomes]
rs72798588	0.97[EUR][1000 genomes]
rs72798589	0.97[EUR][1000 genomes]
rs72798590	0.97[EUR][1000 genomes]
rs72798591	0.97[EUR][1000 genomes]
rs72798592	0.97[EUR][1000 genomes]
rs72798593	0.97[EUR][1000 genomes]
rs72798594	0.97[EUR][1000 genomes]
rs72798595	0.97[EUR][1000 genomes]
rs72798598	0.97[EUR][1000 genomes]
rs72798599	0.97[EUR][1000 genomes]
rs72798601	0.97[EUR][1000 genomes]
rs72798602	0.97[EUR][1000 genomes]
rs72800003	0.97[EUR][1000 genomes]
rs72800004	0.97[EUR][1000 genomes]
rs72800005	0.97[EUR][1000 genomes]
rs72800006	0.97[EUR][1000 genomes]
rs72800007	0.97[EUR][1000 genomes]
rs72800008	0.97[EUR][1000 genomes]
rs72800010	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72800011	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv971871	chr10:21460392-21579987	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21522000-21549600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr10:21522200-21549200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:21524000-21548000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:21524000-21549000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr10:21524000-21549400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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