Variant report

Variant	rs6469748
Chromosome Location	chr8:90051083-90051084
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:39)

rs_ID	r²[population]
rs10087014	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11991355	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1240027	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1240044	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1240056	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1240057	0.87[EUR][1000 genomes]
rs1240063	0.86[EUR][1000 genomes]
rs1240070	0.86[EUR][1000 genomes]
rs1240072	0.86[EUR][1000 genomes]
rs1240080	0.86[EUR][1000 genomes]
rs1240081	0.86[EUR][1000 genomes]
rs1240138	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1240139	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1262791	0.86[EUR][1000 genomes]
rs13266220	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1586140	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1681451	0.86[EUR][1000 genomes]
rs16889783	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16890578	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1733895	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1733896	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1733918	0.84[EUR][1000 genomes]
rs1733950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1733951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1733960	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1922311	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923309	0.83[EUR][1000 genomes]
rs318327	0.83[EUR][1000 genomes]
rs34051706	1.00[ASN][1000 genomes]
rs384160	0.81[EUR][1000 genomes]
rs427521	0.86[EUR][1000 genomes]
rs4507810	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4961112	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62532180	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6981731	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6996186	0.94[EUR][1000 genomes]
rs7016298	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7841364	0.94[EUR][1000 genomes]
rs980020	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023176	chr8:89707267-90154549	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1015363	chr8:89707267-90158090	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1022619	chr8:89709240-90137813	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1032038	chr8:89735634-90068849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv1031054	chr8:89922522-90102748	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1016268	chr8:89927580-90104483	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv539670	chr8:89927580-90104483	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv891177	chr8:89941889-90166429	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv611718	chr8:90019419-90074757	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv982090	chr8:90023438-90094324	Enhancers Weak transcription ZNF genes & repeats Strong transcription	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	chr8:90049400-90053000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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