Variant report

Variant	rs1005431
Chromosome Location	chr2:50682462-50682463
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10048731	0.91[CEU][hapmap];0.94[MEX][hapmap];0.86[TSI][hapmap];0.92[EUR][1000 genomes]
rs10181475	0.86[EUR][1000 genomes]
rs10181522	0.83[MEX][hapmap]
rs10182951	0.93[EUR][1000 genomes]
rs10190857	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11125306	0.91[CEU][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12473243	0.95[CEU][hapmap];0.86[CHB][hapmap];0.83[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12475335	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12475979	0.83[MEX][hapmap]
rs12613343	0.95[CEU][hapmap];0.92[EUR][1000 genomes]
rs12619946	0.87[CEU][hapmap];0.86[CHB][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12620045	0.93[EUR][1000 genomes]
rs12713098	0.83[MEX][hapmap]
rs12713100	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13014251	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13390864	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.92[EUR][1000 genomes]
rs13392422	0.83[MEX][hapmap]
rs13396103	0.91[CEU][hapmap];0.86[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap];0.89[MEX][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13407013	0.92[EUR][1000 genomes]
rs13407657	0.91[CEU][hapmap];0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.90[EUR][1000 genomes]
rs13407788	0.91[EUR][1000 genomes]
rs1520437	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1520438	0.92[EUR][1000 genomes]
rs1520439	0.91[CEU][hapmap];0.86[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1533692	0.80[EUR][1000 genomes]
rs17040600	0.83[MEX][hapmap]
rs17040640	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.93[EUR][1000 genomes]
rs1818715	0.83[MEX][hapmap]
rs1851012	0.95[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap]
rs1971698	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2160443	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.93[EUR][1000 genomes]
rs34846571	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6709865	0.91[CEU][hapmap];0.84[JPT][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];0.92[EUR][1000 genomes]
rs6711307	0.95[CEU][hapmap];0.86[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.93[EUR][1000 genomes]
rs6717441	0.95[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6718809	0.92[EUR][1000 genomes]
rs6738086	0.91[CEU][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6743117	1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6743562	0.92[EUR][1000 genomes]
rs6743584	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.93[EUR][1000 genomes]
rs6744418	0.92[EUR][1000 genomes]
rs6747128	0.95[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs6747258	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.92[EUR][1000 genomes]
rs6756081	0.95[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.92[EUR][1000 genomes]
rs6756219	0.95[CEU][hapmap];0.86[CHB][hapmap];0.93[CHD][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6756479	0.95[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs7423850	0.91[CEU][hapmap];0.86[CHB][hapmap];0.83[JPT][hapmap]
rs7585229	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7585534	0.92[EUR][1000 genomes]
rs9309182	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948548	chr2:50569117-50695100	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv948361	chr2:50611076-50785178	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv933786	chr2:50628354-50780185	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1010510	chr2:50649641-51011565	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv535694	chr2:50649641-51011565	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv532650	chr2:50675808-51136752	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv491644	chr2:50680795-50892906	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv498102	chr2:50680795-50937503	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv934040	chr2:50681850-50711452	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50673800-50684200	Weak transcription	Fetal Brain Male	brain
2	chr2:50677400-50683200	Weak transcription	Brain Germinal Matrix	brain

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