Variant report

No.	Distal block	Cell Line	Cell type
1	chr15:53093578..53096252-chr15:53138309..53141218,2	MCF-7	breast:
2	chr15:53140110..53140838-chr5:122040574..122041537,2	MCF-7	breast:
3	chr15:53139577..53141179-chr15:53147410..53150139,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251538	Chromatin interaction

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12232305	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17709181	0.85[ASN][1000 genomes]
rs2120440	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2120441	0.81[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs2440356	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2456509	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2456510	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28415452	0.92[ASN][1000 genomes]
rs28449533	0.87[ASN][1000 genomes]
rs28489650	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28556805	0.93[ASN][1000 genomes]
rs28566485	0.92[ASN][1000 genomes]
rs28624935	0.88[ASN][1000 genomes]
rs28663272	0.92[EUR][1000 genomes]
rs28713382	0.85[ASN][1000 genomes]
rs56346629	0.84[ASN][1000 genomes]
rs56710422	0.88[ASN][1000 genomes]
rs57094771	0.82[ASN][1000 genomes]
rs57960122	0.88[ASN][1000 genomes]
rs58028943	0.90[ASN][1000 genomes]
rs60407782	0.88[ASN][1000 genomes]
rs60882420	0.88[ASN][1000 genomes]
rs61364465	0.84[ASN][1000 genomes]
rs6493586	0.92[ASN][1000 genomes]
rs7176412	0.94[CHB][hapmap];0.84[ASN][1000 genomes]
rs731607	0.86[ASN][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	nsv471245	chr15:52607262-53187165	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv1041421	chr15:52661342-53148286	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1046970	chr15:53065114-53142386	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a
4	nsv1538	chr15:53110785-53148080	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	nsv1038129	chr15:53111512-53142386	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No data

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