Variant report

Variant	rs35720798
Chromosome Location	chr4:142456431-142456432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs12152590	0.95[EUR][1000 genomes]
rs12505744	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12513220	0.95[EUR][1000 genomes]
rs13106515	0.95[EUR][1000 genomes]
rs13111616	0.89[EUR][1000 genomes]
rs13120181	0.81[EUR][1000 genomes]
rs13122574	0.89[EUR][1000 genomes]
rs13127492	0.94[EUR][1000 genomes]
rs13132563	0.81[EUR][1000 genomes]
rs13133830	0.95[EUR][1000 genomes]
rs13142400	0.87[EUR][1000 genomes]
rs13145587	0.89[EUR][1000 genomes]
rs17362224	0.95[EUR][1000 genomes]
rs1879684	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1949668	0.95[EUR][1000 genomes]
rs1949669	0.95[EUR][1000 genomes]
rs2049181	0.91[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2139992	0.95[EUR][1000 genomes]
rs34124780	0.95[EUR][1000 genomes]
rs34149126	0.91[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs34274316	0.95[EUR][1000 genomes]
rs34422514	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34579838	0.95[EUR][1000 genomes]
rs34865075	0.89[EUR][1000 genomes]
rs34899172	0.95[EUR][1000 genomes]
rs34962680	0.87[EUR][1000 genomes]
rs35308689	0.95[EUR][1000 genomes]
rs35372192	0.95[EUR][1000 genomes]
rs35969143	0.95[EUR][1000 genomes]
rs36043894	0.83[EUR][1000 genomes]
rs36124988	0.94[EUR][1000 genomes]
rs4519867	0.82[EUR][1000 genomes]
rs4956301	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4956302	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62325330	0.88[EUR][1000 genomes]
rs62326618	0.95[EUR][1000 genomes]
rs62326619	0.95[EUR][1000 genomes]
rs62327371	0.89[EUR][1000 genomes]
rs62327372	0.89[EUR][1000 genomes]
rs62327373	0.80[EUR][1000 genomes]
rs62327375	0.89[EUR][1000 genomes]
rs62327376	0.89[EUR][1000 genomes]
rs62327381	0.85[EUR][1000 genomes]
rs67407219	0.95[EUR][1000 genomes]
rs6812199	0.83[EUR][1000 genomes]
rs6837400	0.89[EUR][1000 genomes]
rs6837886	0.81[EUR][1000 genomes]
rs72728300	0.95[EUR][1000 genomes]
rs72730041	0.81[EUR][1000 genomes]
rs7692755	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880172	chr4:142355535-142565089	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830094	chr4:142411738-142567788	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv526989	chr4:142444108-142501053	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1018949	chr4:142451823-142732365	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:142447200-142461200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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