Variant report

Variant	rs9463363
Chromosome Location	chr6:13002629-13002630
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:13000472..13003227-chr6:13006605..13008195,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10807388	0.82[EUR][1000 genomes]
rs11757634	0.83[CHD][hapmap];0.93[GIH][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.85[AMR][1000 genomes]
rs11758659	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11961007	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11963982	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13207062	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34576660	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4132046	0.90[EUR][1000 genomes]
rs4236091	0.93[GIH][hapmap];0.95[MEX][hapmap];0.86[MKK][hapmap];0.84[TSI][hapmap];0.84[AMR][1000 genomes]
rs4236097	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4349811	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4367379	0.81[EUR][1000 genomes]
rs4380742	0.88[AMR][1000 genomes]
rs4432976	0.82[CHD][hapmap]
rs4492189	0.89[EUR][1000 genomes]
rs4711899	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4715016	0.83[CHD][hapmap];0.93[GIH][hapmap];0.86[LWK][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.87[AMR][1000 genomes]
rs4715023	0.83[CHD][hapmap];0.93[GIH][hapmap];0.95[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes]
rs4715032	0.88[AMR][1000 genomes]
rs4715043	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4715045	0.81[JPT][hapmap]
rs4715048	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6458568	0.86[AMR][1000 genomes]
rs6899754	0.85[CHD][hapmap];0.93[GIH][hapmap];0.86[LWK][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.87[AMR][1000 genomes]
rs6900619	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6901563	0.81[ASW][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];0.82[LWK][hapmap];0.95[MEX][hapmap];0.80[MKK][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6916268	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6920970	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6924689	0.88[CEU][hapmap];0.83[CHD][hapmap];0.87[TSI][hapmap];0.89[EUR][1000 genomes]
rs7341250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7739717	0.87[AMR][1000 genomes]
rs7743219	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7760857	0.83[AMR][1000 genomes]
rs7762881	0.80[ASW][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.84[MKK][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes]
rs7770277	0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes]
rs7774403	0.81[AMR][1000 genomes]
rs7774775	0.87[AMR][1000 genomes]
rs9296556	0.87[AMR][1000 genomes]
rs9296580	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9369759	0.91[EUR][1000 genomes]
rs9369760	0.89[EUR][1000 genomes]
rs9369768	0.86[CHD][hapmap];0.80[TSI][hapmap];0.81[EUR][1000 genomes]
rs9369815	0.82[CHD][hapmap]
rs9381636	0.80[ASW][hapmap];0.88[CEU][hapmap];0.89[CHD][hapmap];0.83[GIH][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs9395335	0.90[EUR][1000 genomes]
rs9463337	0.88[AMR][1000 genomes]
rs9463364	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9473113	0.87[AMR][1000 genomes]
rs9473120	0.88[AMR][1000 genomes]
rs9473156	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9473188	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9473198	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9473285	0.86[CHB][hapmap]
rs9473486	0.82[CHD][hapmap]

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	esv3521000	chr6:12561306-13128519	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3521001	chr6:12561306-13128519	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv817350	chr6:12922859-13137655	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv600992	chr6:12961922-13218549	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv981047	chr6:13000303-13002675	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3413947	chr6:13002566-13005664	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12988800-13006000	Weak transcription	Aorta	Aorta
2	chr6:12995600-13004400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:12997400-13011000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:13000200-13004400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:13000400-13004600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:13000600-13002800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:13001600-13003200	Enhancers	Fetal Heart	heart
8	chr6:13001800-13003200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:13002000-13003000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr6:13002200-13003000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:13002400-13003200	Enhancers	Fetal Brain Female	brain
12	chr6:13002400-13003400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:13002600-13006400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links