Variant report

Variant	rs11183101
Chromosome Location	chr12:45932152-45932153
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	chr12:45929552..45932497-chr12:45935767..45937875,2	MCF-7	breast:
2	chr12:45932018..45945296-chr12:46116937..46125620,30	MCF-7	breast:

Variant related genes	Relation type
ENSG00000273015	Chromatin interaction
ENSG00000189079	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10785581	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10880808	0.84[EUR][1000 genomes]
rs10880809	0.85[EUR][1000 genomes]
rs10880810	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10880811	0.83[EUR][1000 genomes]
rs10880813	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10880814	0.81[EUR][1000 genomes]
rs10880815	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11183092	0.84[EUR][1000 genomes]
rs11183094	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11183098	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11183099	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11183100	0.83[EUR][1000 genomes]
rs11183102	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11183103	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11514430	0.85[EUR][1000 genomes]
rs11514431	0.83[EUR][1000 genomes]
rs2408249	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2897908	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3958762	0.88[EUR][1000 genomes]
rs4450222	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4606536	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4768631	0.85[EUR][1000 genomes]
rs4768633	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4768635	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55987675	0.83[EUR][1000 genomes]
rs56295584	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61923980	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7296623	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7297465	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7303050	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7960483	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7970315	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832395	chr12:45841765-46039297	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv691	chr12:45896295-45946455	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv1842210	chr12:45903118-45940761	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3443760	chr12:45913734-45935783	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45926200-45934400	Weak transcription	Thymus	Thymus
2	chr12:45926800-45933800	Weak transcription	Fetal Thymus	thymus

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