Variant report

Variant	rs73151734
Chromosome Location	chr7:80705741-80705742
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:80570369..80572451-chr7:80702280..80705942,3	MCF-7	breast:
2	chr7:80546160..80553330-chr7:80697243..80707851,28	MCF-7	breast:
3	chr7:80657944..80659650-chr7:80705154..80707062,2	K562	blood:
4	chr7:80545266..80555113-chr7:80701488..80708340,14	MCF-7	breast:

Variant related genes	Relation type
ENSG00000075223	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10236945	1.00[EUR][1000 genomes]
rs12669751	1.00[EUR][1000 genomes]
rs12672157	1.00[EUR][1000 genomes]
rs12673730	1.00[EUR][1000 genomes]
rs28844431	1.00[EUR][1000 genomes]
rs35411400	1.00[EUR][1000 genomes]
rs56106210	1.00[EUR][1000 genomes]
rs56118406	1.00[EUR][1000 genomes]
rs56170251	1.00[EUR][1000 genomes]
rs56768210	1.00[EUR][1000 genomes]
rs57142814	1.00[EUR][1000 genomes]
rs59980342	1.00[EUR][1000 genomes]
rs60118096	1.00[EUR][1000 genomes]
rs60727910	1.00[EUR][1000 genomes]
rs61698263	1.00[EUR][1000 genomes]
rs73134411	1.00[EUR][1000 genomes]
rs73134413	1.00[EUR][1000 genomes]
rs73136532	1.00[EUR][1000 genomes]
rs73136536	1.00[EUR][1000 genomes]
rs73136546	1.00[EUR][1000 genomes]
rs73136555	1.00[EUR][1000 genomes]
rs73136559	1.00[EUR][1000 genomes]
rs73136566	1.00[EUR][1000 genomes]
rs73136569	1.00[EUR][1000 genomes]
rs73136575	1.00[EUR][1000 genomes]
rs73136579	1.00[EUR][1000 genomes]
rs73136583	1.00[EUR][1000 genomes]
rs73141414	1.00[EUR][1000 genomes]
rs73141418	1.00[EUR][1000 genomes]
rs73141427	1.00[EUR][1000 genomes]
rs73147062	1.00[EUR][1000 genomes]
rs73147064	1.00[EUR][1000 genomes]
rs73147071	1.00[EUR][1000 genomes]
rs73147085	1.00[EUR][1000 genomes]
rs73147100	1.00[AFR][1000 genomes]
rs73149007	1.00[EUR][1000 genomes]
rs73149331	1.00[EUR][1000 genomes]
rs73149333	1.00[EUR][1000 genomes]
rs73149335	1.00[EUR][1000 genomes]
rs73149341	1.00[EUR][1000 genomes]
rs73149352	1.00[EUR][1000 genomes]
rs73149361	1.00[EUR][1000 genomes]
rs73149486	1.00[EUR][1000 genomes]
rs73149488	1.00[EUR][1000 genomes]
rs73149492	1.00[EUR][1000 genomes]
rs73149498	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73151191	1.00[EUR][1000 genomes]
rs73151194	1.00[EUR][1000 genomes]
rs73151225	1.00[EUR][1000 genomes]
rs73151238	1.00[EUR][1000 genomes]
rs73151244	1.00[EUR][1000 genomes]
rs73151246	1.00[EUR][1000 genomes]
rs73151250	1.00[EUR][1000 genomes]
rs73151703	1.00[EUR][1000 genomes]
rs73151726	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73151743	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73153111	1.00[EUR][1000 genomes]
rs73153114	1.00[EUR][1000 genomes]
rs73153120	1.00[EUR][1000 genomes]
rs73153125	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888524	chr7:80107798-80723062	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv888551	chr7:80620397-80723062	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv888552	chr7:80683308-80755310	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv888553	chr7:80683308-80766407	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv888554	chr7:80695828-80755310	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv888555	chr7:80695828-80766407	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv888556	chr7:80695828-80797794	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80705200-80706200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:80705400-80706000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:80705600-80706200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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