Variant report

Variant	rs11124443
Chromosome Location	chr2:35710649-35710650
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	chr2:35694136..35697118-chr2:35710618..35713142,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000265301	Chromatin interaction
ENSG00000207255	Chromatin interaction
ENSG00000229013	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10495840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11124444	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11124445	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11675868	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11689864	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11692039	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12185698	1.00[CEU][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12464263	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17327905	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17399995	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17469349	0.80[AMR][1000 genomes]
rs62143281	0.80[AMR][1000 genomes]
rs62143282	0.90[AMR][1000 genomes]
rs62143283	0.80[AMR][1000 genomes]
rs62143287	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62143289	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62143291	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62143294	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62143295	0.80[AMR][1000 genomes]
rs62143296	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62143297	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62143298	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62143299	0.80[AMR][1000 genomes]
rs62143300	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62143301	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62143302	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62143303	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62143561	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62143562	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62146622	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62146628	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62146647	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62146649	0.90[EUR][1000 genomes]
rs62146650	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	nsv1014577	chr2:35672382-35714924	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
8	nsv873849	chr2:35684885-35717239	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
9	esv2762480	chr2:35697479-35714936	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv523461	chr2:35702533-35713309	ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	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

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links