Variant report

Variant	rs584147
Chromosome Location	chr1:57737411-57737412
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:57729389..57732670-chr1:57736869..57739478,3	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1149628	0.95[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs1424473	0.88[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1910690	0.97[ASN][1000 genomes]
rs197625	0.95[ASN][1000 genomes]
rs197626	1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs197638	1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs197644	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs197645	0.95[ASN][1000 genomes]
rs197649	0.97[ASN][1000 genomes]
rs2251472	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs2656093	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2656094	1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs2656095	0.81[JPT][hapmap]
rs2764664	0.85[MEX][hapmap]
rs2764665	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs486809	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs487566	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs488405	0.97[ASN][1000 genomes]
rs492781	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.91[ASN][1000 genomes]
rs492905	0.97[ASN][1000 genomes]
rs493846	0.97[ASN][1000 genomes]
rs499397	1.00[CHB][hapmap];0.86[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs511707	0.81[JPT][hapmap]
rs515802	0.97[ASN][1000 genomes]
rs529527	0.95[ASN][1000 genomes]
rs537441	0.90[ASN][1000 genomes]
rs539229	0.94[ASN][1000 genomes]
rs542873	1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs542949	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs561531	0.81[JPT][hapmap]
rs572092	1.00[CHB][hapmap];0.93[CHD][hapmap];0.89[JPT][hapmap];0.97[ASN][1000 genomes]
rs587046	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs593154	0.97[ASN][1000 genomes]
rs595513	0.95[MEX][hapmap];0.83[TSI][hapmap]
rs595568	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs596784	0.86[MEX][hapmap]
rs597941	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.87[ASN][1000 genomes]
rs611276	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs614488	1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs620214	1.00[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs627489	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs627550	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs627936	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs634391	0.81[JPT][hapmap];0.81[MEX][hapmap]
rs642526	0.81[JPT][hapmap]
rs643382	0.81[MEX][hapmap];0.83[TSI][hapmap]
rs648607	0.86[MEX][hapmap]
rs655277	0.97[ASN][1000 genomes]
rs657612	0.89[ASN][1000 genomes]
rs659069	0.86[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs663975	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.83[TSI][hapmap];0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs66894620	0.93[ASN][1000 genomes]
rs669931	0.94[ASN][1000 genomes]
rs674966	0.85[MEX][hapmap]
rs675075	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs686702	0.97[ASN][1000 genomes]
rs693942	0.95[ASN][1000 genomes]
rs706385	1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.91[ASN][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	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2754702	chr1:57716116-57743244	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57735000-57740400	Strong transcription	Fetal Intestine Small	intestine
2	chr1:57735000-57742400	Weak transcription	Fetal Intestine Large	intestine
3	chr1:57735200-57747200	Weak transcription	Esophagus	oesophagus
4	chr1:57735400-57737600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr1:57736000-57738400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:57736400-57737600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:57737000-57737600	Flanking Active TSS	Liver	Liver
8	chr1:57737200-57737600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
9	chr1:57737200-57738000	Weak transcription	Brain Angular Gyrus	brain
10	chr1:57737400-57741400	Weak transcription	Fetal Brain Male	brain
11	chr1:57737400-57746800	Weak transcription	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links