Variant report

Variant	rs10495841
Chromosome Location	chr2:35727295-35727296
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:33621149..33624012-chr2:35726795..35729641,2	MCF-7	breast:
2	chr2:35721064..35722615-chr2:35725696..35727810,2	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11124437	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11124446	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11682230	0.94[ASN][1000 genomes]
rs11688061	0.95[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.90[YRI][hapmap];0.94[ASN][1000 genomes]
rs11693441	0.94[ASN][1000 genomes]
rs11693497	0.93[ASN][1000 genomes]
rs11695142	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12185690	0.98[ASN][1000 genomes]
rs17016746	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17016750	1.00[CEU][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17016797	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4313955	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4399704	0.98[ASN][1000 genomes]
rs4425057	0.88[JPT][hapmap];0.96[ASN][1000 genomes]
rs4619588	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.85[YRI][hapmap];0.98[ASN][1000 genomes]
rs5013113	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5013114	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5013115	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5013116	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5013117	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5013118	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5013119	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5013122	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55728744	0.94[ASN][1000 genomes]
rs56001730	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs56051086	0.90[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs56053627	0.94[ASN][1000 genomes]
rs56235036	0.86[ASN][1000 genomes]
rs56305920	0.88[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs56665199	0.90[ASN][1000 genomes]
rs57242898	0.92[ASN][1000 genomes]
rs58358221	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6749401	0.98[ASN][1000 genomes]
rs72796501	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72796502	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010722	chr2:35072575-35950219	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv519522	chr2:35425529-35861883	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1008651	chr2:35469467-35896486	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv999139	chr2:35483033-35860024	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv535636	chr2:35483033-35860024	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	nsv873848	chr2:35641532-35973963	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949472	chr2:35709203-36447481	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv518450	chr2:35711861-35779358	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35725800-35728000	Enhancers	HUVEC	blood vessel
2	chr2:35727000-35728200	Weak transcription	HMEC	breast
3	chr2:35727200-35728400	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links