Variant report

Variant	rs10200604
Chromosome Location	chr2:56575020-56575021
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10172020	0.92[CHB][hapmap]
rs10175691	0.92[CHB][hapmap]
rs11886381	0.92[CHB][hapmap]
rs11893331	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12467246	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13021782	0.85[CHB][hapmap]
rs13389344	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs13393981	0.93[EUR][1000 genomes]
rs1549031	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs17047851	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs17047854	0.94[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];0.81[EUR][1000 genomes]
rs17047856	0.92[CHB][hapmap]
rs17268785	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];0.80[EUR][1000 genomes]
rs4671278	0.83[CHB][hapmap]
rs4672106	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs4672110	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56140649	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6545572	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];0.86[TSI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6545574	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs6704684	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs6714635	0.85[CHB][hapmap]
rs6735003	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.92[GIH][hapmap];0.86[TSI][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6747380	0.94[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];0.81[EUR][1000 genomes]
rs6748308	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6756427	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6760269	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7355411	0.92[CHB][hapmap];0.83[CHD][hapmap];0.93[JPT][hapmap]
rs7562381	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.92[GIH][hapmap];0.86[TSI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7566597	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs7573049	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7602657	0.84[EUR][1000 genomes]
rs9309278	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530516	chr2:56447922-56633505	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv874170	chr2:56496589-56590865	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv834093	chr2:56538097-56708677	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1004449	chr2:56538460-56715861	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv874171	chr2:56545845-56727178	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv582032	chr2:56551074-56599354	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10200604	RPL23AP32	cis	parietal	SCAN

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56560600-56575400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:56562400-56577600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr2:56566400-56575200	Weak transcription	Fetal Heart	heart
4	chr2:56567000-56575200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:56573600-56575200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:56574600-56586400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:56575000-56575800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:56575000-56575800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:56575000-56575800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr2:56575000-56576000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:56575000-56576000	Strong transcription	HSMM	muscle
12	chr2:56575000-56576200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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