Variant report

Variant	rs7788304
Chromosome Location	chr7:80858011-80858012
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:80852495..80856208-chr7:80856677..80858955,3	K562	blood:

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

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1509917	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1509922	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs179173	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs186609	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2079435	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2136610	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2367229	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs327644	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs327647	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs327649	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs327712	0.93[EUR][1000 genomes]
rs327716	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs327718	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs327719	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs327720	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs327723	0.95[EUR][1000 genomes]
rs327733	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs327734	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs327735	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs327736	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs327737	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs327738	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs327739	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs327742	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs327744	0.87[EUR][1000 genomes]
rs327745	0.87[EUR][1000 genomes]
rs327747	0.87[EUR][1000 genomes]
rs7798237	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7807571	0.94[AMR][1000 genomes];0.94[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	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
2	nsv831044	chr7:80721773-80918591	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv888557	chr7:80813081-80917148	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1023149	chr7:80817550-80928090	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1029034	chr7:80838012-81137146	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv831045	chr7:80841693-81012404	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv888558	chr7:80844667-80917148	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv607686	chr7:80857196-80917148	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80853800-80858800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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