Variant report

Variant	rs4732106
Chromosome Location	chr7:80758187-80758188
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10234328	0.81[EUR][1000 genomes]
rs10239474	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10245648	0.86[ASN][1000 genomes]
rs10247169	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10265624	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10274106	0.88[ASN][1000 genomes]
rs10277023	0.87[EUR][1000 genomes]
rs10277984	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12534374	0.86[ASN][1000 genomes]
rs12538655	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12668893	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1528736	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1919369	0.84[AMR][1000 genomes]
rs2697219	0.87[EUR][1000 genomes]
rs2697221	0.87[ASN][1000 genomes]
rs2697222	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2697224	0.87[ASN][1000 genomes]
rs2697225	0.87[ASN][1000 genomes]
rs2697943	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2697944	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2697945	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2697946	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28627226	0.81[ASN][1000 genomes]
rs28715268	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28796047	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34344876	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35758038	0.81[EUR][1000 genomes]
rs35876610	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3843546	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3891957	0.81[EUR][1000 genomes]
rs3891958	0.81[EUR][1000 genomes]
rs4732107	0.81[EUR][1000 genomes]
rs58692795	0.81[EUR][1000 genomes]
rs61059308	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62467389	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6467574	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67243095	0.85[EUR][1000 genomes]
rs6955164	0.87[ASN][1000 genomes]
rs6959189	0.87[ASN][1000 genomes]
rs6973162	0.87[ASN][1000 genomes]
rs73384423	0.81[EUR][1000 genomes]
rs7786639	0.81[EUR][1000 genomes]
rs7790887	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs949733	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs953190	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs953191	0.81[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	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	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
3	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
4	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
5	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80745200-80762600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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