Variant report

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:53052952..53054757-chr20:53071357..53073043,2	MCF-7	breast:
2	chr20:53059121..53062054-chr20:53071334..53072998,2	MCF-7	breast:
3	chr20:53069456..53072072-chr20:53072246..53075486,5	MCF-7	breast:
4	chr20:53071107..53073077-chr20:53258088..53260075,2	MCF-7	breast:
5	chr20:53062391..53065674-chr20:53071896..53077511,6	MCF-7	breast:
6	chr20:53072717..53074828-chr20:53100189..53102033,2	MCF-7	breast:
7	chr20:53072388..53074660-chr20:53151314..53154004,2	MCF-7	breast:
8	chr20:53067710..53071026-chr20:53071242..53075338,6	MCF-7	breast:
9	chr20:53065974..53067555-chr20:53070867..53073344,2	MCF-7	breast:
10	chr20:52835069..52840886-chr20:53069895..53074543,8	MCF-7	breast:
11	chr20:52740095..52740996-chr20:53072761..53073363,2	MCF-7	breast:
12	chr20:52909396..52910234-chr20:53072554..53073122,2	MCF-7	breast:
13	chr17:57916329..57918216-chr20:53071161..53073624,2	MCF-7	breast:
14	chr20:53067721..53069339-chr20:53072421..53074110,2	MCF-7	breast:
15	chr20:53072470..53073317-chr20:53266144..53266676,2	MCF-7	breast:
16	chr20:53071006..53073926-chr20:53086546..53089088,2	MCF-7	breast:
17	chr20:52844972..52848737-chr20:53072489..53075619,3	MCF-7	breast:
18	chr20:52956974..52957575-chr20:53072780..53073669,2	MCF-7	breast:
19	chr1:121483247..121486373-chr20:53072094..53074537,3	MCF-7	breast:
20	chr20:52823572..52826255-chr20:53070160..53074731,6	MCF-7	breast:
21	chr17:57913216..57918215-chr20:53071385..53076624,7	MCF-7	breast:
22	chr20:52823596..52826138-chr20:53070146..53074337,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000062716	Chromatin interaction
ENSG00000101132	Chromatin interaction

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1477739	1.00[EUR][1000 genomes]
rs16999399	1.00[EUR][1000 genomes]
rs16999732	1.00[EUR][1000 genomes]
rs2219732	1.00[EUR][1000 genomes]
rs2426520	1.00[EUR][1000 genomes]
rs2426521	1.00[EUR][1000 genomes]
rs2616329	1.00[EUR][1000 genomes]
rs2616331	1.00[EUR][1000 genomes]
rs2616334	1.00[EUR][1000 genomes]
rs2616337	1.00[EUR][1000 genomes]
rs2797969	1.00[EUR][1000 genomes]
rs56977264	1.00[EUR][1000 genomes]
rs57927391	1.00[EUR][1000 genomes]
rs6014025	1.00[EUR][1000 genomes]
rs60215168	1.00[EUR][1000 genomes]
rs6023260	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6023271	1.00[EUR][1000 genomes]
rs6091909	1.00[EUR][1000 genomes]
rs6097991	1.00[EUR][1000 genomes]
rs6097995	0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61495423	1.00[EUR][1000 genomes]
rs62214388	1.00[EUR][1000 genomes]
rs793039	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
2	nsv834011	chr20:52858341-53086042	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv834012	chr20:52921007-53097177	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

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

No data

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