Variant report

Variant	rs2511265
Chromosome Location	chr11:73488287-73488288
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:73481369..73483674-chr11:73488207..73490492,2	K562	blood:
2	chr11:73371040..73373257-chr11:73488206..73490585,3	MCF-7	breast:
3	chr11:73470195..73474536-chr11:73485650..73492680,30	MCF-7	breast:

Variant related genes	Relation type
ENSG00000021300	Chromatin interaction
ENSG00000256034	Chromatin interaction
ENSG00000175582	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10898944	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11235903	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12293194	0.86[AFR][1000 genomes]
rs1525750	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1525751	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1621654	0.89[AFR][1000 genomes]
rs1624231	0.88[AMR][1000 genomes]
rs1670548	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1723834	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1723838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1723839	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1723842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1723844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1723845	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1723846	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1723849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1792157	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1792195	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1792196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1880642	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1880643	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1976914	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2037706	0.81[EUR][1000 genomes]
rs2037709	0.92[EUR][1000 genomes]
rs2056649	0.96[EUR][1000 genomes]
rs2366944	0.92[EUR][1000 genomes]
rs2444600	0.82[AFR][1000 genomes]
rs2462617	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2511263	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2511269	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2515091	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4548648	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4551800	0.83[AFR][1000 genomes]
rs4944026	0.92[EUR][1000 genomes]
rs4944027	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs4944030	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs4944854	0.81[EUR][1000 genomes]
rs4944857	0.92[EUR][1000 genomes]
rs4944859	0.90[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs4944860	0.96[EUR][1000 genomes]
rs4944864	0.90[EUR][1000 genomes]
rs4944865	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6592528	0.81[EUR][1000 genomes]
rs6592529	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7396121	0.92[EUR][1000 genomes]
rs7942515	0.92[EUR][1000 genomes]
rs7950472	0.86[AFR][1000 genomes]
rs940831	0.92[EUR][1000 genomes]
rs9634024	0.90[AFR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530624	chr11:73114283-73646329	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv492091	chr11:73285970-73844424	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
3	nsv1045149	chr11:73314565-73581908	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv530641	chr11:73358393-73638725	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	esv3426251	chr11:73461503-73538032	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73481800-73489800	Weak transcription	A549	lung
2	chr11:73482000-73489600	Weak transcription	Hela-S3	cervix
3	chr11:73484600-73489600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:73484600-73489800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:73485400-73489600	Weak transcription	GM12878-XiMat	blood
6	chr11:73486400-73490200	Weak transcription	Thymus	Thymus
7	chr11:73487200-73490200	Weak transcription	Right Atrium	heart
8	chr11:73487400-73489400	Weak transcription	K562	blood
9	chr11:73487400-73489600	Weak transcription	HepG2	liver

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